Publications & Works

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

Induction of apoptosis by metformin and progesterone in estrogen-induced endometrial hyperplasia in rats: involvement of the bcl-2 family proteins.

Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology, vol.34, pp.433-436, 2018 (Journal Indexed in SCI Expanded) identifier identifier identifier

Ten cases with 46,XX testicular disorder of sex development: single center experience.

International braz j urol : official journal of the Brazilian Society of Urology, vol.43, pp.770-775, 2017 (Journal Indexed in SCI Expanded) Creative Commons License identifier identifier identifier

THE EXPRESSION LEVEL OF BRMS1 IN COLON CANCER PATIENTS AND ITS CLINICAL SIGNIFICANCE

CIENCIA E TECNICA VITIVINICOLA, vol.30, pp.148-155, 2015 (Journal Indexed in SCI Expanded)

AN UNCOMMON CAUSE OF INFERTILITY: Y;1 TRANSLOCATION AND PGD TRIAL

GENETIC COUNSELING, vol.25, no.3, pp.353-355, 2014 (Journal Indexed in SCI) identifier identifier

PARTIAL TRISOMY 14q DUE TO MATERNAL t(4;14)(p16;q32) IN A DYSMORPHIC NEWBORN

GENETIC COUNSELING, vol.22, no.3, pp.287-292, 2011 (Journal Indexed in SCI) identifier identifier

Frank-ter Haar syndrome with unusual clinical features

EUROPEAN JOURNAL OF MEDICAL GENETICS, vol.52, no.4, pp.247-249, 2009 (Journal Indexed in SCI) identifier identifier identifier

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

INDIAN JOURNAL OF MEDICAL RESEARCH, vol.128, no.5, pp.666-668, 2008 (Journal Indexed in SCI) identifier identifier

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

ANNALS OF SAUDI MEDICINE, vol.28, no.3, pp.209-212, 2008 (Journal Indexed in SCI) identifier identifier

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

JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, vol.71, no.6, pp.396-404, 2008 (Journal Indexed in SCI) identifier identifier identifier

Prenatal Diagnosis of Unique Translocation t (7;15)(q11. 23;q26. 3) in a Fetus.

Egyptian Journal of Medical Human Genetics, no.8, pp.105-110, 2007 (Journal Indexed in SCI Expanded)

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

TURKISH JOURNAL OF PEDIATRICS, vol.46, no.4, pp.377-379, 2004 (Journal Indexed in SCI) identifier identifier identifier

A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype

ANNALES DE GENETIQUE, vol.45, no.4, pp.181-183, 2002 (Journal Indexed in SCI) identifier identifier

Effect of zinc deficiency on chromosomal abnormalities in mice

TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, vol.179, no.4, pp.247-251, 1996 (Journal Indexed in SCI) Creative Commons License identifier identifier identifier

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

MUTATION RESEARCH-ENVIRONMENTAL MUTAGENESIS AND RELATED SUBJECTS, vol.334, no.2, pp.209-212, 1995 (Journal Indexed in SCI) identifier identifier

Articles Published in Other Journals

Investigation of cytochrome p450 CYP1A2, CYP2D6, CYP2E1 and CYP3A4 gene expressions and polymorphisms in alcohol with-drawal

KLINIK PSIKIYATRI DERGISI-TURKISH JOURNAL OF CLINICAL PSYCHIATRY, vol.24, no.3, pp.298-306, 2021 (Journal Indexed in ESCI) identifier

Parental karyotype and genetic markers for thrombophilia in recurrent miscarriage

J Turkish German Gynecol Assoc, pp.139-143, 2008 (National Refreed University Journal)

Amenoreli Hastaların Sitogenetik Analiz Sonuçlarının Değerlendirilmesi

Türkiye Klinikleri Dergisi, no.18, pp.83-87, 2008 (National Refreed University Journal)

Hipofiz taraması sonucu saptanan izokromozomlu Turner sendromu

Endokrinolojide yönelişler, vol.12, no.1, pp.109-110, 2003 (Other Refereed National Journals)

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

Erciyes Üniversitesi Sağlık Bilimleri Dergisi, vol.4, pp.42-45, 1995 (National Refreed University Journal)

22q+ Variant kromozomlu bir kronik miyeloid lösemi olgusu

Erciyes Üniversitesi Sağlık Bilimleri Dergisi, pp.42-45, 1995 (National Refreed University Journal)

Refereed Congress / Symposium Publications in Proceedings

Molecular pathological evaluationof Alport syndrome

International Participated Erciyes Medical Genetics Days, Kayseri, Turkey, 21 - 23 February 2019

Identification and frequency of CFTR gene variants

International Participated Erciyes Medical Genetics Days, Kayseri, Turkey, 21 - 23 February 2019

Lack of amplification in next generation sequencing? Check for deletions.

European Conference of Human Genetics 2016, Barselona, Spain, 21 - 24 May 2016, vol.24, pp.475-476

EVALUATION OF PON1 GENE L55M POLYMORPHISM IN ABORTED FETUSES

ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016

A CASE OF HABITUAL ABORTION WITH 46 XX T 12 22 Q13 2 Q13 3 TRANSLOCATION

ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016

Evaluatıon Of Laboratory Results In Cystıc Fıbrosıs Patıents

Medical Genetics and Clinical Applications (with International Participation), Kayseri, Turkey, 11 - 13 February 2016

FREQUENCY OF MVK GENE MUTATIONS IN MEVALONATE KINASE DEFICIENCY

ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016

Frequency Of MVK Gene Mutatıons In Mevalonate Kınase Defıcıency

Medical Genetics and Clinical Applications (with International Participation), Kayseri, Turkey, 11 - 13 February 2016

EVALUATION OF LABORATORY RESULTS IN CYSTIC FIBROSIS PATIENTS

ULUSLARARASI KATKILI GEVHER NESİBE TIP GÜNLERİ 2016, Turkey, 11 - 13 February 2016

Evaluatıon Of Laboratory Results In Cystıc Fıbrosıs Patıents

Medical Genetics and Clinical Applications (with International Participation) 11-13 February, 2016, Kayseri, Turkey, 11 - 13 February 2016, vol.1, pp.1

Evaluatıon Of PON1 Gene L55M Polymorphısm In Aborted Fetuses

Medical Genetics and Clinical Applications (with International Participation) 11-13 February, 2016, Kayseri, Turkey, 11 - 13 February 2016, vol.1, pp.1

AML Hastalarında MDM2 SNP309 Polimorfizminin Değerlendirilmesi

10. ULUSAL TIBBİ GENETİK KONGRESİ, Bursa, Turkey, 13 October - 23 December 2012

Prenatally detected de novo 46, XX, t(2121)(p12p12) at chorionic villus sampling

European Biotechnology Congress 2011, İstanbul, Turkey, 28 September - 01 October 2011, vol.22, pp.107 identifier

A case with 49, XXXXY syndrome: rare chromosomal aneuploidies

European Biotechnology Congress 2011, İstanbul, Turkey, 28 September - 01 October 2011, vol.22, pp.106 identifier

MEFV Gene Mutations Screening In Turkish Population.

IX. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 1 - 04 December 2010

Investigation of PAI-1 4G/5G Polymorphism In Turkish FMF Patients.

IX. Ulusal Tıbbi Genetik Kongresi., İstanbul, Turkey, 1 - 04 December 2010

Omalosel ve Gastroşizise etki eden anomaliler

7.Ulusal Jinekoloji ve Obstetrik Kongresi, Turkey, 14 - 19 May 2009, vol.6, pp.54

Hematolojik Malignensilere Moleküler Yaklaşım.

8. ULUSAL TIBBİ GENETİK KONGRESİ, Çanakkale, Turkey, 8 - 09 May 2008

Ailesel Akdeniz Ateşi Olgularında Mutasyon Taranması.

VIII. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 1 - 04 May 2008

Spinal Müsküler Atrofi Ön Tanısıyla Gelen Hastalarda Möleküler Analiz Sonuçları

VII. Ulusal Prenatal Tanı Ve Tıbbi Genetik Kongresi, Kayseri, Turkey, 17 - 20 May 2006, pp.94

Screening Gene Mutation In FMF Disease

VII. Ulusal Prenatal Tanı Ve Tıbbi Genetik Kongresi, Kayseri, Turkey, 17 - 20 May 2006, pp.93

Kistik Fibrosis Hastalarının Mutasyon Analiz Sonuçları

VII. Ulusal Prenatal Tanı Ve Tıbbi Genetik Kongresİ, Kayseri, Turkey, 20 May 2006, pp.90

A novel denovo translocation t 4 7 p 15 p22

VII.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Turkey, 17 - 20 May 2006, pp.163

Fetusta prenatal olarak tesbit edilmiş t 7 15 q11 23 q26 3

VII.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Turkey, 17 - 20 May 2006, pp.135

Maraş otunun P16 Geni DNA Metilasyonuna Etkisinin İncelenmesi

VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.35

Maraş Otu Kullanan Kişilerde P15 ve VHL(Von Hippel-Lindau)Geni Metilasyonunun Araştırılması

VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.34

Maraş Otunun DNA Metilasyonu ve Mikronükleus Üzerine Olan Etkisinin Araştırılması

V. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.33

46,XX,t(1;16)(p22;p13) ve 46,XY,t(1;16)(q24;q24) Kromozom Anomalili Bir Çiftin Aile Araştırması

V. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.14

Other Publications