Şenay Savaş-Erdeve

32PUBLICATIONS
174CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)NanomedicineImmunogenetics (incl. genetic immunology)
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Publications (32)

|Jun 02, 2026
Clinical and genetic spectrum of SHOX deficiency: phenotypic heterogeneity and the "Jumping SHOX" phenomenon.

|Mar 08, 2026
Expanding the Coffin-Siris syndrome spectrum: genetic, dysmorphic, and endocrine findings in eight cases.

Abdulkerim Kolkiran, Melike Ataseven Kulalı, Tuğba Daşar

|Jul 18, 2025
Two New Families With TAF13 Variant Presenting With Syndromic 46,XY Disorder of Sex Development: Expanding the Clinical Phenotype.

Hasan Arı, Ayberk Türkyılmaz, Ayşe Burcu Doğan Arı

|May 06, 2025
Four New Patients of HHAT -Related Multiple Congenital Anomalies Syndrome (Nivelon-Nivelon-Mabille Syndrome) and a Comprehensive Literature Review.

Ayşe Burcu Doğan Arı, Hasan Arı, Ayberk Türkyılmaz

|Feb 15, 2025
DNA ligase IV deficiency identified in a patient with hypergonadotropic hypogonadism: a case report.

Deniz Yasar, Abdullah Sezer, Caner Aytekin

|Dec 23, 2024
Rare Types of Congenital Adrenal Hyperplasias Other Than 21-hydroxylase Deficiency

Mehmet İsakoca, Şenay Erdeve, Semra Çetinkaya

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Frequent Collaborators

22 joint publications

Semra Çetinkaya

12 joint publications

Zehra Aycan

9 joint publications

Gülin Karacan Küçükali

6 joint publications

Melikşah Keskin