Sebahat Yılmaz Ağladıoğlu

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

Tülay Güran, Federica Buonocore, Nurçin Saka et al. · The Journal of Clinical Endocrinology & Metabolism · 2015 · 212 citations · Full text

Medicine, Endocrinology, Pediatrics +16

Prevalence and long‐term follow‐up outcomes of testicular adrenal rest tumours in children and adolescent males with congenital adrenal hyperplasia

Zehra Aycan, Veysel Nijat Baş, Semra Çeti̇nkaya et al. · Clinical Endocrinology · 2012 · 95 citations

Medicine, Endocrinology, Pediatrics +17

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

Medicine, Genetics, Molecular Genetics +15

Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing

Sebahat Yılmaz Ağladıoğlu, Zehra Aycan, Semra Çeti̇nkaya et al. · Journal of Pediatric Endocrinology and Metabolism · 2015 · 41 citations

Life Sciences, Genetics, Molecular Genetics +9

Insulin Oedema in Newly Diagnosed Type 1 Diabetes Mellitus

Veysel Nijat Baş, Semra Çeti̇nkaya, Sebahat Yılmaz Ağladıoğlu et al. · Journal of Clinical Research in Pediatric Endocrinology · 2010 · 34 citations · Full text

Medicine, Endocrinology, Internal Medicine +9