Alper Gezdirici

22PUBLICATIONS
177CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Neonatology
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Publications (22)

|Sep 07, 2026
Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

|Mar 28, 2026
Phenotype-Driven Next-Generation Sequencing and Structure-Based In Silico Analysis Reveal Disease-Specific Diagnostic Yield and Genotype-Phenotype Correlations in Inherited Kidney Diseases.

Savas Baris, Kerem Terali, Serdar Bozlak

|Jan 28, 2026
Clinical and Genetic Characteristics of Pheochromocytoma and Paraganglioma: A Single-Center Experience Including a Rare VHL Variant.

Merve Korkmaz Yilmaz, Ozlem Kandemir Alibakan, Aydeniz Aydin Gumus

|Jan 28, 2026
Biallelic Truncating DNAH14 Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review.

Savas Baris, Mustafa Dogan, Kerem Terali

|Jul 23, 2025
Hypohidrotic Ectodermal Dysplasias: Phenotypic and Genotypic Findings in 32 Cases.

Zeynep Esener, Mehmet Akif Yücesoy, Alper Gezdirici

|Jul 23, 2024
A novel variant of the STAR gene: nonclassical presentation from Turkey.

Emel Hatun Aytaç Kaplan, Alper Gezdirici, Zümrüt Kocabey Sütçü

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Frequent Collaborators

7 joint publications

Mustafa Doğan

6 joint publications

Kerem Teralı

4 joint publications

Elif Yilmaz Gulec

3 joint publications

Akif Ayaz