Bahar Özcabı

Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

Leman Damla Kotan, Gaëtan Ternier, Aydilek Dağdeviren Çakır et al. · Genetics in Medicine · 2021 · 54 citations · Full text

Infertility, Andrology, Female Infertility +14

Vitamin D Deficiency and Hashimoto’s Thyroiditis in Children and Adolescents: a Critical Vitamin D Level for This Association?

Olcay Evliyaoğlu, Manolya Acar, Bahar Özcabı et al. · Journal of Clinical Research in Pediatric Endocrinology · 2015 · 46 citations · Full text

Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene

Bahar Özcabı, Feride Tahmiscioğlu Bucak, Serdar Ceylaner et al. · Journal of Clinical Research in Pediatric Endocrinology · 2015 · 25 citations · Full text

Immunodeficiencies, Immunology, Pathology +18

Evaluation of Adenovirus-36 (Ad-36) antibody seropositivity and adipokine levels in obese children

Bekir Kocazeybek, Harika Öykü Dinç, Sevgi Ergin et al. · Microbial Pathogenesis · 2017 · 25 citations

Obesity, Metabolic Syndrome, Body Composition +11

Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation

Olcay Evliyaoğlu, Oya Ercan, Emel Ataloğlu et al. · Journal of Clinical Research in Pediatric Endocrinology · 2017 · 22 citations · Full text

Genetics, Genetic Epidemiology, Pathology +22