Metrics
Publication
596
Open Access
81
UN Sustainable Development Goals
Announcements & Documents
Thesis Documents
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Education
1996 - 1997
1996 - 1997Expertise In Medicine
Eskisehir Osmangazi University, Tıp Fakültesi, Tıbbi Genetik, Turkey
1990 - 1994
1990 - 1994Doctorate
Glasgow University, Tıp Fakültesi, Tıbbi Genetik, United Kingdom
1978 - 1985
1978 - 1985Undergraduate
Erciyes University, Tıp Fakültesi, Turkey
Foreign Languages
C1 Advanced
C1 AdvancedEnglish
Research Areas
Avesis Research Areas:
Medical Genetics, Biotechnology, Molecular Biology and Genetics
WoS Research Areas:
Molecular Biology & Genetics, Cell Biology, Genetics & Heredity
Scopus Research Areas:
Molecular Biology, Cell Biology, Genetics
Research Areas Based on Academic Activities
Avesis Research Areas
WoS Research Areas
Scopus Research Areas
Managerial Experience
1995 - Present
1995 - PresentHead of Department
Erciyes University, Tıp Fakültesi, Dahili Tıp Bil.
2002 - 2004
2002 - 2004Vice Dean
Erciyes University, Tıp Fakültesi
2002 - 2004
2002 - 2004Head of International Office
Erciyes Üniversitesi, Erciyes Üniversitesi Uluslararası Ofis
Non Academic Experience
2005 - Present
2005 - PresentYönetim Kurulu Başkanı
Non-profit Organisation, European Biotechnology Thematic Network Associaaiton, Yönetim Kurulu Başkanı, Yönetim Kurulu Başkanı
1996 - Present
1996 - PresentYönetim Kurulu Üyesi
Non-profit Organisation, European Society Of Human Genetics, Yönetim Kurulu Üyesi, Yönetim Kurulu Üyesi
2013 - 2018
2013 - 2018Avrupa İnsan Genetiği Derneği Kurul Üyesi
Board Member of European Society of Human Genetics, Avrupa İnsan Genetiği Derneği Kurul Üyesi
2010 - 2016
2010 - 2016Avrupa Öngörücü Önleyici ve bireysel tıp derneği kurul üyesi
European Predictive Preventive personalised medicine association, Avrupa Öngörücü Önleyici ve bireysel tıp derneği kurul üyesi
2009 - 2010
2009 - 2010Yönetim Kurulu Başkanı
Professional Association, Türkiye Tıbbi Genetik Derneği , Yönetim Kurulu Başkanı, Yönetim Kurulu Başkanı
2006 - 2010
2006 - 2010sorumlu öğretim üyesi
İtalya Perugia Üniversitesi, sorumlu öğretim üyesi
2002 - 2005
2002 - 2005Non-profit Organisation, Erciyes Üniversitesi Mezunları Derneği
Supervised Theses
2024
2024Expertise In Medicine
Revealing the sucrase-isomaltase gene variant profile in the turkish population from non-interventional testing data based on new generation sequencing and evaluation of symptoms in variant carriers
Dündar M. (Advisor)
K.USLU(Student)
2024
2024Expertise In Medicine
Examining the genotype of the ABO blood group system using next-generation sequencing method
Dündar M. (Advisor)
Ş.AKTAŞ(Student)
2024
2024Expertise In Medicine
Evaluation of the genetic etiology of early-onset epileptic encephalopathies using current clinical exome sequencing data
Dündar M. (Advisor)
M.YAKUBİ(Student)
2023
2023Postgraduate
Retrospective evaluation of molecular tests studied in adult akute myeloi̇d leukemia patients
Dündar M. (Advisor)
H.FİRDEVS(Student)
2023
2023Doctorate
Investigation of the molecular mechanisms of the role of mesenchymal stem cells of adipose origin used in the treatment of second-degree superficial burns in the inflammation process on burn bullet fluid
Dündar M. (Advisor)
B.SEYHAN(Student)
2023
2023Postgraduate
Comparison of results biochemical screening in fetal pathologies and new generation sequencing based non-invasive prenatal test
Dündar M. (Advisor)
V.MUSLUMOVA(Student)
2022
2022Doctorate
The investigation of therapeutic effect of mirna and targeted genes involved in multidrug resistance in triple negative breast cancer
Dündar M. (Advisor)
S.KENANOĞLU(Student)
2021
2021Expertise In Medicine
Investigation of variant frequency and genotype-phenotype correlation for COL4A3, COL4A4, and COL4A5 genes in patients with alport syndrome in Turkish population
Dündar M. (Advisor)
M.DEMİR(Student)
2021
2021Doctorate
Determination of the synergistic effect of sorafenib and deinoxanthine on the kidney in hepatocellular carcinoma modeled rats
Dündar M. (Advisor)
N.KARASU(Student)
2018
2018Postgraduate
Comparison of expression levels of period geneticsPER1, PER2 and PER3 at insomnia diagnosed individuals and night shift working health care personnel
Dündar M. (Advisor)
R.EMEKLİ(Student)
2018
2018Postgraduate
Investigation of methylenetetrahydrofolate reductaz (MTHFR) c677t and a1298c gen polymorphism in infertile male
Dündar M. (Advisor)
A.KOÇER(Student)
2018
2018Doctorate
The role of interleukin-6 gene in distinction of transudate exudate in pleural effusions
Dündar M. (Advisor)
M.GÜLCİHAN(Student)
2017
2017Postgraduate
The effect of CYP2C19 * 2 and CYP2C19 * 3 polymorphism on clopidogrel resistance in copd patients
Dündar M. (Advisor)
Z.FUNDA(Student)
2017
2017Postgraduate
Primary brain tumors BCL-2, MEG-3 and NRF2 investigation of gene expression profile
Dündar M. (Advisor)
A.ÇÖMERTMAN(Student)
2017
2017Postgraduate
Alzheimer Hastalığında PARP1 ve DNA Pol Beta mRNA ekspresyonlarının araştırılması
DÜNDAR M.
S.Kenanoğlu(Student)
2015
2015Expertise In Medicine
The investigation of role of apobec gene family on lung adenocarcinoma etiology
Dündar M. (Advisor)
M.ENSAR(Student)
2014
2014Postgraduate
Investigation of BAP1 and ANAPC7 genes expressions in patient with acute myeloid leukemia
Dündar M. (Advisor)
M.EREN(Student)
2014
2014Postgraduate
Identification of mutations with increased number of triplet repeats in the fmr1 gene in patients with fragile X syndrome
Dündar M. (Advisor)
Y.ADA(Student)
2014
2014Postgraduate
Frajil X sendromlu hastalarda FMR1 genindeki 3'lü tekrar artış sayı mutasyonlarının belirlenmesi
DÜNDAR M.
Y.Ada(Student)
2013
2013Expertise In Medicine
Investigation of VDR gene polymorphisms, VDR gene expression and VDR gene promoter methylation in children with autistic disorder
Dündar M. (Advisor)
B.BALTA(Student)
2013
2013Postgraduate
Screening of widespread mutations of phenylalanine hydroxylase gene
Dündar M. (Advisor)
Ş.ERDEM(Student)
2013
2013Postgraduate
Fenilalanin Hidroksilaz Geninde Görülen Yaygın Mutasyonların Taranması
DÜNDAR M.
Ş.Altunok(Student)
2012
2012Expertise In Medicine
A study of CDKL5 gene mutations in patients with persistent seizure, autistic disorder and seizure in addition to autistic disorder during infancy and early childhood
Dündar M. (Advisor)
M.ERDOĞAN(Student)
2012
2012Expertise In Medicine
The investigation of the genetic base of the familial nonsyndromic hearing loss in turkish population
Dündar M. (Advisor)
A.SUBAŞIOĞLU(Student)
2012
2012Expertise In Medicine
İnfant ve erken çocukluk döneminde dirençli nöbetleri ve/veya otistik bulguları olan çocuk hastalarda CDKL5 gen mutasyonunun araştırılması
DÜNDAR M.
M.Erdoğan(Student)
2011
2011Doctorate
Searching new gene with linkage analysis in large Turkish family indicating scoliosis, blindness and arachnodactyly
Dündar M. (Advisor)
S.ÖRENAY(Student)
2011
2011Expertise In Medicine
Türk Toplumunda Ailesel Non-Sendromik İşitme Kaybının Genetik Temelinin Araştırılması
DÜNDAR M.
A.UZAK(Student)
2009
2009Postgraduate
Aneuploidy detection in blastomeres of preembryos
Dündar M. (Advisor)
B.ÖZDEMİR(Student)
2009
2009Doctorate
Effects of seperate or simultaneous injection of two different genes (Enhanced green-fluorescence protein gene, human gamma interferon gene) on transgenic mice recovery
Dündar M.
K.ARSLAN(Student)
2007
2007Expertise In Medicine
Quantitative determination, by real-time reverse transcription polymerase chain reaction, of aromatase and 5 alpha reductase mrna, and polymorphisms in the aromatase and 5 alpha reductase genes in idiopathic hirsutism.
Dündar M. (Advisor)
A.OKAY(Student)
2007
2007Postgraduate
To diagnose the phenylalanine hydroxylase enzyme deficiency with the method of molecular gene analysis
Dündar M. (Advisor)
D.ALGAN(Student)
2006
2006Doctorate
Skolyoz, körlük ve araknodaktili gösteren geniş bir türk ailesinde bağlantı
DÜNDAR M.
S.Öranay(Student)
2006
2006Postgraduate
Fenilalalin hidroksilaz enzim eksikliğine moleküler gen analizleri metoduyla tanı konulması
DÜNDAR M.
D.Algan(Student)
2005
2005Postgraduate
Seeing freqency of most common mutation (656G2, I172N, V281L, Q318X, R356V) in congenital adrenal hiperplazia patients
Dündar M. (Advisor)
R.ERÖZ(Student)
2004
2004Postgraduate
Screening of the 3920 T>A (I 1370 K) point mutation on adenomatous polyposis coli (APC) in Turkish population
Dündar M. (Advisor)
H.KARACA(Student)
Articles
All (335)
SCI-E, SSCI, AHCI (181)
SCI-E, SSCI, AHCI, ESCI (274)
ESCI (93)
Scopus (217)
TRDizin (34)
Other Publications (25)
2026
20261. A novel de novo frameshift variant in ZMYM2 expands the neuropsychiatric spectrum of NECRC syndrome: a case report
MAMMADOVA N., HATİPOĞLU N., DÜNDAR M.
Molecular Biology Reports , vol.53, no.1, 2026 (SCI-Expanded, Scopus)
2026
20262. Integrated Biotechnological Strategies for Planetary Health and Ecosystem Restoration
Yildirim D. T., Baki Yildirim A., Martin D., Beccari T., Vicente O., Radecka I., et al.
EUROBIOTECH JOURNAL
, vol.10, no.2, pp.81-102, 2026 (ESCI, Scopus)
2026
20263. Defective RNA Polymerase III sensing of mitochondrial DNA in pulmonary epithelial cells impairs type I IFN immunity to SARS-CoV-2
Møhlenberg M., Jørgensen S. E., van der Sluis R. M., Zillinger T., Hinke D. M., Hollensen A. K., et al.
Proceedings of the National Academy of Sciences of the United States of America , vol.123, no.12, 2026 (SCI-Expanded, Scopus)
2026
20264. Germline Homozygous RAG1 Missense Variant Associated With Epstein-Barr Virus Negative Childhood Burkitt Lymphoma: A Case Report
Mammadova N., YILDIRIM A., GÖKÇE N., ÖZCAN A., KARAKÜKCÜ M., DÜNDAR M.
Journal of pediatric hematology/oncology , vol.48, no.2, 2026 (SCI-Expanded, Scopus)
2026
20265. A Rare Craniosynostosis Phenotype Associated With a Homozygous CYP26B1 Pathogenic Variant in the Absence of Extremity Synostosis
Caliskan B. O., DEMİR M., Oktem S., YILDIRIM S., CANPOLAT M., DÜNDAR M.
American Journal of Medical Genetics, Part A , vol.200, no.2, pp.490-495, 2026 (SCI-Expanded, Scopus)
2026
20266. Bietti crystalline dystrophy in Türkiye: A genetic crossroads between Asia and Europe
Tuncay F. Y., Kahraman N. S., Kayhan G., Çetinkaya Z., DÜNDAR M., Öner A.
Graefe's Archive for Clinical and Experimental Ophthalmology
, 2026 (SCI-Expanded, Scopus)
2026
20267. Genotype–Phenotype Correlations in Phenylketonuria and Hyperphenylalaninemia: A Single-Center Study
GÜNEŞ H., KARDAŞ F., Erdoğan M., Ada Y., ARSLAN S., Sarı Ü. A., et al.
Pediatrics International , vol.68, no.1, 2026 (SCI-Expanded, Scopus)
2026
20268. Assessment of biotinidase activity changes over time in biotinidase deficient patients
Gülbahçe A., Muderrisoglu A., GÜNEŞ H., Erdoğan M., DÜNDAR M., KARDAŞ F.
Frontiers in Pediatrics
, vol.14, 2026 (SCI-Expanded, Scopus)
2026
20269. First Report of a Novel Pathogenic Variant in the RREB1 Gene Associated With Obesity and Metabolic Syndrome
Mammadova N., Yıldırım A., Hatipoğlu N., Dündar M.
Clinical Genetics , vol.109, no.1, pp.130-135, 2026 (SCI-Expanded, Scopus)
2025
202510. A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosis
KİRAZ A., Erdogan M., Balta B., GÜMÜŞ H., Mutlu M. B., MAMMADOVA N., et al.
Neurogenetics , vol.26, no.1, 2025 (SCI-Expanded, Scopus)
2025
202511. COVID-19 related mucormycosis and hemophagocytic lymphohistiocytosis in a child with juvenile myelomonocytic leukemia
ASLAN K., AKKAN H. B., Özçelik F., KÖKOĞLU K., ÖZCAN A., ACIPAYAM C., et al.
Trends in Pediatrics , vol.6, pp.279-283, 2025 (Scopus, TRDizin)
2025
202512. Brain malformation, neurodevelopmental disorder and epilepsy in a case of two rare genetic diseases: overlapping phenotype
Karatas E., Gulec A., Korkmaz M., Karaman Z. F., Kiraz A., Per H., et al.
NEUROGENETICS , vol.26, no.1, 2025 (SCI-Expanded, Scopus)
2025
202513. Deleterious variants in the autophagy-related gene RB1CC1/FIP200 impair immunity to SARS-CoV-2
Hu L., van der Sluis R. M., Castelino K. B., Zhang B., Ronit A., Zillinger T., et al.
Nature Communications , vol.16, no.1, 2025 (SCI-Expanded, Scopus)
2025
202514. Rare X;13 translocation with NR0B1 duplication in partial gonadal dysgenesis: A novel karyotype in DSD cases
KİRAZ A., MAMMADOVA N., Balta B., DEMİRCİ E., DEMİRCİ D., KARADAĞ A., et al.
Molecular biology reports , vol.52, no.1, pp.986, 2025 (SCI-Expanded, Scopus)
2025
202515. Telomere length in sleep disorders
Eşel G., OLGUNER EKER Ö., AMRALIYEV A., ASDEMİR A., BİÇER E. Ö., Badur Mermer D., et al.
Experimental Gerontology , vol.209, 2025 (SCI-Expanded, Scopus)
2025
202516. Co-occurrence of homozygous ALMS1 variant, 17q11.2 mosaic and germline deletions, and VSX2 nonsense variant in a single family
Mammadova N., Yildirim A. B., Sevim D., BOZKURT YOZGATLI T., SEZERMAN O. U., DÜNDAR M.
MOLECULAR BIOLOGY REPORTS
, vol.52, no.1, 2025 (SCI-Expanded, Scopus)
2025
202517. Artificial Intelligence and Humanoid Robotics: Bioethical Implications of Replacing Human Agency in Healthcare and beyond
Feizyab S., Bonetti G., Medori M. C., Micheletti C., Luca I. D., Donato K., et al.
Eurobiotech Journal , vol.9, no.3, pp.238-246, 2025 (ESCI, Scopus)
2025
202518. Messaging malignancy: Tumour-derived exosomes at the nexus of immune escape, vascular remodelling and metastatic competence
Yildirim D. T., Baki Yildirim A., Salzet M., Bertelli M., Beccari T., Prakash S., et al.
EUROBIOTECH JOURNAL , vol.9, no.3, pp.216-237, 2025 (ESCI)
2025
202519. THE DEVELOPMENT OF A FUZZY LOGIC SYSTEM USING MATLAB FOR EARLY DETECTION OF HEREDITARY CANCER IN BRCA1/2 NEGATIVE CASES
Senturk N., Volkan G., Ali B. S., DOĞAN B., Aliyeva L., Sag O., et al.
Balkan Journal of Medical Genetics
, vol.28, no.1, 2025 (SCI-Expanded, Scopus)
2025
202520. Clinical and laboratory aspects of patients diagnosed with various inherited platelet disorders
GÖK V., ÖZCAN A., Mutlu F. T., YILMAZ E., KOÇAK GÖL D., Ozay M., et al.
RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS
, vol.9, no.4, 2025 (SCI-Expanded, Scopus)
2025
202521. Blended Phenotypes of Sexual Development Disorder and Coenzyme Q10 Deficiency, Together with a Sibling with Homozygous Variants in the AHI1 Gene
ATASAY R., YILMAZ L. N., Gulec A., CANPOLAT M., PER H., KARDAŞ F., et al.
MOLECULAR SYNDROMOLOGY
, vol.16, no.3, pp.271-277, 2025 (SCI-Expanded, Scopus)
2025
202522. Protective effect of deinoxanthin in sorafenib-induced nephrotoxicity in rats with the hepatocellular carcinoma model
Karasu N., Kuzucu M., Mat Ö., Gul M., Yay A., Dundar M.
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY , vol.398, no.5, pp.5969-5988, 2025 (SCI-Expanded, Scopus)
2025
202523. Familial hemophagocytic lymphohistiocytosis case in adult age
FİDAN K., ÇİLEK H. G., ÇELİK S., BAYDAR M., ÜNAL A., ÖZÇELİK F., et al.
Journal of Current Hematology & Oncology Research , vol.3, no.2, pp.42-45, 2025 (Peer-Reviewed Journal)
2025
202524. A Novel Mutation in the Androgen Receptor Gene of Female Patients with 46,XY Karyotype
USLU İ. N., GÖKÇE N., AKSOY G., İNANDIKLIOĞLU N., Yuksel B., DÜNDAR M., et al.
Current Issues in Molecular Biology , vol.47, no.5, 2025 (SCI-Expanded, Scopus)
2025
202525. ClioMD: An artificial intelligence model for ciliopathies
Ergören M. Ç., Senturk N., Ali M. S. B., Özcelik I. Ö., Erol K. D., TEMEL Ş. G., et al.
Eurobiotech Journal
, vol.9, no.2, pp.128-137, 2025 (ESCI, Scopus)
2025
202526. A Case Series of Three Patients with Cleidocranial Dysplasia: Clinical Presentation and Diagnostic Considerations
Berber U., Gül Şiraz Ü., Yakubi M., Gök E., Kara L., Kiraz A., et al.
CLEFT PALATE CRANIOFACIAL JOURNAL
, vol.62, no.4, pp.715-719, 2025 (SCI-Expanded, Scopus)
2025
202527. GENE EXPRESSIONS ASSOCIATED WİTH NEUROTRANSMITTER METABOLISM IN CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER
Akalın H., Erdem Y., EROZ R., Şahin İ. O., Gokce N., ÖZMEN s., et al.
MEANDROS MEDICAL AND DENTAL JOURNAL
, vol.26, no.1, pp.19-32, 2025 (ESCI, TRDizin)
2025
202528. A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity
Al Qureshah F., Le Pen J., de Weerd N. A., Moncada-Velez M., Materna M., Lin D., et al.
Journal of Experimental Medicine , vol.222, no.2, 2025 (SCI-Expanded, Scopus)
2025
202529. Oxytocin receptor gene single nucleotide polymorphisms in patients with bipolar disorder
Ünal Demir F., Turan T., AKALIN H., DEMİREL-ÖZSOY S., DÜNDAR M.
International Journal of Psychiatry in Clinical Practice , vol.29, no.1, pp.18-24, 2025 (SCI-Expanded, Scopus)
2024
202430. Recurrent symptomatic urolithiasis in a patient with cystic fibrosis
Yel S., Dursun İ., Köse M., Kiraz A., Poyrazoğlu M. H., Duendar M.
PEDIATRIC NEPHROLOGY
, vol.39, no.12, pp.3467-3469, 2024 (SCI-Expanded, Scopus)
2024
202431. Mesenchymal stem cells from adipose tissue prone to lose their stemness associated markers in obesity related stress conditions
Al-Sammarraie S. H. A., Ayaz-Güner Ş., Acar M. B., Şimşek A., Sınıksaran B. S., Bozalan H. D., et al.
Scientific Reports , vol.14, no.1, 2024 (SCI-Expanded, Scopus)
2024
202432. Insights into multidrug resistance mechanisms: Exploring distinct miRNAs as prospective therapeutic agents in triple negative breast cancer
Kenanoglu S., AKALIN H., ASLAN D., İNANÇ M., ÖZTÜRK F., DÜNDAR M.
Gene Reports , vol.37, 2024 (ESCI, Scopus)
2024
202433. Frequency of Genetic Mutations in Patients With Chronic Lymphocytic Leukemia and Their Effects on Survival
GÖLBAŞI M., ÜNAL A., ÖZKUL Y., DÜNDAR M., Sanli N. M., AKYOL G., et al.
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA , 2024 (SCI-Expanded, Scopus)
2024
202434. Beyond the phenotype: Exploring inherited retinal diseases with targeted next-generation sequencing in a Turkish cohort
ÖZGÜÇ ÇALIŞKAN B., USLU K., Kahraman N. S., ERKILIÇ K., Oner A., DÜNDAR M.
CLINICAL GENETICS , vol.106, no.3, pp.258-266, 2024 (SCI-Expanded, Scopus)
2024
202435. L1 Syndrome-Associated Phenotypes and a Novel L1CAM Variant: A Clinical Report
Paskal Ş., Yavuz F., Per H., Kucuk A., Dundar M.
Journal of Pediatric Neurology , vol.22, no.04, pp.307-310, 2024 (ESCI, Scopus)
2024
202436. The impact and future of artificial intelligence in medical genetics and molecular medicine: an ongoing revolution
Özçelik F., Dundar M., Yıldırım A., Henehan G., Vicente O., Sanchez-Alcazar J. A., et al.
FUNCTIONAL & INTEGRATIVE GENOMICS , vol.24, no.4, 2024 (SCI-Expanded, Scopus)
2024
202437. Molecular analysis of SMN2, NAIP, and GTF2H2 gene deletions and relationships with clinical subtypes of spinal muscular atrophy
Karasu N., Acer H., Akalin H., Turkgenc B., Demir M., Sahin I. O., et al.
JOURNAL OF NEUROGENETICS
, vol.38, no.3, pp.102-111, 2024 (SCI-Expanded, Scopus)
2024
202438. Promoting International Scientific Cooperation: the Role of Scientific Societies
Vrablova M., Bonetti G., Henehan G., Brown R. E., Sykora P., Marks R. S., et al.
EUROBIOTECH JOURNAL
, vol.8, no.3, pp.115-121, 2024 (ESCI, Scopus)
2024
202439. The role of interleukin-6 gene in distinction of transudate-exudate in pleural effusions
Önal M. G., Akalın H., Akkuş A., Önal Ö., Dündar M.
CUKUROVA MEDICAL JOURNAL , vol.49, no.2, pp.391-399, 2024 (ESCI, TRDizin)
2024
202440. Deciphering the host genetic factors conferring susceptibility to severe COVID-19 using exome sequencing
Uslu K., Ozcelik F., Zararsiz G., Eldem V., Cephe A., Sahin I. O., et al.
GENES AND IMMUNITY
, vol.25, no.1, pp.14-42, 2024 (SCI-Expanded, Scopus)
2024
202441. Evaluation of chromosomal abnormalities in the postnatal cohort: A single-center study on 14,242 patients
Sahin I. O., Akalin H., Paskal Ş., Tan B., Yalcinkaya E., Demir M., et al.
JOURNAL OF CLINICAL LABORATORY ANALYSIS
, vol.38, no.1-2, 2024 (SCI-Expanded, Scopus)
2024
202442. Artificial cells: A potentially groundbreaking field of research and therapy
Dundar M. S., Yildirim A., Yildirim D. T., AKALIN H., DÜNDAR M.
EUROBIOTECH JOURNAL
, vol.8, no.1, pp.55-64, 2024 (ESCI)
2024
202443. ABCA4 variant screening in a Turkish cohort with Stargardt disease
KAHRAMAN N. S., Ozguc caliskan B., Kandemir N., Oner A., DÜNDAR M., ÖZKUL Y.
OPHTHALMIC GENETICS , vol.45, no.2, pp.133-139, 2024 (SCI-Expanded, Scopus)
2024
202444. A case of autoimmune lymphoproliferative syndrome with a novel de novo FAS variant
Özçelik F., Aslan K., Gök V., Ari M. B., Özcan A., Eken A., et al.
Pediatric Hematology and Oncology , vol.41, no.4, pp.301-309, 2024 (SCI-Expanded, Scopus)
2024
202445. A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort
Şahin İ. O., KARATAŞ E., DEMİR M., TAN B., PER H., ÖZKUL Y., et al.
Turkish Journal of Medical Sciences
, vol.54, no.1, pp.86-98, 2024 (SCI-Expanded, Scopus, TRDizin)
2023
202346. Achievement of sustainable development goals through the Mediterranean diet
Medori M. C., Donato K., Stuppia L., Beccari T., DÜNDAR M., Marks R. S., et al.
EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES
, vol.27, pp.89-99, 2023 (SCI-Expanded, Scopus)
2023
202347. Unleashing the potential of biotechnology for sustainable development
Donato K., Medori M. C., Stuppia L., Beccari T., DÜNDAR M., Marks R. S., et al.
EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES
, vol.27, pp.100-113, 2023 (SCI-Expanded, Scopus)
2023
202348. Unexpectedly high mutation rate of cyp11b1 compared to cyp21a2 in randomly-selected turkish women: a large screening study
POLAT S., KARABURGU S., ÜNLÜHİZARCI K., DÜNDAR M., ÖZKUL Y., ARSLAN Y. K., et al.
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.46, no.11, pp.2367-2377, 2023 (SCI-Expanded, Scopus)
2023
202349. Impacts of Biotechnologically Developed Microorganisms on Ecosystems
Celebi D., Akalın H., Yılmaz M. T., Dündar M.
Eurobiotech Journal
, vol.7, no.4, pp.196-205, 2023 (ESCI, Scopus)
2023
202350. Current Advances in Breast Cancer: Implications for Developing New Treatment Strategies Through Epi-Drugs on the Road to Modifying the Epigenome
Kenanoglu S., Yuksel E. B., DÜNDAR M.
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2023
202351. A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey
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European Journal of Breast Health
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202352. PPM1K defects cause mild maple syrup urine disease: The second case in the literature
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2023
202353. A Case of Short Stature Caused by a Mutation in the ACAN Gene
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202354. A New Case of Translocation T(2;7)(p23;q35) in Recurrent Pregnancy Loss
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2023
202355. Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.
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2023
202356. Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case of GLIS3 Mutation
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JCRPE Journal of Clinical Research in Pediatric Endocrinology
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202357. Case Report: A Novel Mutation Leading to 11-β Hydroxylase Deficiency in a Female Patient
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ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS
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2022
202258. Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS-CoV-2 from 946 whole-exome sequencing data in the Turkish population
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202259. Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations
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202260. Investigation of Relation Between MDR1 Gene and Ankylosing Spondylitis: Case Control Research MDR1 Geni ile Ankilozan Spondilit Arasındaki İlişkinin İncelenmesi: Olgu Kontrol Araştırması
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Turkiye Klinikleri Journal of Medical Sciences
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2022
202261. CDH5, a Possible New Candidate Gene for Genetic Testing of Lymphedema
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LYMPHATIC RESEARCH AND BIOLOGY , vol.20, pp.496-506, 2022 (SCI-Expanded, Scopus)
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202262. Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey
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202263. Biomarker potential of the GRP78 cell-free RNA in endometrial cancer
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EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS
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2022
202264. Frequency of RPE65 Gene Mutation in Patients with Hereditary Retinal Dystrophy
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TURK OFTALMOLOJI DERGISI-TURKISH JOURNAL OF OPHTHALMOLOGY
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2022
202265. Ethical considerations regarding animal experimentation
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2022
202266. A novel missense mutation outside the DNAJ domain of DNAJC21 is associated with Shwachman-Diamond syndrome
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BRITISH JOURNAL OF HAEMATOLOGY , vol.197, no.6, 2022 (SCI-Expanded, Scopus)
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202267. A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A
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202268. Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
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FUNCTIONAL & INTEGRATIVE GENOMICS
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202269. An overview of the genetic aspects of hair loss and its connection with nutrition
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Journal of preventive medicine and hygiene
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202270. Methodology for clinical research
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202271. Implication of the Mediterranean diet on the human epigenome
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202272. Evaluation of Utilizing the Distinct Genes as Predictive Biomarkers in Late-Onset Alzheimer's Disease
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GLOBAL MEDICAL GENETICS
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202273. Periconceptional Mediterranean diet during pregnancy on children's health
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2022
202274. Diagnosing Alström syndrome in a patient followed up with syndromic obesity for years
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Intractable & Rare Diseases Research
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2022
202275. A teenager boy with a novel variant of Sitosterolemia presented with pancytopenia.
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Clinica chimica acta; international journal of clinical chemistry , vol.529, pp.61-66, 2022 (SCI-Expanded, Scopus)
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202276. MTA FİLLAPEX'İN İN VİTRO GENOTOKSİSİTESİNİN DEĞERLENDİRİLMESİ: SİSTEMATİK İNCELEMESİ
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Türkiye Klinikleri Diş Hekimliği Bilimleri Dergisi , vol.28, pp.372-380, 2022 (TRDizin)
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202277. Reclassification of Hereditary Cancer Genes Variants
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TURK ONKOLOJI DERGISI-TURKISH JOURNAL OF ONCOLOGY
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2021
202178. The effect of cytokine leukemia-inhibitory factor (LIF) and interleukin-11 (IL-11) gene expression on the primary infertility related to polycystic ovary syndrome, Tubal factor, and Unexplained infertility in Turkish women
Alzaidi Z., Menziletoğlu Yıldız Ş. S., Saatçi Ç., Akalin H. U., Müderris İ. İ., Aynekin B., et al.
EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS
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202179. COVID-19 vaccine candidates and vaccine development platforms available worldwide
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JOURNAL OF PHARMACEUTICAL ANALYSIS
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202180. BRCA Variations Risk Assessment in Breast Cancers Using Different Artificial Intelligence Models
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GENES
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202181. A NOVEL MUTATION IN DIACYLGLYCEROL KINASE EPSILON GENE CAUSING STEROID RESISTANT NEPHROTIC SYNDROME
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202182. Propranolol significantly reduced DNA polymerase expression in patients with essential tremor
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202183. Detection of mutations in CML patients resistant to tyrosine kinase inhibitor: imatinib mesylate therapy
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MEDICAL ONCOLOGY
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202184. Propranolol significantly reduced DNA polymerase beta expression in patients with essential tremor
Kandemir N., Kenanoglu S., GÜLTEKİN M., GÖKÇE N., Akalin H., Tascioglu N., et al.
UNIVERSA MEDICINA
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202185. Current and future therapeutic strategies for limb girdle muscular dystrophy type r1: Clinical and experimental approaches
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Pathophysiology
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2021
202186. The Story of a Ship Journey, Malaria, and the HBB Gene IVS-II-745 Mutation: Circassian Immigration to Cyprus
Ergoren M. C., TEMEL Ş. G., Mocan G., DÜNDAR M.
GLOBAL MEDICAL GENETICS
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2021
202187. Possible Role of theRORCGene in Primary and Secondary Lymphedema: Review of the Literature and Genetic Study of Two Rare Causative Variants
Michelini S., Ricci M., Serrani R., Stuppia L., Beccari T., Veselenyiova D., et al.
LYMPHATIC RESEARCH AND BIOLOGY , vol.19, pp.129-133, 2021 (SCI-Expanded, Scopus)
2021
202188. The Age Structure, Stringency Policy, Income, and Spread of Coronavirus Disease 2019: Evidence From 209 Countries
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FRONTIERS IN PSYCHOLOGY
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202189. Editorial
DÜNDAR M., Marova I., Vicente O.
BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT , vol.35, 2021 (SCI-Expanded, Scopus)
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202190. ROMANIAN RED BIOTECHNOLOGY - BLENDING TRADITION WITH STATE OF THE ART IN THE EUROPEAN AND INTERNATIONAL FRAMEWORK
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SCIENTIFIC PAPERS-SERIES D-ANIMAL SCIENCE
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202191. Naturally-occurring and cultured bacteriophages in human therapy
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EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES , vol.25, pp.101-107, 2021 (SCI-Expanded, Scopus)
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202192. A brief overview of global biotechnology
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BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT
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202193. In vitro and clinical studies on the efficacy of alpha-cyclodextrin and hydroxytyrosol against SARS-CoV-2 infection
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EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES
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202194. Are new genome variants detected in SARS-CoV-2 expected considering population dynamics in viruses?
Ergoren M. C., Tulay P., DÜNDAR M.
EUROBIOTECH JOURNAL
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202195. COVID-19 vaccines: Where do we stand?
Tulay P., Ergoren M. C., DÜNDAR M.
EUROBIOTECH JOURNAL
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2021
202196. Investigation of cytochrome p450 CYP1A2, CYP2D6, CYP2E1 and CYP3A4 gene expressions and polymorphisms in alcohol with-drawal
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KLINIK PSIKIYATRI DERGISI-TURKISH JOURNAL OF CLINICAL PSYCHIATRY , vol.24, no.3, pp.298-306, 2021 (ESCI, Scopus, TRDizin)
2021
202197. NOTCH1: Review of its role in lymphatic development and study of seven families with rare pathogenic variants
Michelini S., Ricci M., Serrani R., Barati S., Kenanoglu S., Veselenyiova D., et al.
MOLECULAR GENETICS & GENOMIC MEDICINE , vol.9, no.1, 2021 (SCI-Expanded, Scopus)
2020
202098. A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Answers
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PEDIATRIC NEPHROLOGY
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202099. Identification of unsolved rare genetic cases of North Cyprus
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EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, pp.944, 2020 (SCI-Expanded, Scopus)
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2020100. Enhancer of zeste homolog 2 (EZH2) gene inhibition via 3-Deazaneplanocin A (DZNep) in human liver cells and it is relation with fibrosis
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TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI , vol.45, no.6, pp.737-745, 2020 (SCI-Expanded, Scopus, TRDizin)
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2020101. A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Questions
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2020102. Reflections on Emerging Technologies in Nanomedicine
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Erciyes Medical Journal , vol.42, pp.370-379, 2020 (ESCI, TRDizin)
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2020103. Segregation Analysis of Rare NRP1 and NRP2 Variants in Families with Lymphedema
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GENES , vol.11, no.11, 2020 (SCI-Expanded, Scopus)
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2020104. Two rare PROX1 variants in patients with lymphedema
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MOLECULAR GENETICS & GENOMIC MEDICINE , vol.8, no.10, 2020 (SCI-Expanded, Scopus)
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2020105. Comparing expression levels of PERIOD genes PER1, PER2 and PER3 in chronic insomnia patients and medical staff working in the night shift
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SLEEP MEDICINE , vol.73, pp.101-105, 2020 (SCI-Expanded, Scopus)
2020
2020106. The role of androgen receptor CAG repeat polymorphism in androgen excess disorder and idiopathic hirsutism
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JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
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2020107. RARE PECAM1 VARIANTS IN THREE FAMILIES WITH LYMPHEDEMA
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LYMPHOLOGY , vol.53, no.3, pp.141-151, 2020 (SCI-Expanded, Scopus)
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2020108. TIE1as a Candidate Gene for Lymphatic Malformations with or without Lymphedema
Michelini S., Ricci M., Veselenyiova D., Kenanoglu S., Kurti D., Baglivo M., et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , vol.21, no.18, 2020 (SCI-Expanded, Scopus)
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2020109. Mutations in the ARAP3 Gene in Three Families with Primary Lymphedema Negative for Mutations in Known Lymphedema-Associated Genes
Ricci M., Compagna R., Amato B., Kenanoglu S., Veselenyiova D., Kurti D., et al.
INTERNATIONAL JOURNAL OF GENOMICS , vol.2020, 2020 (SCI-Expanded, Scopus)
2020
2020110. THE EFFECTS OF O-6-METHYL GUANINE DNA-METHYL TRANSFERASE PROMOTOR METHYLATION AND CpG1, CpG2, CpG3 AND CpG4 METHYLATION ON TREATMENT RESPONSE AND THEIR PROGNOSTIC SIGNIFICANCE IN PATIENTS WITH GLIOBLASTOMA
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BALKAN JOURNAL OF MEDICAL GENETICS , vol.23, no.1, pp.33-41, 2020 (SCI-Expanded, Scopus)
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2020111. REVIEW OF THE FUNCTION OF SEMA3A IN LYMPHATIC VESSEL MATURATION AND ITS POTENTIAL AS A CANDIDATE GENE FOR LYMPHEDEMA: ANALYSIS OF THREE FAMILIES WITH RARE CAUSATIVE VARIANTS
Ricci M., Daolio C., Amato B., Kenanoglu S., Veselenyiova D., Kurti D., et al.
LYMPHOLOGY , vol.53, no.2, pp.63-75, 2020 (SCI-Expanded, Scopus)
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2020112. Meeting Reports: Notes and commentaries on Turkish Medical Genetics Association and Cyprus Turkish Genetic Union Meeting
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GAZI MEDICAL JOURNAL , vol.31, no.3, pp.2-5, 2020 (ESCI, Scopus)
2020
2020113. Propranolol decreases DRD3 and SLC1A2 gene expression in patients with essential tremor
KANDEMİR N., GÜLTEKİN M., Kara M., Bayram A., TAŞÇIOĞLU N., MİRZA M., et al.
UNIVERSA MEDICINA , vol.39, no.2, pp.105-112, 2020 (ESCI)
2020
2020114. CYP26B1 AND ITS IMPLICATIONS IN LYMPHANGIOGENESIS: LITERATURE REVIEW AND STUDY OF RARE VARIANTS IN TWO FAMILIES
Ricci M., Serrani R., Amato B., Compagna R., Veselenyiova D., Kenanoglu S., et al.
LYMPHOLOGY , vol.53, no.1, pp.20-28, 2020 (SCI-Expanded, Scopus)
2020
2020115. Bacteriophages presence in nature and their role in the natural selection of bacterial populations
Naureen Z., Dautaj A., Anpilogov K., Camilleri G., Dhuli K., Tanzi B., et al.
Acta Biomedica , vol.91, pp.1-13, 2020 (Scopus)
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2020116. Genetic testing for autonomic dysfunction or dysautonomias
Maltese P. E., Manara E., Beccari T., DÜNDAR M., Capodicasa N., Bertelli M.
Acta Biomedica , vol.91, pp.1-5, 2020 (Scopus)
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2020117. Pilot study for the evaluation of safety profile of a potential inhibitor of SARS-CoV-2 endocytosis
Paolacci S., Ceccarini M. R., Codini M., Manara E., Tezzele S., Percio M., et al.
Acta Biomedica
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2020118. Bacteriophages in food supplements obtained from natural sources
Kiani A. K., Anpilogov K., Dautaj A., Marceddu G., Sonna W. N., Percio M., et al.
Acta Biomedica , vol.91, pp.1-6, 2020 (Scopus)
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2020119. Comparison between American and European legislation in the therapeutical and alimentary bacteriophage usage
Naureen Z., Malacarne D., Anpilogov K., Dautaj A., Camilleri G., Cecchin S., et al.
Acta Biomedica , vol.91, pp.1-7, 2020 (Scopus)
2020
2020120. Natural compounds as inhibitors of SARS-CoV-2 endocytosis: A promising approach against COVID-19
Kiani A. K., Dhuli K., Anpilogov K., Bressan S., Dautaj A., DÜNDAR M., et al.
Acta Biomedica
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2020121. Ethics committees for clinical experimentation at international level with a focus on Italy
Naureen Z., Beccari T., Marks R. S., Brown R., Lorusso L., Pheby D., et al.
Acta Biomedica
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2020122. A pilot study on the preventative potential of alpha-cyclodextrin and hydroxytyrosol against SARS-CoV-2 transmission
Ergoren M. C., Paolacci S., Manara E., Dautaj A., Dhuli K., Anpilogov K., et al.
Acta Biomedica
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2019
2019123. ANADOLU’DAKİ TIBBIN DOĞUŞU, DÜNYADAKİ İLK TIP OKULU OLARAK GEVHER NESİBE TIP MEDRESESİ VE DARÜŞŞİFASI
DÜNDAR M., EMEKLİ R., ŞENER E. F.
Bilimname , vol.3, pp.79-103, 2019 (TRDizin)
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2019124. A Potential Method to Help Predict Genetic Diseases and Arrange Healthcare: Copy Number Variation Analysis
DÜNDAR M., Arslan S. B.
ERCIYES MEDICAL JOURNAL , vol.41, no.4, pp.355-356, 2019 (ESCI, TRDizin)
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2019125. Diagnostic and therapeutic implements based on advanced biotechnology should be available in low-income countries
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Acta Biomedica , vol.90, pp.5-6, 2019 (Scopus)
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2019126. Comprehensive genotyping of Turkish women with hirsutism.
Polat S., Karaburgu S., Ünlühizarcı K., Dündar M., Özkul Y., Arslan Y., et al.
Journal of endocrinological investigation
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2019129. Genetic background, nutrition and obesity: a review
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2019130. The association of endothelin-1 levels with renal survival in polycystic kidney disease patients
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2019131. Current state and prospects of biotechnology in Central and Eastern European countries. Part I: Visegrad countries (CZ, H, PL, SK)
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2019132. Current state and prospects of biotechnology in Central and Eastern European countries. Part II: new and preaccession EU countries(CRO, RO, B&H, SRB)
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2019133. Anadolu’daki Tıbbın Doğuşu, Dünyadaki İlk Tıp Okulu Olarak: Gevher Nesibe Tıp Medresesi ve Darüşşifası
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2018134. Quality assurance of genetic laboratories and the EBTNA practice certification, a simple standardization assurance system for a laboratory network
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2018135. Genetic testing for bicuspid aortic valve
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2018136. Genetic testing for Marfan syndrome
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2018137. Genetic testing for tetralogy of Fallot
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2018138. Genetic testing for vascular Ehlers-Danlos syndrome and other variants with fragility of the middle arteries
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2018139. Genetic testing for aortic valve stenosis
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2018140. Genetic testing for ventricular septal defect
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2018141. Genetic testing for atrial septal defect
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2018142. Genetic testing for Marfan-like disorders
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2018143. The frequencies of Y chromosome microdeletions in infertile males
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2018144. Genetic testing for cerebral cavernous malformations
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2018145. Genetic testing for atrioventricular septal defect
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2018146. Genetic testing for Ebstein anomaly
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2018147. Genetic testing for coarctation of aorta
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2018148. Genetic testing for pulmonary stenosis
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2018149. Genetic testing for hereditary hemorrhagic telangiectasia
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2018150. Increased vitamin D receptor gene expression and rs11568820 and rs4516035 promoter polymorphisms in autistic disorder
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2018151. 47,XXX, 48,XXXX, 49,XXXXX: DIFFERENCES ANDSIMILARITIES
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2018152. A CASE OF SEVERE HYPOCHROMIC ANEMIA: TRISOMY 10p
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2018153. THE INVESTIGATION OF PARP1 AND DNA POL β mRNAEXPRESSIONS ON ALZHEIMER’S DISEASE
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2018154. Editorial Prof. Mariapia Viola-Magni – An Appreciation
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2018155. Scoliosis, blindness and arachnodactyly in a large Turkish family: Is it a new syndrome?
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2017156. Evaluation of aortic intima-media thickness in newborns with Down syndrome
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2017157. Genetic testing for Leber congenital amaurosis
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2017158. Pharmacologically active fractions of Sideritis spp. and their use in inherited eye diseases
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2017159. Genetic testing for central areolar choroidal dystrophy
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2017160. Genetic testing for Sorsby's fundus dystrophy
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2017161. Genetic testing for retinitis punctata albescens/fundus albipunctatus
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2017162. Genetic testing for congenital stationary night blindness
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2017163. Genetic testing for optic atrophy
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2017164. Genetic testing for cone rod dystrophies
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2017165. Genetic testing for ocular albinism and oculocutaneous albinism
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2017166. Erratum: Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, Turkey.
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2017167. Genetic testing for Usher syndrome
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2017168. Genetic testing for gyrate atrophy of the choroid and retina
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2017169. Genetic testing for enhanced S-cone syndrome
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2017170. Genetic testing for Refsum disease
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2017171. Genetic testing for achromatopsia
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EUROBIOTECH JOURNAL , vol.1, pp.11-13, 2017 (ESCI)
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2017172. Genetic testing for Bietti crystalline dystrophy
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2017173. Genetic testing for infantile nystagmus
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2017174. Genetic testing for familial exudative vitreoretinopathy
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2017175. Genetic testing in translational ophthalmology
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EUROBIOTECH JOURNAL
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2017176. Genetic testing for non syndromic retinitis pigmentosa
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2017177. Genetic testing for Norrie disease
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2017178. Genetic testing for Doyne honeycomb retinal dystrophy
Abeshi A., Coppola P., Beccari T., DÜNDAR M., Ziccardi L., Bertelli M.
EUROBIOTECH JOURNAL , vol.1, pp.45-47, 2017 (ESCI)
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2017179. Genetic testing for Mendelian glaucoma
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2017180. Genetic testing for inherited eye misalignment
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2017181. Genetic testing for Bardet-Biedl syndrome
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EUROBIOTECH JOURNAL , vol.1, pp.14-16, 2017 (ESCI)
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2017182. Genetic testing for Mendelian myopia
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2017183. Genetic testing for ocular coloboma
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EUROBIOTECH JOURNAL , vol.1, pp.29-31, 2017 (ESCI)
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2017184. Genetic testing for corneal dystrophies and other corneal Mendelian diseases
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2017185. Genetic testing for X-linked juvenile retinoschisis
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EUROBIOTECH JOURNAL , vol.1, pp.111-113, 2017 (ESCI)
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2017186. Genetic testing for Mendelian cataract
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2017187. Genetic testing for Stargardt macular dystrophy
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2017188. Genetic testing for pattern dystrophies
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2017189. Genetic testing for choroideremia
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2017190. Genetic testing for Senior-Loken syndrome
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2017191. Genetic testing for color vision deficiency
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2017192. Genetic testing for Best vitelliform macular dystrophy
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2017193. NF1 gene variant allele frequencies comparison of Turkish population with databases
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2017194. Prenatal diagnosis of upper extremity malformations with ultrasonography: Diagnostic features and perinatal outcome.
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2017195. The effect of parental 5,10-methylenetetrahydrofolate reductase 677C/T and 1298A/C gene polymorphisms on response to single-dose methotrexate in tubal ectopic pregnancy
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2017196. Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, Turkey
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2017197. Geneticexpressions of thrombophilicfactors in patientswithSheehan ssyndrome GynecolEndocrinol
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2017198. Advances in biotechnology: Genomics and genome editing
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2017199. Genetic tests for low-and middle-income countries: a literature review
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2016201. The Association of Brain-Derived Neurotrophic Factor Gene Polymorphism with Obstructive Sleep Apnea Syndrome and Obesity
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2016205. Clinical Characteristics of Cases with Spinal Muscular Atrophy
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2016207. A Nonvirilized form of Classic 3 beta-Hydroxysteroid Dehydrogenase Deficiency Due to a Homozygous S218P Mutation in the HSD3B2 Gene in a Girl with Classic Phenylketonuria
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2015208. Triplet Pregnancy with Partial Hydatidiform Mole Coexisting with Two Fetuses after Ovulation Induction and Intrauterine Insemination
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2015209. FRAJİL X SENDROMU ÖN TANILI HASTALARDA FMR1 GENİNDEKİ 3'LÜ TEKRAR SAYI MUTASYONLARIN BELİRLENMESİ
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2015210. Expression of ghrelin and GHS-R1a in long term diabetic rat's kidney
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2015212. Is idiopathic hirsutism (IH) really idiopathic? mRNA expressions of skin steroidogenic enzymes in women with IH
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2015213. The effects of NOS3-786 T/C polymorphism and HBB-551 C/T polymorphism and the expression levels of these genes on alpine skiing performance
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2015215. THE EXPRESSION LEVEL OF BRMS1 IN COLON CANCER PATIENTS AND ITS CLINICAL SIGNIFICANCE
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2015216. The Effects of Long-Term Diabetes on Ghrelin Expression in Rat Stomachs
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2015
2015218. Genotoxic Effects of some Antituberculosis Drugs and Mixtures in Rats
ARSLAN K., KANBUR M., KARABACAK M., Sarıca Z., TAŞÇıOĞLU N., İŞCAN K. M., et al.
DRUG RESEARCH , vol.65, no.4, pp.219-222, 2015 (ESCI, Scopus)
2015
2015219. Genetic background of supernumerary teeth.
SUBASIOGLU A., SAVAS S., KUCUKYILMAZ E., KESIM S., YAGCI A., Dundar M.
European journal of dentistry , vol.9, pp.153-8, 2015 (Scopus)
2015
2015220. The effects of streptozotocin-induced diabetes on ghrelin expression in rat testis: biochemical and immunohistochemical study
Sonmez M. F., Karabulut D., Kılıç E., Akalın H., Sakalar C., Gunduz Y., et al.
FOLIA HISTOCHEMICA ET CYTOBIOLOGICA
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2015221. A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia
Mastushita M., Kitoh H., Subasioglu A., Colak F. K., Dundar M., Mishima K., et al.
MOLECULAR SYNDROMOLOGY
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2014
2014222. Effects of ACE expression and I/D polymorphism on alpine skiing performance
POLAT M., ÇOKSEVİM B., TAHERİ S., DÜNDAR M.
Gazzetta Medica Italiana , vol.173, no.12, pp.593-600, 2014 (Peer-Reviewed Journal)
2014
2014223. Circulating microRNAs in patients with non-alcoholic fatty liver disease.
Çelikbilek M., BAŞKOL M., TAHERİ S., ZARARSIZ G., GÜRSOY Ş., ÖZBAKIR Ö., et al.
World J Hepatol , vol.27, no.6, pp.613-620, 2014 (SCI-Expanded)
2014
2014224. A c.1244G>A (p.Arg415Gln) mutation in SH3BP2 gene causes cherubism in a Turkish family: Report of a family with review of the literature
SEKERCI A., Balta B., DÜNDAR M., Hu Y., Reichenberger E., ETOZ O., et al.
MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL
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2014
2014225. ACE EXPRESION I/D POLYMORPHISM IN ALPINE SKIING
POLAT M., Çoksevim B., TAHERİ S., DÜNDAR M.
Gazzetta Medica Italiana-Archivio Per Le Scienze Mediche , vol.173, no.12, pp.593-600, 2014 (Scopus)
2014
2014226. Is there relation between COL4A1/A2 mutations and antenatally detected fetal intraventricular hemorrhage?
Kutuk M. S., Balta B., Kodera H., Matsumoto N., Saitsu H., Doganay S., et al.
CHILDS NERVOUS SYSTEM , vol.30, no.3, pp.419-424, 2014 (SCI-Expanded, Scopus)
2014
2014227. Etiopathogenesis of Sheehan's Syndrome: Roles of Coagulation Factors and TNF-Alpha
Diri H., ŞENER E. F., BAYRAM F., Tascioglu N., Simsek Y., DÜNDAR M.
INTERNATIONAL JOURNAL OF ENDOCRINOLOGY
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2014
2014228. AN UNCOMMON CAUSE OF INFERTILITY: Y;1 TRANSLOCATION AND PGD TRIAL
DÜNDAR M., Balta B., Bahadir O., Acar H., BAYDİLLİ N., Baltaci V., et al.
GENETIC COUNSELING , vol.25, no.3, pp.353-355, 2014 (SCI-Expanded, Scopus)
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2014229. Circulating microRNAs in patients with non-alcoholic fatty liver disease
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World Journal of Hepatology , vol.6, no.8, pp.613-620, 2014 (SCI-Expanded, Scopus)
2014
2014230. SYNDROMES PRESENTING ADDUCTED THUMB WITH/WITHOUT CLUBFOOT AND DUNDAR SYNDROME
Uzak A. S., Fryns J. P., DÜNDAR M.
GENETIC COUNSELING , vol.25, no.2, pp.159-169, 2014 (SCI-Expanded, Scopus)
2013
2013231. Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural EhlersDanlos syndrome
Mueller T., Mizumoto S., Suresh I., Komatsu Y., Vodopiutz J., DÜNDAR M., et al.
HUMAN MOLECULAR GENETICS
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2013
2013232. Progress towards the 'Golden Age' of biotechnology
Gartland K. M. A., Bruschi F., DÜNDAR M., Gahan P. B., Magni M. P. V., Akbarova Y.
CURRENT OPINION IN BIOTECHNOLOGY
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2013
2013233. Progress towards the 'Golden Age' of biotechnology.
DÜNDAR M.
CURRENT OPINION IN BIOTECHNOLOGY , vol.1, pp.6-13, 2013 (SCI-Expanded, Scopus)
2013
2013234. A Novel COL4A3 Mutation Causes Autosomal-Recessive Alport Syndrome in a Large Turkish Family
Uzak A. S., TOKGÖZ B., DÜNDAR M., Tekin M.
GENETIC TESTING AND MOLECULAR BIOMARKERS , vol.17, no.3, pp.260-264, 2013 (SCI-Expanded, Scopus)
2013
2013235. A NEW FINDING IN A PATIENT WITH MOWAT WILSON SYNDROME: PERIPUPILLARY ATROPHY AND GINGIVAL HYPERTROPHY
Kiraz A., Aldemir O., Karabulut Y., TURAN C., DÜNDAR M.
GENETIC COUNSELING , vol.24, no.1, pp.61-68, 2013 (SCI-Expanded, Scopus)
2013
2013236. Atypical presentation and a novel mutation in ALMS1: implications for clinical and molecular diagnostic strategies for Alstrom syndrome
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CLINICAL GENETICS , vol.83, no.1, pp.96-98, 2013 (SCI-Expanded, Scopus)
2013
2013237. The role of TNF-alpha and PAI-1 gene polymorphisms in familial Mediterranean fever
DÜNDAR M., Kiraz A., Balta B., Emirogullari E. F., ZARARSIZ G., Yurci A., et al.
MODERN RHEUMATOLOGY , vol.23, no.1, pp.140-145, 2013 (SCI-Expanded, Scopus)
2013
2013238. The Role of TNF-? and PAI-1 In Familial Mediterranean Fever (FMF)
DÜNDAR M., Kiraz A., BALTA B., ŞENER E. F., ZARARSIZ G., ARSLAN D., et al.
MODERN RHEUMATOLOGY , vol.23, no.1, pp.140-145, 2013 (SCI-Expanded, Scopus)
2012
2012239. Introduction
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JOURNAL OF BIOTECHNOLOGY , vol.161, pp.1-4, 2012 (SCI-Expanded, Scopus)
2012
2012240. Evaluation of the Results of Cases Prenatally Diagnosed as VSD
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2012241. A new syndrome of microtia with unilateral renal agenesis and short stature
Caglayan A. O., Stevens S. J. C., Albrechts J. C. M., DÜNDAR M., Engelen J.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , no.8, pp.1837-1840, 2012 (SCI-Expanded, Scopus)
2012
2012242. A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients
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2012243. DENTAL PROTEZLERDE KULLANILAN MIKNATISLARIN OLUŞTURDUĞU STATİK MANYETİK ALANIN İNSAN GİNGİVAL DOKU FİBROBLASTLARININ MİTOTİK AKTİVİTELERİNE OLAN ETKİLERİNİN İN VİTRO İNCELENMESİ
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Sağlık Bilimleri Dergisi , vol.21, no.1, pp.9-19, 2012 (SCI-Expanded, TRDizin)
2012
2012244. A NEW SYNDROME: MULTIPLE CONGENITAL ABNORMALITIES AND MENTAL RETARDATION IN TWO BROTHERS
DÜNDAR M., Ozdemir S. Y., Fryns J. P.
GENETIC COUNSELING , vol.23, no.1, pp.13-18, 2012 (SCI-Expanded, Scopus)
2012
2012245. Biotechnology, Cloning and Ethics.
DÜNDAR M., ŞENER E. F.
Global Bioethics , vol.27, pp.179-182, 2012 (Scopus)
2011
2011246. Common Familial Mediterranean Fever gene mutations in a Turkish cohort
DÜNDAR M., Emirogullari E. F., Kiraz A., TAHERİ S., BAŞKOL M.
MOLECULAR BIOLOGY REPORTS , vol.38, no.8, pp.5065-5069, 2011 (SCI-Expanded, Scopus)
2011
2011247. Biotechnology worldwide and the 'European Biotechnology Thematic Network' Association (EBTNA)
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CURRENT OPINION IN BIOTECHNOLOGY
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2011248. Current State of Biotechnology in Turkey
DÜNDAR M., Akbarova Y.
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2011249. Idiopathic hirsutism: local and peripheral expression of aromatase (CYP19A) and 5 alpha-reductase genes (SRD5A1 and SRD5A2)
Caglayan A. O., DÜNDAR M., TANRIVERDİ F., Baysal N. A., ÜNLÜHİZARCI K., Ozkul Y., et al.
FERTILITY AND STERILITY , vol.96, no.2, pp.479-482, 2011 (SCI-Expanded, Scopus)
2011
2011250. Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases.
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The EPMA Journal , no.2, pp.181-195, 2011 (Peer-Reviewed Journal)
2011
2011251. Loss of Dermatan-4-sulfotransferase 1 (D4ST1/CHST14) Function Represents the First Dermatan Sulfate Biosynthesis Defect, "Dermatan Sulfate-Deficient Adducted Thumb-Clubfoot Syndrome''
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HUMAN MUTATION , vol.32, no.4, pp.484-485, 2011 (SCI-Expanded, Scopus)
2011
2011252. Expression of Biologically Active Human Interferon Gamma in the Milk of Transgenic Mice Under the Control of the Murine Whey Acidic Protein Gene Promoter
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BIOCHEMICAL GENETICS , vol.49, pp.251-257, 2011 (SCI-Expanded, Scopus)
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2011253. Türkiye de Yatırımcıya ve sanayiciye çağrı
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Kayseri İli Yardım Derneği İstanbul Şubesi-Bizim Kayseri , pp.60-61, 2011 (Non Peer-Reviewed Journal)
2011
2011254. PARTIAL TRISOMY 14q DUE TO MATERNAL t(4;14)(p16;q32) IN A DYSMORPHIC NEWBORN
Dundar M., Uzak A., SAATÇİ Ç., AKALIN H.
GENETIC COUNSELING
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2011
2011255. PARTIAL TRISOMY 3q IN A CHILD WITH SACROCOCCYGEAL TERATOMA AND CORNELIA DE LANGE SYNDROME PHENOTYPE
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2011
2011256. Hayatın Sempatik Yüzleri Down Sendromlu çocuklar
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Dr. Dergisi , no.1, pp.13-14, 2011 (Non Peer-Reviewed Journal)
2011
2011257. Fetal Genetik Hastalıklar
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Türkiye Klinikleri Dergisi , vol.4, no.1, pp.1-7, 2011 (Peer-Reviewed Journal)
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2010258. Genetik ve Genetik Hastalıklar
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Erciyes Tıp Haber Bülteni , no.2, 2010 (Non Peer-Reviewed Journal)
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2010259. Unbalanced 3;22 Translocation With 22q11 and 3p Deletion Syndrome
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AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.152A, no.11, pp.2791-2795, 2010 (SCI-Expanded, Scopus)
2010
2010260. GDO ya dair her şey
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Türkiye Yeni Ufuklar Dergisi , no.7, pp.38-41, 2010 (Non Peer-Reviewed Journal)
2010
2010261. Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency
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DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY , vol.52, no.9, pp.868-872, 2010 (SCI-Expanded, Scopus)
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2010262. Genetik Yapısı Değiştirilmiş Gıdalar
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Kayseri İli Yardım Derneği İstanbul Şubesi-Bizim Kayseri , pp.64-65, 2010 (Non Peer-Reviewed Journal)
2010
2010263. Genetic Approach to the Case with Amniotic Band Sequence
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Erciyes Medical Journal , vol.32, no.1, pp.61-64, 2010 (ESCI, TRDizin)
2010
2010264. Amniyotik Bant Sekanslı Olguya Genetik Yaklaşım
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ERCİYES TIP DERGİSİ , vol.32, no.1, pp.61-64, 2010 (TRDizin)
2010
2010265. The prevalence of non-classic adrenal hyperplasia among Turkish women with hyperandrogenism
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GYNECOLOGICAL ENDOCRINOLOGY
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2010266. A CASE WITH A RARE CHROMOSOMAL ABNORMALITY: ISOCHROMOSOME 18p
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GENETIC COUNSELING , vol.21, no.1, pp.69-74, 2010 (SCI-Expanded, Scopus)
2010
2010267. A UNIQUE CASE OF A PATIENT WITH PARTIAL TRISOMY 22 AND LIPODYSTROPHY: IS IT A NEW SYNDROME DUE TO AN IGF-IR MUTATION?
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GENETIC COUNSELING , vol.21, no.2, pp.187-197, 2010 (SCI-Expanded)
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2010268. Türkiyede Nadir Hastalıklar ve Yetim İlaçlar Medikal ve Sosyal Problemler
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Erciyes Tıp Dergisi , vol.32, no.3, pp.195-200, 2010 (TRDizin)
2010
2010269. Amniyotik Band Sekanslı Olguya Genetik Yaklaşım
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Erciyes Tıp Dergisi , vol.32, no.1, pp.9-14, 2010 (TRDizin)
2009
2009270. Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome
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AMERICAN JOURNAL OF HUMAN GENETICS
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2009271. The Deletion Polymorphism of the Angiotensin-Converting Enzyme Gene Is Associated with Acute Aortic Dissection
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TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE
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2009272. Effects of seperate or sımultaneous ınjectıon of two dıfferent genes Enhanced green fluorescence proteın gene Human gamma ınterferon gene on Transgenıc mice recovery
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Sağlık Bilimleri Dergisi (Journal of Health Sciences , vol.18, no.2, pp.43-52, 2009 (TRDizin)
2009
2009273. Effects Of Seperate Or Simultaneous İnjection Of Two Different Genes (Enhanced Green-Fluorescence Protein Gene, Human Gamma İnterferon Gene) On Transgenic Mice Recovery
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E.Ü.Journal of Health Sciences , vol.18, no.2, pp.43-52, 2009 (Peer-Reviewed Journal)
2009
2009274. Frank-ter Haar syndrome with unusual clinical features
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EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.52, no.4, pp.247-249, 2009 (SCI-Expanded, Scopus)
2009
2009275. Detection of p16 promotor hypermethylation in "Maras powder" and tobacco users
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CANCER EPIDEMIOLOGY
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2009276. Inherited diseases and syndromes leading to aortic aneurysms and dissections
ÇAĞLAYAN A. O., DÜNDAR M.
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY
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2009
2009277. The Frequency of CYP 21 Gene Mutations in Turkish Women with Hyperandrogenism
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EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
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2009
2009278. Lack of Association of the Glu298Asp Polymorphism of Endothelial Nitric Oxide Synthase with Coronary Slow Flow in the Turkish Population.
ÇAĞLAYAN A. O., KALAY N., SAATÇİ Ç., YALÇIN A., AKALIN H., DÜNDAR M.
CANADIAN JOURNAL OF CARDIOLOGY , vol.25, pp.69-72, 2009 (SCI-Expanded, Scopus)
2009
2009279. Lack of association between the Glu298Asp polymorphism of endothelial nitric oxide synthase and slow coronary flow in the Turkish population
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CANADIAN JOURNAL OF CARDIOLOGY
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2009
2009280. İki farklı genin Güçlendirilmiş Yeşil Floresan protein geni İnsan gamma interferon geni ayrı ayrı veya birlikte mikroenjeksiyonunun transgenik fare eldesi üzerine etkilerinin araştırılması
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Sağlık Bilimleri Dergisi (Journal of Health Sciences) , vol.18, no.2, pp.43-52, 2009 (Peer-Reviewed Journal)
2009
2009281. FLUORESCENCE IN SITU HYBRIDIZATION AND SINGLE NUCLEOTIDE POLYMORPHISM OF A NEW CASE WITH INV DUP DEL(8p)
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GENETIC COUNSELING , vol.20, no.4, pp.333-340, 2009 (SCI-Expanded)
2008
2008282. İnvazif Prenatal Tanı Yöntemleri Uygulanan 2295 Olgunun Retrospektif Analizi
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PERİNATOLOJİ DERGİSİ , pp.116-119, 2008 (TRDizin)
2008
2008283. Down syndrome like appearance with a novel de novo translocation t(6;21)(q21;q13)
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INDIAN JOURNAL OF MEDICAL RESEARCH , vol.128, no.5, pp.666-668, 2008 (SCI-Expanded, Scopus)
2008
2008284. Apolipoprotein E3/E3 Genotype Decreases the Risk of Pituitary Dysfunction after Traumatic Brain Injury due to Various Causes: Preliminary Data
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JOURNAL OF NEUROTRAUMA
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2008285. Facial findings in fetuses with nonchromosomal syndromes diagnosed by prenatal ultrasound
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ULTRASOUND IN OBSTETRICS & GYNECOLOGY , vol.32, pp.363, 2008 (SCI-Expanded, Scopus)
2008
2008286. Parental karyotype and genetic markers for thrombophilia in recurrent miscarriage
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J Turkish German Gynecol Assoc , pp.139-143, 2008 (Peer-Reviewed Journal)
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2008287. Amenoreli Hastaların Sitogenetik Analiz Sonuçlarının Değerlendirilmesi
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Türkiye Klinikleri Dergisi , no.18, pp.83-87, 2008 (Peer-Reviewed Journal)
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2008288. Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2)
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ANNALS OF SAUDI MEDICINE , vol.28, no.3, pp.209-212, 2008 (SCI-Expanded, Scopus)
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2008289. Genotype-phenotype correlation in children with familial Mediterranean fever in a Turkish population
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PEDIATRICS INTERNATIONAL , vol.50, no.2, pp.208-212, 2008 (SCI-Expanded, Scopus)
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2008290. Megarbane Syndrome; Second Report.
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Indian Journal of Human Genetic , vol.14, pp.27-29, 2008 (SCI-Expanded)
2008
2008291. ICR1 epimutations in 11p15 are restricted to patients with Silver-Russell syndrome features
Eggermann T., Meyer E., Caglayan A. O., DÜNDAR M., Schoenherr N.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
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2008
2008292. The effect of maras powder on DNA methylation and micronucleus formation in human buccal tissue
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JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES
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2008
2008293. Klonlama
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Kayseri İli Yardım Derneği İstanbul Şubesi-Bizim Kayseri , pp.61, 2008 (Non Peer-Reviewed Journal)
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2008294. Hastalıklarda Genetik Faktörlerin Rolü
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Kayseri İli Yardım Derneği İstanbul Şubesi-Bizim Kayseri , pp.65, 2008 (Non Peer-Reviewed Journal)
2008
2008295. SCOLIOSIS, BLINDNESS AND ARACHNODACTYLY IN A LARGE TURKISH FAMILY: IS IT A NEW
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GENETIC COUNSELING , vol.19, no.3, pp.319-330, 2008 (SCI-Expanded, Scopus)
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2007296. A case of partial trisomy 13 with features similar to ‘C’ Syndrome. Bulguları C sendromuna benzeyen parsiyel trizomi
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ERCİYES TIP DERGİSİ , pp.159-163, 2007 (TRDizin)
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2007297. Sexing Greater Flamingo chicks from feather bulb DNA
Balkiz O., Danol S., BARBRAUD C., Tekin S., Oezesmi U., Duendar M., et al.
WATERBIRDS , vol.30, no.3, pp.450-453, 2007 (SCI-Expanded, Scopus)
2007
2007298. How the I1307K adenomatous polyposis coli gene variant contributes in the assessment of risk of colorectal cancer, but not stomach cancer, in a Turkish population
Dundar M., Caglayan A. O., Saatci C., Karaca H., Baskol M., Tahiri S., et al.
CANCER GENETICS AND CYTOGENETICS
, vol.177, no.2, pp.95-97, 2007 (SCI-Expanded, Scopus)
2007
2007299. Genetik Anomalisi Olmayan İki Oligodonti Olgusu
ŞİŞMAN Y., Tarım Ertaş E., DÜNDAR M.
Erciyes Üniversitesi Sağlık Bilimleri Degisi , vol.16, pp.180-185, 2007 (Peer-Reviewed Journal)
2007
2007300. Frequency of the common G985A mutation in the medium-chain acyl-coa dehydrogenase gene in Turkish population
DÜNDAR M., TAHERİ S., SAATÇİ Ç., ÖZKUL Y., ÇAĞLAYAN O.
SAĞLIK BİLİMLERİ DERGİSİ , vol.29, pp.263-267, 2007 (TRDizin)
2007
2007301. Prenatal Diagnosis of Unique Translocation t (7;15)(q11. 23;q26. 3) in a Fetus.
Saatci C., Caglayan A., ÖZKUL Y., Dundar M.
Egyptian Journal of Medical Human Genetics , no.8, pp.105-110, 2007 (SCI-Expanded, Scopus)
2007
2007302. Sacrococcygeal teratoma in a fetus with prenatally diagnosed partial trisomy 10q (10q24.3 -> qter) and partial monosomy 17p (p13.3 -> pter)
BATUKAN C., Ozgun M. T., Basbug M., ÇAĞLAYAN O., Dundar M., Murat N.
PRENATAL DIAGNOSIS , vol.27, no.4, pp.365-368, 2007 (SCI-Expanded, Scopus)
2007
2007303. Prenatal diagnosis of a fetus with partial trisomy 7p
Ozgun M. T., Batukan C., Basbug M., Akgun H., ÇAĞLAYAN O., Dundar M.
FETAL DIAGNOSIS AND THERAPY , vol.22, no.3, pp.229-232, 2007 (SCI-Expanded, Scopus)
2007
2007304. Ülkemiz ve Biyoteknoloji Kayseri İli Yardım Derneği İstanbul Şubesi
DÜNDAR M.
Kayseri İli Yardım Derneği İstanbul Şubesi-Bizim Kayseri , pp.47, 2007 (Non Peer-Reviewed Journal)
2007
2007305. A case of partial trisomy 13 with features similar to C Syndrome Bulguları C sendromuna benzeyen parsiyel trizomi 13
DÜNDAR M.
Erciyes Tıp Dergisi , vol.29, no.2, pp.159-163, 2007 (TRDizin)
2006
2006306. Adrenal axis functions in patients with familial Mediterranean fever
Sav T., ÖZBAKIR Ö., KELEŞTEMUR H. F., GÜRSOY Ş., BAŞKOL M., KULA M., et al.
Journal of Clinical Rheumatology , vol.25, pp.458-461, 2006 (SCI-Expanded, Scopus)
2006
2006307. Circulating testosterone regulates the local GnRH-II expression in peripheral lymphocytes: An in vivo interaction in patients with idiopathic hypogonadotrophic hypogonadism (IHH).
Tanriverdi F., Demirkoparan U., Akalın H., ÇAĞLAYAN O., ÖZKUL Y., Dundar M., et al.
FRONTIERS IN NEUROENDOCRINOLOGY , no.27, pp.107, 2006 (SCI-Expanded, Scopus)
2005
2005308. 5,10-Methylenetetrahydrofolate reductase C677T gene polymorphism in Behcet's patients with or without ocular involvement
Ozkul Y., Evereklioglu C., Borlu M., Taheri S., Calis M., Dundar M., et al.
BRITISH JOURNAL OF OPHTHALMOLOGY
, vol.89, no.12, pp.1634-1637, 2005 (SCI-Expanded, Scopus)
2005
2005309. İnsan Genomu Kromozomlar
DÜNDAR M.
urkiye Klinikleri J Pediatr Sci , vol.1, no.2, pp.11-17, 2005 (Peer-Reviewed Journal)
2005
2005310. Familial Mediterranean fever (FMF) in Turkey - Results of a nationwide multicenter study
Tunca M., Akar S., Onen F., Ozdogan H., Kasapcopur O., Yalcinkaya F., et al.
MEDICINE , vol.84, no.1, pp.1-11, 2005 (SCI-Expanded, Scopus)
2005
2005311. Hereditary isolated ankyloblepharon filiforme adnatum
Ozyazgan I., Eskitascioglu T., Dundar M., Karaci S.
PLASTIC AND RECONSTRUCTIVE SURGERY , vol.115, no.1, pp.363-364, 2005 (SCI-Expanded, Scopus)
2004
2004312. Isolated congenital anonychia cases with coincident chromosomal fragility
Ozyazgan I., Ozyazgan I., Dundar M.
ANNALES DE GENETIQUE , vol.47, no.4, pp.381-386, 2004 (SCI-Expanded, Scopus)
2003
2003313. Associated anomalies in asymmetric crying facies and 22q11 deletion
Akçakuş M., Ozkul Y., Gunes T., Kurtoglu S., Çetin N., KISAARSLAN A. F., et al.
GENETIC COUNSELING , vol.14, no.3, pp.325-330, 2003 (SCI-Expanded, Scopus)
2002
2002314. A family with two different chromosomal translocations
Ozkul Y., Dundar M.
ANNALES DE GENETIQUE , vol.45, no.4, pp.185-187, 2002 (SCI-Expanded, Scopus)
2002
2002315. A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype
Ozkul Y., ATABEK M. E., Dundar M., Kurtoglu S., Saatci C.
ANNALES DE GENETIQUE , vol.45, no.4, pp.181-183, 2002 (SCI-Expanded, Scopus)
2001
2001316. A case with adducted thumb and club foot syndrome
Dundar M., Kurtoglu S., ELMAS B., DEMİRYILMAZ F., CANDEMİR Z., Ozkul Y., et al.
CLINICAL DYSMORPHOLOGY , vol.10, no.4, pp.291-293, 2001 (SCI-Expanded, Scopus)
2001
2001317. A novel acropectoral syndrome maps to chromosome 7q36
Dundar M., Gordon T., Ozyazgan I., Oguzkaya F., Ozkul Y., Cooke A., et al.
JOURNAL OF MEDICAL GENETICS
, vol.38, no.5, pp.304-309, 2001 (SCI-Expanded, Scopus)
2001
2001318. . Detection of Mutations in the RB1 Gene by Single Strand Conforaıation Polynıorphism (SSCP) Analysis, Amplifıcation Mismatch Detection (AMD) Analysis and Polymerase Chain Reaction Sequencing
DÜNDAR M., LANYON G., CONNOR M. J.
Proceedings of the National Science Council, Republic of China. Part B, Life sciences , vol.25, pp.166-173, 2001 (SCI-Expanded)
2001
2001319. A case of ambiguous genitalia presenting with a 45,X/46,Xr(Y)(p11.2;q11.23)/47,X,idic(Y)(p11.2),idic(Y)(p11.2) karyotype
Dundar M., LOWTHER G., ACAR H., Kurtoglu S., Demiryılmaz F., Kucukaydin M.
ANNALES DE GENETIQUE , vol.44, no.1, pp.5-8, 2001 (SCI-Expanded, Scopus)
2001
2001320. A case with Waardenburg syndrome presenting with two separate translocations - one reciprocal and one complex
Dundar M., Lowther G., Colgan J., Ozkul Y., Candemir Z., Saatci C., et al.
CLINICAL DYSMORPHOLOGY , vol.10, no.1, pp.65-66, 2001 (SCI-Expanded, Scopus)
2000
2000321. Cystic hygroma occuring in a twin pregnancy
Yaşasın Z., Başbuğ M., Dündar M., SERİN I. S., Tayyar M., Narin N.
Gynecol Obstet Reprod Med , vol.6, pp.219-220, 2000 (Peer-Reviewed Journal)
2000
2000322. Female-to-male transsexual with 47,XXX karyotype
TURAN M. T., ESEL E., DUNDAR M., CANDEMIR Z., Basturk M., SOFUOGLU S., et al.
BIOLOGICAL PSYCHIATRY , vol.48, no.11, pp.1116-1117, 2000 (SCI-Expanded, Scopus)
2000
2000323. A locus for preaxial polydactyly with sternal abnormalities maps to chromosome 7q36
Gordon T., Dundar M., Cooke A., Ozyazgan I., Oguzkaya F., ÖZKUL Y., et al.
JOURNAL OF MEDICAL GENETICS , no.37, pp.81, 2000 (SCI-Expanded, Scopus)
2000
2000324. Patient with Weismann-Netter and Stuhl (toxopachyosteosis) syndrome with communicant hydrocephalus and arachnoid cyst
Kurtoglu S., Dundar M., Kumandas S., Gunduz Z., Uzum K., Durak A. C., et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.13, no.2, pp.211-215, 2000 (SCI-Expanded, Scopus)
1999
1999325. A case with two separate complex translocations 46,XY,t(1;8)(q32.3;q24.1), t(4;7)->(7ter -> p13 :: 7q34 -> q31.2 :: 4p15.2 -> qter), (7qter -> q34 :: 7p13 -> q31.2 :: 4p15.2 -> pter)
ÖZKUL Y., DÜNDAR M., Candemir Z., SAATÇİ Ç., Colgan J., Lowther G., et al.
CYTOGENETICS AND CELL GENETICS , no.85, pp.159, 1999 (SCI-Expanded)
1997
1997326. Polycystic kidney disease, biliary dysgenesis in a patient with Larsen's syndrome
Kurtoglu S., Dundar M., HALLAÇ I. K., Uzum K., OKUMUŞ Y., Oktem T.
CLINICAL GENETICS , vol.51, no.6, pp.408-411, 1997 (SCI-Expanded, Scopus)
1997
1997327. Identification of classic and complex t (15;17) and/or RAR alpha/ PML gene fusion in APL by cytogenetic and dual color FISH techniques
Acar H., DÜNDAR M., Stewart J.
Proceedings of the National Science Council, Republic of China. Part B, Life sciences , vol.21, pp.54-60, 1997 (SCI-Expanded)
1997
1997328. Bloom sendromu Bir hastanın sunulması
DÜNDAR M.
Medical Network Klinik Bilimler ve Doktor , vol.3, no.4, pp.573-575, 1997 (Peer-Reviewed Journal)
1997
1997329. An autosomal recessive adducted thumb club foot syndrome observed in Turkish cousins
Dundar M., Demiryılmaz F., Demiryilmaz I., Kumandas S., Erkilic K., Kendirci M., et al.
CLINICAL GENETICS , vol.51, no.1, pp.61-64, 1997 (SCI-Expanded, Scopus)
1997
1997330. A seventeen years old patient presenting with X linked agammaglobulinemia
DÜNDAR M.
Türkiye Tıp Dergisi , vol.3, no.4, pp.171-174, 1997 (Peer-Reviewed Journal)
1996
1996331. Congenital alacrima in a patient with G (Opitz frias) syndrome
Dundar M., Erkilic K., Demiryılmaz F., Kucukaydin M., Kendirci M., Okur H., et al.
HUMAN GENETICS , vol.97, no.4, pp.540-542, 1996 (SCI-Expanded, Scopus)
1996
1996332. Detection of a germline mutation in the RB1 gene
DÜNDAR M.
The New Journal of Medicine , vol.13, no.1, pp.28-29, 1996 (Peer-Reviewed Journal)
1996
1996333. Screening of RB1 gene mutations in breast and bladder tumours
DÜNDAR M.
The New Journal of Medicine , vol.13, no.2, pp.82-84, 1996 (Peer-Reviewed Journal)
1993
1993334. SCOTTISH FREQUENCY OF THE COMMON G985 MUTATION IN THE MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) GENE AND THE ROLE OF MCAD DEFICIENCY IN SUDDEN-INFANT-DEATH-SYNDROME (SIDS)
DÜNDAR M., Lanyon W., Connor J.
JOURNAL OF INHERITED METABOLIC DISEASE , vol.16, no.6, pp.991-993, 1993 (SCI-Expanded, Scopus)
1990
1990335. Anadolu nun Genetik yapısı üzerine araştırmalar XX 8 ölü doğumlu ailelerde yeni gebelikten beklentiler
DÜNDAR M.
Erciyes Tıp Dergisi , vol.12, pp.215-223, 1990 (Scopus)
Papers Presented at Peer-Reviewed Scientific Conferences
2025
20251. Kronik Lenfositer Lösemi Hastalarında Görülen Genetik Mutasyonların Sıklığı ve Surveye Etkisi
GÖLBAŞI M., ÜNAL A., ÖZKUL Y., DÜNDAR M., MANDACI ŞANLI N., AKYOL G., et al.
7. HEMATOLOJIK NADIR HASTALIKLAR KONGRESI, Girne, Cyprus (Kktc), 22 - 25 February 2025, (Summary Text)
2025
20252. Genetically Confirmed 46 Patients WithInherited Thrombocytopenia: A City Experience FromTürkiye
GÖK V., ÖZCAN A., Mutlu F. T., YILMAZ E., KOÇAK GÖL D., MUTLU M. B., et al.
18th Annual Congress of the European Association for Haemophilia and Allied Disorders, Milan, Italy, 4 - 07 February 2025, vol.31, pp.187, (Summary Text)
2024
20243. Frequency of Genetic Mutations in Patients With Chronic Lymphocytic Leukemia and Their Effects on Survival
GÖLBAŞI M., ÜNAL A., ÖZKUL Y., DÜNDAR M., MANDACI ŞANLI N., AKYOL G., et al.
11th SOHO Türkiye Meeting, İstanbul, Turkey, 28 - 30 April 2024, vol.24, pp.345, (Summary Text)
2023
20234. Blended Phenotype in a Case with Brain Malformation, Neurodevelopmental Disorder and Epilepsy
KARATAŞ E., KİRAZ A., KARAMAN Z. F., PER H., DÜNDAR M.
8th INTERNATIONAL CONGRESS OF MEDICAL GENETICS, 21 - 23 September 2023, (Summary Text)
2022
20225. Nadir bir hipogonadotropik hipogonadizm nedeni: Boucher-Neuhauser sendromu
KALANYUVA D., KARA C. Ş., ÖKÇESİZ İ., DÜNDAR M., BAYRAM F.
43. Türkiye Endokrinoloji ve Metabolizma Hastalıkları Kongresi, Turkey, 18 - 22 May 2022, (Summary Text)
2021
20216. Two novelKMT2Dvariants in a series of 7 patients with Kabuki syndrome
Özçelik F., Duman N., KİRAZ A., Öz Ö., GÖKÇE N., Çiçek D., et al.
6.Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Turkey, 16 September 2021, pp.24-25, (Summary Text)
2021
20217. Short stature caused by ACAN gene mutation; a case report
KARATAŞ E., ÖZÇELİK F., DEMİR M., KARA L., AKYÜREK E., HATİPOĞLU N., et al.
6.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ, Kayseri, Turkey, 16 - 18 September 2021, pp.36, (Summary Text)
2021
20218. A case of rare CYP26B1-related craniosynostosis in a Turkish female patient
DEMİR M., Özgüç B., ÖZTÜRK M. A., ÖZKUL Y., DÜNDAR M.
6.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ, Kayseri, Turkey, 16 September 2021, pp.29, (Summary Text)
2021
20219. Clinical and Molecular Evaluation of MEFV Gene Variants in the Turkish Population: A study by the National Genetics Consortium
FAHRİOĞLU U., DÜNDAR M.
6. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Turkey, 16 September 2021, pp.3, (Summary Text)
2021
202110. Investigation of the Effects of Obesity on the Pluripotency Feature of Mouse Adipose Tissue Originated Mesenchymal Stem Cells
Ahmed Al Sammarraie S. H., GÜNAYDIN Z., SINIKSARAN B. S., DÜNDAR M., ÖZCAN S.
6.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ, Kayseri, Turkey, 16 - 18 September 2021, pp.48, (Summary Text)
2021
202111. A novel homozygous variant inSUOXgene causes classic isolated sulfite oxidase deficiency: a case report
USLU K., GÜLEÇ A., ARSLAN S., BAŞGÖZ N., KARDAŞ F., PER H., et al.
6.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ, Kayseri, Turkey, 16 September 2021, pp.30, (Summary Text)
2021
202112. A case report of Alstrom syndrome in a Turkish girl with syndromic obesity
YAKUBİ M., DEMİR M., ÇİÇEK D., HATİPOĞLU N., ÖZKUL Y., DÜNDAR M.
6.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ, Kayseri, Turkey, 15 September 2021, pp.30, (Summary Text)
2021
202113. Evaluation of chimerism test and genetic translocation results in ALL, AML and CML patients
TAN B., ŞAHİN İ. O., EKİNCİ Ö. G., YILMAZ E., ÖZCAN A., KARAKÜKCÜ M., et al.
6.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ, Kayseri, Turkey, 15 December 2021, pp.30, (Summary Text)
2021
202114. Molecular evaluation of patients with pre-diagnosed Dravet Syndrome
GÖKÇE N., MERMER D. B., MAMMADOVA N., AKALIN H., BAŞGÖZ N., AKYÜREK E., et al.
6.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ, Kayseri, Turkey, 16 - 18 September 2021, pp.36-37, (Summary Text)
2021
202115. A novel homozygous mutation inCYP11A1gene in 46, XX patient with P450scc deficiency
KULAK ABAY H., HATİPOĞLU N., GÜL ŞİRAZ Ü., ÖZKUL Y., DÜNDAR M.
6.Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Turkey, 16 September 2021, pp.29, (Summary Text)
2021
202116. 6.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ
ŞAHİN İ. O., KARATAŞ E., DEMİR M., GÖKÇE N., ÖZKUL Y., DÜNDAR M.
6.ULUSLARARASI ERCİYES TIP TİBBİ GENETİK KONGRESİ, Kayseri, Turkey, 16 - 18 September 2021, pp.35, (Summary Text)
2021
202117. A cleft palate with 49, XXXXY karyotype: A case report
Ekinci Ö. G., Kenanoğlu S., Küçük T. Y., Özgüç B., Tan B., Babacan S., et al.
6.Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Turkey, 16 - 18 September 2021, pp.27-28, (Summary Text)
2021
202118. Novel variant detected in the FAS gene of a patient with Autoimmune Lymphoproliferative Syndrome
ARI M. B., YAMAN T., ÇALIŞKAN Ç., ÖZÇELİK F., ÖZCAN A., ÖZKUL Y., et al.
6.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ, Kayseri, Turkey, 16 - 18 September 2021, pp.56, (Summary Text)
2021
202119. Clinical studies on the efficacy of alpha-cyclodextrin and hydroxytyrosol against SARS-CoV-2 infection: North Cyprus ExperienceNorth Cyprus Experience
ERGÖREN M. Ç., Paolacci S., Manara E., TUNCEL G., Dhuli K., Camilleri G., et al.
EUROPEAN BIOTECHNOLOGY CONGRESS 2021, Sofija, Bulgaria, 23 - 25 September 2021, vol.5, pp.49, (Summary Text)
2021
202120. Molecular investigation ofpatients diagnosed with Crouzen Syndrome by next-generation sequencing method
MERMER D. B., GÖKÇE N., ÖZÇELİK F., AKALIN H., CANPOLAT M., GÜMÜŞ H., et al.
6.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ, Kayseri, Turkey, 16 - 18 September 2021, pp.55, (Summary Text)
2020
202021. A novel variant in the EFTUD2 gene is associated with mandibulofacial dysostosis with microcephaly in a Turkish patient and her mother
KIRANATLIOĞLU K., DOĞAN M. E., Kazımlı U., Akyürek E., CANPOLAT M., ÖZKUL Y., et al.
V. Uluslararası Erciyes Tıp Genetik Günleri, 20 - 22 February 2020, vol.31, (Summary Text)
2020
202022. A novel variant in the SLC2A2 gene associated with glycogen storage disease type XI
Özçelik F., KADIOĞLU YILMAZ B., BAYSAL K., KARASU N., DOĞAN M. E., KARDAŞ F., et al.
V. Uluslararası Erciyes Tıp Genetik Günleri, 20 - 22 February 2020, vol.31, (Summary Text)
2020
202023. A novel EDAR gene variant causing autosomal dominant hypohidrotic ectodermal dysplasia
BAYSAL K., DOĞAN M. E., Kazımlı U., Boyyadoğlu Ç., COŞKUN N., Akkuş M., et al.
V. Uluslararası Katılımlı Erciyes Tıp Genetik Günleri Kongresi, Nevşehir, Turkey, 20 - 22 February 2020, vol.31, pp.1, (Full Text)
2020
202024. Therapeutic approach to DMD with HSP70-hom and HSP70-2
Aynekin B., Akalın H., COŞKUN N., BAYSAL K., GÜMÜŞ H., PER H., et al.
V. Uluslararası Katılımlı Erciyes Tıp Genetik Günleri Kongresi, Nevşehir, Turkey, 20 - 22 February 2020, vol.31, pp.1, (Full Text)
2020
202025. Recent Developments in Biotechnology and European BiotechnologyNetwork Association
DÜNDAR M., Karasu N.
Bio Turkey 2020 Uluslararası Biyoteknoloji Kongresi, İstanbul, Turkey, 5 - 07 March 2020, (Summary Text)
2020
202026. The sexual and psychological conditions of male patients with klinefelter syndrome and vasal agenesis
BAYDİLLİ N., DEMİRTAŞ A., ÖZKAYA M., SABUR V., AKINSAL E. C., DÜNDAR M., et al.
V. Uluslararası Katılımlı Erciyes Tıp Genetik Günleri Kongresi, Nevşehir, Turkey, 20 - 22 February 2020, (Summary Text)
2020
202027. Developing evidence based computerized diagnostic tools for breast cancer early prediction
ŞENTÜRK N., TUNCEL G., KÖSEOĞLU S., DOĞAN B., ÖZEMRİ SAĞ Ş., MOCAN G., et al.
V. Uluslararası Katılımlı Erciyes Tıp Genetik Günleri Kongresi, Turkey, 20 - 22 February 2020, (Summary Text)
2019
201928. Application of high-throughput DNA sequencing to score population-specific variants for rare disorders
Ergören M., Manara E., Paolucci S., Temel S., Mocan G., DÜNDAR M., et al.
European Biotechnology Congress, 11 - 13 April 2019, vol.305, pp.25, (Summary Text)
2019
201929. Investigation of the effect of propranolol treatment on HTRA2, DRD3, SLC1A2 genes expression in the patients with essential tremor of the hands
Kandemir N., Bayramov R., Gültekin M., DÜNDAR M.
European Biotechnology Congress, 11 - 13 April 2019, vol.305, pp.28, (Summary Text)
2019
201930. A case of cockayne syndrome: a novel homozygous missense variant
Kandemir N., Karaduman N., Arslan S., Baysal K., DÜNDAR M.
European Biotechnology Congress, 11 - 13 April 2019, vol.305, pp.88, (Summary Text)
2019
201931. Future Biotechnology
DÜNDAR M., Prakash S., Lal R., Martin D.
European Biotechnology Congress, 11 - 13 April 2019, vol.305, pp.1-2, (Summary Text)
2019
201932. Quality assurance of genetic laboratories and the EBTNA practice certification
Manara E., Precone V., DÜNDAR M., Beccari T., Cecchin S., Marceddu G., et al.
European Biotechnology Congress, 11 - 13 April 2019, vol.305, pp.7, (Summary Text)
2019
201933. A novel nonsense variant in COL1A1 gene in a family with clinical symptoms of osteogenesis imperfecta
Kandemir N., Kazımlı U., Dirican Ö., DÜNDAR M.
European Biotechnology Congress, 11 - 13 April 2019, vol.305, pp.88, (Summary Text)
2019
201934. Investigation of the Effects of Propranolol on DRD3, SLC1A2 and HTRA2 Gene Expression in Patients with Essential Tremor
Gultekin M., Kandemir N., Mirza M., Kara M., Tascioglu N., Dundar M.
International Congress of Parkinson's Disease and Movement Disorders, Nice, France, 22 - 26 September 2019, vol.34, (Summary Text)
2019
201935. Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency
Aghayeva A., Turan H., Toksoy G., Cakir A. D., Berkay E., Gunes N., et al.
58th Annual ESPE meeting, 19 - 21 September 2019, vol.91, pp.361-362, (Summary Text)
2018
201836. Familial Mediterranean fever looking into ten years’xx experience
BAYRAMOV R., DOĞAN M. E., AYNEKİN B., EMEKLİ R., YAVUZ F., CERRAH GÜNEŞ M., et al.
51st European Society of Human GeneticsConference, Milan, Italy, 16 - 19 June 2018, vol.27, pp.903, (Summary Text)
2018
201837. Familial Mediterranean fever; looking into ten years' experience
BAYRAMOV R., DOĞAN M., Aynekin B., Emekli R., Yavuz F., Gunes M. C., et al.
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.903, (Summary Text)
2019
201938. A case with multiple dislocations associated Larsen Syndrome a novel variant of FLNB gene
ARSLAN S. B., Acar Dirican Ö., CERRAH GÜNEŞ M., DOĞAN M. E., PER H., DÜNDAR M.
13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, (Summary Text)
2019
201939. A de novo novel frameshift variant in the penultimate exon of FBN1 gene cause of rare Marfan lipodystrophy syndrome
DOĞAN M. E., DÜNDAR M.
13th Balkan Congress of Human Genetics, 17 - 20 April 2019, vol.22, pp.69, (Summary Text)
2019
201940. A novel missense variant in the homogentisate 1,2-dioxygenase (HGD) gene in a patient with clinical symptoms of alkaptonuria.
KAZIMLI U., DOĞAN M. E., BAYSAL K., ÖZKUL Y., ŞENEL S., DÜNDAR M.
13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.166, (Summary Text)
2019
201941. Molecular Analysis of Hotspot Mutation Sites in Chronic Myeloid Leukemia (CML) Patients with Imatinib Mesylate Drug Resistance
KARASU N., Akalın H., GÖKÇE N., ÇELİK S., ESER B., DÜNDAR M.
Uluslararası 7. İlaç Kimyası: İlaç Etkin Maddesi Tasarımı, Sentezi, Üretimi ve Standardizasyonu Kongresi, Antalya, Turkey, 14 - 17 March 2019, vol.1, pp.1, (Full Text)
2019
201942. Molecular pathological evaluationof Alport syndrome
BAŞGÖZ N., DOĞAN M. E., COŞKUN N., ÖNAL M. G., SİPAHİOĞLU M. H., DURSUN İ., et al.
International Participated Erciyes Medical Genetics Days, Kayseri, Turkey, 21 - 23 February 2019, (Summary Text)
2019
201943. Identification and frequency of CFTR gene variants
KENANOĞLU S., BOZ M., NESLİHAN B., COŞKUN N., BADUR MERMER D., ÖNAL M. G., et al.
International Participated Erciyes Medical Genetics Days, Kayseri, Turkey, 21 - 23 February 2019, (Summary Text)
2018
201844. How Today’s Biotechnology Modifying Future and EBTNA
DÜNDAR M., Bayramov R., Gartland K.
42. 3rd International Conference On Applied Biotechnology (3rd ICAB), Tirane, Albania, 23 - 24 November 2018, (Summary Text)
2018
201845. THE ASSOCIATION OF BRAIN-DERIVED NEUROTROPHIC FACTOR GENE POLYMORPHISM WITH OBSTRUCTIVE SLEEP APNEA SYNDROME and OBESITY
TUTAR N., yüksekkaya m., DÜNDAR M., YILMAZ İ., GÜLMEZ İ., OYMAK F. S., et al.
european respiratory society congress 2018, 15 - 19 September 2018, (Full Text)
2018
201846. Gene variants of Congenital Adrenal Hyperplasia in Anatolian population
BAYRAMOV R., DÜNDAR A., DOĞAN M. E., AKKUŞ M., POLAT S., HATİPOĞLU N., et al.
European Biotechnology Congress 2018, Atina, Greece, 26 - 28 April 2018, vol.280, pp.21, (Summary Text)
2018
201847. Two novel missense variants of FGFR2 gene in two patients with Pfeiffer Syndrome Type 3
Doğan M. E., Dundar B., Gunes M. C., Bayramov R., Karaduman N. K., Per H., et al.
European Biotechnology Congress, Athens, Greece, 26 - 28 April 2018, vol.280, (Summary Text)
2018
201848. Biotechnological opportunities
Gartland K. M., DÜNDAR M., Beccari T., Gartland J. S.
European Biotechnology Congress, ATİNA, Greece, 26 - 28 April 2018, vol.280, pp.3, (Summary Text)
2018
201849. In memory of Mariapia Viola-Magni, Founder of European Biotechnology Thematic Network Association
DÜNDAR M., Beccari T., Vicente O., Slavica A., Bayramov R., Dundar M. S., et al.
European Biotechnology Congress, Athens, Greece, 26 - 28 April 2018, vol.280, (Summary Text)
2018
201850. Recent Developments and Oppurtunities in Biotechnology
DÜNDAR M.
SECOND INTERNATIONAL BIOMEDICAL ENGINEERING CONGRESS, 24 - 27 May 2018, (Summary Text)
2018
201851. The Association of Endothelin-1 Levels With Renal Survival in Polycystic Kidney Disease Patients
EROĞLU E., KOÇYİĞİT İ., KAYNAR A. S., KOÇER D., ZARARSIZ G., BAYRAMOV R., et al.
55th ERA-EDTA Congress, 24 - 27 May 2018, vol.33, pp.64, (Summary Text)
2017
201752. The frequencies of Y chromosome microdeletions in infertile men from Middle Anatolia, Turkey
AKINSAL E. C., BAYDİLLİ N., DÜNDAR M., EKMEKÇİOĞLU O.
10th Meeting of the EAU Section of Andrological Urology, Malmö, Sweden, 24 - 25 November 2017, vol.16, pp.2995-2996, (Full Text)
2017
201753. Medical Genetics Course and Biotechnology MAGI Balkan and EBTNA European Biotechnology Thematic Network Association
DÜNDAR M.
Medical Genetics Course and Biotechnology MAGI Balkan and EBTNA European Biotechnology Thematic Network Association, 21 - 24 September 2017
2017
201754. kolanjiokarsinom hücre hattında SAHA’xxnın transciptional enhancer factors gen ekspresyonları üzerine etkisi
yasemin a., güneş f., özel m., uçar ç., doğru b. n., BAŞKOL G., et al.
Uluslararası Biyokimya Kongresi, 19 - 23 September 2017, (Summary Text)
2017
201755. kolanjiokarsinoma hücre hattında histon deasetilaz inhibitörü SAHA’xxnın transforming growth factor beta yolağı üzerine etkisi
güneş f., özel m., doğru b. n., uçar ç., BAŞKOL G., BAŞKOL M., et al.
uluslararası Biyokimya kongresi, 19 - 23 September 2017, (Summary Text)
2017
201756. karaciğer fibrosis hücre hattında histon deasetilaz inhibitörü olan SAHA’xxnınepitel hücrelerin mezankimal hücrelere dönüşümü üzerine olan etkisinin araştırılması
özel m., uçar ç., doğru b. n., güneş f., BAŞKOL G., BAŞKOL M., et al.
uluslararası biyokimya kongresi, 19 - 23 September 2017, (Full Text)
2017
201757. European biotechnology thematic network association
DÜNDAR M.
Smart Specialization Strategy in the Field of Biotechnologies in Europe: A Challenge for CEE Region, Bratislava, Slovakia, 4 - 06 September 2017
2017
201758. Prenatal diagnosis of a foetus with partial monosomy 4p and partial trisomy 13q
DOĞAN M. E., Kutuk M. S., BAYRAMOV R., SAATÇİ Ç., ÖZKUL Y., DÜNDAR M.
European Biotechnology Congress, Dubrovnik, Croatia, 25 - 27 May 2017, vol.256, (Summary Text)
2017
201759. Retrospective results of 18 years prenatal diagnosis cases and its evaluation
BAYRAMOV R., Kutuk M. S., KENANOGLU S., GUNES M. C., DOĞAN M. E., ÖZKUL Y., et al.
European Biotechnology Congress, Dubrovnik, Croatia, 25 - 27 May 2017, vol.256, (Summary Text)
2017
201760. The correlation of genotype-phenotype of FMF disease and its review of statistical data
YAVUZ F., BAYRAMOV R., KENANOGLU S., DOĞAN M. E., GUNES M. C., BOZ M., et al.
European Biotechnology Congress, Dubrovnik, Croatia, 25 - 27 May 2017, vol.256, (Summary Text)
2017
201761. Frequency of chromosome variants in families with recurrent pregnancy loss and statistical analysis of infertility
GUNSILI B., BAYRAMOV R., KENANOGLU S., DOĞAN M. E., GUNES M. C., SAATÇİ Ç., et al.
European Biotechnology Congress, Dubrovnik, Croatia, 25 - 27 May 2017, vol.256, (Summary Text)
2017
201762. Association of the thrombophilia factors with breast and/or ovarian cancer risk
Badur Mermer D., COŞKUN N., Akalın H., Bayramov R., ÖNAL M. G., SAATÇİ Ç., et al.
JOURNAL OF BIOTECHNOLOGY, Dubrovnik, Croatia, 25 - 27 May 2017, (Full Text)
2017
201763. NF1 gene variant allele frequencies comparison of Turkish population with databases
BAYRAMOV R., DOĞAN M. E., GUNES M. C., UNAL M. G., BOZ M., ADA Y., et al.
European Biotechnology Congress, Dubrovnik, Croatia, 25 - 27 May 2017, vol.256, (Summary Text)
2017
201764. GENERAL REVIEW OF STATISTICAL DATA IN FMF DISEASEAND GENOTYPE-PHENOTYPE CORRELATION
YAVUZ F., BAYRAMOV R., DOĞAN M. E., CERRAH GÜNEŞ M., BOZ M., SAATÇİ Ç., et al.
ERCİYES MEDİCAL GENETİCS DAYS 2017, Turkey, 11 - 13 May 2017, (Summary Text)
2017
201765. The mutation spectrum of DHCR7 gene and two novel mutations
IŞIK E., ONAY H., AKGÜN B., ATİK T., AYKUT A., DURMAZ A., et al.
The European Society of Human Genetics 2017, 27 - 30 May 2017, (Summary Text)
2017
201766. Developments in biotechnology
DÜNDAR M.
European Biotechnology Congress 2017, Dubrovnik, Croatia, 25 - 27 May 2017, pp.7, (Full Text)
2017
201767. Association of the thrombopholia panel with breast and/or ovarian cancer risk
DÜNDAR M.
European Biotechnology Congress 2017, Dubrovnik, Croatia, 25 - 27 May 2017, pp.80, (Full Text)
2017
201768. The Effect of CYP2C19*2 Polymorphism on Clopidogrel Resistance In COPD Patients
DÜNDAR M.
European Biotechnology Congress 2017, Dubrovnik, Croatia, 25 - 27 May 2017, pp.80, (Full Text)
2017
201769. NCAH prevalance with novel CYP21A2 and CYP11B1 mutations in hirsut turkish women
POLAT S., karaburgu s., ÜNLÜHİZARCI K., DÜNDAR M., ÖZKUL Y., ÖZDAMAR KARACA Z. C., et al.
19th European Congress of Endocrinology, 20 - 23 May 2017, (Summary Text)
2017
201770. HEPG2 HÜCRE HATTINDA DZNEP’İN COLONİ-FORMİNG UNİT (CFU), APOPİTOZ, CELL CYCLE VE HÜCRE CANLILIĞI ÜZERİNE ETKİSİ
BAŞKOL G., ÖZEL M., UÇAR Ç., DOĞRU B. N., GÜNEŞ F., GÜVEN İ., et al.
XVII. Klinik Biyokimya Kongresi, Girne, Cyprus (Kktc), 4 - 07 May 2017, vol.15, pp.121, (Full Text)
2017
201771. Assessment of subclinical inflammation in children with mefv mutation and fmf patients in remission.
Gündüz Z., Esen A., SÖZERİ B., PAÇ KISAARSLAN A., KILIÇ H., ŞAHİN N., et al.
9th International Congress of Familial Mediterranean Fever and Systemic Auto Inflamatory Diseases, 4 - 07 May 2017, (Summary Text)
2017
201772. İNSAN KARACIĞER STELLAT HÜCRE HATLARINDA (LX2), ENHANCER OF ZESTE HOMOLOG2 GENİNİN İNHİBİSYONUNUN, FİBROZİS İLE İLİŞKİSİ
BAŞKOL G., KILIÇ E., DÜNDAR M., Özel M., Güven İ.
Türk Klinik Biyokimya Kongresi 04-07 Mayıs 2017 Acapulco Otel Girne, KKTC, Girne, Cyprus (Kktc), 4 - 07 May 2017, pp.77, (Summary Text)
2017
201773. İnsan karaciğer stellat hücre hatlarında (LX2), enhancer of zeste homolog2 geninin inhibisyonunun fibrozis ile ilişkisi.
BAŞKOL G., KILIÇ E., DÜNDAR M., Özel M., Güven İ.
Uluslararası katılımlı XVII. Klinik Biyokimya Kongresi, 4 - 07 May 2017, (Summary Text)
2017
201774. HepG2 hücre hattında DZNE’xxin EMT sinyal yolağında rol oynayan genler üzerine olan etkisi
özel m., uçar ç., doğru b. n., güneş f., güven i., DÜNDAR M., et al.
Uluslararası katılımlı XVII. Klinik Biyokimya Kongresi, 4 - 07 May 2017, (Summary Text)
2017
201775. İnsan karaciğer stellat hücre hatlarında (LX2), enhancer of zeste homolog2 geninin inhibisyonunun, fibrozis ile ilşkisi
BAŞKOL G., KILIÇ E., DÜNDAR M., özel m., güven i.
Uluslararası katılımlı XVII. Klinik Biyokimya Kongresi, 4 - 07 May 2017, (Summary Text)
2017
201776. HEPG2 HÜCRE HATTINDA DZNEP’İN EMT SİNYAL YOLAĞINDA ROL OYNAYAN GENLER ÜZERİNE OLAN ETKİSİ
BAŞKOL G., OZEL M., UÇAR Ç., DOĞRU B. N., GÜNEŞ F., GÜVEN İ., et al.
XVII. Klinik Biyokimya Kongresi, Girne, Cyprus (Kktc), 4 - 07 May 2017, vol.15, pp.170, (Full Text)
2017
201777. Dündar sendromu ve CHST14 gen mutasyonları
DÜNDAR M.
2. Uluslararası Katılımlı Ulusal Nadir Hastalıklar ve Yetim İlaçlar Sempozyumu, İstanbul, Turkey, 23 - 24 March 2017
2017
201778. Smith Lemli Opitz Sendromu’ndan Sorumlu DHCR7 Geni Mutasyon Spektrumu ve İki Yeni Mutasyon
IŞIK E., ONAY H., AKGÜN B., ATİK T., AYKUT A., DURMAZ A., et al.
2. Ege Endokrin Hastalıkları ve Genetik Sempozyumu, Turkey, 23 - 25 February 2017, (Summary Text)
2016
201679. Presentation of EBTNA Scientific Society
DÜNDAR M.
MAGI EUREGIO, Perugia, Italy, 28 October 2016
2016
201680. Prenatal diagnosis of upper extremity malformations with ultrasonography diagnostic features and perinatal outcome
KÜTÜK M. S., altun ö., tutuş ş., DOĞAN M. E., ÖZGÜN M. T., DÜNDAR M.
26th World Congress on Ultrasound in Obstetrics and Gynecology, Roma, 24 - 28 September 2016, vol.48, pp.315, (Summary Text)
2016
201681. CURRENT STATE OF BIOTECHNOLOGY AND EUROPEAN BIOTECHNOLOGY THEMATIC NETWORK ASSOCIATION
DÜNDAR M.
ONE HEALTH-The 1st European Interregional Conference 2016, Bükreş, Romania, 22 - 24 September 2016
2016
201682. Perspectives of biotechnology
Gartland K. M. A., DÜNDAR M., BECCARI T., MAGNI M. V., Gartland J. S.
European Biotechnology Conference, Latvia, 5 - 07 May 2016, vol.231, (Summary Text)
2016
201683. A novel nonsense mutation in GALNS gene in family with MPS4A diagnosed child
GUNES M. C., BAYRAMOV R., BOYUKOGLAN R., DOĞAN M. E., BAYRAMOV K. K., DÜNDAR M.
European Biotechnology Conference, Latvia, 5 - 07 May 2016, vol.231, (Summary Text)
2016
201684. A case of XYY male patient with micropenis
Bayramov R., GUNES M. C., DOĞAN M. E., BOYUKOGLAN R., BAYRAMOV K. K., DÜNDAR M.
European Biotechnology Conference, Latvia, 5 - 07 May 2016, vol.231, (Summary Text)
2016
201685. Fmf Hastalarının Kardeşlerinde Klinik Ve Subklinik Özellikler Ve Mefv Mutasyon Dağılımları
Gündüz Z., Esen A., SÖZERİ B., PAÇ KISAARSLAN A., KILIÇ H., DÜŞÜNSEL R., et al.
3. çocuk Romatoloji Kongresi, Turkey, 21 April - 24 June 2016, (Summary Text)
2016
201686. New applications in medical genetics
DÜNDAR M.
EBTNA-National Academy of Sciences of Belarus-European Biotechnology School, Minsk, Belarus, 30 May - 04 June 2016
2016
201687. Lack of amplification in next generation sequencing? Check for deletions.
Bayramov R., DOĞAN M. E., CERRAH GÜNEŞ M., Korkmaz Bayramov K., ADA Y., SAATÇİ Ç., et al.
European Conference of Human Genetics 2016, Barselona, Spain, 21 - 24 May 2016, vol.24, pp.475-476, (Summary Text)
2016
201688. Evaluatıon Of Laboratory Results In Cystıc Fıbrosıs Patıents
KILIK Z. F., ÖNAL M. G., AKALIN H., COŞKUN N., BADUR MERMER D., BAYRAMOV R., et al.
Medical Genetics and Clinical Applications (with International Participation), Kayseri, Turkey, 11 - 13 February 2016, (Summary Text)
2016
201689. POLYMORPHISMS IN THE METHYLENETETRAHYDROFOLATE REDUCTASE GENE MTHFR ARE ASSOCIATED WITH ACUTE MYELOID LEUKEMIA IN A TURKISH POPULATION
KENANOĞLU S., TAŞCIOĞLU N., AKALIN H., ÜNAL A., SAATÇİ Ç., ÖZKUL Y., et al.
ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016
2016
201690. EVALUATION OF PON1 GENE L55M POLYMORPHISM IN ABORTED FETUSES
BADUR MERMER D., AKALIN H., KILIK Z. F., COŞKUN N., ÇÖMERTMAN A., ÜNAL N., et al.
ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016
2016
201691. EVALUATION OF LABORATORY RESULTS IN CYSTIC FIBROSIS PATIENTS
COŞKUN N., KILIK Z. F., CERRAH GÜNEŞ M., BADUR MERMER D., ÇÖMERTMAN A., BAYRAMOV R., et al.
ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016
2016
201692. DETERMINATION OF DELETIONS WITH LACK OF AMPLIFICATION IN NEXT GENERATION SEQUENCING
BAYRAMOV R., DOĞAN M. E., CERRAH GÜNEŞ M., KORKMAZ BAYRAMOV K., ADA Y., SAATÇİ Ç., et al.
ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016
2016
201693. A CASE OF HABITUAL ABORTION WITH 46 XX T 12 22 Q13 2 Q13 3 TRANSLOCATION
HEJAZİ N., GÜNDÜZ C., SAATÇİ Ç., ÖZKUL Y., DÜNDAR M.
ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016
2016
201694. FREQUENCY OF MVK GENE MUTATIONS IN MEVALONATE KINASE DEFICIENCY
KILIK Z. F., ÖNAL M. G., AKALIN H., COŞKUN N., BADUR MERMER D., BAYRAMOV R., et al.
ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016
2016
201695. A RARE CASE OF 14Q31 DELETION LOSS OF NRXN3 GENE IN PATIENT DIAGNOSED WITH AUTISM SPECTRUM DISORDER
KARADUMAN N., BAYRAMOV R., DOĞAN M. E., CERRAH GÜNEŞ M., HEJAZİ N., BÜYÜKOĞLAN R., et al.
ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016
2016
201696. Evaluatıon Of Laboratory Results In Cystıc Fıbrosıs Patıents
GÖKÇE N., Kılık Z. F., CERRAH GÜNEŞ M., Badur Mermer D., Çömertman A., Bayramov R., et al.
Medical Genetics and Clinical Applications (with International Participation) 11-13 February, 2016, Kayseri, Turkey, 11 - 13 February 2016, vol.1, pp.1, (Full Text)
2012
201297. Alcohol withdrawal investigation of Cytochrome P450 CYP1A2 CYP2D6 CYP2E1 and CYP3A4 expression and gene polymorphism
DÜNDAR M.
Journal of Biotechnology, 1 - 03 November 2012, vol.161, pp.28, (Summary Text)
2015
201598. The levels of NOS in rat testicular tissue damage created by diabtes and pentoxifyline therapy
SÖNMEZ M. F., KILIÇ E., karabulut d., çilenk k. t., DELİGÖNÜL E., DÜNDAR M.
acta physiologica lithuania 26-29 2015 kongre, 26 - 29 August 2015, (Full Text)
2015
201599. The levels of NOS in rat testicular tissue damage created by diabetes and pentoxifylline therapy
mf s., kılç e., karabulut d., çilenk k., deligönül e., DÜNDAR M.
ACTA PHYSIOLOGICA HUNGARICA, 2 - 04 November 2015, vol.215, pp.85, (Summary Text)
2015
2015100. Kromozomal anomalilerin yerel populasyondaki sıklığı
DÜNDAR M.
2. Ulusal Çocuk Genetik Sempozyumu, Turkey, 22 - 24 October 2015, (Summary Text)
2015
2015101. On Beşinci Kromozomun Parsiyel Tetrazomi ve Trizomisi ile Otizm Spektrum Bozuklukları Arasındaki İlişki
DÜNDAR M.
2. Ulusal Çocuk Genetik Sempozyumu, Samsun, Turkey, 22 - 24 October 2015, (Summary Text)
2015
2015102. Evaluaton of In Vitro Genotoxicity of MTA Fillapex
ARSLAN S., ÜSTÜN Y., NAZİFE T., SAĞSEN B., MÜGE Ö., AKBAROVA Y., et al.
47th MEETİNG OF CED-IADR, 15 - 17 October 2015
2015
2015103. Clinical and subclinical features and MEFV mutation distrubiotion in of FMF patient's siblings
GÜNDÜZ Z., SÖZERİ B., ESEN A., PAÇ KISAARSLAN A., KILIÇ H., DÜŞÜNSEL R., et al.
8th International Congress of Familial Mediterrannean Fever and systemic autoinflammatory diseases, Dresden, Germany, 30 September - 03 October 2015, vol.13, pp.63, (Full Text)
2015
2015104. Clinical and subclinical features and MEFV mutation distribution in of FMF patients siblings
GÜNDÜZ Z., SÖZERİ B., esen a., PAÇ KISAARSLAN A., hü k., DÜŞÜNSEL R., et al.
8th International Congress of FamilialMediterranean Fever and SystemicAutoinflammatory Diseases, 30 September - 03 October 2015, (Summary Text)
2015
2015105. A case of SRY positive 46, XX male with speaking disorder
Bayramov R., Gunes M. C., Erdem Y., DÜNDAR M.
European Biotechnology Congress, Bucharest, Romania, 7 - 09 May 2015, vol.208, (Summary Text)
2015
2015106. Investigation of BAP1 and ANAPC7 genes expression in patients with acute myeloid leukemia
Erdem Y., KORKMAZER M. E., Akalın H., Ozdemir M. A., ÖZKUL Y., DÜNDAR M.
European Biotechnology Congress, Bucharest, Romania, 7 - 09 May 2015, vol.208, (Summary Text)
2015
2015107. Innovations in biotechnology
GARTLAND K., BECCARİ T., BRUSCHİ F., DÜNDAR M.
Journal of Biotechnology, 2 - 04 August 2015, vol.208, pp.5, (Summary Text)
2015
2015108. Novel FBN1 gene frameshift mutation in patient with type 1 Chiari malformation
GÜNEŞ M., BAYRAMOV R., ERDEM Y., DÜNDAR M.
Journal of Biotechnology, 2 - 04 August 2015, vol.208, pp.86, (Summary Text)
2015
2015109. Expression of ghrelin and GHS R1a in long term diabetic rat s kidney
DÜNDAR M.
ACTA PHYSIOLOGICA HUNGARICA, 2 - 04 November 2015, vol.215, pp.117, (Summary Text)
2014
2014110. Türk (Kayseri-Türkiye) Popülasyonunun Somatik STR Lokuslarındakş Alel Frekansları
Ada Y., GÖKÇE N., ÖZKUL Y., DÜNDAR M.
1.Uluslararası Adli Biyoloji ve Genetik Kongresi, Ankara, Turkey, 27 - 28 November 2014, vol.1, pp.1, (Full Text)
2014
2014111. Novel technologies and their applications in biotechnology and the life sciences
DÜNDAR M.
Journal of Biotechnology, 1 - 03 September 2014, vol.185, pp.12, (Summary Text)
2014
2014112. Sheehan Sendromunun Etiyolojisinde ACE I/D ve TLR2 Gen Polimorfizmlerinin Araştırılması.
ŞENER E. F., DİRİ H., BAYRAM F., DÜNDAR M.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.1, (Full Text)
2014
2014113. Frajil X Sendrom Şüphesiyle Gelen Hastalarda FMR1 Genindeki CGG Tekrar Sayılarının Ve Metilasyon Durumlarının İncelenmesi
Ada Y., GÖKÇE N., GÜMÜŞ H., DÜNDAR M.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, vol.1, pp.1, (Full Text)
2014
2014114. Triplet pregnancy with partial hydatidiform mole coexisting with two fetuses after ovulation induction and intrauterine insemination
KÜTÜK M. S., DOLANBAY M., AKALIN H., ÖZGÜN M. T., ÖKTEM T., DÜNDAR M., et al.
24th World Congress on Ultrasound in Obstetrics and Gynecology in Barcelona, 14 - 17 September 2014
2014
2014115. Diyabetin sıçan testis dokusunda oluşturduğu hasarda NOS'ların rolü ve pentoksifillinin etkisi
SONMEZ M. F., KILIÇ E., DÜNDAR M., KARABULUT D., CILENK K., DELIGONUL E.
40. Ulusal Fizyoloji Kongresi, Kayseri, Turkey, 2 - 06 September 2014, pp.145, (Full Text)
2013
2013116. A de nova SRCAP Mutation Associated with Floating-Harbor Syndrome.
SUBAŞIOĞLU UZAK A., Murray J. E., Bicknell L. S., Jackson A. P., DÜNDAR M.
European Biotechnology Congress, Slovakia, 1 - 04 July 2013, (Full Text)
2013
2013117. A Study df CDKL5 Gene Mutations in Pediatric Patients with Persistent Seizure, Autistic Disorder and Seizure in Addition to Autistic Disorder During Infancy and Early Childhood
SUBAŞIOĞLU UZAK A., DÜNDAR M., Erdoğan M.
European Biotechnology Congress, Slovakia, 1 - 04 July 2013, (Full Text)
2013
2013118. Analysing the role of MDM2 SNP309 in patients with glioblastoma multiforme
Akbarova Y., DÜNDAR M., Akalin H., ASLAN D., CANÖZ Ö., Ada Y., et al.
European Biotechnology Congress, Bratislava, Slovakia, 16 - 18 May 2013, vol.24, no.1, (Summary Text)
2013
2013119. Polymorphisms of TNF-alpha and coagulation genes in the etiopathogenesis of Sheehan's Syndrome
Tascioglu N., ŞENER E. F., Onal M. G., Diri H., BAYRAM F., DÜNDAR M.
European Biotechnology Congress, Bratislava, Slovakia, 16 - 18 May 2013, vol.24, (Summary Text)
2013
2013120. The effects of streptozotocin-induced diabetes on ghrelin expression in rat testis.
SONMEZ M. F., AKKUŞ D., KILIÇ E., DÜNDAR M., ŞAKALAR Ç., GÜNDÜZ Y., et al.
49.Ulusal Diyabet Kongresi, Antalya, Turkey, 17 - 21 April 2013, (Full Text)
2012
2012121. AML Hastalarında MDM2 SNP309 Polimorfizminin Değerlendirilmesi
AKALIN H., ÖNAL M. G., AKBAROVA Y., SAR Ş., ÜNAL E., KAYNAR L., et al.
10. ULUSAL TIBBİ GENETİK KONGRESİ, Bursa, Turkey, 13 October - 23 December 2012, (Summary Text)
2012
2012122. Ailevi Akdeniz Ateşi nde MEFV Geninde M680V Mutasyonunun Tanımlanması
ÖZDEMİR S. Y., ŞENER E. F., BOZ M., KORKMAZ K., DEĞİRMENCİ B., SAATÇİ Ç., et al.
10. Ulusal Tıbbi Genetik Kongresi, Turkey, 19 - 23 December 2012
2010
2010123. Kolorektal kanserlerde K-Ras mutasyon analizlerinin değerlendirilmesi
ÖNAL M. G., AKALIN H., ADA Y., POLAT İNANÇ M., ÖZKAN M., ÖZKUL Y., et al.
10. ULUSAL TIBBİ GENETİK KONGRESİ, Bursa, Turkey, 19 December 2010 - 23 December 2012, (Summary Text)
2012
2012124. Epidermolysis Bullosa Dystrophica’lı Bir Olgu Sunumu.
Özdemir S. Y., ŞENER E. F., DÜNDAR M.
10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 1 - 04 December 2012, (Full Text)
2012
2012125. Türk Toplumunda MEFV Geninde M694K Mutasyonunun Tanımlanması.
ŞENER E. F., Korkmaz K., DÜNDAR M., Özdemir S. Y., ÖZKUL Y.
10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 1 - 04 December 2012, (Full Text)
2012
2012126. Fenilketonüri Hastalarında Fenilalanin Hidroksilaz Geninde Görülen Yaygın Mutasyonların Taranması
SUBAŞIOĞLU UZAK A., DÜNDAR M.
10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 1 - 04 December 2012, (Full Text)
2012
2012127. McKusick-Kaufman Sendromlu Bir Olgu Sunumu.
Özdemir S. Y., ŞENER E. F., ÖZKUL Y., DÜNDAR M.
10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 1 - 04 December 2012, (Full Text)
2012
2012128. Ailesel Nonsendromik İşitme Kaybının Genetik Temelinin Araştırılması
DÜNDAR M., SUBAŞIOĞLU UZAK A.
10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 1 - 04 December 2012, (Full Text)
2012
2012129. A Novel FGFR3 Mutation in Hypochondroplasia
SUBAŞIOĞLU UZAK A., DÜNDAR M.
10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 1 - 04 December 2012, (Full Text)
2012
2012130. MEFV Geninde Yeni Bir Mutasyonun Tanımlanması: R717H.
Özdemir S. Y., ŞENER E. F., Korkmaz K., DÜNDAR M., ÖZKUL Y.
10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 1 - 04 December 2012, (Full Text)
2012
2012131. Genotoxic effects of some antituberculosis drug and mixtures in rats
ARSLAN K., KANBUR M., TAŞÇIOĞLU N., KARABACAK M., SARICA SOYER Z., DÜNDAR M., et al.
8. Uluslararası Katılımlı Türk Toksikoloji Derneği Kongresi, Turkey, 15 - 18 November 2012, (Summary Text)
2012
2012132. Genotoxic efects of some antituberculosis drug and mixturesın rats
ARSLAN K., KANBUR M., TAŞCIOĞLU N., KARABACAK M., SOYER SARICA Z., DÜNDAR M., et al.
8.Uluslararası Katılımlı Türk Toksikoloji Derneği Kongresi, Turkey, 15 - 18 November 2012
2012
2012133. The Investigation of Relation Between Alpine Skiing Success and ACE, NOS3, HBB Gene Polymorphisms and Expression Levels
POLAT M., ÇOKSEVİM B., TAHERİ S., DÜNDAR M.
XXXII WORLD CONGRESS of SPORTS MEDICINE, Sports Medicine, the challenge for global health: Quo Vadis?, Roma, Italy, 27 - 30 September 2012, no.59, pp.54, (Full Text)
2012
2012134. O6-metil guanin DNA-metil transferaz promoter metilasyonu olan glioblastomalı olgularda CpG 1, CpG 2, CpG 3 ve CpG 4 metilasyonunun tedavi cevabına etkisi
ASLAN D., YILDIZ O. G., CANÖZ Ö., DÜNDAR M., GÜNDOĞ M., SOYUER S.
10. Ulusal Radyasyon Onkolojisi Kongresi, Turkey, 19 - 23 April 2012, (Summary Text)
2011
2011135. The increasing importance of Medical Genetics in Turkey
POLAT S., Karabulut S. Y., BAHADIR O., DÜNDAR M.
European Biotechnology Congress 2011, İstanbul, Turkey, 28 October - 01 November 2011, vol.22, pp.90, (Summary Text)
2011
2011136. Prenatally detected de novo 46, XX, t(2121)(p12p12) at chorionic villus sampling
DOĞAN M. E., Çolak F., SUBAŞIOĞLU A., Erdoğan M., ÖZDEMİR S. Y., Balta B., et al.
European Biotechnology Congress 2011, İstanbul, Turkey, 28 September - 01 October 2011, vol.22, pp.107, (Summary Text)
2011
2011137. A case of 46, XX, t(217)(q37.1q25) with recurrent miscarriage
ÇOLAK F., DOĞAN M. E., SUBAŞIOĞLU A., ERDOĞAN M., ÖZDEMİR S. Y., BALTA B., et al.
European Biotechnology Congress 2011, İstanbul, Turkey, 28 September - 01 October 2011, vol.22, pp.107, (Summary Text)
2011
2011138. A case with 49, XXXXY syndrome: rare chromosomal aneuploidies
ERDOĞAN M., SUBAŞIOĞLU A., ÖZDEMİR S. Y., BAHADIR O., ÇOLAK F., DOĞAN M. E., et al.
European Biotechnology Congress 2011, İstanbul, Turkey, 28 September - 01 October 2011, vol.22, pp.106, (Summary Text)
2011
2011139. Determination of human interferon gamma in the transgenic mice milk by modified Kynurenine bioassay test
BAĞIŞ H., AKTOPRAKLIGİL D., GÜNEŞ Ç., AKKOÇ T., ÇETİNKAYA G., KANKAVİ O., et al.
European Biotechnology Congress, 28 September - 01 October 2011, vol.22, pp.53, (Summary Text)
2011
2011140. Association of PAI-1 and TNF-? Gene Polymorphisms In Familial Mediterranean Fever (FMF) Patients.
DÜNDAR M., Kiraz A., Balta B., EMİROĞULLARI E. F., YURCİ M. A., BAŞKOL M.
9th Balkan Congress of Medical Genetics, Romania, 1 - 04 September 2011, (Full Text)
2010
2010141. Investigation of PAI-1 4G/5G Polymorphism In Turkish FMF Patients.
ŞENER E. F., TAHERİ S., POLAT S., ZARARSIZ G., SAATÇİ Ç., ÖZKUL Y., et al.
IX. Ulusal Tıbbi Genetik Kongresi., İstanbul, Turkey, 1 - 04 December 2010, (Full Text)
2010
2010142. Seckel syndrome: acconpanied by semilobar holoprosencephaly.
Çoban D., Akın M. A., Kara A., Doğanay S., KURTOĞLU S., Uzak A., et al.
9th National Genetics Congress of Turkish Medical Genetics Society with International Participation, Turkey, 1 - 04 December 2010, pp.96, (Full Text)
2010
2010143. MEFV Gene Mutations Screening In Turkish Population.
DÜNDAR M., POLAT S., ŞENER E. F., TAHERİ S., Kiraz A., SAATÇİ Ç., et al.
IX. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 1 - 04 December 2010, (Full Text)
2010
2010144. Survivin (BIRC5) Gen Ekspresyonunun Minimal Rezidüel Hastalık (MRH) Takibindeki Önemi
ÖZKUL Y., ŞIVGIN H., PEHLİVAN M., ŞIVGIN S., ÖNAL M. G., KAYNAR L., et al.
36. ULUSAL HEMATOLOJİ KONGRESİ, Antalya, Turkey, 3 - 07 October 2010, (Summary Text)
2010
2010145. Association Between Polymorphisms of Interleukins and Pathogenesis of Pituiary Deficiency caused by Head Trauma
DÜNDAR M., POLAT S., ŞENER E. F., TAHERİ S., KİRAZ A., SAATÇİ Ç., et al.
Clinical Genetics, 5 - 07 May 2010
2009
2009146. HİPOTİROİDİ BİRLİKTELİĞİNİN GÖZLENDİĞİ RUBİNSTEİN-TAYBİ SENDROMLU İKİZ OLGULAR
Kiraz A., ÖZDEMİR S. Y., TUBAŞ F., GÜNEŞ T., KURTOĞLU S., DÜNDAR M.
ENDOKRİN HASTALIKLAR VE GENETİK SEMPOZYUMU, Turkey, 8 - 10 October 2009, (Summary Text)
2009
2009147. Effects of seperate or simultaneous injection of two different genes Enhanced Green Fluorescence Protein Gene Human Gama Interferon Gene on transgenic mice recovery
ARSLAN K., BAĞIŞ H., DÜNDAR M.
Mediterranean Medical Genetics Meeting, 28 June - 01 July 2009, pp.26
2009
2009148. Rubinstein Taybi Syndrome in two siblings
DÜNDAR M., SUBAŞIOĞLU UZAK A., ARSLAN K., KARABULUT Y., ERDOĞAN M., ASLIHAN K.
Mediterranean Medical Genetics Meeting, 28 June - 01 July 2009, pp.48
2009
2009149. Coffin Lowry Syndrome in two siblings with a new findings
DÜNDAR M., ÇAĞLAYAN A. O., ARSLAN K.
Mediterranean Medical Genetics Meeting, 28 June - 01 July 2009, pp.47
2009
2009150. Unusual Dysmorphic Features in two siblings with Riley Day Syndrome
DÜNDAR M., SUBAŞIOĞLU UZAK A., ARSLAN K., KARABULUT Y.
Mediterranean Medical Genetics meeting, 28 June - 01 July 2009, pp.48
2009
2009151. A case of Hallermann Streiff Syndrome with an unusual MR findings
DÜNDAR M., KARABULUT Y., SUBAŞIOĞLU UZAk A., ARSLAN K., ERDOĞAN M., DÜNDAR G., et al.
Medditerranean Medical Genetics Meeting, 28 June - 01 July 2009, pp.48
2009
2009152. The analyze of azospermia factor and cystic fibrozis gene mutations in male infertile individuals with congenital unilateral or bilateral vas deferens agenesis.
ÖNAL M. G., KARABULUT Y., EKMEKÇİOĞLU O., SAATÇİ Ç., ÖZKUL Y., DÜNDAR M.
8th Balkan Meeting on Human Genetics, 14 - 17 May 2009, (Summary Text)
2009
2009153. Partial trisomy of 14q resulting from balanced maternal translocation
UZAK A., KARABULUT Y., AKALIN H., ARSLAN K., TAŞDEMİR Ş., KİRAZ A., et al.
8th Balcan Meeting on Human genetics, 14 - 17 May 2009, pp.101, (Summary Text)
2008
2008154. Transgenik fare eldesi çalışmalarında iki farklı gen konstraktının enjeksiyonunun doğum oranları ve transgenik fare yüzdeleri üzerine etkisi
BAĞIŞ H., AKTOPRAKLIGİL D., GÜNEŞ Ç., AKKOÇ T., ARSLAN K., ÇETİNKAYA G., et al.
III. Veteriner Jinekoloji Kongresi Uluslararası Katılımlı, Turkey, 23 - 26 October 2008
2008
2008155. Application of EGFP as a reporter gene for selection of transgenic mouse embryos
BAĞIŞ H., ARSLAN K., AKTOPRAKLIGİL D., ÇETİNKAYA G., DÜNDAR M., ARAT S.
National Histology And Embryology Congress With International Contribution, Turkey, 20 - 23 May 2008, pp.109
2008
2008156. Hematolojik Malignensilere Moleküler Yaklaşım.
ÖNAL M. G., AKALIN H., SAATÇİ Ç., ESER B., ALTUNTAŞ F., ÖZKUL Y., et al.
8. ULUSAL TIBBİ GENETİK KONGRESİ, Çanakkale, Turkey, 8 - 09 May 2008, (Summary Text)
2008
2008157. Spinal Musküler Atrofi Ön Tanısı İle Gelen Hastaların Moleküler Analiz Sonuçları
TAHERİ S., EMİROĞULLARI E. F., SAATÇİ Ç., ÖZKUL Y., DÜNDAR M.
VIII. Ulusal Tıbbi Genetik Kongresi, 6 - 09 May 2008
2008
2008158. Kronik Miyeloid Lösemi’li Hastaların Tanı Ve Takibinde RT-PCR Kantitatif PCR Ve FISH Yöntemlerinin Analizi.
AKALIN H., ÖNAL M. G., TAŞDEMİR Ş., SAATÇİ Ç., ALTUNTAŞ F., KAYNAR L., et al.
8. ULUSAL TIBBİ GENETİK KONGRESİ, Çanakkale, Turkey, 6 - 09 May 2008, (Summary Text)
2008
2008159. Tromboz Eğilimi Olan Hastalarda Faktör V (G1691A), Protrombin (G20210A) ve MTHFR (C677T) Gen Mutasyonlarının Sıklığı.
Taşdemir Ş., ŞENER E. F., ÖZKUL Y., DÜNDAR M., SAATÇİ Ç.
VIII. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 1 - 04 May 2008, (Full Text)
2008
2008160. Ailesel Akdeniz Ateşi Olgularında Mutasyon Taranması.
ŞENER E. F., TAHERİ S., SAATÇİ Ç., ÖZKUL Y., DÜNDAR M.
VIII. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 1 - 04 May 2008, (Full Text)
2006
2006161. Kronik Miyeloid Lösemili Hastaların Takibinde RT_PCR Kantitatif PCR ve FISH Yöntemlerinin Analizi
AKALIN H., ŞAHİN A., ALTUNTAŞ F., ÖNAL M. G., TAŞDEMİR Ş., SAATÇİ Ç., et al.
32. ULUSAL HEMATOLOJİ KONGRESİ, Antalya, Turkey, 8 - 12 November 2006, (Summary Text)
2006
2006162. Tıbbi Genetik Anabilim Dalı nda Kistik Fibrosis Hastalarının Mutasyon Analiz Sonuçları
TAHERİ S., SAATÇİ Ç., ERÖZ R., ÖZKUL Y., DÜNDAR M.
VII. Ulusal Prenatal Tanı Ve Tıbbi Genetik Kongresi. Kayseri, Turkey, 17 - 20 May 2006
2006
2006163. Screening Gene Mutation In FMF Disease
ŞIVGIN H., TAHERİ S., SAATÇİ Ç., ÖZKUL Y., DÜNDAR M.
VII. Ulusal Prenatal Tanı Ve Tıbbi Genetik Kongresi, Kayseri, Turkey, 17 - 20 May 2006, pp.93, (Full Text)
2006
2006164. Tıbbi Genetik Anabilim Dalı nda Duchenne Becker Muscular Distrofi Hastalarında Polimeraz Zincir Reaksiyonu ile Delesyon Analizi Sonuçları
TAHERİ S., SAATÇİ Ç., ERÖZ R., ÖZKUL Y., DÜNDAR M.
VII. Ulusal Prenatal Tanı Ve Tıbbi Genetik Kongresi. Kayseri, Turkey, 17 - 20 May 2006
2006
2006165. Spinal Müsküler Atrofi Ön Tanısıyla Gelen Hastalarda Möleküler Analiz Sonuçları
TAHERİ S., SAATÇİ Ç., ERÖZ R., ÖZKUL Y., DÜNDAR M.
VII. Ulusal Prenatal Tanı Ve Tıbbi Genetik Kongresi, Kayseri, Turkey, 17 - 20 May 2006, pp.94, (Summary Text)
2006
2006166. Duchenne/Becker Muscular Distrofi Hastalarında Polimeraz Zincir Reaksiyonu ile Delesyon Analizi Sonuçları
TAHERİ S., SAATÇİ Ç., ERÖZ R., ÖZKUL Y., DÜNDAR M.
VII. Ulusal Prenatal Tanı Ve Tıbbi Genetik Kongresi, Kayseri, Turkey, 17 - 20 May 2006, pp.72, (Full Text)
2006
2006167. Kistik Fibrosis Hastalarının Mutasyon Analiz Sonuçları
SAATÇİ Ç., TAHERİ S., ÖZKUL Y., DÜNDAR M., ERÖZ R.
VII. Ulusal Prenatal Tanı Ve Tıbbi Genetik Kongresİ, Kayseri, Turkey, 20 May 2006, pp.90, (Full Text)
2006
2006168. Fetusta prenatal olarak tesbit edilmiş t 7 15 q11 23 q26 3
SAATÇİ Ç., ÇAĞLAYAN A. O., ARSLAN K., ÖZKUL Y., TAŞCIOĞLU N., DÜNDAR M.
VII.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Turkey, 17 - 20 May 2006, pp.135
2006
2006169. Down syndrome like apperance with a novel denovo translocation t 6 21 p21 13
ÇAĞLAYAN A. O., SAATÇİ Ç., ARSLAN K., ÖZKUL Y., VURAL Ö., DÜNDAR M.
VII.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Turkey, 17 - 20 May 2006, pp.163
2006
2006170. A novel denovo translocation t 4 7 p 15 p22
ÇAĞLAYAN A. O., SAATÇİ Ç., ARSLAN K., ÖZKUL Y., VURAL Ö., DÜNDAR M.
VII.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Turkey, 17 - 20 May 2006, pp.163
2004
2004171. Maraş Otu Kullanan Kişilerde P15 ve VHL(Von Hippel-Lindau)Geni Metilasyonunun Araştırılması
TEKİN S., ÖZKUL Y., SAATÇİ Ç., DÜNDAR M.
VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.34, (Full Text)
2004
2004172. Maraş otunun P16 Geni DNA Metilasyonuna Etkisinin İncelenmesi
SAATÇİ Ç., ÖZKUL Y., TEKİN S., DÜNDAR M.
VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.35, (Full Text)
2003
2003173. Kronik miyoloid lösemi Sitogenetik ve moleküler yaklaşımlar
AKALIN H., ÖZKUL Y., DÜNDAR M., ÇETİN M., TAHERİ S.
XXX.Ulusal Hematoloji Kongresi, Turkey, 10 - 14 October 2003, (Summary Text)
2003
2003174. The effect of Maras powder on DNA methylation and micronucleus in blood lymphocyte and buccal tissues
ÖZKUL Y., SAATÇİ Ç., TAHERİ S., TURHAN A. B., DÜNDAR M.
European Human Genetics Conference, 4 - 06 September 2003
2003
2003175. Duchhene/Becker Musküler Distrofi Hastalarında Polimeraz Zincir Reaksiyonu İle Delesyon Analizi
TAHERİ S., ŞENER E. F., SAATÇİ Ç., ÖZKUL Y., DÜNDAR M.
VIII. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 1 - 04 May 2003, (Full Text)
2003
2003176. The Effect of Turkish propolis on Micronucleus and Mitotic index in Peripheral Blood Lymphocytes
SİLİCİ S., ÖZKUL Y., Eroğlu E., DÜNDAR M.
2. Internationalen Deutschen Kongress für Bienenprodukte und Apitherapie, Passau, Germany, 28 - 30 March 2003, pp.23, (Summary Text)
2002
2002177. Kistik Fibrozis Mutasyon Dağılımı
DÜNDAR M., TEKİN S., ÖZKUL Y.
V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.8, (Full Text)
2002
2002178. Orta Zincir Acil –KoA Dehidrogenaz Enzim Eksikliğinin Türk Toplumundaki İnsidansı
TEKİN S., DÜNDAR M., ÖZKUL Y., AKALIN H.
V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.27, (Full Text)
2002
2002179. Maraş Otunun DNA Metilasyonu ve Mikronükleus Üzerine Olan Etkisinin Araştırılması
SAATÇİ Ç., ÖZKUL Y., TEKİN S., TURHAN A., DÜNDAR M.
V. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.33, (Full Text)
2002
2002180. Kronik Miyoloid Lösemide Sitogenetik ve Moleküler Yaklaşımlar
AKALIN H., ÖZKUL Y., DÜNDAR M., ÇETİN M., TEKİN S.
V. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.8, (Full Text)
2002
2002181. Adenomatous Polipozis Coli’de 3920TA(13307K) Mutasyon Analizleri
DÜNDAR M., ÖZKUL Y., ÖZBAKIR Ö., BAŞKOL M., TEKİN S., KARACA H.
V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.40, (Full Text)
2002
2002182. Apoliprotein –E Lokus Allel Profili
DÜNDAR M., ÖZKUL Y., ÖZTOPRAK S., BAŞKOL M., ÖZBAKIR Ö., TEKİN S.
V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.23, (Full Text)
2002
2002183. 46,XX,t(1;16)(p22;p13) ve 46,XY,t(1;16)(q24;q24) Kromozom Anomalili Bir Çiftin Aile Araştırması
ÖZKUL Y., DÜNDAR M., SAATÇİ Ç., AKALIN H., TEKİN S.
V. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.14, (Full Text)
1998
1998184. Klinefelter sendromu : bir 48XXYY variyantı vakası
Kendirci M., Dündar M., Özkul Y., KURTOĞLU S., Gündüz Z.
3. Ulusal Pediatrik Endokrinoloji Kongresi, Adana, Turkey, 1 - 04 October 1998, pp.306, (Full Text)
1998
1998185. Erciyes Üniversitesi Prenatal Tanı Ünitesinin sitogenetik amaçlı invaziv girişimlerinde iki yılın değerlendirilmesi
BAŞBUĞ M., TAYYAR M., DÜNDAR M., Oğur G., ALTUNTAŞ H.
Perinatoloji Kongresi, Antalya, Turkey, 10 - 13 May 1998, (Full Text)
1997
1997186. A case of Weismann-Netter and Stuhl ( Toxopachyosteosis ) syndrome with communicant hydrocephalusi arachnoid cyst and corpus callosum abnormalities.
KURTOĞLU S., Dündar M., Kumandaş S., Caksen H., Üzüm K., Durak A. C., et al.
5th Joint Meeting ESPE/LWPES Pediatric Endocrinology 1997, Sweden, 1 - 04 June 1997, vol.48, pp.66, (Full Text)
Books
2024
20241. FMF Hastalığında Genetik Danışmanlık
Kılıç E., Akalın H., Dündar M.
in: Sorularla FMF, Doç.Dr.Soner Şenel, Editor, EMA Tıp Kitapevi, İstanbul, pp.69-74, 2024
2024
20242. Nadir Hastalıklarda Yeni Nesil Dizilemenin Klinik Kullanım Alanları
Akalın H., Özçelik F., Dündar M.
in: Yeni Nesil Dizileme ve Klinikteki Uygulamaları, Prof.Dr.Ahmet Okay Çağlayan,Dr. Zafer YÜKSEL, Editor, Güneş Tıp Kitabevi, İstanbul, pp.13-23, 2024
2023
20233. CINSIYET GELISIM BOZUKLUKLARI
Akalın H., Dündar M.
Türk Üroloji Derneği, İstanbul, 2023
2023
20234. Konjenital Anomalilerde Kök Hücre ve Transamniyotik Kök Hücre Tedavisi
Kiraz A., Aydın M. M., Dündar M.
in: ÇOCUK NÖROLOJISI PRATIĞINDE KÖK HÜCRE MULTIDISIPLINER YAKLAŞIM, MEHMET CANPOLAT, Editor, Akademisyen Yayınevi Kitabevi, Ankara, pp.361-370, 2023
2023
20235. Oncogenic Genomic Changes in Cancer
Yıldırım A., Akalın H., Dündar M.
in: Oncology: Genomics, Precision Medicine and Therapeutic Targets, Hardeep Singh Tuli,Mükerrem Betül Yerer Aycan, Editor, Springer, London/Berlin , London, pp.25-38, 2023
2023
20236. Gonadal Gelisim, Cinsiyet Farklılasma Bozuklugunun Moleküler Temeli
Akalın H., Dündar M.
in: Cinsiyet Gelisim Bozuklukları , Nihal Hatipoğ,Numan Baydilli,Esra Demirci,Ateş Kadıoğlu, Editor, Türk Üroloji Derneği, İstanbul, pp.127-134, 2023
2022
20227. MDR1 Geni ile Ankilozan Spondilit Arasındaki İlişkinin İncelenmesi: Olgu Kontrol Araştırması
Dündar M.
in: Türkiye Klinikleri tıp bilimleri dergisi, Prof. Dr. Hikmet AKGÜL,Prof. Dr. Ahmet AKGÜL, Editor, Türkiye Klinikleri Yayınevi, Ankara, pp.213-220, 2022
2022
20228. MTA Fillapex’in İn Vitro Genotoksisitesinin Değerlendirilmesinin Sistematik İncelemesi
Dündar M.
in: Türkiye Klinikleri DİŞ HEKİMLİĞİ BİLİMLERİ, Prof. Dr. Orhan GÜVEN, Editor, Türkiye Klinikleri Yayınevi, Ankara, pp.372-380, 2022
2022
20229. Türk Dismorfoloji Tarihçesi ve Anadolu'da Tanımlanan Sendromlar
Dündar M.
in: Türkiye Klinikleri TIBBİ GENETİK ÖZEL KONULAR, Prof. Dr. C. Nur SEMERCİ GÜNDÜZ, Editor, Türkiye Klinikleri Yayınevi, Ankara, pp.5-14, 2022
2021
202110. Biotechnological Therapies for Rare Diseases
Özçelik F., Yıldırım A., Aynekin B., Alzaıdı Z., Dündar M.
in: Türkiye klinikleri Tıbbi Genetik, Özbek U., Editor, Türkiye Klinikleri Yayınevi, Ankara, pp.78-90, 2021
2018
201811. Tıbbi Genetiğe Genel Bakış ve Konjenital Göğüs Duvarı Deformitelerinde Genetik
CERRAH GÜNEŞ M., GÖKÇE N., DÜNDAR M.
in: Göğüs Duvarı Deformiteleri, Prof.Dr. Mehmet BİLGİN Prof.Dr. Berkant ÖZPOLAT, Editor, 2018 Ankara Nobel Tıp Kitabevleri Ltd. Şti, Ankara, pp.5-20, 2018
2018
201812. Tıbbi Genetiğe Genel Bakışve Konjenital Göğüs Duvarı Deformitelerinde Genetik
DÜNDAR M., COŞKUN N., CERRAH M.
in: Göğüs Duvarı Deformiteleri, Mehmet Bilgin, Berkant Özpolat, Editor, Ankara Nobel Tıp Kitabevleri, Ankara, pp.5-20, 2018
2018
201813. Kök hücre ve kök hücre tedavisi
YAPIŞLAR H., DÜNDAR M., Bayramov R., Bayramov Korkmaz K.
in: Güncel biyoteknoloji ve uygulamaları, Munis Dündar, Haydar Bağış, Editor, Mgrup Matbaacılık, Kayseri, pp.81-95, 2018
2017
201714. Güncel Biyoteknoloji ve Uygulamaları
BAĞIŞ H., DÜNDAR M., ARAT S., TALAS OĞRAŞ T., KESMEN Z., SAYİTOĞLIU M., et al.
MGRUP MATBAACILIK KAYSERİ, Kayseri, 2017
2017
201715. Biyoteknolojik Terimler
DÜNDAR M., BAĞIŞ H., GÖKÇE N.
in: GÜNCEL BİYOTEKNOLOJİ VE UYGULAMALARI, Prof.Dr. MUNİS DÜNDAR Prof.Dr. HAYDAR BAĞIŞ, Editor, Erciyes Üniversitesi Yayınları, Kayseri, pp.609-625, 2017
2017
201716. YENİ NESİL DİZİLEME TEKNOLOJİLERİ
DOĞAN M. E., BAYRAMOV R., DÜNDAR M.
in: GÜNCEL BİYOTEKNOLOJİ VE UYGULAMALARI, Dündar M., Bağış H., Editor, Erciyes Üniversitesi Yayınları, Kayseri, pp.371-394, 2017
2017
201717. Biyoteknolojiye Genel Bakış ve Tarihi Süreç
DÜNDAR M., ŞENER E. F.
in: Güncel Biyoteknoloji Uygulamaları, Dündar M, Bağış H, Editor, Erciyes Üniversitesi, Kayseri, pp.1-23, 2017
2017
201718. Biyoteknolojik Terimler
DÜNDAR M., BAĞIŞ H., gökçe N.
in: ”Güncel Biyoteknolojoji ve Uygulamaları”, Dündar M, Bağış Haydar, Editor, MGRUP Matbaacılık, Kayseri, pp.609-626, 2017
2017
201719. Biyoteknolojik Terimler
DÜNDAR M., BAĞIŞ H., GÖKÇE N.
in: Güncel Biyoteknoloji Ve Uygulamaları, Dündar Munis, Bağış Haydar, Editor, Erciyes Üniversitesi, Kayseri, pp.609-625, 2017
2016
201620. Tıbbi Genetik ve Klinik Uygulamaları-Cilt 1
DÜNDAR M.
Mgrup Matbaacılık Kayseri, Kayseri, 2016
2016
201621. Entellektüel Yetersizlik - Anlıksal Yetiyitimi
DÜNDAR M.
in: Tıbbi Genetik ve Klinik Uygulamaları-Cilt 2, Dündar M., Editor, Mgrup Matbaacılık Kayseri, Kayseri, pp.821-832, 2016
2016
201622. Nöromusküler Hastalıklar ve Genetiği
DÜNDAR M.
in: Tıbbi Genetik ve Klinik Uygulamaları-Cilt 2, Dündar M., Editor, Mgrup Matbaacılık Kayseri, Kayseri, pp.839-873, 2016
2016
201623. Bireysel Tıp
DÜNDAR M.
in: Tıbbi Genetik ve Klinik Uygulamaları-Cilt 2, Dündar M., Editor, Mgrup Matbaacılık Kayseri, Kayseri, pp.1147-1160, 2016
2016
201624. Tarihçe
DÜNDAR M.
in: Tıbbi Genetik ve Klinik Uygulamaları-Cilt 1, Dündar M., Editor, Mgrup Matbaacılık Kayseri, Kayseri, pp.1-24, 2016
2016
201625. Genetik Hastalıklarda Antropometrik Ölçümler ve Yorumlanması
DÜNDAR M.
in: Tıbbi Genetik ve Klinik Uygulamaları-Cilt 2, Dündar M., Editor, Mgrup Matbaacılık Kayseri, Kayseri, pp.1213-1221, 2016
2016
201626. Genetik Hastalıklarda Antropometrik Ölçümler ve Yorumlanması
GÜL Ü., HATİPOĞLU N., MAZICIOĞLU M. M., KURTOĞLU S., DÜNDAR M.
in: Tıbbi Genetik ve Klinik Uygulamaları, Muhnis Dündar, Editor, MGRUP MATBAACILIK, Kayseri, pp.1213-1222, 2016
2016
201627. Tarihçe
DÜNDAR M.
in: Tıbbi Genetik Ve Klinik Uygulamaları, Munis Dündar, Editor, Mgrup Matbaacılık, Kayseri, pp.1-22, 2016
2016
201628. Bireysel Tıp
DÜNDAR M., DOĞAN M. E.
in: Tıbbi Genetik ve Klinik Uygulamaları, munis dündar, Editor, mgrup matbaacılık, Kayseri, pp.1147-1162, 2016
2016
201629. Genetik Hastalıklarda Antropometrik Ölçümler ve Yorumlaması
GÜL Ü., HATİPOĞLU N., MAZICIOĞLU M. M., KURTOĞLU S., DÜNDAR M.
in: Tıbbi Genetik ve Klinik Uygulamaları, munis dündar, Editor, mgrup matbaacılık, Kayseri, pp.1213-1222, 2016
2016
201630. Genetik hastalıklarda antropometrik ölçümler ve yorumlanması
Gül Ü., Hatipoğlu N., Mazıcıoğlu M. M., Kurtoğlu S., Dündar M.
in: Tıbbi genetik ve klinik uygulamaları, Munis Dündar, Editor, Mgrup Matbaacılık, Kayseri, pp.1213-1222, 2016
2016
201631. Entelektüel Yetersizlik - Anlıksal Yetiyitimi
KAÇAR BAYRAM A., BÜYÜKOĞLAN R., PER H., DÜNDAR M.
in: Tıbbi Genetiik ve Klinik Uygulamaları, Dündar Munis, Editor, Mgrup Matbaacılık, Kayseri, pp.821-832, 2016
2016
201632. Nöromüsküler Hastalıklar ve Genetiği
DÜNDAR M., düzcan f., cerrah güneş m.
in: Tıbbi Genetik ve Klinik Uygulamaları, munis dündar, Editor, mgrup matbaacılık, Kayseri, pp.839-879, 2016
2015
201536. HISTORY OF BIOTECHNOLOGY
DÜNDAR M., ÖNAL M. G., Erdem Y.
in: CURRENT APPLİCATİONS OF BİOTECHNOLOGY, Dündar M, Editor, Mgrup, Kayseri, pp.1-8, 2015
2015
201537. Chapter 1- History of Biotechnology
DÜNDAR M., ÖNAL M., ERDEM Y.
in: Current Applications of Biotechnology, Dündar Munis, Bruschi Fabrizio, Gartland Kevan MA, Magni Mariapia Viola, Gahan Peter, Deeni Yusuf, Editor, Erciyes University, Kayseri, pp.1-8, 2015
2012
201238. Overview of the Healthcare System in Turkey
DÜNDAR M., ÖZDEMİR S. Y.
in: Advances in Predictive, Preventive and Personalised Medicine, Golubnitschaja O., Editor, Epma/Springer, Brüksel, pp.167-189, 2012
2011
201139. Dismorfik Çocuk ve Endokrin Sorunlar
DÜNDAR M.
in: Yenidoğan Dönemi Endokrin Hastalıkları, Kurtoğlu S., Editor, Nobel Tıp Kitapevleri, İstanbul, pp.129-141, 2011
2010
201040. Modern Biyoteknoloji Ve Uygulamalar
DÜNDAR M.
Erciyes Üniversitesi Yayınları, Kayseri, 2010
2010
201041. 1.Kök Hücre ve Kök Hücre Tedavisi
DÜNDAR M.
in: Modern Biyoteknoloji ve Uygulamaları, Dündar M.,Bağış H., Editor, Erciyes Üniversitesi Yayınları, Kayseri, pp.91-111, 2010
2010
201042. Biyoteknolojiye Genel Bakış ve Tarihi Süreç
DÜNDAR M.
in: Modern Biyoteknoloji ve Uygulamaları, Dündar M.,Bağış H., Editor, Erciyes Üniversitesi Yayınları, Kayseri, pp.7-14, 2010
2008
200843. Lomber Dejeneratif Disk Hastalığında Genetik Etiopatogenez ve Güncel Genetik Tedavi Yöntemleri
DÜNDAR M.
in: Lomber Dejeneratif Disk Hastalığı, Koç RK., Editor, Türk Nöroşirürji Derneği, Ankara, pp.16-29, 2008
2008
200844. Hastalıkların Moleküler Temeli
DÜNDAR M.
in: Andreoli and Carpenter’s Cecil Essentials of Medicine 7th Edition, Editor, Thomas E Andreoli, Çeviri, Bölüm 1, Hastalıkların Moleküler Temeli, 3-15,, mıstık s., Editor, Güneş Tıp Kitapevi Yayınları, Kayseri, pp.3-15, 2008
Expert Reports
Other Publications
2023
20231. Genetic Counseling in Nucleotide Repeat Expansion Diseases
Aktaş Paskal Ş., Dundar M.
Other, pp.75-80, 2023
2011
20112. A case of 46, XX, t(2;17)(q37.1;q25) with recurrent miscarriage. Current Opinion in Biotechnology, Volume 22, Supplement 1, European Biotechnology Congress
Colak F., Dogan M., Uzak A., Erdogan M., Karabulut S., Balta B., et al.
Other, pp.107, 2011
2009
20093. A Patient With an Isodicentric Y Chromosome, Mediterranean Medical Genetics Meeting, Bilkent-Ankara, Turkey
TAŞDEMİR Ş., AKALIN H., Saatci C., ÖZKUL Y., Dundar M.
Other, pp.49, 2009
2009
20094. The analyze of azospermia factor and cystic fibrozis gene mutations in male infertile individuals with congenital unilateral or bilateral vas deferens agenesis. 8th Balkan Meeting On Human Genetics, Dubrovnik Croatia
Onal M. G., Karabulut S., Ekmekcioglu O., Saatci C., ÖZKUL Y., Dundar M.
Other, pp.72, 2009
2009
20095. Partial trisomy of 14q resulting from balanced maternal translocation. 8th Balkan Meeting On Human Genetics, Dubrovnik Croatia
Uzak A., Karabulut S., AKALIN H., Arslan K., TAŞDEMİR Ş., KİRAZ A., et al.
Other, pp.101, 2009
2009
20096. No relationship among aromatase and 5-alpha reductase genes polymorphisms and idioptic hirsutizm. 8th Balkan Meeting On Human Genetics Dubrovnik Croatia
Dundar M., Caglayan A., Baysal N. A., Tanriverdi F., ÖZKUL Y., Unluhizarci K., et al.
Other, pp.62, 2009
2008
20087. Quantitative determination of aromatase and 5-? reductase mRNA and polymorphisms in the aromatase and 5-? reductase genes in idiopathic hirsutism. ıÜüEndocrine Abstracts
Dundar M., Caglayan A., Baysal N. A., Tanriverdi F., ÖZKUL Y., Unluhizarci K., et al.
Other, pp.610, 2008
2007
20078. Normalization of serum testosterone level alters local GnRH-II and IL-2R mRNA expression in peripheral lymphocytes in patients with idiopathic hypogonadotrophic hypogonadism (IHH). European Congress of Endocrinology
Tanriverdi F., AKALIN H., Caglayan A., Demirkoparan U., ÖZKUL Y., Dundar M., et al.
Other, pp.10, 2007
2000
20009. A locus for preaxial polydactyly with sternal abnormalities Maps to chromosome 7q36. (Abstract and programme). Journal of Medical Genetics
Gordon T., Dundar M., Cooke A., Ozyazgan I., Oguzkaya F., ÖZKUL Y., et al.
Other, pp.11-13, 2000
2000
200010. Female-to-male transsexual with 47, XXX karyotype: A case report. Abstracts from the XXIInd CINP Congress Brussely
Turan M., Esel E., Dundar M., Candemir Z., Basturk M., Sofuoglu S., et al.
Other, pp.17-22, 2000
1999
199911. A case with two separate complex translocations 46,XY, t(l;8)(q32.3;q24.1), t(4;7) (7ter->pl3::7q34->q31.2::4pl5.2->qter), (7qter->q 34::7pl3-»q31.2::4pl5.2-»pter). Abstrcts of the second European Cytogenetics Conference.
ÖZKUL Y., Dundar M., Candemir Z., Saatci C., Colgan J., Lowther G., et al.
Other, pp.670, 1999
Funded Projects
2022 - 2024
2022 - 2024Üveiti olan Behçet Hastalarında Oksidatif stresle ilişkisi bilinen OXR1 OSGIN2 ve SOD2 genlerinin ekspresyon düzeylerinin araştırılması
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), ERCAN M.
2022 - 2024
2022 - 2024Investigation of the Relationship Between Football Skills and BDNF, COMT and DRD2 Genes in Young Football Players
TUBITAK Project , 1001 - Program for Supporting Scientific and Technological Research Projects
(Project Final Report)
Akkurt S. (Executive), Akalın H., Sucan S. (Executive), Karakuş M. (Executive), Öztürk A., Kafadar İ. H., et al.
2021 - 2023
2021 - 2023
Covid-19'a Bağlı Akut Solunum Sıkıntısı Sendromunda Prolil Hidroksilaz 2, HIF1 ve HIF2 Polimorfizmi ve Sağkalım ile İlişkisi
Project Supported by Higher Education Institutions , BAP Research Project
DÜNDAR M. (Executive), SAATÇİ Ç., SİPAHİOĞLU H., YÜKSEL R. C., ELAY G., EREN E.
2021 - 2023
2021 - 2023
COVID19 hastalık şiddetini etkileyebilecek konak genetik varyantlarının araştırılması
Project Supported by Higher Education Institutions , BAP Research Project
DÜNDAR M. (Executive), GÜNDOĞAN K., KARAYOL AKIN A., TUTAR N., ZARARSIZ G., AKALIN H., et al.
2020 - 2023
2020 - 2023II Derece Yüzeyel Yanık Tedavisinde Kullanılan Adipoz Kökenli Mezenkimal Kök Hücrelerin İnflamasyon Sürecinde Yanık Bül Sıvısı Üzerinden Oynadığı Rolün Moleküler Mekanizmalarının Araştırılması
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), SEYHAN SINIKSARAN B.
2020 - 2022
2020 - 2022
Triple Negatif Meme Kanserinde çoklu ilaç direncinde rol alan miRNA ve hedeflediği genlerin terapötik etkisinin araştırılması
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), KENANOĞLU S.
2020 - 2022
2020 - 2022Hepatosellüler Karsinom Modellenmiş Ratlarda Sorafenibin Deinoksantin ile Böbrek Üzerindeki Sinerjik Etkisinin Belirlenmesi
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), KARASU N.
2019 - 2020
2019 - 2020Elde esansiyel tremoru olan hastalarda PARP1 ve DNA Pol genlerinin ekspresyonunun araştırılması
Project Supported by Higher Education Institutions , BAP Research Project
DÜNDAR M. (Executive), KÖSEOĞLU E., GÜLTEKİN M., KANDEMİR N., KENANOĞLU S., MİRZA M., et al.
2018 - 2019
2018 - 2019İnsomnia tanılı bireylerde ve gece vardiyasında çalışan sağlık personellerinde Period ailesi genlerinden PER1 PER2 ve PER3 genlerinin ekspresyon düzeylerinin karşılaştırılması
Project Supported by Higher Education Institutions , BAP MSc
DÜNDAR M. (Executive), EMEKLİ R.
2016 - 2019
2016 - 2019Elde Esansiyel Tremoru olan hastalarda Propranolol tedavisinin LINGO1 HS1BP3 HTRA2 DRD3 TENM4 SLC1A2 genlerinin üzerindeki etkisinin araştırılması
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), MİRZA M., GÜLTEKİN M., HEJAZI N., KARA M., TAŞÇIOĞLU N.
2017 - 2018
2017 - 2018Plevral efüzyonlarda transuda eksuda ayrımında İnterlökin-6 genin rolü
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), ÖNAL M. G.
2017 - 2018
2017 - 2018İNSAN KARACIĞER STELLAT HÜCRE HATLARINDA LX2 ENHANCER OF ZESTE HOMOLOG 2 GENİNİN İNHİBİSYONUNUN FİBROZİS İLE OLAN İLİŞKİSİNİN ARAŞTIRILMASI
Project Supported by Higher Education Institutions , BAP Research Project
BAŞKOL G. (Executive), KILIÇ E., DÜNDAR M., BAŞKOL M.
2016 - 2018
2016 - 2018Alzheimer Hastalığında PARP1 ve DNA Pol Beta mRNA ekspresyonlarının araştırılması
Project Supported by Higher Education Institutions , BAP MSc
DÜNDAR M. (Executive), KENANOĞLU S., KÖSEOĞLU E., GÖL M. F., AKALIN H.
2016 - 2017
2016 - 2017Primer Beyin Tümörlerinde BCL2 MEG3 ve NRF2 gen ifade profillerinin araştırılması
Project Supported by Higher Education Institutions , BAP MSc
DÜNDAR M. (Executive), AKBAROVA Y., CANÖZ Ö., ÇÖMERTMAN A., AKALIN H.
2016 - 2017
2016 - 2017BİPOLAR AFFEKTİF BOZUKLUĞU OLAN HASTALARDA OKSİTOSİN POLİMORFİZMLERİ VE AGRESYON VE CİNSEL İŞLEVLERİ İLE İLİŞKİSİ
Project Supported by Higher Education Institutions , BAP PhD
TURAN M. T. (Executive), DÜNDAR M., ÜNAL F., AKALIN H.
2015 - 2017
2015 - 2017KOAH hastalarında CYP2C192 CYP2C193 polmorfizimin Klopidogrel direnci üzerine etkisi
Project Supported by Higher Education Institutions , BAP MSc
DÜNDAR M. (Executive), AKALIN H., GÜLMEZ I., KILIK Z. F.
2015 - 2017
2015 - 2017İNSAN KARACIĞER STELLAT HÜCRE HATLARINDA (LX2), ENHANCER OF ZESTE HOMOLOG 2 GENİNİN İNHİBİSYONUNUN, FİBROZİS İLE OLAN İLİŞKİSİNİN ARAŞTIRILMASI
TUBITAK Project , 1001 - Program for Supporting Scientific and Technological Research Projects
BAŞKOL G. (Executive), KILIÇ E., DÜNDAR M., ÖZCAN S.
2012 - 2017
2012 - 2017MTA Fillapex'in İn Vitro Genotoksisitesinin Değerlendirilmesi
Project Supported by Higher Education Institutions , BAP Research Project
SAĞSEN B. (Executive), ÜSTÜN Y., Taşçıoğlu N., DÜNDAR M., ARSLAN S.
2014 - 2016
2014 - 2016PREMENAPOZAL HİRSUT/HİPERANDROJENİZMLİ KADINLARDA CYP21A2, CYP11B1, HSD3ß2 VE NR3C4 (AR) LOKUSLARINA AİT GENETİK DEĞİŞİKLİKLERİN ARAŞTIRILMASI
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), KELEŞTEMUR H. F., POLAT S., ÖZKUL Y.
2013 - 2016
2013 - 2016Metilentetrahidrofolat Redüktaz Genindeki 667C>T ve 1298 A>C Polimorfizmlerinin Ektopik Gebelik Hastalarında Uygulanan Metotreksat Tedavisine Etkilerinin Araştırılması
Project Supported by Higher Education Institutions , BAP Research Project
KÜTÜK M. S. (Executive), SUBAŞIOĞLU UZAK A., ÖZGÜN M. T., ULUDAĞ S. Z., DÜNDAR M., TAŞÇIOĞLU N.
2014 - 2015
2014 - 2015
BEYİN KÖKENLİ NÖROTROFİK FAKTÖR GEN POLİMORFİZMİNİN OBSTRÜKTİF UYKU APNE SENDROMU ve OBEZİTE İLE İLİŞKİSİ
Project Supported by Higher Education Institutions , BAP PhD
TUTAR N. (Executive), YÜKSEKKAYA M., DÜNDAR M.
2014 - 2015
2014 - 2015Akciğer Adenokarsinomlarının Etiyolojisinde APOBEC (apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like) Gen Ailesinin Rolünün Araştırılması
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), AKALIN H., CANÖZ Ö., KARACA H., DOĞAN M. E., AKBAROVA Y.
2014 - 2015
2014 - 2015Otomatik Metafaz Tarama ve Görüntü Analiz Sistemi ile Nadir Mozaik Vakaların Belirlenmesi
Project Supported by Higher Education Institutions , BAP Guided
DÜNDAR M. (Executive), SAATÇİ Ç., DOĞAN M. E., AKALIN H.
2014 - 2015
2014 - 2015Hirsut/Hiperandrojenemili Kadın Hastalarda Fenotip-Genotip İlişkisinin Araştırılması
Project Supported by Higher Education Institutions , BAP Research Project
KELEŞTEMUR H. F. (Executive), ARIBAŞ S., DÜNDAR M., ÖZDAMAR KARACA Z. C., POLAT S., ÖZKUL Y., et al.
2014 - 2015
2014 - 2015
Diyabetin Sıçan Testis Dokusunda Oluşturduğu Hasar Üzerine Pentoksifilin’in Etkilerinin Araştırılması
Project Supported by Higher Education Institutions , BAP Research Project
SÖNMEZ M. F.(Executive), KILIÇ E., DÜNDAR M.
2013 - 2015
2013 - 2015Akut Myeloid Lösemi Hastalarında BAP1 ve ANAPC7 Gen Ekspresyonlarının Araştırılması.
Project Supported by Higher Education Institutions , BAP MSc
DÜNDAR M. (Executive), AKBAROVA Y., KORKMAZER M. E., AKALIN H., ÖZKUL Y., ÖZDEMİR M. A.
2012 - 2015
2012 - 2015İdiyopatik Hirsutizmli hastalarda Östrojen ve Androjen Metabolizmasında Görevli Genlerin mRNA Ekspresyonlarının Araştırılması
Project Supported by Higher Education Institutions , BAP Research Project
ÜNLÜHİZARCI K. (Executive), TAHERİ S., ÖZGÜN M. T., BORLU M., TANRIVERDİ F., ÖZDAMAR KARACA Z. C., et al.
2012 - 2014
2012 - 2014Sheehan Sendromunun Etiyolojisinde Hipofiz Organogenezisi ve Otoimmunite ile İlgili Genetik Faktörlerin Rolünün Değerlendirilmesi
Project Supported by Higher Education Institutions , BAP Research Project
BAYRAM F. (Executive), DİRİ H., DÜNDAR M., EMİROĞULLARI E. F.
2012 - 2014
2012 - 2014Sheehan Sendromunun Etiyolojisinde Kraniyal Kemiklerinin Gelişimi ve Trombofili ile İlgili Genetik Faktörlerin Rolünün Değerlendirilmesi
Project Supported by Higher Education Institutions , BAP PhD
BAYRAM F. (Executive), EMİROĞULLARI E. F., DİRİ H., DÜNDAR M.
2012 - 2014
2012 - 2014Fragile X sendromlu hastalarda FMR1 genindeki 3'lü tekrar artış sayı mutasyonlarının belirlenmesi
Project Supported by Higher Education Institutions , BAP MSc
DÜNDAR M. (Executive), KARABULUT S. Y., ADA Y., AKBAROVA Y. Y.
2012 - 2014
2012 - 2014FARKLI DOKU İSKELELERİ ÜZERİNDE EX VİVO OLUŞTURULAN BAĞ DOKUSU EŞ DEĞERLERİNİN HİSTOLOJİK OLARAK İNCELENMESİ
Project Supported by Higher Education Institutions , BAP PhD
ALKAN B. A. (Executive), TAŞÇIOĞLU N., KOLAY M., DÜNDAR M., BALCIOĞLU E., ÖZDAMAR S.
2012 - 2014
2012 - 2014Fenilalanin Hidroksilaz Geninde Görülen Yaygın Mutasyonların Taranması
Project Supported by Higher Education Institutions , BAP MSc
DÜNDAR M. (Executive), KENDİRCİ M., KARDAŞ F., AKBAROVA Y. Y., SUBAŞIOĞLU UZAK A., ALTUNOK Ş.
2012 - 2013
2012 - 2013Otistik Bozukluklu Çocuk Hastalarda VDR Gen Polimorfizmi, VDR Gen Ekspresyonu ve VDR Geni Promotor Metilasyonunun Araştırılması
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), TAHERİ S., GÜMÜŞ H., BALTA B., ÖZTOP D. B.
2012 - 2013
2012 - 2013Avrupa Tarım Biyoteknoloji Sempozyumu
Project Supported by Higher Education Institutions , BAP Other
DÜNDAR M. (Executive), BAŞKOL G., DEMİRHAN İ., GÜRCAN K., ARSLAN K., İMAMOĞLU ŞİRVANLI N. N., et al.
2011 - 2013
2011 - 2013SEPSİSTE TLR-2, TLR-4 GEN POLİMORFİZMLERİ VE mRNA EKSPRESYONU
Project Supported by Higher Education Institutions , BAP PhD
SUNGUR M. (Executive), TAHERİ S., DÜNDAR M., KARAKAŞ S., GÜNDOĞAN K.
2011 - 2013
2011 - 2013
Diyabetik Sıçan Testis Dokusunda Ghrelin Ekspresyonunun Araştırılması
Project Supported by Higher Education Institutions , BAP Research Project
SÖNMEZ M. F.(Executive), AKKUŞ D., KARA A., DÜNDAR M., KILIÇ E.
2011 - 2013
2011 - 2013
İnsan Meme Epitel Hücrelerinin, Göğüs Kanseri Kök Hücrelerine Transisyonunda Piwil2 Rolünün Araştırılması
Project Supported by Higher Education Institutions , BAP Research Project
DİNÇ G. (Executive), ÖZBİLGE H., EKİZER A., ÖZCAN S., ÖZKUL Y., ÇETİN M., et al.
2011 - 2013
2011 - 2013Ailesel hiperkolesterolemili hastalarda LDL-reseptör (LDLR), Apolipoprotein B-100 (ApoB-100) ve PCSK9 (proprotein convertase subtilin kexin 9) gen mutasyonlarının tespiti
Project Supported by Higher Education Institutions , BAP PhD
KENDİRCİ M. (Executive), POLAT S., KARDAŞ F., DÜNDAR M.
2010 - 2013
2010 - 2013ELİT ALP DİSİPLİNİ KAYAKÇILARININ BAZI GENETİK MATERYALLERİ İLE YETENEK SEÇİMLERİNİN BELİRLENMESİ
Project Supported by Higher Education Institutions , BAP PhD
ÇOKSEVİM B. (Executive), DÜNDAR M., POLAT M.
2010 - 2013
2010 - 2013BAZI ANTİTÜBERKÜLOZ İLAÇ VE KARIŞIMLARININ RATLARDA GENOTOKSİK ETKİLERİ
Project Supported by Higher Education Institutions , BAP Research Project
ARSLAN K. (Executive), AKÇAY A., KARABACAK M., İŞCAN K. M., TAŞÇIOĞLU N., SOYER SARICA Z., et al.
2011 - 2012
2011 - 2012İNFANT VE ERKEN ÇOCUKLUK DÖNEMİNDE DİRENÇLİ NÖBET, OTİSTİK BOZUKLUK VE NÖBETİN EŞLİK ETTİĞİ OTİSTİK HASTALARDA CDKL5 GEN MUTASYONLARININ ARAŞTIRILMASI
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), ERDOĞAN M., GÜMÜŞ H., ÖZTOP D. B., SUBAŞIOĞLU UZAK A.
2011 - 2012
2011 - 2012Glioblastome multiforme (GBM) olgularında izositrat dehidrogenaz 1 (IDH1), izositrat dehidrogenaz 2 (IDH2), izositrat dehidrogenaz 3 (IDH3) gen mutasyonlarının prognostik önemi
Project Supported by Higher Education Institutions , BAP PhD
YILDIZ O. G. (Executive), LALE A., CANÖZ Ö., DÜNDAR M.
2011 - 2012
2011 - 2012Türk Toplumunda Ailesel Non-Sendromik İşitme Kaybının Genetik Temelinin Araştırılması
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), TEKİN M., SUBAŞIOĞLU UZAK A.
2010 - 2012
2010 - 2012NON-ALKOLİK YAĞLI KARACİĞER HASTALARINDA SERUM MİKRO RNA DÜZEYLERİ
Project Supported by Higher Education Institutions , BAP PhD
BAŞKOL M. (Executive), ÇELİKBİLEK M., DÜNDAR M., TAHERİ S., DENİZ K.
2010 - 2012
2010 - 2012Glioblastomalı hastalarda O6-metil guanin metil transferaz geninin promoter metilasyonunun tedavi cevabına etkisi ve prognostik önemi
Project Supported by Higher Education Institutions , BAP PhD
YILDIZ O. G. (Executive), ASLAN D., CANÖZ Ö., DÜNDAR M.
2009 - 2011
2009 - 2011ALKOL YOKSUNLUĞUNDA SİTOKROM(CYP) 1A2,2D6,2E1 VE 3A4 ENZİMLERİNİN EKSPRESYON VE POLİMORFİZİMLERİNİN ARAŞTIRILMASI
Project Supported by Higher Education Institutions , BAP PhD
SAATÇİ Ç. (Executive), TAŞCIOĞLU N., ÖZKUL Y., EŞEL E., DÜNDAR M.
2009 - 2011
2009 - 2011SKOLYOZ, KÖRLÜK VE ARAKNODAKTİLİ GÖSTEREN GENİŞ BİR TÜRK AİLESİNDE BAĞLANTI
Project Supported by Higher Education Institutions , BAP Research Project
DÜNDAR M. (Executive), ÖRENAY S.
2009 - 2011
2009 - 2011TRAVMATİK BEYİN HASARINA BAĞLI HİPOFİZ YETMEZLİĞİNDE TNF-ALFA, IL-1 ALFA, IL-1 BETA VE IL-6 GEN POLİMORFİZİMLERİNİN REAL-TİME PCR YÖNTEMİYLE ARAŞTIRILMASI
Project Supported by Higher Education Institutions , BAP Research Project
KELEŞTEMUR H. F. (Executive), TAHERİ S., TANRIVERDİ F., ÜNLÜHİZARCI K., DÜNDAR M., ÖRENAY S.
2008 - 2009
2008 - 2009PRE-EMBRİYOLARDAN ELDE EDİLEN BLASTOMER HÜCRELERİNDE ANÖPLOİDİK PATOLOJİLERİN SAPTANMASI
Project Supported by Higher Education Institutions , BAP MSc
DÜNDAR M. (Executive), AYGEN E. M., YAKAN B., AKALIN H., ÖZKUL Y., SAATÇİ Ç., et al.
2006 - 2009
2006 - 2009İdiopatik Hirşutizmli Vakalarda CYP19 Geni ve SRD5A2 Geni Polimorfizmlerinin ve Bunların Lokal Olarak Androjene Duyarlı Dokudaki Ekspresyonlarının Araştırılması
TUBITAK Project
DÜNDAR M. (Executive), BORLU M., ÇAĞLAYAN A., ÖZKUL Y., TANRIVERDİ F., ÜNLÜHİZARCI K.
2006 - 2007
2006 - 2007FENİLALALİN HİDROKSİLAZ ENZİM EKSİKLİĞİNE MOLEKÜLER GEN ANALİZLERİ METODUYLA TANI KONULMASI.
Project Supported by Higher Education Institutions , BAP MSc
DÜNDAR M. (Executive), KENDİRCİ M., ALGAN D.
2005 - 2007
2005 - 2007Türk Toplumunda Hirsutizm İle Başvuran Hastalarda 21 Hidroksilaz Enzim Eksikliği Prevalansının Araştırılması
TUBITAK Project
ÜNLÜHİZARCI K. (Executive), TANRIVERDİ F., DÜNDAR M., KULA M.
2006 - 2006
2006 - 2006KONJENİTAL ADRENAL HİPERPLAZİLİ HASTALARDA MOLEKÜLER PATOLOJİKLERİN ARAŞTIRILMASI.
Project Supported by Higher Education Institutions , BAP PhD
DÜNDAR M. (Executive), ŞAHİN A.
2005 - 2006
2005 - 2006MULTİPL MYELOMALI HASTALARDA WT1 GENİNİN EKSPRESYONUNUN VE DE 13Q NUN ARAŞTIRILMASI
Project Supported by Higher Education Institutions , BAP Research Project
SAATÇİ Ç. (Executive), ÇAĞLAYAN A. O., DÜNDAR M., ESER B., ÖZKUL Y., ÇETİN M.
2004 - 2006
2004 - 2006HİPOGONADİZMLİ HASTALARDA KONVANSİYONEL TEDAVİNİN PERİFERAL LENFOSİTLERDE IL-2R,GNRH-1 VE GNRH-2 MRNA EKSPRESYONU ÜZERİNE ETKİSİ VE SERUM IL-2 DÜZEYİ VE LENFOSİT SUBTİP DEĞİŞİKLERİNİN SAPTANMASI
Project Supported by Higher Education Institutions , BAP Research Project
BAYRAM F. (Executive), PATIROĞLU T., TANRIVERDİ F., DÜNDAR M., ÖZKUL Y., KELEŞTEMUR H. F., et al.
2005 - 2005
2005 - 2005İDİOPATİK HİRŞUTİZMLİ VAKALARDA CYP19 GENİ VE SRD5A2 GENİ POLİFORFİZMLERİNİN VE BUNLARIN LOKAL OLARAK ANDROJENE DUYARLI DOKUDAKİ EKSPRESYONLARININ ARAŞTIRILMASI.
Project Supported by Higher Education Institutions , BAP PhD
ÇAĞLAYAN A. O. (Executive), BORLU M., ÜNLÜHİZARCI K., DÜNDAR M.
2004 - 2005
2004 - 2005KONJENTİAL ADRENAL HİPERPLAZİ HASTALARINDA EN YAYGIN (656G, II72N, V28IL, Q318X, R356V VB)
Project Supported by Higher Education Institutions , BAP MSc
DÜNDAR M. (Executive), KURTOĞLU S., ERÖZ R., ÖZKUL Y.
Patent
2024
2024TAZE KESİLMİŞ MEYVE VE SEBZELERİ RAF ÖMÜRLERİ BOYUNCA GERÇEK ZAMANLI PAKET ÜZERİNDE İZLEME
Patent
Registered / Approved, The Invention Registration Number: 2024/06/21 , Standard Registration
2023
2023Composition for the prevention of infection by sars-cov-2
Patent
Registered / Approved, The Invention Registration Number: US20230372264A1 , Standard Registration
Activities in Scientific Journals
2013 - Present
2013 - PresentGlobal Bioethics
Editor
2013 - Present
2013 - PresentFrontiers
Editor
2013 - Present
2013 - PresentFrontiers in Child and Neurodevelopmental Psychiatry
Publication Committee Member
2013 - Present
2013 - PresentThe EPMA Journal
Publication Committee Member
2012 - Present
2012 - PresentTurkish Journal of Medical Science
Editor
2012 - Present
2012 - PresentInternational Journal of Anthropology
Editor
2011 - Present
2011 - PresentHuman Evolution
Editor
2011 - Present
2011 - PresentMoleküler Tanı Dergisi
Assistant Editor/Section Editor
2010 - Present
2010 - PresentInternational Journal of Anthropology
Publication Committee Member
2010 - Present
2010 - PresentSağlık Bilimleri Dergisi
Publication Committee Member
Memberships and Roles in Scientific Organizations
2011 - Present
2011 - PresentAvrupa Biyoteknoloji Derneği
Chairman
2005 - Present
2005 - PresentEuropean Association of Predictive Preventive Personalised Medicine
Member
2005 - Present
2005 - PresentEuropean Cytogenetics Association
Member
2004 - Present
2004 - PresentErciyes Üniversitesi Deneysel ve Klinik Araştırma Derneği
Member
2015 - 2015
2015 - 2015British Society of Human Genetics
Member
2010 - 2015
2010 - 2015European Society of Human Genetics
Member
2009 - 2011
2009 - 2011Türkiye Tıbbi Genetik Derneği başkanı
Chairman
2007 - 2009
2007 - 2009Türkiye Tıbbi Genetik Derneği
Co-chairman
2002 - 2005
2002 - 2005Erciyes Üniversitesi Mezunları Derneği
Chairman
Peer Reviews in Scientific Publications
June 2018
June 2018CLINICAL GENETICS
SCI Journal
November 2016
November 2016Frontiers in Neuroscience
Other journals
November 2016
November 2016Frontiers in Neurogysection Autonomic Neuroscience
Other journals
October 2016
October 2016Frontiers in Pediatrics
Other journals
July 2016
July 2016Frontier Pediatrics
Other journals
July 2016
July 2016Fırat Tıp Dergisi
National Scientific Refreed Journal
July 2016
July 2016Journal of Biotechnology
Other journals
July 2016
July 2016Neuropediatrics
Other journals
July 2016
July 2016Erciyes Medical Journal
National Scientific Refreed Journal
July 2016
July 2016Journal of Human Genome Variation Society
Other journals
July 2016
July 2016Neuropediatrics
Other journals
June 2016
June 2016İzmir Eğitim ve Araştırma Hastanesi Tıp Dergisi
National Scientific Refreed Journal
June 2016
June 2016Frontiers in Neuroscience
Other journals
May 2016
May 2016Frontiers in Neuroscience
Other journals
April 2016
April 2016Frontiers in Neuroscience
National Scientific Refreed Journal
April 2016
April 2016Frontiers in Pediatrics
Other journals
April 2016
April 2016Frontiers in Neuroscience
Other journals
April 2016
April 2016Frontiers in Neuroscience
Other journals
March 2016
March 2016Frontiers in Neuroscience
National Scientific Refreed Journal
March 2016
March 2016Frontiers in Neuroscience
National Scientific Refreed Journal
March 2016
March 2016Journal of Assisted Reproduction and Genetics
National Scientific Refreed Journal
March 2016
March 2016Frontiers in Neuroscience
National Scientific Refreed Journal
March 2016
March 2016Journal of Assisted Reproduction and Genetics
Other journals
March 2016
March 2016Türkiye Klinikleri
National Scientific Refreed Journal
February 2016
February 2016Frontiers in Pediatrics
National Scientific Refreed Journal
January 2013
January 2013Molecular Biology Reports
SCI Journal
January 2013
January 2013Child and Neurodeveloppmental Psychiatry
Other journals
January 2013
January 2013The Application of Clinical Genetics
Other journals
January 2013
January 2013Journal of Assisted Reproduction and Genetic
SCI Journal
January 2013
January 2013Iranian Journal of Pediatrics
SCI Journal
January 2012
January 2012The EPMA Journal
Other journals
Scientific Project Refereeing
April 2016
April 2016TUBITAK Project
Scientific Consultations
2013 - Present
2013 - PresentOther
NHLS RESEARCH TRUST, Güney Afrika Cumhuriyeti
Erciyes University, Tıp Fakültesi, Dahili Tıp Bil., Turkey
2011 - Present
2011 - PresentProject Consultancy
TUBİTAK
Erciyes University, Tıp Fakültesi, Dahili Tıp Bil., Turkey
2010 - Present
2010 - PresentOther
Sağlık Bakanlığı Tıbbi Genetik Uzmanlığı Müfredatı Komisyonu
Erciyes University, Tıp Fakültesi, Dahili Tıp Bil., Turkey
2010 - Present
2010 - PresentScientific Consultancy
YÖK
Erciyes University, Tıp Fakültesi, Dahili Tıp Bil., Turkey
Congress and Symposium Activities
01 March 2019 - 01 March 2019
01 March 2019 - 01 March 20193. Ege Endokrin Hastalıklar ve Genetik Sempozyumu
Attendee
İzmir-Turkey
01 March 2019 - 01 March 2019
01 March 2019 - 01 March 20195. Adana Genetik Günleri “Nörogenetik Sempozyumu"
Attendee
Adana-Turkey
01 March 2019 - 01 March 2019
01 March 2019 - 01 March 2019TOTBİD – TOTEK Ortapedi ve Travmatoloji XVIII. Temel Bilimler ve Araştırma Okulu
Attendee
Kayseri-Turkey
01 February 2019 - 01 February 2019
01 February 2019 - 01 February 2019Uluslararası Katılımlı Erciyes Tıp Genetik Günleri
Attendee
Kayseri-Turkey
01 February 2019 - 01 February 2019
01 February 2019 - 01 February 2019BRCAkademi
Attendee
İstanbul-Turkey
01 November 2018 - 01 November 2018
01 November 2018 - 01 November 201813. Uluslararası Katılımlı Ulusal Tıbbi Genetik Kongresi
Attendee
Antalya-Turkey
01 March 2018 - 01 March 2018
01 March 2018 - 01 March 2018Adnan Menderes Üniversitesi, Rekombinant DNA ve Protein Araştırma ve Uygulama Merkezi Konferansı
Attendee
Aydın-Turkey
01 March 2018 - 01 March 2018
01 March 2018 - 01 March 2018Erciyes Tıp Genetik Günleri
Attendee
Kayseri-Turkey
01 February 2018 - 01 February 2018
01 February 2018 - 01 February 20183. Hematolojik Genetik Sempozyumu
Attendee
İzmir-Turkey
01 October 2017 - 01 October 2017
01 October 2017 - 01 October 20173. Ulusal Çocuk Genetik Sempozyumu
Attendee
Antalya-Turkey
01 September 2017 - 01 September 2017
01 September 2017 - 01 September 2017Medical Genetics Course and Biotechnology MAGI Balkan and EBTNA European Biotechnology Thematic Network Association
Attendee
Tiranë-Albania
01 May 2017 - 01 May 2017
01 May 2017 - 01 May 2017Erciyes Tıp Genetik Günleri 2017
Attendee
Kayseri-Turkey
01 February 2017 - 01 February 2017
01 February 2017 - 01 February 20172. Ege Endokrin Hastalıklar ve Genetik Sempozyumu
Attendee
İzmir-Turkey
01 November 2016 - 01 November 2016
01 November 2016 - 01 November 20162. Uluslararası Katılımlı Ulusal Nadir Hastalıklar ve Yetim İlaçlar Sempozyumu
Attendee
İstanbul-Turkey
01 October 2016 - 01 October 2016
01 October 2016 - 01 October 2016Magi Euregio
Attendee
Perugia-Italy
01 September 2016 - 01 September 2016
01 September 2016 - 01 September 2016One Health Inter-Regional European Conference
Attendee
Bucuresti-Romania
01 June 2016 - 01 June 2016
01 June 2016 - 01 June 2016European Biotechnology School
Attendee
Minsk-Belarus
01 May 2016 - 01 May 2016
01 May 2016 - 01 May 2016European Human Genetics Conference 2016
Attendee
Barcelona-Spain
01 March 2016 - 01 March 2016
01 March 2016 - 01 March 20163. Nörometabolik Dismorfoloji Sempozyumu
Attendee
İstanbul-Turkey
01 March 2016 - 01 March 2016
01 March 2016 - 01 March 201613. Uludağ Ortopedi ve Travmatoloji Günleri
Attendee
Bursa-Turkey
01 February 2016 - 01 February 2016
01 February 2016 - 01 February 2016II. Hematolojik Genetik Sempozyumu
Attendee
İzmir-Turkey
01 December 2015 - 01 December 2015
01 December 2015 - 01 December 2015Euroasia genç bilim insanları toplantısı
Attendee
Minsk-Belarus
01 December 2015 - 01 December 2015
01 December 2015 - 01 December 2015Biyoinformatik ve Genetikteki Uygulamaları
Attendee
İstanbul-Turkey
01 September 2015 - 01 September 2015
01 September 2015 - 01 September 2015Avrupa biyoteknolojisi ve Rusya işbirliğ
Attendee
Saransk-Russia
01 March 2015 - 01 March 2015
01 March 2015 - 01 March 2015KKTC Yakın Doğu Üniversitesi Uluslararası Biyomedikal Kongresi
Attendee
-Cyprus (Kktc)
01 March 2014 - 01 March 2014
01 March 2014 - 01 March 2014İ.Ü. Genetik Kulübü "11. Uluslararası Katılımlı Moleküler Biyoloji ve Genetik Kış Okulu"
Invited Speaker
İstanbul-Turkey
01 March 2014 - 01 March 2014
01 March 2014 - 01 March 201411. Uluslararası Katılımlı Moleküler Biyoloji ve Genetik Kış Okulu
Attendee
İstanbul-Turkey
01 December 2013 - 01 December 2013
01 December 2013 - 01 December 2013I. Hematolojik Genetik Sempozyumu
Attendee
İzmir-Turkey
01 September 2013 - 01 September 2013
01 September 2013 - 01 September 2013I. Ulusal Çocuk Genetik Sempozyumu
Attendee
İzmir-Turkey
01 June 2013 - 01 June 2013
01 June 2013 - 01 June 20139. Ulusal Hepatoloji Kongresi
Attendee
İstanbul-Turkey
01 May 2013 - 01 May 2013
01 May 2013 - 01 May 2013European Biotechnology Congress
Attendee
Bratislava-Slovakia
01 December 2012 - 01 December 2012
01 December 2012 - 01 December 201210. Ulusal Tıbbi Genetik Kongresi
Attendee
Bursa-Turkey
01 November 2012 - 01 November 2012
01 November 2012 - 01 November 2012International Conference on Genetic Syndromes & Gene Therapy
Attendee
San Antonio-United States Of America
01 November 2012 - 01 November 2012
01 November 2012 - 01 November 2012OMICS Kongresi
Attendee
Texas-United States Of America
01 September 2012 - 01 September 2012
01 September 2012 - 01 September 2012European Biotechnology Week in Valencia
Attendee
Valencia-Spain
01 April 2012 - 01 April 2012
01 April 2012 - 01 April 2012
EUROBIOTECH 2012 Agriculture Symposium
Attendee
Kayseri-Turkey
01 December 2011 - 01 December 2011
01 December 2011 - 01 December 2011Toraks İç Anadolu Derneği Toplantısı
Attendee
-Turkey
01 October 2011 - 01 October 2011
01 October 2011 - 01 October 2011BIOTECH 2011 2. Ulusal Biyoteknoloji Öğrenci Kongresi
Attendee
İstanbul-Turkey
01 May 2011 - 01 May 2011
01 May 2011 - 01 May 2011V. Dismorfoloji Günleri 2011
Attendee
İstanbul-Turkey
01 December 2010 - 01 December 2010
01 December 2010 - 01 December 20109. Ulusal Tıbbi Genetik Kongresi
Attendee
İstanbul-Turkey
01 September 2010 - 01 September 2010
01 September 2010 - 01 September 20101.Uluslararası Katılımlı Kök Hücre Sempozyumu
Attendee
Samsun-Turkey
01 October 2009 - 01 October 2009
01 October 2009 - 01 October 2009Tıbbi Genetik Sempozyumu
Attendee
Bolu-Turkey
01 October 2009 - 01 October 2009
01 October 2009 - 01 October 2009İSTANBUL ÜNİVERSİTESİ ve TIBBİ GENETİK DERNEĞİ işbirliği ile Hibrid Kursu
Attendee
İstanbul-Turkey
01 June 2009 - 01 June 2009
01 June 2009 - 01 June 2009MediMedGen 2009 Toplantısı ve Mediterrenean Medical Genetics Congress
Attendee
-Turkey
01 May 2009 - 01 May 2009
01 May 2009 - 01 May 2009Uluslarası Katılımlı X. Ulusal Metabolik Hastalıklar ve Beslenme Kongresi
Attendee
Kayseri-Turkey
01 May 2006 - 01 May 2006
01 May 2006 - 01 May 2006