Gönül Öçal

Phenotypical, Biological, and Molecular Heterogeneity of 5α-Reductase Deficiency: An Extensive International Experience of 55 Patients

Laurent Maı̈moun, Pascal Philibert, B. Cammas et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 213 citations

Medicine, Endocrinology, Genetics +17

Severe Growth Hormone Insensitivity Resulting from Total Absence of Signal Transducer and Activator of Transcription 5b

Vivian Hwa, Brian M. Little, Pelin Adıyaman et al. · The Journal of Clinical Endocrinology & Metabolism · 2005 · 150 citations · Full text

Medicine, Endocrinology, Endocrine Genetics +11

Adherence to Growth Hormone Therapy: Results of a Multicenter Study

Banu Küçükemre Aydın, Zehra Aycan, Zeynep Şıklar et al. · Endocrine Practice · 2013 · 87 citations

Pharmacy, Endocrinology, Pharmacotherapy +11

Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

Sarah E. Flanagan, Weijia Xie, Richard Caswell et al. · The American Journal of Human Genetics · 2012 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Vitamin D Deficiency in Turkish Mothers and Their Neonates and in Women of Reproductive Age

Ayça Törel Ergür, Merih Berberoğlu, Begüm Atasay et al. · Journal of Clinical Research in Pediatric Endocrinology · 2009 · 80 citations · Full text

Medicine, Endocrinology, Maternal Health +15