Abdelhamid Barakat
Institut Pasteur du Maroc(MA)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Genomics and Rare Diseases, Vestibular and auditory disorders, Connexins and lens biology, Mitochondrial Function and Pathology
Most-Cited Works
- → A Mutation in PNPT1, Encoding Mitochondrial-RNA-Import Protein PNPase, Causes Hereditary Hearing Loss(2012)97 cited
- → Consanguinity and Inbreeding in Health and Disease in North African Populations(2019)79 cited
- → Y-Chromosome Analysis in Egypt Suggests a Genetic Regional Continuity in Northeastern Africa(2002)75 cited
- → Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies(2015)73 cited
- → Chromosomal abnormalities in couples with recurrent spontaneous miscarriage: a 21-year retrospective study, a report of a novel insertion, and a literature review(2018)61 cited
- → Mutations in TPRN Cause a Progressive Form of Autosomal-Recessive Nonsyndromic Hearing Loss(2010)59 cited
- → Mutations in the protamine locus: association with spermatogenic failure?(2009)57 cited
- → Novel Mutations Involving the INSL3 Gene Associated With Cryptorchidism(2007)56 cited
- → AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men(2007)54 cited
- → The gene distribution of the maize genome.(1995)51 cited