Redouane Boulouiz

A Mutation in PNPT1, Encoding Mitochondrial-RNA-Import Protein PNPase, Causes Hereditary Hearing Loss

Simon von Ameln, Geng Wang, Redouane Boulouiz et al. · The American Journal of Human Genetics · 2012 · 97 citations · Full text

Mitochondrial Function, Genetic Disorder, Genetics +7

Mutations in TPRN Cause a Progressive Form of Autosomal-Recessive Nonsyndromic Hearing Loss

Yun Li, Esther Pohl, Redouane Boulouiz et al. · The American Journal of Human Genetics · 2010 · 59 citations · Full text

Developmental Biology, Genetic Disorder, Progressive Form +10

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 · 54 citations · Full text

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

Mendelian Disorder, Genetic Disorder, Medicine +9

Distribution and features of hematological malignancies in Eastern Morocco: a retrospective multicenter study over 5 years

Mounia Elidrissi Errahhali, Manal Elidrissi Errahhali, Redouane Boulouiz et al. · BMC Cancer · 2016 · 35 citations · Full text