Abdelhamid Barakat

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

Y-Chromosome Analysis in Egypt Suggests a Genetic Regional Continuity in Northeastern Africa

Franz Manni, Pascal Leonardi, Abdelhamid Barakat et al. · Human Biology · 2002 · 75 citations

Genetics, Y Chromosome, Genetic Analysis +17

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies

Claire Angebault, Pierre‐Olivier Guichet, Yasmina Talmat-Amar et al. · The American Journal of Human Genetics · 2015 · 72 citations · Full text

Rtn4ip1 Cause Isolated, Mendelian Disorder, Genetic Disorder +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

Mutations in the protamine locus: association with spermatogenic failure?

Laila Imken, Hassan Rouba, Brahim El Houate et al. · Molecular Human Reproduction · 2009 · 57 citations

Fertility, Genetics, Genetic Epidemiology +17