Ahmet Cevdet Ceylan

18PUBLICATIONS
120CO-AUTHORS
Developmental genetics (incl. sex determination)NeurogeneticsCancer geneticsNeonatologyHaematological tumours
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Publications (18)

|Oct 23, 2026
The clinical spectrum of MECP2 variants in males: a multicenter Turkish cohort of 22 probands, with implications for diagnosis and variant interpretation.

|Oct 12, 2026
Phenotypic spectrum of 1q21.1 copy number variants in 42 children: genotype-phenotype correlations and clinical implications.

|Sep 25, 2026
Clinical impact of ENIGMA-based variant reclassification on genotype-phenotype analyses in BRCA1- and BRCA2-associated hereditary breast and ovarian cancer.

|Sep 18, 2026
Pediatric Familial Cerebral Cavernous Malformation Associated With a Novel KRIT1 Initiation-Region Frameshift Variant.

|Sep 16, 2026
Dnmt3b and Dnmt3l knockdown reduces blastocyst development in early mouse embryos.

|Aug 14, 2026
Interstitial Lung Disease in Children: Rare Genetic Variants Beyond Surfactant Dysfunction.

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Frequent Collaborators

3 joint publications

Güzin Cinel

2 joint publications

Figen Gülen

2 joint publications

Melih Hangül

2 joint publications

Sanem Eryılmaz Polat