Merih Berberoğlu

Human and mouse<i>TPIT</i>gene mutations cause early onset pituitary ACTH deficiency

Anne-Marie Pulichino, Sophie Vallette-Kasic, Catherine Couture et al. · Genes & Development · 2003 · 215 citations · Full text

Different Tpit Mutations, Developmental Biology, Pituitary Gland +11

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 · 210 citations

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 · 149 citations · Full text

Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by<i>TPIT</i>Gene Mutations

Sophie Vallette-Kasic, Thierry Brue, Anne-Marie Pulichino et al. · The Journal of Clinical Endocrinology & Metabolism · 2005 · 125 citations · Full text

Genetics, Pathology, Tpit Mutation +17

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 · 86 citations · Full text