Prof. Dr. Zeynep Ocak graduated from Atatürk University Faculty of Medicine in 2001. She completed her specialization education at the same university in 2007. Her Specialization Thesis was "Connexin 26 gene studies in non-syndromic hearing loss.". Between 2011 and 2014, Dr.Ocak worked as the Deputy Chief Physician of Abant İzzet Baysal University Faculty of Medicine Hospital and the head of the Genetic Diseases Diagnosis Center. Between 2013 and 2014, she worked at the Center for Genomic Medicine, Saitama Medical University in Japan, on diagnosis and treatment methods of mitochondrial diseases, molecular genetic techniques, and gene therapy. Dr. Ocak, who received the title of Associate Professor of Medical Genetics and Genetic Diseases in 2013, worked as the Director and responsible manager of the Genetic Diseases Diagnosis Center of Kanuni Sultan Süleyman Training and Research Hospital between 2014-2017. Between 2015-2016, she worked on HLA Tissue Typing, Flowcytometry and Transplantation at Dışkapı Yıldırım Beyazıt Training and Research Hospital Transplantation immunology, Tissue Typing and Transplantation Center. Between 2017-2019, she worked as a faculty member at Istanbul Yeni Yüzyıl University Faculty of Medicine Gaziosmanpaşa Hospital, Department of Medical Biology and Genetics and as the Head of the Genetic Diseases Diagnosis Center. Dr. Ocak, who received the Young Researcher Awards from the European Society of Human Genetics (ESHG) in 2009 in Vienna, Austria and in 2016 in Kyoto, Japan, has been involved in many multi-center studies in Japan, Europe and the USA. contributed to the elucidation of the genetic cause of many diseases. She has more than seventy articles published in international refereed journals and many book chapters. Research and interests; clinical genetics, cancer genetics, preimplantation genetic diagnosis, cell culture, microarray, SNParray, aCGH, NGS, epigenetics, sequencing, expression-based studies.
Araştırma Alanları
- Genetics
- Medical Genetics
- Cancer
Çalışma Alanları
- Sağlık Bilimleri Temel Alanı
- Tıbbi Genetik
- HETEROZYGOUS PATHOGENIC MASP2 VARIANT ASSOCIATED WITH INFANTILE GIANT CELL HEPATITIS WITH AUTOIMMUNE HAEMOLYTIC ANAEMIA IN A CHILD, 2024
- Left Ventricular Systolic Dysfunction Related to Adrenal Insufficiency in a Case due to Autoimmune Polyendocrine Syndrome Type 1 with a Novel Variant, 2023
- Left Ventricular Systolic Dysfunction Related to Adrenal Insufficiency in a Case due to Autoimmune Polyendocrine Syndrome Type 1 with a Novel Variant, 2023
- Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability, 2022
- Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability, 2022
- Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability, 2022
- Is There an Association Between Nasal Polyposis and ADAMTS Genes Expressions?, 2021
- The relationship between genotype and phenotype in primary ciliary dyskinesia patients, 2021
- Is There an Association Between Nasal Polyposis and ADAMTS Genes Expressions?, 2021
- The Relationship between Genotype and Phenotype in Primary Ciliary Dyskinesia Patients, 2021
- The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance, 2019
- The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance, 2019
- The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance., 2019
- The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance, 2019
- A Case of Sotos Syndrome with Congenital Sacrococcygeal Teratoma, 2019
- The Genomics of Arthrogryposis, a Complex Trait:Candidate Genes and Further Evidence for Oligogenic Inheritance, 2019
- Toll-Like Receptor Gene Expression in Nasal Polyp, 2016
- Association of Toll like receptors 2 3 and 4 genes polymorphisms with periapical pathosis risk, 2016
- Serum and aqueous xanthine oxidase levels, and mRNA expression in anterior lens epithelial cells in pseudoexfoliation, 2015
- Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype, 2015
- Clinical and cytogenetic results of a large series of amniocentesis cases from Turkey: Report of 6124 cases, 2014
- The effects of salidrosid on DIABLO and XAF1 gene expression in PC3 prostat cancer cells, 2014
- The effects of hypericin on ADMTS and p53 gene expression in MCF 7 breast cancer cells, 2014
- Frequency Of Y Chromosome Microdeletions And Chromosomal Abnormalities In Infertile Turkish Men, 2013
- Prenatal detection of Pai syndrome without cleft lip and palate: a case report., 2013
- MOLECULAR CYTOGENETIC CHARACTERIZATION OF A CASE OF PRIMARY AMENORRHEA WITH INTRACHROMOSOMAL TRIPLICATION OF THE X CHROMOSOME Q ARM, 2012
- Walker-Warburg syndrome with persistent hyperplastic primary vitreous detected by prenatal ultrasonography, 2010
- Becker musküler distrofili geniş bir ailede moleküler ve klinik değerlendirme, 2010
- Primary Hypogonadism, Partial Alopecia, and Mullerian Hypoplasia: Report of a Third Family and Review, 2009
- Geunotoxic effect of albendazole in pediatric patients with hepatic hydatid disease, 2007
- Whole-exom sequencing: Discovering genetic causes of Granulomatous Mastitis,
- Assesment of Pathological Variations Associated with Autoimmunity and Inflammation through Whole Exome Sequencing in Granulomatous Mastitis Disease, 2023
- Whole exome sequencing reveals potential oligogenic inheritance and candidate novel genes in patients with arthrogryposis, 2017
- Whole exome sequencing reveals potential oligogenic inheritance and candidate novel genes in patients with arthrogryposis., 2017
- Velocardiofacial Syndrome: Review of the Five Years Experience, 2015
- Mosaic Tetraploidy in a Liveborn, 2014
- Osteogenezis İmperfecta Tanılı Çocukta Düşük Enerjili Kafa Travması Sonrasında Kranyum Fraktürü, 2015
- Role of Gene Variations of Toll like Receptors 2, 3 and 4on Genetic Susceptibility to Periapical Pathosis, 2013
- Analysis of HPV Incidence, Genotype and Age Distribution in aTraining and Research Hospital in Istanbul and Comparison of Results with Previous Literature from Turkey, 2015
- Mozaik olmayan 49 XYYYY karyotipli bir vaka, 2008
- Hipogonadizm parsiyel alopezi ve mullerian hipoplazisi olan bir aile, 2008
- Familial t 2 5 in a Patient with micropenis, 2007
- Nazal Polip Dokusunda IL 1A IL 10 ADAMTS 5 ADAMTS 8 ve ADAMTS 9 genlerinin expresyon analizleri, 2014