Tahir Atik

23PUBLICATIONS
157CO-AUTHORS
Gene mappingGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Molecular targetsRespiratory diseases
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Publications (23)

|Aug 19, 2026
Sotos and Malan Syndromes in Childhood: Molecular and Clinical Findings From a Nationwide Cohort of 48 Patients.

|May 15, 2026
Expanding the Neurodevelopmental Spectrum of Xia-Gibbs Syndrome: New Clinical Entities and Novel Variants From a Turkish Cohort.

|Apr 16, 2026
Optical genome mapping identifies previously undetected causal variants in early-onset developmental epileptic encephalopathies.

|Mar 19, 2026
CDK4 and CDK6 variants in patients with primary microcephaly lead to cell cycle defects and mitochondria-induced apoptosis.

Esra Isik, Mohammad Faraz Zafeer, Guney Bademci

|Dec 08, 2025
GNE Mutation-related Congenital Thrombocytopenia in 2 Siblings: Case Reports and Literature Review.

Yeter Düzenli Kar, Melike Sezgin Evim, Ugur Cem Mete

|Oct 09, 2025
Mucolipidosis type II and III: clinical spectrum, genetic landscape, and longitudinal outcomes in a pediatric cohort with six novel mutations.

Fehime Erdem, Ebru Canda, Havva Yazıcı

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Frequent Collaborators

8 joint publications

Özgür Çoğulu

8 joint publications

Esra Işık

7 joint publications

Samim Özen

7 joint publications

Hüseyin Onay