Ahmet Kablan

9PUBLICATIONS
30CO-AUTHORS
NeonatologyAnimal growth and developmentGene expression (incl. microarray and other genome-wide approaches)European history (excl. British, classical Greek and Roman)Gene mapping
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Publications (9)

|Sep 15, 2026
ADNP-Related Neurodevelopmental Disorder: The First Turkish Case Series with Novel Variants and Reduced Intrafamilial Penetrance.

|Aug 19, 2026
ACAN-Related Short Stature and Skeletal Dysplasia: Expanding the Phenotypic and Genotypic Spectrum in a 47 Patient Cohort From Turkey.

|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

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Frequent Collaborators

5 joint publications

Elifcan Tasdelen

4 joint publications

Melike Ataseven Kulalı

4 joint publications

Abdulkerim Kolkıran

4 joint publications

Abdullah Sezer