Publications & Works

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

Prenatal diagnosis of campomelic dysplasia due to SOX9 deletion

JOURNAL OF OBSTETRICS AND GYNAECOLOGY, vol.39, no.8, pp.1175-1176, 2019 (Journal Indexed in SCI) identifier identifier identifier

Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region

TURKISH JOURNAL OF PEDIATRICS, vol.60, no.1, pp.94-98, 2018 (Journal Indexed in SCI) Creative Commons License identifier identifier identifier

Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses

JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, vol.30, no.13, pp.1579-1583, 2017 (Journal Indexed in SCI) identifier identifier identifier

MECP2 DUPLICATION SYNDROME WITH ADDITIONAL FINDINGS

GENETIC COUNSELING, vol.27, no.4, pp.471-478, 2016 (Journal Indexed in SCI) identifier identifier identifier

AN INTERCHANGE TRISOMY RESULTED IN DOWN SYNDROME

GENETIC COUNSELING, vol.27, no.3, pp.429-431, 2016 (Journal Indexed in SCI) identifier identifier identifier

CRANIORACHISCHISIS, GASTROSCHISIS, AND A BRANCHIAL SINUS DEFECT: A CASE REPORT

GENETIC COUNSELING, vol.25, no.2, pp.237-240, 2014 (Journal Indexed in SCI) identifier identifier identifier

Unique variant of Adams-Oliver syndrome with dilated cardiomyopathy and heart block

PEDIATRICS INTERNATIONAL, vol.55, no.4, pp.508-512, 2013 (Journal Indexed in SCI) identifier identifier identifier

Mapping of Microsatellite Instability in Endoscopic Normal Colon

GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.16, no.5, pp.388-395, 2012 (Journal Indexed in SCI) identifier identifier identifier

Harlequin Syndrome With Hemifacial Atrophy: A Case Study

TURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY, vol.46, no.1, pp.50-52, 2012 (Journal Indexed in SCI) identifier identifier

Cochlear involvement in Familial Mediterranean Fever: A new feature of an old disease

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, vol.76, no.2, pp.244-247, 2012 (Journal Indexed in SCI) identifier identifier identifier

A patient with 9q subtelomeric deletion syndrome with additional findings.

Genetic counseling (Geneva, Switzerland), vol.23, no.4, pp.465-71, 2012 (Journal Indexed in SCI Expanded) identifier identifier identifier

THROMBOPHILIA GENE MUTATIONS IN OCULOAURICULOVERTEBRAL SPECTRUM

GENETIC COUNSELING, vol.23, no.1, pp.65-72, 2012 (Journal Indexed in SCI) identifier identifier identifier

THE IMPACT OF THE D727E POLYMORPHISM HAS NO SIGNIFICANT ROLE IN MULTI NODULAR GOITER

BALKAN JOURNAL OF MEDICAL GENETICS, vol.15, no.2, pp.67-71, 2012 (Journal Indexed in SCI) Creative Commons License identifier identifier identifier

A TURKISH PATIENT WITH LARGE 17p11.2 DELETION PRESENTING WITH SMITH MAGENIS SYNDROME

GENETIC COUNSELING, vol.22, no.1, pp.11-19, 2011 (Journal Indexed in SCI) identifier identifier identifier

Relationship Between the IL-12B Promoter Polymorphism and Allergic Rhinitis, Familial Asthma, Serum Total IgE, and Eosinophil Level in Asthma Patients

JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY, vol.19, no.1, pp.21-26, 2009 (Journal Indexed in SCI) identifier identifier identifier

Interleukin-10 gene promoter polymorphism in patients with schizophrenia in a region of East Turkey

WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, vol.10, no.4, pp.461-468, 2009 (Journal Indexed in SCI) identifier identifier identifier

Spondyloepiphyseal dysplasia tarda with progressive arthropathy with delayed diagnosis

TURKISH JOURNAL OF MEDICAL SCIENCES, vol.38, no.1, pp.83-89, 2008 (Journal Indexed in SCI) identifier identifier

Effects of long-term inhaled steroid use on bone mineral density in asthma patients

JOURNAL OF INVESTIGATIONAL ALLERGOLOGY & CLINICAL IMMUNOLOGY, vol.11, no.4, pp.300-302, 2001 (Journal Indexed in SCI) identifier identifier identifier

Articles Published in Other Journals

Prenatal and Postnatal Clinical Spectrum of a Mosaic Small Supernumerary Marker Chromosome 22

International Journal of Pediatrics and Child Health, vol.7, pp.36-39, 2019 (Refereed Journals of Other Institutions)

Prenatal Sitogenetik Analizde Gerçek ve Yalancı Mozaisizmler

Turkiye Klinikleri J Med Genet-Special Topics, vol.3, no.1, pp.48-52, 2018 (Other Refereed National Journals)

Clinical findings in patients with9q deletion encompasing the 9q21 11q21 32 region

Erciyes Medical Journal, vol.38, no.1, pp.14, 2016 (Refereed Journals of Other Institutions)

Farklı bulguları olan spina bifida ve renal anomalili iki olgu sunumu

J Kartal TR, vol.26, no.3, pp.272-276, 2015 (Other Refereed National Journals)

Batı Karadeniz Bölgesindeki Pulmoner Tromboemboli Vakalarında Faktör V Faktör II ve MTHFR Mutasyonlarının Sıklığı

Turkiye Klinikleri Journal of Cardiovascular Sciences, vol.22, no.2, pp.185-192, 2010 (Other Refereed National Journals) identifier

MikroRNA lar ve İnsan Hastalıkları

Abant İzzet Baysal Üniversitesi İzzet Baysal Tıp Fakültesi Dergisi, vol.3, no.1, pp.24-28, 2008 (Other Refereed National Journals)

Asbest maruziyeti ve malign mezotelyomada etyopatogenez ve epidemiyolojik özellikler tümör supressör gen ilişkileri

Türkiye Klinikleri Tıp Bilimleri Dergisi, vol.25, no.3, pp.436-444, 2005 (Other Refereed National Journals)

Kistik fibrozis ve moleküler genetik yaklaşımlar

Türk Toraks Dergisi, vol.4, pp.198-204, 2003 (Other Refereed National Journals)

Refereed Congress / Symposium Publications in Proceedings

Prenatal Dönemde Saptanan 48,XXYY Sendromlu Olgu

XIII. Uluslararası Katılımlı Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018

Determination of IL-28B Polymorphism and IL-28B serum levels in Turkish patients with Hepatitis B and Hepatitis C

XIII. Uluslararası Katılımlı Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018

The Relation between micropenis in childhood and CAG with GGN repeat polymorphisms in the androgen reseptor gene

12th National Medical Genetics Congress of Turkish Sciety of Medical Genetics (with international participation), Turkey, 5 - 09 October 2016, vol.2, pp.261

Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived from Chromosome 15

Medical genetic and Clinical Applications, Erciyes Medical Journal, Turkey, 11 - 13 February 2016, vol.38, pp.35

MECP2 Duplication Syndrome with Additional Findings

Medical Genetics and Clinical Applications, Turkey, 11 - 13 February 2016, vol.38, pp.35

Prenatal dönemde tanısı konulan Trizomi 18 ve Klinefelter Sendromunun birlikte olduğu çift anöploidi 48 XXY 18 olgusu

Türkiye Maternal Fetal Tıp ve Perinatoloji Derneği Perinatal Medicine 2015 Kongresi, İstanbul, Turkey, 23 - 25 April 2015

Ectrodactyly-Ectodermal Dysplasia-Clefting (EEC) Syndrome: Variable clinical presentations in a family

7th European Cytogenetics Conference, Stockholm, Sweden, 4 - 07 July 2009, vol.17, pp.45-46 identifier

Meningomyelocele and Renal Hypoplasia: A Rare Case Report

7th European Cytogenetics Conference, Stockholm, Sweden, 4 - 07 July 2009, vol.17, pp.57 identifier

Books & Book Chapters

Pontoserebellar Açı Tümörlerinde Genetik Etyoloji

in: Pontoserebellar Açı Tümörlerinde Tedavi Seçimi ve Cerrahi Yaklaşımlar, Kaymaz AM, Editor, Digital Akademi, Ankara, pp.20-26, 2018