Department of Medical Genetics
Assoc. Prof. Ozlem SEZER
Internal Medicine, Department of Medical Genetics, Samsun University Faculty of Medicine
Education: Ondokuz Mayıs University Faculty of Medicine (1994-2000), Ankara Private Public Polyclinic (2000-2001), Ankara Baskent University/Neurosurgery- Assistant Doctor (2001), Ondokuz Mayıs University Faculty of Medicine/ Internal Medicine Sciences, Medical Genetics Department- Assistant Doctor (2002-2009), Samsun Gynecology and Pediatrics Hospital (2009-20013), Baylor Hopkins Center for Mendelian Genetics, BCM Baylor College of Medicine (2013), Samsun Training and Research Hospital (2013-2023), Samsun University Faculty of Medicine /Internal Medical Sciences, Department of Medical Genetics- Associate Professor (2023).
Research Areas: Children with mental and physical special needs and their families, couples with reproductive problems, recurrent pregnancy losses, infertility, couples with failures in in vitro fertilization, hematological and oncological cancers, familial cancer cases such as breast, ovarian and colon cancer, FMF, ankylosing spondylitis, behçet such as rheumatological and autoinflammatory diseases, Individuals with a genetic disease previously diagnosed in the family, Muscle and nerve diseases, Young cases with stroke and cardiological problems, cases with a history of recurrent deep vein thrombi and embolism, and cases with coagulation disorders, especially in pregnant women with anomaly detected in fetal ultrasonography pregnant women and those with high risk in screening tests. Current study and research topics include COVID-19, infertility, microbiota, familial and somatic cancers, dysmorphism, syndromes, rheumatological and metabolic diseases.
Selected Studies: She wrote his specialty thesis in medicine titled “Determination of mesenchymal stem cell characteristics in cultured amniotic cells: morphological typing, surface antigen expression (Immunophenotyping) and osteogenic, adipogenic, chondrogenic differentiation”(2009). International works are original articles in SCI/E journals. He has international book chapter authors and projects. It consists of original articles whose national works are in the UAK/TR directory. Major works: “YIF1B-related Kaya-Barakat-Masson Syndrome: Report of a new patient and literature review”(2023);“Clock 3111 T/C and Period3 VNTR gene polymorphisms and proteins, and melatonin levels in women with infertility”( 2023);“Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia”(2023);“The effect of a 18 bp deletion/insertion variant of VEGF gene on the FMF development”(2022);“Possible effect of genetic background in thrombophilia genes on clinical severity of patients with coronavirus disease-2019: A prospective cohort study”(2022);“Oocyte maturation abnormalities – A systematic review of the evidence and mechanisms in a rare but difficult to manage fertility pheneomina”(2022); “Derangements of vaginal and cervical canal microbiota determined with real-time PCR in women with recurrent miscarriages”(2022);“Analysis ofACE2 and TMPRSS2 coding variants as a risk factor for SARS‐CoV‐2 from 946 whole‐exome sequencing data in the Turkish population”(2022);“Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium”(2022); “Assessment of vaginal and endometrial microbiota by real-time PCR in women with unexplained infertility”(2022);“Analysis of Endotheal Nitric Oxide Synthase Gene VNTR Variant in Turkish FMF Patients”(2022); “The assessment of mesenchymal stem cells characteristics in cultured amniotic fluid cells”(2022);“The Spectrum of MEFV Gene Mutations and Genotypes in Patients with Familial Mediterranean Fever in Black Sea Region of Turkey”(2021);“High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population”(2021);“Angiotensin-converting enzyme-1 gene insertion/deletion polymorphism may be associated with COVID-19 clinical severity: a prospective cohort study”(2021);“Genetic Management Algorithm in High -Risk Fabry Disease Cases especially in Female Indexes with Mutations”(2020);
Office Samsun Health Application and Research Centre (Samsun Training and Research Hospital)
e-mail:[email protected]
Tel: +90 (362) 311 15 00
Google Academic YÖKAKADEMIC