Author

Madoussou Toure

Institution: Institut Pasteur du Maroc

Observed institutions: Institut Pasteur du Maroc, University of Hassan II Casablanca

ORCID: 0009-0001-7827-9027

Observed ORCID: 0009-0001-7827-9027

OpenAlex ID: A5093413591

First report of an Ivorian family with nonsyndromic hearing loss caused by GJB2 compound heterozygous variants

2024 · Madoussou Toure, Ghita Amalou, et al. · Annals of Human Genetics · 1

Expanding the genetic spectrum of neurogenetic disorders in moroccan families by exome sequencing: identification of candidate variants in RYR3, POLR3A, and LAMA2

2026 · Fatima Ezzahra Chentoufi, Assia Idyahia, et al. · Molecular Biology Reports

Computational study of deleterious missense SNPs in the USH1G gene implicated in Usher syndrome

2025 · Kenza El Khair, Madoussou Toure, et al. · Journal of Biomolecular Structure and Dynamics

In-silico assessment of the potential impact of missense SNPs in SYNE4 and SUN1 on the LINC complex and their association with hearing loss

2023 · Madoussou Toure, Salaheddine Redouane, et al. · Human Gene

Works count: 4

Citation count: 1

H-index: 1

I10-index: