Eyyüp Üçtepe

4PUBLICATIONS
27CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Gene mapping
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Publications (4)

|Aug 13, 2026
Novel Compound Heterozygous Variants in SLC13A3 Associated With ARLIAK: A Case Report and Review of the Literature.

|Mar 13, 2026
Biallelic Novel SKOR2 Variants in Individuals With Cerebellar Hypoplasia and Intellectual Disability, Expanding the Phenotypic Spectrum of Valence-Farazi Cerebellar Ataxia Syndrome.

Aya Abu-El-Haija, Allan Bayat, Hanifenur Mancılar

|Mar 10, 2026
De Novo 3q27.1 Microdeletion Refines the Critical Region and Implicates PSMD2 Haploinsufficiency in Growth and Neurodevelopmental Abnormalities.

Eyyup Uctepe, Fatma Nisa Esen, Hanifenur Mancilar

|Dec 01, 2025
Revisiting Wiedemann-Steiner Syndrome: Novel KMT2A Variants and Broadened Clinical Spectrum.

Zehra Manav Yiğit, Aydan Mengübaş Erbaş, Ayberk Türkyılmaz

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Frequent Collaborators

2 joint publications

Hanifenur Mancılar

1 joint publications

Zehra Manav Yiğit

1 joint publications

Aydan Mengübaş Erbaş

1 joint publications

Ayberk Türkyılmaz