Halima Nahili

AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men

Laila Imken, Brahim El Houate, Abdelaziz Chafik et al. · Asian Journal of Andrology · 2007 · 56 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation

Omar Abidi, Redouane Boulouiz, Halima Nahili et al. · International Journal of Pediatric Otorhinolaryngology · 2007 · 39 citations

Life Sciences, Genetics, Molecular Genetics +13

The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population

Majida Charif, Safaa Bounaceur, Omar Abidi et al. · Molecular Biology Reports · 2012 · 27 citations

Life Sciences, Genetics, Molecular Genetics +12

Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees

Amina Bakhchane, Majida Charif, Sara Salime et al. · PLoS ONE · 2015 · 27 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility

Hicham Charoute, Halima Nahili, Omar Abidi et al. · European Journal of Human Genetics · 2013 · 24 citations

Life Sciences, Genetics, Molecular Genetics +13