Faculty / Medical Geneticists

Abdullatif Bakır

Associate Professor of Medical Genetics

Educational Faculty

Department: Department of Medical Genetics, Ankara Etlik City Hospital

Departmental publications

Records from the department’s publication database linked to this researcher. The count above and this list come from the same index as the Publications page, so the figure matches that page’s author filter exactly. Author strings are reproduced from the source record and are not rewritten.

Distribution of HFE Gene Variants in Patients Undergoing Genetic Testing in Türkiye: A Retrospective Analysis of 643 Cases

Kablan A; Sezer A; Bakır A; Güneş AK; Taşdelen E; Dinçsoy Bir F; Erdem HB; Saat H; Erdal H; Alay MT; Coşkun Y

The Eurasian Journal of Medicine · 2026

DOI PubMed

Rare Disease Genetics Metabolic, Mitochondrial & Cardiovascular Genetics

Identification of a novel KISS1R ( GPR54 ) gene variant (c.505+2T>G) in a patient with congenital hypogonadotropic hypogonadism: A case report and literature review

Burak Menekşe, Enes Üçgül, Abdüllatif Bakır, Sema Hepşen, İlknur Öztürk Ünsal, Muhammed Kızılgül, Takako Araki, Erman Çakal

Experimental and Therapeutic Medicine · 2026

DOI PubMed

Phenotypic spectrum in patients with 16p11.2 deletion: a single tertiary centre experience in Türkiye

Kablan A; Bakır A; Taşdelen E; Dinçsoy Bir F; Kolkıran A; Kulalı MA; Atasoy E; Menderes D; Efe A; Kılıç M; Erdal İ

The Turkish Journal of Pediatrics · 2026

DOI PubMed

Rare Disease Genetics Cytogenomics & Structural Variation

Decoding Genomic Variants in a Turkish Cohort of Patients with Spasticity

Bakir A; Saat H; Erdem HB; Sezer A; Tasdelen E; Dincsoy-Bir F; Önder H; Çomoglu SS; Kazan HH

Bratislava Medical Journal · 2025

DOI

Rare Disease Genetics Neurogenetics & Neurodevelopmental Disorders

Evaluation of Mutation Profiles of Cardiomyopathy Patients in the Turkish Cohort

Bakir A; Saat H; Erdem HB; Tolunay H; Kazan HH

Bratislava Medical Journal · 2025

DOI

Rare Disease Genetics Metabolic, Mitochondrial & Cardiovascular Genetics

Expanding the Genetic Spectrum of PPM1K-Related Maple Syrup Urine Disease: A Novel Mutation

Kılıç M; Sayar E; İcil S; Doğan S; Gökçe-Altaş G; Koşukçu C; Bakır A; Sezer A

American Journal of Medical Genetics Part A · 2025

DOI PubMed

Rare Disease Genetics Metabolic, Mitochondrial & Cardiovascular Genetics

Multilocus Disease-Causing Genomic Variations for Genetic Disorders: Single Tertiary Centre Experience From Türkiye

Kablan A; Sezer A; Bakır A; Taşdelen E; Dinçsoy Bir F; Erdem HB; Saat H; Alay MT; et al.

Clinical Genetics · 2025

DOI PubMed

Rare Disease Genetics Cytogenomics & Structural Variation

Prenatally Diagnosed De Novo Interstitial Duplication in 2p21p24.3 with Unique Manifestations: Case Report

Kablan A; Sezer A; Bakir A; Kolkiran A; Saat H

Molecular Syndromology · 2025

DOI PubMed

Rare Disease Genetics Cytogenomics & Structural Variation

The Diagnostic Utility of Prenatal Microarray in High-Risk Pregnancies: A Single-Center Experience in Enhancing Reproductive Care and Risk Stratification

Bakır A; Alay MT; Tekbaş UC; Sucu S; Kalay I; Saat H

Diagnostics · 2025

DOI PubMed

Rare Disease Genetics Cytogenomics & Structural Variation

The Role of the T790M Mutation in Lung Cancer: A Molecular Perspective Based on Genetic Data

Abdullatif Bakır, Esma Ertürkmen Aru

Acta haematologica oncologica Turcica. · 2024

DOI