Ahmet Okay Çağlayan

10PUBLICATIONS
52CO-AUTHORS
Ngā kaiwhakawhānau me te mātai mate tamariki o te Māori (Māori midwifery and paediatrics)Medical infection agents (incl. prions)Haematological tumoursAdolescent healthImmunogenetics (incl. genetic immunology)
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Publications (10)

|Aug 26, 2026
The First Case Series of Malattia Leventinese/Doyne Honeycomb Retinal Dystrophy in Türkiye Identified with EFEMP1 Gene Mutation.

|May 15, 2026
Elucidating the Genetic Landscape, Phenotypic Spectrum, and Pathogenic Mechanisms in a Turkish Cohort with Primary Microcephaly.

|Jan 01, 2025
Dysregulation of mTOR signalling is a converging mechanism in lissencephaly.

Ce Zhang, Dan Liang, A Gulhan Ercan-Sencicek

|May 20, 2024
Peripheral Expression of MACROD2 Gene Is Reduced Among a Sample of Turkish Children with Autism Spectrum Disorder.

Alper Alnak, İpek Kuşcu Özücer, Ahmet Okay Çağlayan

|May 20, 2024
Peripheral Expression of ADORA2A Is Increased and Is Correlated with Autism Spectrum Disorder Severity in a Sample of Turkish Children.

Hilal Akköprü, Alper Alnak, Zeynep Nur Karadoğan

|Sep 01, 2023
Genetic, serological and clinical evaluation of childhood myasthenia syndromes- single center subgroup analysis experience in Turkey.

Özlem Özsoy, Tayfun Cinleti, Çağatay Günay

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Frequent Collaborators

2 joint publications

Murat Coşkun

2 joint publications

Alper Alnak

2 joint publications

Murat Gunel

2 joint publications

Cengiz Yalçınkaya