Ahmet Cevdet Ceylan

16PUBLICATIONS
83CO-AUTHORS
Cancer geneticsNeonatologyHaematological tumoursGene expression (incl. microarray and other genome-wide approaches)Liquid biopsies
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Publications (16)

|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.

|Jun 12, 2026
Homozygous TP53 alterations: a case of a biallelic splice variant and a brief review of the literature.

|Mar 08, 2026
MLPA-Detected CFTR Exon Deletions in Children With Inconclusive CFTR Sequencing: A Single-Center Experience From Türkiye.

Sanem Eryılmaz Polat, Çelebi Yıldırım, Hande Yetişgin

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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