Serkan Bilge Koca

23PUBLICATIONS
80CO-AUTHORS
Developmental genetics (incl. sex determination)Women's studies (incl. girls' studies)Adolescent healthGene mappingSexualities
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Publications (23)

|Jun 24, 2026
Long-term clinical outcomes of primary adrenal insufficiency caused by homozygous CYP11A1 p.R451W variant.

|Apr 15, 2026
Bioelectrical Impedance Analysis to Identify the Affected Body Component in Girls With Celiac Disease.

Arzu Gülseren, Esra Eren, Serkan Bilge Koca

|Apr 11, 2026
The role of Spexin and Phoenixin-20 in girls during puberty.

Serkan Bilge Koca, Tarık Kırkgöz, Leyla Kara

|Nov 15, 2025
A novel homozygous c.301T > C, p.Y101H variant in the GNA11 gene is implicated in familial hypocalciuric hypercalcemia type 2 in a proband with the heterozygous variant present in mother and father - A case report.

Serkan Bilge Koca, Burhan Balta

|Nov 10, 2025
Bioelectrical impedance analysis and hormonal assessment in adolescents with pubertal gynecomastia.

Tarık Kırkgöz, Serkan Bilge Koca

|Oct 13, 2025
Diabetes Insipidus as an Early Clinical Indicator of Wolfram Syndrome Type 1: Evidence From a Symptom-Based Screening Approach.

Ozge Beyza Gundogdu Ogutlu, Atilla Cayır, Ayşe Sena Donmez

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Frequent Collaborators

8 joint publications

Gönül Büyükyılmaz

4 joint publications

Keziban Toksoy Adıgüzel

4 joint publications

Mehmet Boyraz

4 joint publications

Tarık Kırkgöz