Faculty / Medical Geneticists

Haktan Bağış Erdem

Professor of Medical Genetics

Clinical Education and Administrative Lead

Professor, Health Sciences University, Gülhane Faculty of Medicine, Department of Medical Genetics

Department: Department of Medical Genetics, Ankara Etlik City Hospital
E-mail: haktanbagis.erdem@sbu.edu.tr

Professional profiles

Biography

Professor Haktan Bağış Erdem is a medical geneticist whose clinical and research work spans cancer genetics and rare-disease genomics. His interests include hereditary cancer predisposition, tumor genomics, liquid biopsy, precision oncology, molecular hematology, neurogenetics and neurodevelopmental disorders, cytogenomics, genotype–phenotype relationships, and the clinical interpretation of germline and somatic variants.

His work focuses on translating genomic technologies into clinically meaningful diagnostic and molecular-stratification approaches, while contributing to medical genetics residency education, research supervision and genomic laboratory development.

Publications listing this author

Full database

Records from the department’s publication database whose author list includes this name. Author strings are reproduced from the source record and are not rewritten.

Comparative prognostic performance of ELN 2022 and ELN 2024 risk classifications in a Turkish cohort of acute myeloid leukemia patients receiving hypomethylating agents and BCL-2 inhibitors

Etlik Hematology team; includes Erdem HB

Acta Medica · 2026

DOI

Cancer Genetics Hematologic Malignancy Genomics

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

Professional profiles

Biography

Publications listing this author

Comparative prognostic performance of ELN 2022 and ELN 2024 risk classifications in a Turkish cohort of acute myeloid leukemia patients receiving hypomethylating agents and BCL-2 inhibitors

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

Efficacy of risperidone and behavioral delineation in METTL5-related syndrome: a pooled analysis of literature and report of a novel variant

Integrated Clinical, Molecular, and Machine Learning Assessment of Familial Hypercholesterolemia

Monoallelic germline RAD51C, RAD51D, and BRIP1 variants in hereditary cancer testing: Variant spectrum and clinical counselling implications

Monoallelic NTHL1 p.(Gln90*) and cancer risk: evidence from a large Turkish cohort

Prognostic Impact of Serum Albumin Levels at Diagnosis in Patients with Chronic Lymphocytic Leukemia

PRR11 expression in early ER+/HER2-low breast cancer: Association with estrogen receptor positivity and exploratory analysis of prognostic significance

Rare Coexistence of Hidradenitis Suppurativa and Hyper-IgD Syndrome With Homozygous MVK V377I and Compound Heterozygous MEFV (M680I/E148Q) Mutations

Spinocerebellar Ataxia Type 40 Presenting with Isolated Cervical Dystonia: Expanding the Phenotypic Spectrum

Unveiling Mitochondrial DNA Copy Number Alterations: Insights into Progression from Cervical Intraepithelial Neoplasia to Cervical Cancer

Attenuated Form of Nijmegen Breakage Syndrome: Case Report of the Oldest Patient

Decoding Genomic Variants in a Turkish Cohort of Patients with Spasticity

Design, Development, and Clinical Validation of a Novel Kit for Cell-Free DNA Extraction

Evaluation of Mutation Profiles of Cardiomyopathy Patients in the Turkish Cohort

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

Oromandibular Dystonia as the First Reported Presentation of SCA43 Due to MME c.94_95dup (p.Val33Argfs*10)

Effects of BRCA variation on prognosis in patients with nonmetastatic breast cancer

Higher TP53 somatic mutation prevalence from liquid biopsy analysis in ever smoker non-small-cell lung cancer patients

Uncommon variants detected via hereditary cancer panel and suggestions for genetic counseling