Author

Özlem Sezer

Observed names: O Sezer, Ozlem SEZER, Ozlem Sezer, Ozlem Turkeli Sezer, Ö Sezer, Özlem SEZER, Özlem Sezer Türkeli, Özlem Türkeli Sezer

Institution: Samsun University

Observed institutions: Sivas Cumhuriyet Üniversitesi, Ministry of Health, Hakkari University, Baylor College of Medicine, Ondokuz Mayıs University, Samsun University, Sağlık Bilimleri Üniversitesi, Izmir Tepecik Eğitim ve Araştırma Hastanesi

ORCID: 0000-0001-5727-7965

Observed ORCID: 0000-0001-5727-7965

OpenAlex ID: A5014944431

Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease

2015 · Ender Karaca, Tamar Harel, et al. · Neuron · 320

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High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population

2021 · Tadahiro Mitani, Sedat Isikay, et al. · The American Journal of Human Genetics · 101

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Angiotensin-converting enzyme-1 gene insertion/deletion polymorphism may be associated with COVID-19 clinical severity: a prospective cohort study

2021 · Ozgur Gunal, Ozlem Sezer, et al. · Annals of Saudi Medicine · 38

Assessment of vaginal and endometrial microbiota by real‐time PCR in women with unexplained infertility

2021 · Ozlem Sezer, Canan Soyer Çalışkan, et al. · Journal of obstetrics and gynaecology research · 23

Clınical, demographic and histopathological prognostic factors for urothelial carcinoma of the bladder

2015 · Ulku Kucuk, Emel Ebru Pala, et al. · Editor-in-Chief s Voice List of Authors is an Important Element in a Scientific Publication · 22

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

2022 · Munis Dundar, Umut Fahrioglu, et al. · Functional & Integrative Genomics · 20

Oocyte maturation abnormalities - A systematic review of the evidence and mechanisms in a rare but difficult to manage fertility pheneomina

2022 · Şafak Hatırnaz, Ebru Saynur Hatırnaz, et al. · Journal of Turkish Society of Obstetric and Gynecology · 19

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Derangements of vaginal and cervical canal microbiota determined with real-time PCR in women with recurrent miscarriages

2022 · Canan Soyer Caliskan, Nazan Yurtcu, et al. · Journal of Obstetrics and Gynaecology · 16

Association between colchicine resistance and vitamin D in familial Mediterranean fever

2015 · Ismail Ozer, Turkan Mete, et al. · Renal Failure · 15

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Fibular aplasia, tibial campomelia, and oligosyndactyly: a further patient with a 2-year follow-up

2014 · Ozlem Sezer, Ismet Gebesoglu, et al. · Clinical Dysmorphology · 14

Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS‐CoV‐2 from 946 whole‐exome sequencing data in the Turkish population

2022 · Nilgun Duman, Gulten Tuncel, et al. · Journal of Medical Virology · 13

Contribution of genotypes in Prothrombin and Factor V Leiden to COVID‐19 and disease severity in patients at high risk for hereditary thrombophilia

2023 · Aslıhan Kiraz, Ozlem Sezer, et al. · Journal of Medical Virology · 11

Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study

2024 · Dilek Cavusoglu, Gulten Ozturk, et al. · The Cerebellum · 9

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Effect of vitamin D receptor gene BsmI polymorphism on hospitalization of SARS-CoV-2 positive patients

2023 · Recai Aci, Adem Keskin, et al. · Nucleosides Nucleotides & Nucleic Acids · 8

Interleukin-1Ra rs2234663 and Interleukin-4 rs79071878 Polymorphisms in Familial Mediterranean Fever

2016 · Ayse Feyda Nursal, Akin Tekcan, et al. · Gene · 8

Hyperekplexia: A Single-Center Experience

2024 · Merve Hilal Dolu, Gökçen Öz Tunçer, et al. · Journal of Child Neurology · 7

Genetic Management Algorithm in High-Risk Fabry Disease Cases; Especially in Female Indexes with Mutations

2020 · Ozlem Sezer, Serdar Ceylaner · Endocrine Metabolic & Immune Disorders - Drug Targets · 7

MTHFR gene C677T and A1298C variants are associated with FMF risk in a Turkish cohort

2017 · Ayse Feyda Nursal, Süheyla Kaya, et al. · Journal of Clinical Laboratory Analysis · 7

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The IL4-VNTR P1 Allele, IL4-VNTR P2P2 Genotype, and IL4-VNTR_IL6-174CG P2P1-GG Genotype Are Associated with an Increased Risk of Brucellosis

2016 · Ozgur Gunal, Serbulent Yigit, et al. · Japanese Journal of Infectious Diseases · 7

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Evaluation of Full Blood Count–Derived Inflammatory Indices (SII, SIRI, PIV, NLR) in Behçet’s Disease Patients and Healthy Controls

2025 · Recai Aci, Adem Keskin, et al. · OBM Genetics · 6

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Evaluating interleukin-6 levels and the rs1800795 variant in Turkish patients with COVID-19: a prospective cohort study

2023 · Ozlem Sezer, Ayse Feyda Nursal, et al. · Nucleosides Nucleotides & Nucleic Acids · 6

TUBB8 mutations as a cause of oocyte maturation abnormalities: presentation of oocyte and embryo profiles and novel mutations

2023 · Hatirnaz Ebru, Michael H. Dahan, et al. · Reproductive BioMedicine Online · 6

Cytopathologic differential diagnosis of low-grade urothelial carcinoma and reactive urothelial proliferation in bladder washings: a logistic regression analysis

2017 · Ebru Cakir, Ulku Kucuk, et al. · Apmis · 6

Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders

2024 · Elisa Cali, Tania Quirin, et al. · Genetics in Medicine · 5

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Diagnostic Utility of Chromosomal Microarray Analysis in a Turkish Pediatric Cohort: Insights from 1,022 Patients with Neurodevelopmental Disorders and Congenital Anomalies

2025 · Aslihan Sanri, Mehmet Burak Mutlu, et al. · Cytogenetic and Genome Research · 4

Works count: 62

Citation count: 741

H-index: 11

I10-index: 12