Maha Abdulhadi‐Atwan

XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription

David Zangen, Yotam Kaufman, Sharon Zeligson et al. · The American Journal of Human Genetics · 2011 · 117 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Novel De Novo Mutation in Sulfonylurea Receptor 1 Presenting as Hyperinsulinism in Infancy Followed by Overt Diabetes in Early Adolescence

Maha Abdulhadi‐Atwan, Jeremy D. Bushman, Sharona Tornovsky-Babaey et al. · Diabetes · 2008 · 57 citations · Full text

Medicine, Endocrinology, Pediatrics +17

Autosomal recessive familial neurohypophyseal diabetes insipidus: onset in early infancy

Abdulsalam Abu‐Libdeh, Floris Levy‐Khademi, Maha Abdulhadi‐Atwan et al. · European Journal of Endocrinology · 2009 · 49 citations

Medicine, Endocrinology, Genetics +17

Role of a Founder c.201_202delCT Mutation and New Phenotypic Features of Congenital Lipoid Adrenal Hyperplasia in Palestinians

Maha Abdulhadi‐Atwan, Amy M. Jean, Wendy K. Chung et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 37 citations · Full text

Life Sciences, Endocrinology, Genetics +17

A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitalia

Oded Breuer, Maha Abdulhadi‐Atwan, Sharon Zeligson et al. · European Journal of Endocrinology · 2012 · 18 citations · Full text

Medicine, Endocrinology, Molecular Genetics +17