Liat de Vries

Exome Sequencing Reveals SYCE1 Mutation Associated With Autosomal Recessive Primary Ovarian Insufficiency

Liat de Vries, Doron M. Behar, Pola Smirin‐Yosef et al. · The Journal of Clinical Endocrinology & Metabolism · 2014 · 179 citations

Life Sciences, Genetics, Molecular Genetics +17

Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study

Kanetee Busiah, Séverine Drunat, Laurence Vaivre‐Douret et al. · The Lancet Diabetes & Endocrinology · 2013 · 113 citations

Medicine, Genetics, Pediatrics +17

Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity

Sharona Tornovsky, Ana Crane, Karen E. Cosgrove et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 86 citations

Life Sciences, Genetics, Molecular Genetics +17

Treated and untreated women with idiopathic precocious puberty: long‐term follow‐up and reproductive outcome between the third and fifth decades

Liora Lazar, Joseph Meyerovitch, Liat de Vries et al. · Clinical Endocrinology · 2013 · 80 citations

Medicine, Endocrinology, Gynecology +13

Treated and Untreated Women With Idiopathic Precocious Puberty: BMI Evolution, Metabolic Outcome, and General Health Between Third and Fifth Decades

Liora Lazar, Yael Lebenthal, Michal Yackobovitch‐Gavan et al. · The Journal of Clinical Endocrinology & Metabolism · 2015 · 78 citations · Full text

Medicine, Endocrinology, Reproductive Endocrinology +14