Namik Kaya

23PUBLICATIONS
30CO-AUTHORS
NeurogeneticsCell and nuclear divisionAutonomic nervous systemNeurology and neuromuscular diseasesNeonatology
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Publications (23)

|Aug 27, 2026
Biallelic EZH1 Nonsense Novel Variant in Two Siblings with Neurodevelopmental Disorder and Central Precocious Puberty: A Case Report from a Consanguineous Saudi Family.

|Aug 13, 2026
A Novel SLC25A4 Variant Causing Mitochondrial Dysfunction, Myopathy and Cardiomyopathy: A Functional and Molecular Characterization.

|Dec 31, 2025
Clinical and Genetic Characterization of Hereditary Sensory and Autonomic Neuropathy Type IV in a Consanguineous Population: Identification of Novel NTRK1 Variants and Expansion of Phenotypic Spectrum.

Amal AlHashem, Hanan AlQudairy, Jana Raed

|Aug 08, 2025
Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness.

Hanan AlQudairy, Mohammad A AlMuhaizea, Mohamed Tohary

|Jun 13, 2025
A Report of a Child with SEC31A-Related Neurodevelopmental Disorder.

Ruqaiah AlTassan, Hanan AlQudairy, Biam Saydo

|Dec 17, 2024
Identification of Diagnostic and Prognostic Subnetwork Biomarkers for Women with Breast Cancer Using Integrative Genomic and Network-Based Analysis.

Olfat Al-Harazi, Achraf El Allali, Namik Kaya

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Frequent Collaborators

12 joint publications

Dilek Colak

5 joint publications

Stefan T Arold

3 joint publications

Mohammad AlMuhaizea

2 joint publications

Tahsin Stefan Barakat