Prof. Dr. YUSUF ÖZKUL

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Experimentally altering microRNA levels in embryos alters adult phenotypes

Sukranli Z. Y., Bayram K. K., TAHERİ S., Cuzin F., ÖZKUL Y., HASSANZADEH FAALASLI M.

SCIENTIFIC REPORTS , cilt.14, sa.1, 2024 (SCI-Expanded)

Evaluation of HOTAIR, HOXD8, HOXD9, HOXD11 gene expression levels in Turkish patients with acute and chronic myeloid leukemia: A single center experience.

Saraymen E., Erdem Y., Akalın H., Taşçıoğlu N., Saraymen B., Çelik S., et al.

Cellular and molecular biology (Noisy-le-Grand, France) , cilt.70, sa.11, ss.39-45, 2024 (SCI-Expanded)

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)

Trans Species RNA Activity: Sperm RNA of the Father of an Autistic Child Programs Glial Cells and Behavioral Disorders in Mice

Yilmaz Sukranli Z., Korkmaz Bayram K., Mehmetbeyoglu E., DOĞANYİĞİT Z., BEYAZ F., ŞENER E. F., et al.

Biomolecules , cilt.14, sa.2, 2024 (SCI-Expanded)

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 , cilt.25, sa.1, ss.14-42, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma

Nano-based drug delivery systems in hepatocellular carcinoma

Abtahi M. S., Fotouhi A., Rezaei N., AKALIN H., ÖZKUL Y., Hossein-Khannazer N., et al.

JOURNAL OF DRUG TARGETING , cilt.32, sa.9, ss.977-995, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma

<i>ABCA4</i> 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 , cilt.45, sa.2, ss.133-139, 2024 (SCI-Expanded)

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 , cilt.54, sa.1, ss.86-98, 2024 (SCI-Expanded)

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 , cilt.41, sa.4, ss.301-309, 2024 (SCI-Expanded)

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 , cilt.38, sa.1-2, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma

From Data to Insights: Machine Learning Empowers Prognostic Biomarker Prediction in Autism.

Mehmetbeyoglu E., Duman A., Taheri S., Ozkul Y., Rassoulzadegan M.

Journal of personalized medicine , cilt.13, sa.12, 2023 (SCI-Expanded)

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 , cilt.46, sa.11, ss.2367-2377, 2023 (SCI-Expanded)

Heterozygous Cc2d1a mice show sex-dependent changes in the Beclin-1/p62 ratio with impaired prefrontal cortex and hippocampal autophagy

Şener E. F., Dana H., Tahtasakal R., Hamurcu Z., Taheri S., Delibasi N., et al.

Progress in Neuro-Psychopharmacology and Biological Psychiatry , cilt.125, 2023 (SCI-Expanded)

Safety and efficacy of mesenchymal stromal cell therapy for multi-drug-resistant acute and late-acute graft-versus-host disease following allogeneic hematopoietic stem cell transplantation

Keklik M., Deveci B., Celik S., Deniz K., Gonen Z. B., Zararsiz G., et al.

ANNALS OF HEMATOLOGY , cilt.102, sa.6, ss.1537-1547, 2023 (SCI-Expanded) Sürdürülebilir Kalkınma

PPM1K defects cause mild maple syrup urine disease: The second case in the literature

ÖZÇELİK F., ARSLAN S., Ozguc Caliskan B., KARDAŞ F., ÖZKUL Y., DÜNDAR M.

American Journal of Medical Genetics, Part A , cilt.191, sa.5, ss.1360-1365, 2023 (SCI-Expanded)

A Case of Short Stature Caused by a Mutation in the ACAN Gene

KARATAŞ E., DEMİR M., ÖZÇELİK F., KARA L., Akyurek E., BERBER U., et al.

MOLECULAR SYNDROMOLOGY , cilt.14, sa.2, ss.123-128, 2023 (SCI-Expanded)

EVs vs. EVs: MSCs and Tregs as a source of invisible possibilities

Heydari Z., Peshkova M., GÖNEN Z. B., Coretchi I., Eken A., YAY A. H., et al.

Journal of Molecular Medicine , cilt.101, sa.1-2, ss.51-63, 2023 (SCI-Expanded) Sürdürülebilir Kalkınma

A pilot study for treatment of severe COVID-19 pneumonia by aerosolized formulation of convalescent human immune plasma exosomes (ChipEXO™)

GÜL F., GÖNEN Z. B., Jones O. Y., Taşlı N. P., ZARARSIZ G., ÜNAL E., et al.

FRONTIERS IN IMMUNOLOGY , cilt.13, 2022 (SCI-Expanded)

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

DÜNDAR M., FAHRİOGLU U., Yildiz S. H., Bakir-Gungor B., TEMEL Ş. G., AKIN H., et al.

FUNCTIONAL & INTEGRATIVE GENOMICS , cilt.22, sa.3, ss.291-315, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Mouse neuronal cells outperform in a novel galactonamide molecular gel rather than in neurosphere; comparison of neurogenesis and neuronal differentiation mRNA markers

KORKMAZ BAYRAM K., Fitremann J., Bayram A., Yilmaz Z., Mehmetbeyoglu E., ÖZKUL Y., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.30, sa.SUPPL 1, ss.259, 2022 (SCI-Expanded)

Preclinical Studies on Convalescent Human Immune Plasma-Derived Exosome: Omics and Antiviral Properties to SARS-CoV-2.

Taşlı N. P., Gönen Z. B., Kırbaş O. K., Gökdemir N. S., Bozkurt B. T., Bayrakçı B., et al.

FRONTIERS IN IMMUNOLOGY , cilt.13, ss.1-15, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Impact of K-ras Mutation and C-myc Overexpression on the Prognosis of Diffuse Large B-Cell Lymphomas

Ertas S. K., ÜNAL A., Akalin H., BARAN M., CANÖZ Ö., KONTAŞ O., et al.

UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI , cilt.32, sa.1, ss.16-22, 2022 (SCI-Expanded)

Assessment of genes involved in behavior, learning, memory, and synaptic plasticity following status epilepticus in rats

Gol M. F., ERDOĞAN F. F., Bayramov K. K., Mehmetbeyoglu E., ÖZKUL Y.

EPILEPSY & BEHAVIOR , cilt.98, ss.101-109, 2019 (SCI-Expanded)

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 , cilt.42, sa.9, ss.1077-1087, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

The molecular basis and genotype-phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population.

DÜNDAR A., BAYRAMOV R., ÖNAL M. G., AKKUŞ M., DOĞAN M. E., KENANOĞLU S., et al.

Molecular biology reports , cilt.46, sa.4, ss.3677-3690, 2019 (SCI-Expanded)

FOXM1 plays a role in autophagy by transcriptionally regulating Beclin-1 and LC3 genes in human triple-negative breast cancer cells

Hamurcu Z., Delibaşı N., Nalbantoglu U., Şener E. F., Nurdinov N., Taşçı B., et al.

JOURNAL OF MOLECULAR MEDICINE-JMM , cilt.97, sa.4, ss.491-508, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

Altered Global mRNA Expressions of Pain and Aggression Related Genes in the Blood of Children with Autism Spectrum Disorders

Şener E. F., Taheri S., Şahin M., Bayramov K. K., Maraşlı M. K., Zararsız G., et al.

JOURNAL OF MOLECULAR NEUROSCIENCE , cilt.67, sa.1, ss.89-96, 2019 (SCI-Expanded)

Targeting LC3 and Beclin-1 autophagy genes suppresses proliferation, survival, migration and invasion by inhibition of Cyclin-D1 and uPAR/Integrin beta 1/ Src signaling in triple negative breast cancer cells

HAMURCU Z., DELIBASI N., GECENE S., ŞENER E. F., Donmez-Altuntas H., ÖZKUL Y., et al.

JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY , cilt.144, sa.3, ss.415-430, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma

NF1 gene variant allele frequencies comparison of Turkish population with databases

BAYRAMOV R., DOĞAN M. E., CERRAH GÜNEŞ M., ÖNAL M. G., BOZ M., ADA Y., et al.

Journal Of Biotechnology , 2017 (SCI-Expanded)

INHERITED PROTHROMBOTIC RISK FACTORS IN TURKISH CHILDREN WITH HEREDITARY ANJIOEDEMA. SINGLE CENTER EXPERIENCE

PATIROĞLU T., CANSEVER M., ÖZCAN A., TAHAN F., ÖZKUL Y.

HLA , cilt.89, sa.6, ss.475, 2017 (SCI-Expanded)

Serum micro-rna profiles in patients with autosomal dominant polycystic kidney disease according to hypertension and renal function

KOÇYİĞİT I., TAHERİ S., ŞENER E. F., EROĞLU E., Ozturk F., ÜNAL A., et al.

BMC NEPHROLOGY , cilt.18, 2017 (SCI-Expanded)

Effect of sodium benzoate on DNA breakage, micronucleus formation and mitotic index in peripheral blood of pregnant rats and their newborns

SAATÇİ Ç., Erdem Y., BAYRAMOV R., Akalin H., Tascioglu N., ÖZKUL Y.

BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT , cilt.30, sa.6, ss.1179-1183, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

Dendritic Cell Production from Allogeneic Donor Cd34+ Stem Cells and Mononuclear Cells; Cancer Vaccine Ali Unal, Ayse Birekul, Mehmet Cagri Unal, Esen Karakus, Yavuz Köker, Yusuf Ozkul ve Faruk Metin Comu

ÜNAL A., BİREKUL A., ÜNAL M. Ç., KÖKER M. Y., ÖZKUL Y., KARAKUŞ E., et al.

BLOOD , cilt.128, sa.225723, ss.5723, 2016 (SCI-Expanded)

Subretinal adipose tissue-derived mesenchymal stem cell implantation in advanced stage retinitis pigmentosa: a phase I clinical safety study

ÖNER A., GÖNEN Z. B., Sinim N., ÇETİN M., ÖZKUL Y.

STEM CELL RESEARCH & THERAPY , cilt.7, 2016 (SCI-Expanded)

The Impact of Epigenetics on Mesenchymal Stem Cell Biology

ÖZKUL Y., Galderisi U.

JOURNAL OF CELLULAR PHYSIOLOGY , cilt.231, sa.11, ss.2393-2401, 2016 (SCI-Expanded)

Investigation of the promoter polymorphisms of the growth hormone (GH1), growth hormone receptor (GHR), insulin-like growth factor (IGF-I), and prolactin (PRL) genes and the correlation between gene expression and milk

ARSLAN K., TAHERİ S., ŞENER E. F., AKYÜZ B., AKÇAY A., ÖZKUL Y., et al.

TURKISH JOURNAL OF VETERINARY & ANIMAL SCIENCES , cilt.40, ss.1-7, 2016 (SCI-Expanded)

The roles of CC2D1A and HTR1A gene expressions in autism spectrum disorders

ŞENER E. F., UYTUN M. C., BAYRAMOV K. K., ZARARSIZ G., Oztop D. B., CANATAN H., et al.

METABOLIC BRAIN DISEASE , cilt.31, sa.3, ss.613-619, 2016 (SCI-Expanded)

Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing Technology.

Sener E. F., Canatan H., Ozkul Y.

Psychiatry investigation , cilt.13, ss.255-64, 2016 (SCI-Expanded)

Expression of Glutamate Transporters in Alcohol Withdrawal

DEMİREL-ÖZSOY S., ASDEMİR A., KARAASLAN Ö., Akalın H., ÖZKUL Y., EŞEL E.

Pharmacopsychiatry , cilt.49, ss.14-17, 2016 (SCI-Expanded)

Investigation of the promoter polymorphisms of the growth hormone (GH1), growth hormone receptor (GHR), insulin-like growth factor (IGF-I), and prolactin (PRL) genes and the correlation between gene expression and milk yields in Holstein cattle raised in Central Anatolia

ARSLAN K., TAHERİ S., ŞENER E. F., AKYÜZ B., AKÇAY A., ÖZKUL Y., et al.

TURKISH JOURNAL OF VETERINARY & ANIMAL SCIENCES , cilt.40, sa.5, ss.609-615, 2016 (SCI-Expanded)

mRNA Expression Level of Interleukin Genes in the Determining Phases of Behcet's Disease

Taheri S., BORLU M., EVEREKLİOĞLU C., Ozdemir S. Y., ÖZKUL Y.

ANNALS OF DERMATOLOGY , cilt.27, sa.3, ss.291-297, 2015 (SCI-Expanded)

Otistik spektrum bozukluklarında SLC6A4 geni ekspresyonunun araştırılması

ŞENER E. F., Korkmaz K., ÖZTOP D. B., ÖZKUL Y.

Journal of Clinical and Experimental Investigations (Eski Adı: Klinik ve Deneysel Araştırmalar Dergisi) , cilt.6, sa.2, ss.165-169, 2015 (SCI-Expanded)

Does the Level of WT1 Expression Predict the Outcome in Philadelphia-Negative Myeloproliferative Neoplasms?

Tasdemir S., ŞENER E. F., Akalın H., Keklik M., Kaynar L., ÖZKUL Y.

GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.19, sa.4, ss.222-224, 2015 (SCI-Expanded)

Erythropoietin improves brain development in short-term hypoxia in rat embryo cultures

TORUN Y. A., Ozdemir M. A., ÜLGER H., NİSARİ M., AKALIN H., PATIROĞLU T., et al.

BRAIN & DEVELOPMENT , cilt.36, sa.10, ss.864-869, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

Association of TNF-alpha 2308 G > A and ACE I/D gene polymorphisms in hemodialysis patients with arteriovenous fistula thrombosis

ŞENER E. F., TAHERİ S., Korkmaz K., ZARARSIZ G., Serhatlioglu F., ÜNAL A., et al.

INTERNATIONAL UROLOGY AND NEPHROLOGY , cilt.46, sa.7, ss.1419-1425, 2014 (SCI-Expanded)

Identification of Mycobacterium Species from BACTEC MGIT (TM) Positive Cultures with Oligo-FISH and PNA-FISH Methods

Borekci G., Aslan G., Aydin E., Fiandaca M. J., Stender H., Lee N. M., et al.

MIKROBIYOLOJI BULTENI , cilt.48, sa.3, ss.385-401, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

The role of endothelial nitric oxide synthase gene G894T and intron 4 VNTR polymorphisms in hemodialysis patients with vascular access thrombosis

ŞENER E. F., EMİROĞULLARI Ö. N., Serhatlioglu F., ÖZKUL Y.

ANADOLU KARDIYOLOJI DERGISI-THE ANATOLIAN JOURNAL OF CARDIOLOGY , cilt.14, sa.3, ss.239-243, 2014 (SCI-Expanded)

Anthrax Lethal Factor as an Immune Target in Humans and Transgenic Mice and the Impact of HLA Polymorphism on CD4(+) T Cell Immunity

Ascough S., Ingram R. J., Chu K. K., Reynolds C. J., Musson J. A., DOĞANAY M., et al.

PLOS PATHOGENS , cilt.10, sa.5, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

Diagnosis of allergic rhinitis: inter-rater reliability and predictive value of nasal endoscopic examination: a prospective observational study

Eren E., Aktas A., Arslanoglu S., Kopar A., Ciger E., ÖZKUL Y., et al.

CLINICAL OTOLARYNGOLOGY , cilt.38, sa.6, ss.481-486, 2013 (SCI-Expanded)

Mutations in IDH1, IDH2, PON1 genes in patients with diffuse large b-cell lymphoma

AKALIN H., Ertas S., AKBAROVA Y., ÖZKUL Y., Unal A.

CURRENT OPINION IN BIOTECHNOLOGY , sa.24, ss.98, 2013 (SCI-Expanded)

The Role of Endothelial Nitric Oxide Synthase Gene G894T and Intron 4 VNTR Polymorphisms In Hemodialysis Patients With Vascular Access Thrombosis: An Observational Study.

ŞENER E. F., TAHERİ S., ZARARSIZ G., SERHATLIOĞLU F., ÜNAL A., EMİROĞULLARI Ö. N., et al.

ANADOLU KARDIYOLOJI DERGISI-THE ANATOLIAN JOURNAL OF CARDIOLOGY , cilt.1, 2013 (SCI-Expanded)

The prevalence of primary hereditary hemochromatosis in central Anatolia

Karaca H., GÜVEN K., Onal M., GÜRSOY Ş., BAŞKOL M., ÖZKUL Y.

TURKISH JOURNAL OF GASTROENTEROLOGY , cilt.24, sa.1, ss.43-50, 2013 (SCI-Expanded)

The effect of levetiracetam therapy on the autonomous nervous system in epilepsy patients

Ekmekci K., Altun Y., Tumay Y., ÖZKUL Y.

EUROPEAN JOURNAL OF NEUROLOGY , sa.19, ss.138, 2012 (SCI-Expanded)

Do thrombophilic gene mutations have a role on thromboembolic events in cancer patients?

ÖZKAN M., Sivgin S., KOÇYİĞİT I., Emirogullari F., Dikilitas M., KAYNAR L., et al.

ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY , cilt.8, sa.3, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients

DÜNDAR M., Kiraz A., Emirogullari E. F., SAATÇİ Ç., Taheri S., BAŞKOL M., et al.

ANNALS OF SAUDI MEDICINE , cilt.32, sa.4, ss.343-348, 2012 (SCI-Expanded)

Comment on "Frequency of Epitope-Specific Naive CD4(+) T Cells Correlates with Immunodominance in the Human Memory Repertoire"

ASCOUGH S., INGRAM R. J., Metan G., MAILLERE B., DOĞANAY M., ÖZKUL Y., et al.

JOURNAL OF IMMUNOLOGY , cilt.188, sa.11, ss.5205-5206, 2012 (SCI-Expanded)

Radioprotective Effects of Melatonin on Bone Marrow Cells in Total Body Irradiated Mice

Kaplan B., EROĞLU C., ÖZKUL Y., HALICI M.

ASIAN JOURNAL OF CHEMISTRY , cilt.24, sa.5, ss.1945-1948, 2012 (SCI-Expanded)

Inherited Prothrombotic Risk Factors in Turkish Children With Acute Lymphoblastic Leukemia: Significance of Concomitant Genetic Mutation

TORUN Y. A., PATIROĞLU T., Ozdemir M. A., ÖZKUL Y., Ekici A., KARAKÜKCÜ M.

CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS , cilt.18, sa.2, ss.218-221, 2012 (SCI-Expanded)

Association Between Apolipoprotein E Polymorphism and Subclinic Atherosclerosis in Patients with Type 1 Diabetes Mellitus

Atabek M. E., Özkul Y., Eklioglu B. S., Kurtoglu S., Baykara M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.4, sa.1, ss.8-13, 2012 (SCI-Expanded)

KARYOLOGICAL COMPARISONS OF THE EUROPEAN HARE (LEPUS EUROPAEUS PALLAS, 1778) FROM THE ASIAN PART OF TURKEY, WITH MORPHOLOGICAL CONTRIBUTIONS

Tez C., Özkul Y., İbiş O.

ARCHIVES OF BIOLOGICAL SCIENCES , cilt.64, ss.935-942, 2012 (SCI-Expanded)

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 , cilt.96, sa.2, ss.479-482, 2011 (SCI-Expanded)

Identification of Candida Species from Blood Cultures with Fluorescent In Situ Hybridization (FISH), Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) and Conventional Methods

Borekci G., Ersoz G., Otag F., Ozturhan H., Sen S., Soylemez F., et al.

TRAKYA UNIVERSITESI TIP FAKULTESI DERGISI , cilt.27, sa.2, ss.183-191, 2010 (SCI-Expanded)

Kan Kültürü Örneklerinden Candida Türlerinin Floresan In Situ Hibridizasyon (FISH), Polimeraz Zincir Reaksiyonu-Restriksiyon Fragment Uzunluk Polimorfizmi (PCR-RFLP) ve Konvansiyonel Yöntemlerle İdentifikasyonu

Borekci G., Ersoz G., Otag F., Ozturhan H., Sen S., Soylemez F., et al.

TRAKYA UNIVERSITESI TIP FAKULTESI DERGISI , ss.183-191, 2010 (SCI-Expanded)

An Epitope of Bacillus anthracis Protective Antigen That Is Cryptic in Rabbits May Be Immunodominant in Humans

Ingram R. J., Chu K. K., Metan G., Maillere B., DOĞANAY M., ÖZKUL Y., et al.

INFECTION AND IMMUNITY , cilt.78, sa.5, ss.2353, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma

Natural Exposure to Cutaneous Anthrax Gives Long-Lasting T Cell Immunity Encompassing Infection-Specific Epitopes

INGRAM R. J., METAN G., MAILLERE B., DOĞANAY M., ÖZKUL Y., KIM L. U., et al.

JOURNAL OF IMMUNOLOGY , cilt.184, sa.7, ss.3814-3821, 2010 (SCI-Expanded)

GnRH-II mRNA expression in tumor tissue and peripheral blood mononuclear cells (PBMCs) in patients with malignant and benign ovarian tumors

SERİN I. S., TANRIVERDİ F., Ata C. D., Akalin H., ÖZÇELİK B., ÖZKUL Y., et al.

EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY , cilt.149, sa.1, ss.92-96, 2010 (SCI-Expanded)

Expression of WT1 gene in multiple myeloma patients at diagnosis: is WT1 gene expression a useful marker in multiple myeloma?

SAATÇİ Ç., Caglayan A. O., KOÇYİĞİT I., Akalin H., KAYNAR L., Altuntas F., et al.

HEMATOLOGY , cilt.15, sa.1, ss.39-42, 2010 (SCI-Expanded)

In Vitro Genotoxic Effects of Four Helichrysum Species in Human Lymphocytes Cultures

Eroglu E. H., Hamzaoglu E., Aksoy A., Budak U., ÖZKUL Y.

BIOLOGICAL RESEARCH , cilt.43, sa.2, ss.177-182, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma

Detection of p16 promotor hypermethylation in "Maras powder" and tobacco users

SAATÇİ Ç., Çağlayan A. O., ÖZKUL Y., Tahiri S., Turhan A. B., DÜNDAR M.

CANCER EPIDEMIOLOGY , cilt.33, sa.1, ss.47-50, 2009 (SCI-Expanded)

Frank-ter Haar syndrome with unusual clinical features

DÜNDAR M., SAATÇİ Ç., Taşdemir S., AKÇAKUŞ M., ÇAĞLAYAN A. O., ÖZKUL Y.

EUROPEAN JOURNAL OF MEDICAL GENETICS , cilt.52, sa.4, ss.247-249, 2009 (SCI-Expanded)

Down syndrome like appearance with a novel de novo translocation t(6;21)(q21;q13)

DÜNDAR M., ÇAĞLAYAN A. O., SAATÇİ Ç., ARSLAN K., ÖZKUL Y.

INDIAN JOURNAL OF MEDICAL RESEARCH , cilt.128, sa.5, ss.666-668, 2008 (SCI-Expanded)

Apolipoprotein E3/E3 Genotype Decreases the Risk of Pituitary Dysfunction after Traumatic Brain Injury due to Various Causes: Preliminary Data

TANRIVERDİ F., TAHERİ S., ULUTABANCA H., Caglayan A. O., ÖZKUL Y., DÜNDAR M., et al.

JOURNAL OF NEUROTRAUMA , cilt.25, sa.9, ss.1071-1077, 2008 (SCI-Expanded) Sürdürülebilir Kalkınma

Methylation status of CpG islands at sites-59 to+96 in exon 1 of the BRCA2 gene varies in mammary tissue among women with sporadic breast cancer

CÜCER N., TAHERİ S., Ok E., ÖZKUL Y.

JOURNAL OF GENETICS , cilt.87, sa.2, ss.155-158, 2008 (SCI-Expanded) Sürdürülebilir Kalkınma

Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2)

Çağlayan A., Köklü E., Saatci C., GÜNEŞ T., ÖZKUL Y., NARİN N., et al.

ANNALS OF SAUDI MEDICINE , cilt.28, sa.3, ss.209-212, 2008 (SCI-Expanded)

CAN THE CLASSICAL EUCHROMATIC VARIANTS OF 9q12/qh+ CAUSE RECURRENT ABORTIONS?

Duadar M., Caglaian A. O., SAATÇİ Ç., Batukan C., BAŞBUĞ M., ÖZKUL Y.

GENETIC COUNSELING , cilt.19, sa.3, ss.281-286, 2008 (SCI-Expanded)

The effect of maras powder on DNA methylation and micronucleus formation in human buccal tissue

SAATÇİ Ç., ÖZKUL Y., Tahiri S., Çağlayan A. O., Turhan A. B., DÜNDAR M.

JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES , cilt.71, sa.6, ss.396-404, 2008 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.177, sa.2, ss.95-97, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , sa.8, ss.105-110, 2007 (SCI-Expanded)

Thrombosis and cancer: Clinical, laboratuary and genetic evaluation.

ÖZKAN M., Dikilitas M., KOÇYİĞİT I., Er O., SARI İ., Dogu G., et al.

ANNALS OF ONCOLOGY , sa.17, ss.301, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

Genotoxic potential of Turkish propolis in peripheral blood lymphocytes

Ozkul Y., Eroglu H. E., Ok E.

PHARMAZIE , cilt.61, sa.7, ss.638-640, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , sa.27, ss.107, 2006 (SCI-Expanded)

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 , cilt.89, sa.12, ss.1634-1637, 2005 (SCI-Expanded)

The anticarcinogenic effect of propolis in human lymphocytes culture

OZKUL Y., Silici S., EROGLU E.

PHYTOMEDICINE , cilt.12, sa.10, ss.742-747, 2005 (SCI-Expanded) Sürdürülebilir Kalkınma

Desflurane anaesthesia increases sister chromatid exchanges in human lymphocytes.

Akin A., Ugur F., Ozkul Y., Esmaoglu A., Gunes I., Ergul H.

Acta anaesthesiologica Scandinavica , cilt.49, sa.10, ss.1559-61, 2005 (SCI-Expanded)

An epidermoid carcinoma case developed on old surgical scar in an epidermodysplasia verruciformis patient

OZYAZGAN İ., Kontas O., GOKAHMETOGLU S., OZKUL Y.

JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY , cilt.19, sa.5, ss.640-642, 2005 (SCI-Expanded)

Radioprotective and radiocovery effects of melatonin on bone marrow cells in total body irradiated mice.

ÖZKUL Y.

CHROMOSOME RESEARCH , sa.13, ss.106, 2005 (SCI-Expanded)

The effects of brucella, Levafloxacine and Doxycycline on mitotics index and micronucleus.

ÖZKUL Y., Oguzkaya M., Artan C., Tekin S., AKALIN H.

Hamdard Medicus , sa.48, ss.145-147, 2005 (SCI-Expanded)

No effects of long-term sildenafil treatment on ocular functions

Oguz H., Verit A., ÖZKUL Y., Gurkan T., Ciftci H.

ANNALS OF OPHTHALMOLOGY , cilt.37, sa.2, ss.85-90, 2005 (SCI-Expanded)

Evaluation of the nucleolar organizer regions in Alzheimer's disease

Donmez-Altuntas H., AKALIN H., Karaman Y., Demirtas H., Imamoglu N. N., Ozkul Y.

GERONTOLOGY , cilt.51, sa.5, ss.297-301, 2005 (SCI-Expanded)

Localization of C04107 marker, CTR1 and Wilson (ATP7B) BAC clones on dog chromosomes

Ozkul Y.

TURKISH JOURNAL OF VETERINARY & ANIMAL SCIENCES , cilt.29, sa.4, ss.945-949, 2005 (SCI-Expanded)

Triple-X syndrome accompanied by congenital adrenal hyperplasia: case report

Kurtoglu S., Atabek M., Akçakuş M., Özkul Y., Saatçi C.

TURKISH JOURNAL OF PEDIATRICS , cilt.46, sa.4, ss.377-379, 2004 (SCI-Expanded)

Asymmetric crying facies associated with congenital hypoparathyroidism and 22q11 deletion

Akçakuş M., Güneş T., Kurtoglu S., Çetin N., Özkul Y., Narin N., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.46, sa.2, ss.191-193, 2004 (SCI-Expanded)

"Trichorhinophalangeal syndrome type I": A Turkish case

KENDİRCİ M., Keskin M., ARSLAN D., COŞKUN A., ÖZKUL Y.

Turkish Journal of Medical Sciences , cilt.33, sa.4, ss.259-263, 2003 (SCI-Expanded)

Non-myeloablative stem cell transplantation for the treatment of hematologic malignancies and metastatic solid tumors: a single center experience

Cetin M., Unal A., ESER B., ALTUNTAŞ F., Er O., PATIROĞLU T., et al.

BONE MARROW TRANSPLANTATION , sa.31, ss.158-159, 2003 (SCI-Expanded)

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 , cilt.14, sa.3, ss.325-330, 2003 (SCI-Expanded)

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 , cilt.45, sa.4, ss.181-183, 2002 (SCI-Expanded)

A family with two different chromosomal translocations

Ozkul Y., Dundar M.

ANNALES DE GENETIQUE , cilt.45, sa.4, ss.185-187, 2002 (SCI-Expanded)

Genotoxic effects of formaldehyde on the cultured human lymphocytes

Liman B. C., Liman N., Ozkul Y., Hamurcu Z.

INDIAN VETERINARY JOURNAL , cilt.79, sa.7, ss.661-664, 2002 (SCI-Expanded)

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 , cilt.10, sa.4, ss.291-293, 2001 (SCI-Expanded)

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 , cilt.38, sa.5, ss.304-309, 2001 (SCI-Expanded)

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 , cilt.10, sa.1, ss.65-66, 2001 (SCI-Expanded)

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 , cilt.48, sa.11, ss.1116-1117, 2000 (SCI-Expanded)

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 , sa.37, ss.81, 2000 (SCI-Expanded)

The effect of medroxyprogesterone acetate on bone marrow and testis during cytotoxic chemotherapy

Cetin M., Ozkul Y., Unal A., Eser B., Ozturk O., Kutlubay R., et al.

CELL BIOLOGY AND TOXICOLOGY , cilt.16, sa.6, ss.385-390, 2000 (SCI-Expanded)

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 , sa.85, ss.159, 1999 (SCI-Expanded)

Localization of C04107 marker CTR1 and Wilson ATP7B BAC clones on dogs chromosomes

ÖZKUL Y.

Cytogenetics and Cell Genetics , cilt.85, 1999 (SCI-Expanded)

The detection of bcr-abl and abl-bcr mRNA transcripts in Philadelphia-positive, Philadelphia-negative and variant Philadelphia chronic myeloid leukemia

ÖZKUL Y., Tuszynski A., Menevse A., Lillington D., Dhut S., Lister T., et al.

TURKISH JOURNAL OF HEMATOLOGY , sa.15, ss.33-38, 1998 (SCI-Expanded)

Increased sister chromatid exchanges in workers exposed to occupational lead and zinc

Donmez H., Dursun N., Ozkul Y., Demirtas H.

BIOLOGICAL TRACE ELEMENT RESEARCH , cilt.61, sa.1, ss.105-109, 1998 (SCI-Expanded) Sürdürülebilir Kalkınma

Induction of micronuclei by smokeless tobacco on buccal mucosa cells of habitual users

Ozkul Y., Donmez H., Erenmemisoglu A., Demirtas H., Imamoglu N. N.

MUTAGENESIS , cilt.12, sa.4, ss.285-287, 1997 (SCI-Expanded) Sürdürülebilir Kalkınma

Increased frequency of sister chromatid exchange inHelicobacter pylori infection

ÖZKUL Y., ALTUNTAŞ H., GÜVEN K.

Infection , cilt.25, ss.53-54, 1997 (SCI-Expanded)

Increased frequency of sister chromatid exchange in Helicobacter pylori infection

Ozkul Y., Guven K., Donmez H.

INFECTION , cilt.25, sa.1, ss.53-54, 1997 (SCI-Expanded)

Induction of micronuclei by smokeless tobacco on buccal mucosa cells of habitual users

ERENMEMİŞOĞLU A., ÖZKUL Y., ALTUNTAŞ H., Demirtaş H., İMAMOĞLU ŞİRVANLI N. N.

CYTOGENETICS AND CELL GENETICS , cilt.77, ss.64, 1997 (SCI-Expanded)

Induction of micronuclei by smokeless tobacco on buccal mucosa cells of habitual users

Erenmemisoglu A., Ozkul Y., Donmez H., Demirtas H., Imamoglu N.

CYTOGENETICS AND CELL GENETICS , cilt.77, 1997 (SCI-Expanded)

Sister chromatid exchange in lymphocytes after to occupational exposure to lead and zinc

Donmez H., Dursun N., Ozkul Y., Demirtas H.

CYTOGENETICS AND CELL GENETICS , cilt.77, 1997 (SCI-Expanded)

Sister chromatid exchange frequency in inhabitants exposed to asbestos in Turkey

Donmez H., Ozkul Y., Ucak R.

MUTATION RESEARCH-ENVIRONMENTAL MUTAGENESIS AND RELATED SUBJECTS , cilt.361, ss.129-132, 1996 (SCI-Expanded) Sürdürülebilir Kalkınma

Effect of zinc deficiency on chromosomal abnormalities in mice

Ozkul Y., Dursun N., Erenmemisoglu A., Suer C., Saatci C.

TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE , cilt.179, sa.4, ss.247-251, 1996 (SCI-Expanded)

Do non-steroidal anti-inflammatory drugs induce sister chromatid exchanges in T lymphocytes?

Ozkul Y., Erenmemisoglu A., Ekecik A., Saatci C., Özdamar S., Demirtas H.

JOURNAL OF INTERNATIONAL MEDICAL RESEARCH , cilt.24, sa.1, ss.84-87, 1996 (SCI-Expanded)

SISTER-CHROMATID EXCHANGE INDUCING EFFECT OF SMOKELESS TOBACCO USING ON T-LYMPHOCYTE CHROMOSOMES

OZKUL Y., ERENMEMISOGLU A., CUCER N., Menevse A., SAATCI C.

MUTATION RESEARCH-ENVIRONMENTAL MUTAGENESIS AND RELATED SUBJECTS , cilt.334, sa.2, ss.209-212, 1995 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

Evaluation of HOTAIR, HOXD8, HOXD9, HOXD11 Gene Expression Levels in Turkish Patients with Acute Myeloid Leukemia and Chronic Myeloid Leukemia: A Single Center Experience

Saraymen E., Erdem Y., Akalın H., Taşçıoğlu N., Saraymen B., Çelik S., et al.

medRxiv , ss.1-19, 2023 (Hakemsiz Dergi)

An overview of the genetic aspects of hair loss and its connection with nutrition

GÖKÇE N., Basgoz N., Kenanoglu S., AKALIN H., ÖZKUL Y., Ergoren M. C., et al.

Journal of preventive medicine and hygiene , cilt.63, sa.2, 2022 (Scopus) Sürdürülebilir Kalkınma

Diagnosing Alström syndrome in a patient followed up with syndromic obesity for years

Yakubi M., Çiçek D., Demir M., Yıldırım A., Hatipoğlu N., Özkul Y., et al.

Intractable & Rare Diseases Research , cilt.11, sa.2, ss.1-3, 2022 (ESCI)

Otizm Spektrum Bozukluğu Olan Hastalarda Öğrenme ve Hafıza Bozukluklarının NEURL1 ve RGS14 Genleri ile İlişkisi

ECİROĞLU H., ŞENER E. F., ÖZTOP D. B., ÖZMEN S., KAAN D., ÖZKUL Y.

ACTA MEDICA ALANYA , cilt.6, sa.2, ss.207-213, 2022 (Hakemli Dergi)

The Effect of Gene Mutations on Metastasis and Overall Survival in Metastatic and Nonmetastatic Colon Cancers.

Ozdemir Y., Cag M., Colak E., Coskun N., Başgöz N., Sarici H., et al.

Asian Pacific journal of cancer prevention : APJCP , cilt.22, sa.12, ss.3839-3846, 2021 (Scopus) Sürdürülebilir Kalkınma

Polymorphisms that affect propofol metabolism and their clinical effects

ÜLGEY A., ŞENER E. F., GÜNAY CANPOLAT D., ÇAPAR A., PEHLİVAN S. S., ÖZKUL Y.

Advance Research Journal of Medical and Clinical Sciences , cilt.5, sa.12, ss.39-45, 2019 (Hakemli Dergi)

Increased EGFR mRNA Expression Levels in Non-Small Cell Lung Cancer

Tasdemir S., TAHERİ S., AKALIN H., KONTAŞ O., ÖNAL Ö., ÖZKUL Y.

EURASIAN JOURNAL OF MEDICINE , cilt.51, sa.2, ss.177-185, 2019 (ESCI)

Inherited prothrombotic risk factors in children with hereditary angioedema

CANSEVER M., ÖZCAN A., ÖZKUL Y., PATIROĞLU T.

Annals of Medical Research , cilt.26, ss.1700-1703, 2019 (Hakemli Dergi)

Investigation of Interleukin 1 Alpha GenePromoter Polymorphism in hemodialysis patientswith arteriovenous fistula thrombosi

EMİROĞULLARI Ö. N., TUNÇAY A., ŞENER E. F., TAHERİ S., ÜNAL A., ÖZKUL Y.

Erciyes Tıp Dergisi/Erciyes Med J , 2018 (Hakemli Dergi)

Investigation of Interleukin 1 Alpha Gene Promoter Polymorphism in Hemodialysis Patients with Arteriovenous Fistula Thrombosis

EMİROĞULLARI Ö. N., TUNÇAY A., ŞENER E. F., TAHERİ S., ÜNAL A., ÖZKUL Y.

ERCIYES MEDICAL JOURNAL , ss.18-22, 2018 (ESCI)

THE INVESTIGATION OF PARP1 AND DNA POL β mRNAEXPRESSIONS ON ALZHEIMER’S DISEASE

Kenanoğlu S., Akalın H., Göl M. F., Bayramov R., KÖSEOĞLU E., SAATÇİ Ç., et al.

Erciyes Medical Journal , 2018 (Hakemli Dergi)

47,XXX, 48,XXXX, 49,XXXXX: DIFFERENCES ANDSIMILARITIES

Bayramov R., DOĞAN M. E., Korkmaz Bayramov K., Cerrah Güneş M., SAATÇİ Ç., ÖZKUL Y., et al.

Erciyes Medical Journal , 2018 (Hakemli Dergi)

A CASE OF SEVERE HYPOCHROMIC ANEMIA: TRISOMY 10p

Cerrah Güneş M., DOĞAN M. E., Bayramov R., SAATÇİ Ç., ÖZKUL Y., DÜNDAR M.

Erciyes Medical Journal , 2018 (Hakemli Dergi)

Cytogenetic Features of Elderly Turkish Myelodysplastic Syndrome Patients

Keklik M., Buyukoglan R., Sivgin S., ESER B., KAYNAR L., ÇETİN M., et al.

ERCIYES MEDICAL JOURNAL , cilt.38, sa.3, ss.95-98, 2016 (ESCI)

MTHFR gene C677T polymorphism in autism spectrum disorders

ŞENER E. F., Oztop D. B., ÖZKUL Y.

Genetics Research International , cilt.2014, 2014 (Scopus)

Otizmin Genetik Temelleri

ŞENER E. F., ÖZKUL Y.

Erciyes Üniversitesi Sağlık Bilimleri Dergisi (Journal of Health Sciences) , ss.86-92, 2013 (Hakemli Dergi)

Tümör Nekrosis Faktör-? -308(A/G) Gen Polimorfizminin Behçet Hastalığının Aktif ve İnaktif Fazlarında Araştırılması

TAHERİ S., BORLU M., TAŞDEMİR Ş., EVEREKLİOĞLU C., SAATÇİ Ç., ÖZKUL Y.

SAĞLIK BİLİMLERİ DERGİSİ , cilt.21, ss.75-81, 2012 (Hakemli Dergi)

Tümör Nekrosis Faktör alfa 308 A G Gen Polimorfizminin Behçet Hastalığının Aktif ve İnaktif Fazlarında Araştırılması

TAHERİ S., BORLU M., TAŞDEMİR Ş., EVEREKLİOĞLU C., SAATÇİ Ç., ÖZKUL Y.

SAĞLIK BİLİMLERİ DERGİSİ , cilt.21, sa.2, ss.75-81, 2012 (Hakemli Dergi)

Tıbbi Genetiğin Günümüz Yaşamındaki Uygulama Alanı

ÖZKUL Y.

Melikşah Üniversitesi Hukuk Fakültesi Dergisi Gen Hukuku Özel Sayısı , ss.1-4, 2012 (Hakemli Dergi)

Nekrosis Faktör 308 A G Gen Polimorfizminin Behçet Hastalığının Aktif Ve İnaktif Fazlarında Araştırılması

ÖZKUL Y.

Sağlık Bilimleri Dergisi (Journal of Health Sciences) , cilt.21, ss.75-81, 2012 (Hakemli Dergi)

Prothrombin Factor V Leiden and Plasminogen Activator Inhibitor Type 1 Gene Polymorphisms in Hemodialysis Patients with without Arteriovenous Fistula Thrombosis

ÖZKUL Y.

Nephro Urol Mon , cilt.2, ss.314-319, 2010 (Scopus)

Prothrombin, factor-V Leiden, and plasminogen activator ınhibitor type 1 gene polymorphisms in hemodialysis patients with/without arteriovenous fistula thrombosis

EMİROĞULLARI E. F., SAATÇİ Ç., ÜNAL A., ÖZKUL Y.

Nephro-Urology Monthly , cilt.2, sa.2, ss.314-319, 2010 (Scopus)

İnvazif Prenatal Tanı Yöntemleri Uygulanan 2295 Olgunun Retrospektif Analizi

Saatci C., ÖZKUL Y., TAŞDEMİR Ş., KİRAZ A., Müderris İ., Taşcıoğlu N., et al.

PERİNATOLOJİ DERGİSİ , ss.116-119, 2008 (Hakemli Dergi)

Parental karyotype and genetic markers for thrombophilia in recurrent miscarriage

Saatci C., Öner G., TAŞDEMİR Ş., KİRAZ A., ÖZKUL Y., Dundar M., et al.

J Turkish German Gynecol Assoc , ss.139-143, 2008 (Hakemli Dergi)

Amenoreli Hastaların Sitogenetik Analiz Sonuçlarının Değerlendirilmesi

Saatci C., ÖZKUL Y., Müderris İ., KİRAZ A., TAŞDEMİR Ş., Caglayan A., et al.

Türkiye Klinikleri Dergisi , sa.18, ss.83-87, 2008 (Hakemli Dergi)

A case of partial trisomy 13 with features similar to ‘C’ Syndrome. Bulguları C sendromuna benzeyen parsiyel trizomi

Caglayan A., Koklu E., Saatci C., KURTOĞLU S., ÖZKUL Y., Dundar M.

ERCİYES TIP DERGİSİ , ss.159-163, 2007 (Hakemli Dergi)

Arteriyo-Venöz Fistül Trombozu Gelişen Ve Gelişmeyen Kronik Böbrek Yetmezliği Olan Hastalarda Metilentetrahidrofolat Redüktaz Polimorfizmlerinin Araştırılması.

ŞENER E. F., SAATÇİ Ç., ÜNAL A., ÖZKUL Y.

Erciyes Üniversitesi Sağlık Bilimleri Dergisi , cilt.16, sa.3, ss.121-128, 2007 (Hakemli Dergi)

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 , cilt.29, ss.263-267, 2007 (Hakemli Dergi)

Gastrointestinal sistem kanserlerinde Metilentetrahidrofolat Redüktaz Geni 677C/T Polimorfizmlerinin İncelenmesi

TAŞÇIOĞLU N., TAHERİ S., SAATÇİ Ç., ÖZKUL Y.

SAĞLIK BİLİMLERİ DERGİSİ , cilt.15, ss.41-45, 2006 (Hakemli Dergi) Sürdürülebilir Kalkınma

The karyotype of the Goitred Gazelle, Gazella subgutturosa, from Turkey

TEZ C., ÖZKUL Y., Yıldız H., Dursun M., Gündüz I.

ZOOLOGY IN THE MIDDLE EAST , sa.36, ss.105-107, 2005 (Scopus)

Mesane kanserli doku kültürlerindeki mikronükleus üzerine propolis ve Mitomisin-C’nin etkileri

eroğlu h., TATLIŞEN A., ÖZKUL Y.

Erciyes Üniversitesi Sağlık Bilimleri Dergisi , sa.13, ss.15-20, 2004 (Hakemli Dergi) Sürdürülebilir Kalkınma

Determination of the genotoxic activity of Furazolidone by micronuclei test

Liman B. C., ÖZKUL Y., Liam N., Hamurcu Z.

Erciyes University Journal of Health Sciences , ss.57-60, 2002 (Hakemli Dergi)

Variable expression and hypermethylation of p16 gene in patients with T-ALL and cell lines Leukemia

ÖZKUL Y., Jurickoc I., Gu L., Fİndley H.

Turk J Haematol , ss.391-397, 1998 (Hakemli Dergi)

Helikobakter Pilori İnfeksiyonu ve Artmış Kardeş Kromatid Değişimi (Helicobacter pylori infection and increased sister chromatid exchange)

ÖZKUL Y., GÜVEN K., ALTUNTAŞ H.

Turkiye Klinikleri J Gastroenterohepatol , cilt.7, sa.1, ss.10-12, 1996 (Hakemli Dergi)

HELICOBACTER PYLORI INFECTION AND INCREASED SISTER CHROMATID EXCHANGE Helikobakter Pilori İnfeksiyonu ve Artmış Kardeş Kromatid Değişimi

ÖZKUL Y., GÜVEN K., ALTUNTAŞ H.

Turkiye Klinikleri Journal of Gastroenterohepatology , cilt.7, ss.10-12, 1996 (Hakemli Dergi)

22q+ varyant ph1 kromozomlu bir kronik miyeloid lösemi olgusu.

Ceylaner S., CÜCER N., ÜNAL A., Özyazgan I., SAATÇİ Ç., ÖZKUL Y.

Erciyes Üniversitesi Sağlık Bilimleri Dergisi , cilt.4, ss.42-45, 1995 (Hakemli Dergi)

Effects of radiation on the bone marrow and germinative tissue chromosomes in mice.

ÖZKUL Y., CÜCER N., Temoçin K., ÖZDAMAR S., Yaray K., Öztürk S.

Tr J Of Medical Sciences , cilt.17, sa.3, ss.271-274, 1995 (Hakemli Dergi)

Çeşitli antiseptik maddelerin değişik sürelerde cild florası üzerinde anti-mikrobiyal etkileri

Saatci C., Beyatlı Y., Sumerkan B., ÖZKUL Y., Özcan M.

ERCİYES TIP DERGİSİ , ss.246-249, 1995 (Hakemli Dergi)

Philadelphia kromozomu pozitif lösemilerin moleküler analizleri

ÖZKUL Y.

Gaziantep Üniversitesi Tıp Fakültesi Dergisi , ss.219-226, 1995 (Hakemli Dergi)

22q+ Variant kromozomlu bir kronik miyeloid lösemi olgusu

Ceylaner S., CÜCER N., Unal A., Ozyazgan I., Saatci C., ÖZKUL Y.

Erciyes Üniversitesi Sağlık Bilimleri Dergisi , ss.42-45, 1995 (Hakemli Dergi)

Fankoni anemisinde sitogenetik ve klinik bulgular.

ÖZKUL Y., PATIROĞLU T., CÜCER N.

Türk Hematoloji-Onkoloji Dergisi , cilt.5, ss.91-96, 1994 (Hakemli Dergi)

İnsan kromozomlarında farklı G-bandlama yöntemlerinin denenmesi ve karşılaştırılması

ÖZKUL Y., Demirtas H.

Erciyes Üniversitesi Sağlık Bilimleri Dergisi , ss.5-11, 1994 (Hakemli Dergi)

Mobilya boyacılığında çalışanlar üzerinde kardeş kromatid değişim sıklığının incelenmesi

ÖZKUL Y., Şaylı A., Menevse A.

ERCİYES TIP DERGİSİ , ss.483-485, 1992 (Scopus)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler

GENE RESISTANCE IN CHRONIC MYELOID LEUKEMIA

OKTEN EKIZ H., TAN B., KEKLİK M., ÜNAL A., MANDACI ŞANLI N., ÖZKUL Y.

X. Uluslararası Katılımlı Deneysel Hematoloji Kongresi, Gaziantep, Türkiye, 30 Ağustos 2024, (Özet Bildiri)

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, Türkiye, 16 Eylül 2021, ss.24-25, (Özet Bildiri)

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, Türkiye, 16 - 18 Eylül 2021, ss.56, (Özet Bildiri)

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, Türkiye, 16 Eylül 2021, ss.29, (Özet Bildiri)

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, Türkiye, 16 - 18 Eylül 2021, ss.36-37, (Özet Bildiri)

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, Türkiye, 15 Aralık 2021, ss.30, (Özet Bildiri)

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, Türkiye, 16 Eylül 2021, ss.30, (Özet Bildiri)

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, Türkiye, 15 Eylül 2021, ss.30, (Özet Bildiri) Sürdürülebilir Kalkınma

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, Türkiye, 16 - 18 Eylül 2021, ss.35, (Özet Bildiri)

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, Türkiye, 16 - 18 Eylül 2021, ss.36, (Özet Bildiri)

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, Türkiye, 16 Eylül 2021, ss.29, (Özet Bildiri)

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, Türkiye, 16 - 18 Eylül 2021, ss.27-28, (Özet Bildiri)

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, Türkiye, 16 - 18 Eylül 2021, ss.55, (Özet Bildiri)

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 Şubat 2020, cilt.31, (Özet Bildiri)

genome variation and precision medicine

ÖZKUL Y.

usmf.md / congres.usmf.md, Moldova, 21 - 23 Ekim 2020, (Tam Metin Bildiri)

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, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.903, (Özet Bildiri)

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, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.903, (Özet Bildiri)

Assessment of genes involved in behavior, learning, memory and synaptic plasticity following status epilepticus in rats

Gol M. F., ERDOĞAN F. F., Bayramov K. K., Mehmetbeyoglu E., ÖZKUL Y., Deconinck N.

5th Congress of the European-Academy-of-Neurology (EAN), Oslo, Norveç, 29 Haziran - 02 Temmuz 2019, ss.413, (Özet Bildiri)

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, Türkiye, 17 - 20 Nisan 2019, cilt.22, ss.166, (Özet Bildiri)

Can long non-coding RNA HOTAIR be a novel biomarker in the diagnosis of CML

BENTLİ E., AKBAROVA Y., AKALIN H., TAŞCIOĞLU N., SARAYMEN B., ÇETİN M., et al.

VI.Uluslararası Katılımlı Deneysel Hematoloji Kongresi, Türkiye, 19 - 21 Nisan 2019, (Özet Bildiri)

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, Türkiye, 21 - 23 Şubat 2019, (Özet Bildiri)

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, Türkiye, 21 - 23 Şubat 2019, (Özet Bildiri)

Beta Talesemili Hastalarda C282Y ve H63D Gen Mutasyonları Arasındaki İlişki

Seyhan Sınıksaran B., Başgöz N., Akalın H., GÖKÇE N., KAYNAR L., KARAKÜKCÜ M., et al.

44. Ulusal Hematoloji Kongresi, Antalya, Türkiye, 31 Ekim - 04 Kasım 2018, cilt.1, ss.1, (Tam Metin Bildiri)

GVHH Hastalarında Steroid Cevabı ve Kortikosteroid Direnci Arasındaki İlişkinin Araştırılması

GÖKÇE N., Badur Mermer D., ERMİŞ TURAK E., KARAKÜKCÜ M., KAYNAR L., GALDERISI U., et al.

44. Ulusal Hematoloji Kongresi, Antalya, Türkiye, 31 Ekim - 04 Kasım 2018, cilt.1, ss.1, (Tam Metin Bildiri)

ULK1 geninin agresif meme kanser hücrelerinde rolü

HAMURCU Z., Delibaşı N., ŞENER E. F., ÖZKUL Y., ALTUNTAŞ H., CANATAN H., et al.

7. Multidisipliner Kanser Araştırma ve 1. Temel Onkoloji Kongresi., İzmir, Türkiye, 11 - 14 Ekim 2018, (Özet Bildiri) Sürdürülebilir Kalkınma

Oner A, Gonen ZB, Sevim DG, Sinim N, Cetin M, Ozkul Y. First year results of subretinal adipose tissue derived mesenchymal stem cell implantation in advanced stage retinitis pigmentosa. 18th Euretina Congress, 20-23

ÖNER A., GÖNEN Z. B., GÜLMEZ SEVİM D., Sinim N., ÇETİN M., ÖZKUL Y.

Euretina, 20 - 23 Eylül 2018, (Özet Bildiri)

First year results of subretinal adipose tissue derivedmesenchymal stem cell implantation in advanced stage retinitis pigmentosa

ÖNER A., GÖNEN Z. B., GÜLMEZ SEVİM D., ÇETİN M., ÖZKUL Y., sinim n.

Euretina, 20 - 23 Eylül 2018, (Özet Bildiri)

Complications may occur in stem cell based therapies of retinitis pigmentosa.

ÖNER A., GÖNEN Z. B., GÜLMEZ SEVİM D., Sinim N., ÇETİN M., ÖZKUL Y.

European Vitreoratinal Surgery, Prag, Çek Cumhuriyeti, 30 Ağustos - 02 Eylül 2018, ss.92, (Tam Metin Bildiri)

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, Yunanistan, 26 - 28 Nisan 2018, cilt.280, ss.21, (Özet Bildiri)

Oner A, Gonen ZB, Sevim DG, Sinim N, Cetin M, Ozkul Y. Complications may occur in stem cell based therapies of retinitis pigmentosa. European Vitreoretinal Society (EVRS) Meeting, 30 August- 2 September 2018, Prague, Czech Republic. (Sözlü Bildiri).

ÖNER A., GÖNEN Z. B., GÜLMEZ SEVİM D., Sinim N., ÇETİN M., ÖZKUL Y.

EVRS, 30 Ağustos - 02 Eylül 2018, (Özet Bildiri)

SIÇANLARDA STATUS EPİLEPTİKUS SONRASI DAVRANIŞ, ÖĞRENME, HAFIZA VE SİNAPTİK PLASTİSİTEDE ROL ALAN GEN EKSPRESYONLARININ DEĞERLENDİRİLMESİ

GÖL M. F., ERDOĞAN F. F., ÖZKUL Y.

11.ULUSAL EPİLEPSİ KONGRESİ, Muğla, Türkiye, 3 - 06 Mayıs 2018, ss.33, (Tam Metin Bildiri)

RATLARDA STATUS EPİLEPTİKUS SONRASI SİNAPTİK PLASTİSİTE VE DAVRANIŞ, ÖĞRENME, HAFIZANIN DEĞERLENDİRİLMESİ

GÖL M. F., ERDOĞAN F. F., ÖZKUL Y.

53. ULUSAL NÖROLOJİ KONGRESİ, Antalya, Türkiye, 24 - 30 Kasım 2017, ss.14, (Tam Metin Bildiri)

İleri evre retinitis pigmentosalı olgularda kök hücre uygulaması: 1 yıllık sonuçlar.

ÖNER A., GÖNEN Z. B., ÇETİN M., ÖZKUL Y.

TOD 51. Ulusal Kongresi, Antalya, Türkiye, 24 - 29 Ekim 2017, (Tam Metin Bildiri)

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, Hırvatistan, 25 - 27 Mayıs 2017, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

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, Hırvatistan, 25 - 27 Mayıs 2017, cilt.256, (Özet Bildiri)

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, Hırvatistan, 25 - 27 Mayıs 2017, cilt.256, (Özet Bildiri)

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, Hırvatistan, 25 - 27 Mayıs 2017, cilt.256, (Özet Bildiri)

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, Hırvatistan, 25 - 27 Mayıs 2017, cilt.256, (Özet Bildiri)

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, Hırvatistan, 25 - 27 Mayıs 2017, cilt.256, (Özet Bildiri)

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, Türkiye, 11 - 13 Mayıs 2017, (Özet Bildiri)

INHERITED PROTHROMBOTIC RISK FACTORS IN TURKISH CHILDREN WITH HEREDITARY ANGIOEDEMA. SINGLE CENTER

PATIROĞLU T., Cansever M., ÖZCAN A., TAHAN F., ÖZKUL Y.

22nd Congress of the European-Hematology-Association, Madrid, İspanya, 22 - 25 Haziran 2017, cilt.102, ss.584, (Özet Bildiri)

INHERITED PROTHROMBOTIC RISK FACTORS IN TURKISH CHILDREN WITH HEREDITARY ANGIODEMA:SINGLE CENTER

PATIROĞLU T., CANSEVER M., ÖZCAN A., ÖZKUL Y.

22ND CONGRESS OF THE EUROPAN HEMATOLOGY ASSOCİATİON, 22 - 25 Haziran 2017, (Özet Bildiri)

INHERITED PROTHROMBOTIC RISK FACTORS IN TURKISH CHILDREN WITH HEREDITARY ANJIOEDEMA. SINGLE CENTER EXPERIENCE

PATIROĞLU T., CANSEVER M., ÖZCAN A., TAHAN F., ÖZKUL Y.

Abstracts for the 31st European Immunogenetics and Histocompatibility Conference (EFI) 25th Annual Meeting of the German Society for Immunogenetics (DGI) Mannheim/Heidelberg, Germany 30 May-2 June 2017, 30 Mayıs - 02 Haziran 2017, (Özet Bildiri)

The osteogenic differentiation via conditioned medium of human dental pulp mesenchymal stem cell: an experimental study

ERGEN E., GÖNEN Z. B., SALKIN H., ÖZKUL Y.

European Human Genetics Conference, Denmark, Kopenhag, Danimarka, 27 - 30 Mayıs 2017, (Tam Metin Bildiri)

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 Mayıs 2017, (Özet Bildiri) Sürdürülebilir Kalkınma

CIRCADIAN CLOCK-REGULATED DNA REPAİR GENE XPA IS DOWNREGULATED IN METASTATIC OF LUNG CANCER

YILMAZ S., ATAR E., CANÖZ Ö., GÜNDOĞ M., ÖZKUL Y., SEZER G.

ERCİYES TIP GENETİK GÜNLERİ, Kayseri, Türkiye, 11 - 13 Mayıs 2017, (Özet Bildiri) Sürdürülebilir Kalkınma

CIRCADIAN CLOCK-REGULATED DNA REPAIR GENE XPA ISDOWNREGULATED IN METASTATIC OF LUNG CANCER

YILMAZ S., ATAR E., CANÖZ Ö., GÜNDOĞ M., ÖZKUL Y., SEZER G., et al.

ERCİYES MEDİCAL GENETİCS DAYS 2017, Türkiye, 11 - 13 Mayıs 2017, (Özet Bildiri) Sürdürülebilir Kalkınma

HEREDİTER ANGİOÖDEMİ OLAN ÇOCUKLARDA HEREDİTER PROTROMBOTİK RİSK FAKTÖRLERİ. TEK MERKEZ DENEYİMİ

PATIROĞLU T., CANSEVER M., ÖZCAN A., ÖZKUL Y.

11.ULUSAL PEDİATRİK HEMATOLOJİ KONGRESİ, Türkiye, 4 - 07 Mayıs 2017, (Özet Bildiri)

Ratlarda kırık kaynaması ve non-union modellerinde RANK, RANKL ve OPG gen ekspresyon düzeylerinin karşılaştırılması

OLÇAR H. A., KAFADAR İ. H., HALICI M., ÖZKUL Y.

KemikEklem 2017 (Uluslararası katılımlı), 27 Nisan - 01 Mayıs 2017, (Özet Bildiri)

Dendritic Cell Production from Allogeneic Donor Cd34+Stem Cells and Mononuclear Cells; Cancer Vaccine

ÜNAL A., BİREKUL A., ÜNAL M. Ç., Karakus E., Koker Y., ÖZKUL Y., et al.

58th Annual Meeting and Exposition of the American-Society-of-Hematology (ASH), California, Amerika Birleşik Devletleri, 3 - 06 Aralık 2016, cilt.128, (Özet Bildiri) Sürdürülebilir Kalkınma

Evaluation of microRNA profiles in patients with autosomal dominant polycystic kidney disease

KOÇYİĞİT I., TAHERİ S., ŞENER E. F., EROĞLU E., ÖZTÜRK F., ÜNAL A., et al.

Kidneyweek 2016, Chicago, Amerika Birleşik Devletleri, 15 - 20 Kasım 2016, (Tam Metin Bildiri)

Dendritic Cell Production from Allogeneic Donor Cd34 Stem Cells and Mononuclear Cells Cancer Vaccine

ÜNAL A., ÜNAL M. Ç., BİREKUL A., KÖKER M. Y., ÖZKUL Y., COMU F. M., et al.

ESMO Symposium on Immuno-Oncology 2016, 4 - 06 Kasım 2016, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

Dendritic cell production from allogenenic donor Cd34 stem cells and mononuclear cells Cancer vaccine

ÜNAL A., birekul a., MC Ü., karakuş e., KÖKER M. Y., ÖZKUL Y., et al.

ESMO Symposium on Immuno-Oncology 2016, 05 Kasım 2016 Sürdürülebilir Kalkınma

Dendritic cell production from allogenenic donor Cd34+stem cells and mononuclear cells: Cancer vaccine

ÜNAL A., BİREKUL A., ÜNAL M. Ç., KARAKUŞ E., Koker Y., ÖZKUL Y., et al.

ESMO Symposium on Immuno-Oncology, Lausanne, İsviçre, 4 - 06 Kasım 2016, cilt.27, (Özet Bildiri) Sürdürülebilir Kalkınma

Subretinal adipose tissue derived mesenchymal stem cell implantation in advanced stage retinitis pigmentosa A Phase I clinical safety study

ÖNER A., GÖNEN Z. B., SİNİM N., ÇETİN M., ÖZKUL Y.

16th Euretina Congress, 8 - 12 Eylül 2016, (Özet Bildiri)

The role of circadian clock genes in metastatic lung cancer: the potential of per1 for early diagnosis

YILMAZ S., Atar E., CANÖZ Ö., ÖZKUL Y., SEZER G., Sercin O., et al.

41st FEBS Congress on Molecular and Systems Biology for a Better Life, Kusadasi, Türkiye, 3 - 08 Eylül 2016, cilt.283, ss.46, (Özet Bildiri) Sürdürülebilir Kalkınma

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, İspanya, 21 - 24 Mayıs 2016, cilt.24, ss.475-476, (Özet Bildiri)

Otistik Spektrum Bozukluğunda DRD4 Gen Ekspresyonunun Saldırganlık İle İlişkisinin Araştırılması.

ŞENER E. F., TAHERİ S., Şahin M., Topaloğlu T., Korkmaz Bayramov K., ZARARSIZ G., et al.

14. Sinir Bilim Kongresi, Ankara, Türkiye, 26 - 29 Mayıs 2016, cilt.10, sa.1, (Tam Metin Bildiri)

CAN WE USE PIWIL2 GENE IN SCREENING PROSTATE CANCER ASA NEW MARKER

tosun H., akalın H., ÖZKUL Y., DEMİRTAŞ A.

CAN WE USE PIWIL2 Medical Genetics and Clinical Applications (with International Participation)11-13 February, 2016, Kayseri, Turkey, Türkiye, 11 - 13 Şubat 2016, (Özet Bildiri) Sürdürülebilir Kalkınma