Serdar Bozlak

6PUBLICATIONS
47CO-AUTHORS
Genetic immunologyEpigenetics (incl. genome methylation and epigenomics)Gene mappingNeurogeneticsPaediatrics not elsewhere classified
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Publications (6)

|Sep 29, 2026
Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

|Sep 26, 2026
Novel Homozygous LAMC3 Frameshift Variant Associated with Confluent Leukoencephalopathy and Low-Grade Tectal Glioneuronal Tumor: Expanding the Phenotypic Spectrum with Bioinformatic Characterization.

|Aug 13, 2026
Neurovascular Involvement in Arterial Tortuosity Syndrome Associated with a Homozygous SLC2A10 p.(Trp162Ter) Variant: Clinical, Molecular, and In Silico Characterization.

|Jul 28, 2026
Reclassification of PAPSS2 Missense Variants in Turkish Patients with Brachyolmia Type 4: Multi-Modal Computational and Structural Biology Evidence for APS-Kinase Domain Dysfunction.

|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

|Aug 23, 2025
Atypical pediatric presentation of hyperparathyroidism: CDC73 gene mutation and parathyroid carcinoma.

Emel Hatun Aytaç Kaplan, Mehmet Çakmak, M Banu Yilmaz Özgüven

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Frequent Collaborators

4 joint publications

Cuneyd Yavas

2 joint publications

Tunay Dogan

2 joint publications

Alper Gezdirici

1 joint publications

Emel Hatun Aytaç Kaplan