Ahmet Kablan

7PUBLICATIONS
22CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)European history (excl. British, classical Greek and Roman)Gene mappingGene and molecular therapyEnvironmental epidemiology
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Publications (7)

|Mar 08, 2026
Expanding the Coffin-Siris syndrome spectrum: genetic, dysmorphic, and endocrine findings in eight cases.

Abdulkerim Kolkiran, Melike Ataseven Kulalı, Tuğba Daşar

|Oct 11, 2025
Founder Variants of the Turkish.

Ahmet Kablan

|Aug 10, 2025
A Founder Allele in SGCG Combining Missense Variant and Multi-Exon Duplication in Turkish Patients With Sarcoglycanopathy.

Abdullah Sezer, Afife Büke, Hasan Hüseyin Kazan

|Apr 07, 2025
Multilocus Disease-Causing Genomic Variations for Genetic Disorders: Single Tertiary Centre Experience From Türkiye.

Ahmet Kablan, Abdullah Sezer, Abdullatif Bakır

|Nov 11, 2024
Expanding the Genetic and Phenotypic Spectrum of Mowat-Wilson Syndrome: A Study of 10 Turkish Patients With an Intrafamilial Recurrence Caused by First Intragenic Large Deletion.

Ahmet Kablan, Esma Ertürkmen Aru, Süleyman Atar

|Jun 05, 2024
Novel homozygous frameshift insertion variant in the last exon of the EDARADD causing hypohidrotic ectodermal dysplasia in two siblings: case report and review of the literature.

Ahmet Kablan, Elifcan Tasdelen

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Frequent Collaborators

3 joint publications

Elifcan Tasdelen

2 joint publications

Fatma Silan

2 joint publications

Melike Ataseven Kulalı

2 joint publications

Abdulkerim Kolkıran