Bilgen Bilge Geckinli - Genetics Department, Zeynep Kamil Women's and Children's Research and Training Hospital

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论文共 73 篇作者统计合作学者相似作者

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Assessment of Genetic Variants Linked to Susceptibility to Mechanical Prosthetic Valve Thrombosis

Semih Kalkan,M. Ozan Gursoy,Ahmet Guner,Semra Gursoy,Macit Kalcik,Bilge Bilgen Geckinli,Kenan Delil,Esra Arslan Ates, Eylem Gokmeydan Erdogan,Sezin Canbek,Emrah Bayam, A. Cagri Aykan,Mehmet Ayturk,Sabahattin Gunduz,Mehmet Ozkan

AMERICAN JOURNAL OF CARDIOLOGY (2025): 22-29

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Genetic Characterization of Turkish Patients with Pituitary Neuroendocrine Tumors

Ceren Alavanda,Ozcan Sonmez,Bilgen Bilge Geckinli,Fatih Bayrakli,Ahmet Ilter Guney

Turkish neurosurgeryno. 2 (2025): 319-320

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Identification of Novel Variants in the NHS in Four Turkish Patients with Nance-Horan Syndrome

Ceren Alavanda,Esra Arslan Ates,Senol Demir,Hamza Polat, Onur Hanoglu,Ahmet Arman,Bilgen Bilge Geckinli

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2025)

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NKX2-5 Gene Variants Associated with Congenital Heart Defects in Turkish Population

Bilgen Bilge Geckinli, Gozde Girgin Ozgumus,Senol Demir,Ayberk Turkyilmaz,Figen Akalin

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICSno. 3 (2024): 158-162

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A Case of Carvajal Syndrome Presenting with Dilated Cardiomyopathy

Sule Arici,Figen Akalin,Bilgen Bilge Geckinli

Cardiology in the Youngpp.1-3, (2024)

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PHARC Syndrome Which an Ultra-Rare Syndrome with Retinitis Pigmentosa and Cataracts: Case Report and Review of the Literature

Senol Demir,Mehmet Orkun Sevik,Aysenur Ersoy,Bilgen Bilge Geckinli,Ozlem Sahin,Esra Arslan Ates

Ophthalmic Geneticsno. 2 (2024): 113-119

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Pubertal Virilization in Individuals with Partial Gonadal Dysgenesis Attributable to Dhh Mutation: A Case Report

Aylin Gunay,Ilknur Kurt, Burcu Ayaz,Ahsen Karagozlu Akgul,Aysenur Ersoy,Bilgen Bilge Geckinli,Zehra Yavas Abali, Mehmet Nuri Ozbek,Tulay Guran

HORMONE RESEARCH IN PAEDIATRICS (2024): 449-449

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The Spondylocarpotarsal Synostosis Syndrome Case with Ventricular Septal Defect Caused by a Homozygous Frameshift Variation in FLNB

Esra Dirimtekin,Esra Arslan Ates,Hamza Polat,Eda Almus,Bilgen B. Geckinli

Journal of Pediatric Genetics (2024)

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OP-104 Utilizing Lactate Dehydrogenase and Aspartate Transaminase As Diagnostic Biomarkers in GM2 Gangliosidoses

Muhammet Terzioğlu,Dilşad Türkdoğan, Emine Genç, Emel Yılmaz Gümüş,Gülten Öztürk,Şenol Demir,Bilgen Bilge Geçkinli, Enver Yaya, Burcu Hişmi, Sebile Kılavuz

Oral Presentation (2024)

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Severe Adrenal Insufficiency in Six Neonates with Normal Newborn Screening for CAH

Ilknur Kurt,Metin Eser,Ahmet Kahveci,Ahmet Ucar,Derya Bulus,Bahar Ozcabi,Omer Guran, Selen Karagozlu,Aysenur Ersoy,Senol Demir,Bilge Geckinli,Tulay Guran

Clinical Endocrinologyno. 2 (2024): 108-113

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