Fatimetou M. Veten - Publications

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

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: December 08, 2025

Impact of TNF-α (- 308G>A and - 857 C>T) promoter variants on susceptibility to chronic hepatitis B virus infection in a cohort of Mauritanian patients: pilot study.

Journal: BMC microbiology

Published: November 24, 2025

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

Journal: Journal of applied genetics

Published: February 14, 2024

Genetic variation of TLR3 gene is associated with the outcome of hepatitis b infection in mauritanian patients: case control study.

Journal: BMC infectious diseases

Published: August 01, 2023

Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness.

Journal: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery

Published: September 30, 2022

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

Journal: Molecular vision

Published: December 01, 2018

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

Journal: European journal of ophthalmology

Published: October 31, 2018

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

Journal: BMC medical genetics

Published: September 08, 2017

Etiology and associated GJB2 mutations in Mauritanian children with non-syndromic hearing loss.

Journal: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery

Published: October 15, 2015

Occurrence of the Codon 24 (A > T) Mutation in the Mauritanian Population.

Journal: Hemoglobin

Published: June 06, 2015

Type 2 diabetes in Mauritania: prevalence of the undiagnosed diabetes, influence of family history and maternal effect.

Journal: Primary care diabetes

Published: September 12, 2012

Hb S [β6(A3)Glu→Val, GAG>GTG] and β-globin gene cluster haplotype distribution in Mauritania.

Journal: Hemoglobin

Published: May 26, 2012