Nisrine Aboussair

Treacher Collins syndrome: a clinical and molecular study based on a large series of patients

Marie Vincent, David Geneviève, Agnès Ostertag et al. · Genetics in Medicine · 2015 · 162 citations

Medicine, Clinical Sciences, Molecular Genetics +3

Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II

S. Gerber, Sylvain Hanein, Isabelle Perrault et al. · Human Mutation · 2007 · 30 citations · Full text

Medicine, Genetics, Ophthalmology +17

Genetic testing and first presymptomatic diagnosis in Moroccan families at high risk for breast/ovarian cancer

Fatima Zahra Laarabi, Imane Cherkaoui Jaouad, Karim Ouldim et al. · Oncology Letters · 2011 · 26 citations · Full text

Life Sciences, Genetics, Oncology +17

Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype

Isabelle Perrault, Alejandro Estrada‐Cuzcano, Irma López et al. · PLoS ONE · 2013 · 21 citations · Full text

Medicine, Genetics, Molecular Genetics +12

Cytogenetic Analysis of 5572 Patients Referred for Suspected Chromosomal Abnormalities in Morocco

Nisrine Aboussair, Imane Cherkaoui Jaouad, Souad Cherkaoui Dequaqui et al. · Genetic Testing and Molecular Biomarkers · 2012 · 16 citations

Life Sciences, Genetics, Cytogenetics +16