Sinem Kocagil

5PUBLICATIONS
39CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Cancer geneticsAnimal welfareNeurology and neuromuscular diseases
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Publications (5)

|Aug 10, 2026
An episignature informed systematic analysis to ascertain the clinical significance and consequences of CHD8 missense variants.

|Jul 23, 2025
Hypohidrotic Ectodermal Dysplasias: Phenotypic and Genotypic Findings in 32 Cases.

Zeynep Esener, Mehmet Akif Yücesoy, Alper Gezdirici

|Jul 04, 2025
A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia.

Abdullah Sezer, Sukru S Oner, Hanife Saat

|Mar 31, 2022
Spectrum of PAH gene mutations and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Turkey.

Müge Çınar, Gonca Kılıç Yıldırım, Sinem Kocagil

|Sep 25, 2021
NDE1-related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly.

Hasan Bas, Suzan Saylisoy, Oguz Cilingir

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Frequent Collaborators

2 joint publications

Hasan Bas

1 joint publications

Müge Çınar

1 joint publications

Gonca Kılıç Yıldırım

1 joint publications

Oğuz Çilingir