Mustafa Dogan

12PUBLICATIONS
40CO-AUTHORS
NeurogeneticsNeurology and neuromuscular diseasesGene and molecular therapyGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (12)

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

Savas Baris, Mustafa Dogan, Kerem Terali

|Nov 03, 2025
Delineating the Adult Phenotype of PGM2L1 -Related Neurodevelopmental Disorder.

Pelin Ercoskun, Ekrem Akbulut, Cuneyd Yavas

|Sep 04, 2025
Juvenile Hyaline Fibromatosis Syndrome: A Novel Variant in the ANTXR2 Gene Causing Severe Phenotype.

Ilayda Akyon, Ozgenur Ozen, Mustafa Dogan

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

Zeynep Esener, Mehmet Akif Yücesoy, Alper Gezdirici

|Apr 26, 2024
Discovery of a novel homozygous SOD1 truncating variant bolsters infantile SOD1 deficiency syndrome.

Mustafa Dogan, Kerem Teralı, Recep Eroz

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Frequent Collaborators

7 joint publications

Alper Gezdirici

5 joint publications

Kerem Teralı

4 joint publications

Cüneyd Yavaş

3 joint publications

Recep Eröz