Haktan B. Erdem
Ankara, Turkey
Last Updated: 09/26/2026
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Found 42 publications
Monoallelic germline RAD51C, RAD51D, and BRIP1 variants in hereditary cancer testing: Variant spectrum and clinical counselling implications.
Journal: Mutation research
Published: March 02, 2026
Efficacy of risperidone and behavioral delineation in METTL5-related syndrome: a pooled analysis of literature and report of a novel variant.
Journal: Acta neurologica Belgica
Published: February 24, 2026
Integrated Clinical, Molecular, and Machine Learning Assessment of Familial Hypercholesterolemia.
Journal: Life (Basel, Switzerland)
Published: February 24, 2026
Monoallelic NTHL1 p.(Gln90*) and cancer risk: evidence from a large Turkish cohort.
Journal: Familial cancer
Published: January 26, 2026
Prognostic Impact of Serum Albumin Levels at Diagnosis in Patients with Chronic Lymphocytic Leukemia.
Journal: Journal of clinical medicine
Published: December 11, 2025
Dramatic clonazepam response in dystonic head tremor associated with PEX10-related peroxisomal biogenesis disorder.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: October 06, 2025
PRR11 expression in early ER+/HER2-low breast cancer: Association with estrogen receptor positivity and exploratory analysis of prognostic significance.
Journal: Oncology letters
Published: September 25, 2025
Unveiling mitochondrial DNA copy number alterations: Insights into progression from cervical intraepithelial neoplasia to cervical cancer.
Journal: Oncology letters
Published: September 06, 2025
Spinocerebellar ataxia type 40 presenting with isolated cervical dystonia: expanding the phenotypic spectrum.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: August 27, 2025
Design, Development, and Clinical Validation of a Novel Kit for Cell-Free DNA Extraction.
Journal: Diagnostics (Basel, Switzerland)
Published: June 08, 2025
Rare Coexistence of Hidradenitis Suppurativa and Hyper-IgD Syndrome With Homozygous MVK V377I and Compound Heterozygous MEFV (M680I/E148Q) Mutations.
Journal: Pediatric dermatology
Published: May 21, 2025
Last Updated: 09/26/2026