Sukran Poyrazoglu

30PUBLICATIONS
188CO-AUTHORS
Adolescent healthNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Infant and child health
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Publications (30)

|Aug 06, 2026
Assessment of cardiometabolic risk using single point insulin sensitivity estimator (SPISE) in pediatric Bardet-Biedl Syndrome: a pilot study.

|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

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Frequent Collaborators

19 joint publications

Firdevs Baş

18 joint publications

Feyza Darendelıler

10 joint publications

Aslı Kardelen

8 joint publications

Esin Karakılıc Ozturan