Sukran Poyrazoglu

29PUBLICATIONS

185CO-AUTHORS

NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Infant and child healthCancer therapy (excl. chemotherapy and radiation therapy)

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Publications (29)

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|May 27, 2026

Identifying Genetic Factors Contributing to Non-Syndromic Early-Onset Childhood Obesity Utilizing Whole-Exome Sequencing in Consanguineous Families.

|Feb 06, 2026

Evaluation of rare NR1D2 variants in MODY-X: clinical, genetic, and in silico insights.

Cagatay Aydogan, Deniz Kanca-Demirci, Nurdan Gul

|May 29, 2025

Comparison of the clinical characteristics of children with Silver-Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study.

İlker Tolga Özgen, Tuğçe Kandemir, Melek Yıldız

|Jun 25, 2024

Whole Exome Sequencing Revealed Paternal Inheritance of Obesity-related Genetic Variants in a Family with an Exclusively Breastfed Infant

Hazal Banu Olgun Çelebioğlu, Ayşe Pınar Öztürk, Şükran Poyrazoğlu

|Apr 26, 2024

Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study

Zeynep Şıklar, Elif Özsu, Sirmen Kızılcan Çetin

|Feb 17, 2024

Novel variants ensued genomic imprinting in familial central precocious puberty.

V Karaman, E Karakilic-Ozturan, S Poyrazoglu

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Frequent Collaborators

18 joint publications

Firdevs Baş

17 joint publications

Feyza Darendelıler

9 joint publications

Aslı Kardelen

8 joint publications

Esin Karakılıc Ozturan

Ayşe Pınar Öztürk

Melek Yıldız

Merih Berberoğlu

Zehra Yavaş Abalı