Faculty / Medical Geneticists

Özge Beyza Gündoğdu-Öğütlü

Portrait of Özge Beyza Gündoğdu-Öğütlü

Medical Genetics Specialist

Department
Department of Medical Genetics, Ankara Etlik City Hospital

Professional profiles

Departmental publications

3 records in the database

Records from the department’s publication database linked to this researcher. The count above and this list come from the same index as the Publications page, so the figure matches that page’s author filter exactly. Author strings are reproduced from the source record and are not rewritten.

Benchmarking five large language models in medical genetics: a bilingual comparative evaluation using published and novel expert-authored questions

Özge Beyza Gündoğdu Öğütlü, Benjamin D. Solomon, Yusuf Selman Çelik

Frontiers in Medicine · 2026

Efficacy of risperidone and behavioral delineation in METTL5-related syndrome: a pooled analysis of literature and report of a novel variant

Gündoğdu Öğütlü ÖB; Baştan F; Sever Erdem Z; Öğütlü H; Erdem HB

Acta Neurologica Belgica · 2026

Rare Disease Genetics Neurogenetics & Neurodevelopmental Disorders

Rare Disease Genetics

Integrating Optical Genome Mapping into the Genetic Diagnostic Algorithm: Clinical Utility in Unresolved Autosomal Recessive Disorders from a Large Cohort

Özge Beyza Gündoğdu Öğütlü, Hasan Hüseyin Kazan, Mehmet Burak Mutlu, Mehmet Ali Ergün, Sengul Özdek, Gülsüm Kayhan

Cytogenetic and Genome Research · 2026

Earlier work at previous institutions

13 records

Publications verified as this researcher’s own, carried out before joining the Department of Medical Genetics at Ankara Etlik City Hospital or at another institution. They are listed here as part of their individual record and are deliberately not counted as departmental output.

De novo interstitial 3p21.31p14.2 duplication in a boy with esophageal atresia, talipes equinovarus, and global developmental delay: a case report

Özge Beyza Gündoğdu Öğütlü, Kezban Karabağ

Molecular Syndromology · 2026

Familial Presentation of a Rare NCKAP1 Splice‐Site Variant Associated With a Neurodevelopmental Disorder and Cutaneous Manifestations

Özge Beyza Gündoğdu Öğütlü, Berrin Demır, Zeynep Utlu, Merve Karabak, Filiz Keskin, Oğuzhan Yaralı

American Journal of Medical Genetics Part A · 2026

Structural Variant and Repeat Expansion Findings Identified by Optical Genome Mapping in Complex Autism Spectrum Disorder With Concomitant Neurodevelopmental Disorders

Mehmet Burak Mutlu, Özge Beyza Gündoğdu Öğütlü, Özlem Öz, Fahrettin Duymuş, Serhat Seyhan, Ayşe Gül Bayrak, Mustafa Esad Tezcan, Hakan Öğütlü, Fatma Demiryılmaz, Nurcan Silahtarlıoğlu, Kader Bilgil, Sümeyye Elma, Murat Erdoğan, Hakan Gümüş, Sefer Kumandaş, Fethiye Kılıçaslan

Human Mutation · 2026

Diabetes Insipidus as an Early Clinical Indicator of Wolfram Syndrome Type 1: Evidence From a Symptom‐Based Screening Approach

Özge Beyza Gündoğdu Öğütlü, Atilla Çayır, Ayşe Sena Donmez, Serkan Bilge Koca, Oğuzhan Yaralı, Hüseyin Demirbilek

Pediatric Diabetes · 2025

Eating disorders: clinical update

D. Lynch, Hakan Öğütlü, Özge Beyza Gündoğdu Öğütlü, Elizabeth Barrett, Fiona McNicholas

Irish Journal of Psychological Medicine · 2025

Genetic and clinical characteristics of children with mody: insights into novel HNF4A variants and genotype–phenotype correlation

Meltem Buhur Pirimoglu, Özge Beyza Gündoğdu Öğütlü, Hatice Nursoy, Hüseyin Önay, Şebnem Özemri Sağ, Şehime Gülsün Temel, Erdal Eren

Irish Journal of Medical Science (1971 -) · 2025

Genetic insights and biochemical profiles in hyperlipidemia: a cohort study from Eastern Anatolia

Oğuzhan Yaralı, Muharrem Bayrak, Özge Beyza Gündoğdu Öğütlü, Erdal Kurnaz, Sezai Arslan, Engin Şebin, Mustafa Can Güler

Endocrine Research · 2025

Investigation of BRCA1-BRCA2 Gene Variations in Breast Cancer Patients in the Eastern Anatolian Region of Turkey: A Study of Genetic Predisposition and Clinical Outcomes

Oğuzhan Yaralı, Özge Beyza Gündoğdu Öğütlü, İrfan Buğday, Mustafa Can Güler, Ali Kaan Şanal, Muharrem Bayrak

Akdeniz Medical Journal · 2025

A retrospective study on biotinidase deficiency: analysis of the Eastern Anatolia region patient cohort

Oğuzhan Yaralı, Sezai Arslan, Özge Beyza Gündoğdu Öğütlü, Mustafa Can Güler, Büşra Nur Akgül

Scandinavian Journal of Clinical and Laboratory Investigation · 2024

Epilepsy genetics in the paediatric population of the Eastern Anatolia region of Turkey

Oğuzhan Yaralı, Özge Beyza Gündoğdu Öğütlü, Serdar Saritaş, Mustafa Can Güler, Filiz Keskin, Ayberk Türkyılmaz

Journal of Neurogenetics · 2024

Clinicopathological importance of Ki-67, p27, and p53 expression in gastric cancer

Muhammet Çalık, Elif Demirci, Eren Altun, İlknur Çalık, Özge Beyza Gündoğdu Öğütlü, Nesrin Gürsan, Betül Gündoğdu, Mevlüt Albayrak

TURKISH JOURNAL OF MEDICAL SCIENCES · 2015

Hydatid Cyst Cases with Different Localization: Region of Erzurum

Elif Demirci, Eren Altun, Muhammet Çalık, İrmak Durur-Subasi, Sare Şipal, Özge Beyza Gündoğdu Öğütlü

Turkish Journal of Parasitology · 2015

A new hypothesis about hematopoietic Pbx-interaction protein (HPIP): Can it be a key factor in neurodegeneration in the post-menopausal period?

Murat Karameşe, Selina Aksak, Özge Beyza Gündoğdu Öğütlü, Bünyami Ünal

Medical Hypotheses · 2013