Author

Mouna Hadrami

Institution: Université de Nouakchott

Observed institutions: Université des Sciences, de Technologie et de Médecine, Université de Nouakchott

OpenAlex ID: A5032562792

HLA class I (-A, -B, -C) and class II (-DR, -DQ) polymorphism in the Mauritanian population

2018 · Cheikh Tijani Hamed, Ghlana Meiloud, et al. · BMC Medical Genetics · 11

Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma.

2019 · Mouna Hadrami, Crystel Bonnet, et al. · PubMed · 9

A novel missense mutation of GJA8 causes congenital cataract in a large Mauritanian family

2018 · Mouna Hadrami, Crystel Bonnet, et al. · European Journal of Ophthalmology · 9

Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment

2024 · Malak Salame, Crystel Bonnet, et al. · Journal of Applied Genetics · 2

Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity

2025 · Zied Riahi, Sophie Boucher, et al. · Proceedings of the National Academy of Sciences · 1

Works count: 5

Citation count: 32

H-index: 3

I10-index: 1