İhsan Turan

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

CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

İhsan Turan, B. Ian Hutchins, Bülent Hacıhamdioğlu et al. · The Journal of Clinical Endocrinology & Metabolism · 2017 · 38 citations · Full text

Changes in the presentation of newly diagnosed type 1 diabetes in children during the COVID-19 pandemic in a tertiary center in Southern Turkey

Fatih Gürbüz, İhsan Turan, Can Celiloğlu et al. · Journal of Pediatric Endocrinology and Metabolism · 2021 · 35 citations

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1

Leman Damla Kotan, Charlton Cooper, Şükran Darcan et al. · Journal of Clinical Research in Pediatric Endocrinology · 2016 · 27 citations · Full text

Prevalence and associated phenotypes of <i>PLXNA1</i> variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism

Leman Damla Kotan, İhsan Turan, Eda Mengen et al. · Clinical Genetics · 2018 · 24 citations

Genetics, Genetic Epidemiology, Pathology +17