Rita Menassa

Functional variants of POC5 identified in patients with idiopathic scoliosis

Patricia Margaritte‐Jeannin, Jean‐Claude Bernard, Eudéline Alix et al. · Journal of Clinical Investigation · 2015 · 116 citations · Full text

Spinal Cord Injury, Genetic Disorder, Genetics +13

New Management Strategy of Pregnancies at Risk of Congenital Adrenal Hyperplasia Using Fetal Sex Determination in Maternal Serum: French Cohort of 258 Cases (2002–2011)

Véronique Tardy-Guidollet, Rita Menassa, Jean‐Marc Costa et al. · The Journal of Clinical Endocrinology & Metabolism · 2014 · 96 citations · Full text

Phenotype-Genotype Correlations of 13 Rare CYP21A2 Mutations Detected in 46 Patients Affected with 21-Hydroxylase Deficiency and in One Carrier

Véronique Tardy, Rita Menassa, V. Sulmont et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 71 citations · Full text

Mutational spectrum of cystic fibrosis in the Lebanese population

Chantal Farra, Rita Menassa, Johnny Awwad et al. · Journal of Cystic Fibrosis · 2010 · 43 citations · Full text

Fibrosis, Mendelian Disorder, Genetic Disorder +4

p.H62L, a Rare Mutation of the CYP21 Gene Identified in Two Forms of 21-Hydroxylase Deficiency

Rita Menassa, Véronique Tardy, F Despert et al. · The Journal of Clinical Endocrinology & Metabolism · 2008 · 37 citations