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Fatimetou Veten

Observed names: Fatimetou M. Veten, Fatimetou VETEN, Fatimetou Vetten
OpenAlex ID: A5064055719
Etiology and associated GJB2 mutations in Mauritanian children with non-syndromic hearing loss
2016 · Ely Cheikh Mohamed Moctar, Zied Riahi, et al. · European Archives of Oto-Rhino-Laryngology · 22
Type 2 diabetes in Mauritania: Prevalence of the undiagnosed diabetes, influence of family history and maternal effect
2013 · Ghlana Meiloud, Imen Arfa, et al. · Primary care diabetes · 17
Hb S [β6(A3)Glu→Val, GAG>GTG] and β-Globin Gene Cluster Haplotype Distribution in Mauritania
2012 · Fatimetou M. Veten, Isselmou O. Abdelhamid, et al. · Hemoglobin · 12
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
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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
Genetic variation of TLR3 gene is associated with the outcome of hepatitis b infection in mauritanian patients: case control study
2024 · Tetou Soumbara, Crystel Bonnet, et al. · BMC Infectious Diseases · 4
Occurrence of the Codon 24 (A > T) Mutation in the Mauritanian Population
2015 · Fatimetou Veten, Sidi Ghaber, et al. · Hemoglobin · 4
Epidemiological and Clinicopathological Features of Breast Cancer in Mauritania
2021 · Selma MOHAMED BRAHIM, Cheikh Tijani HAMED, et al. · Research Square · 3
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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
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Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness
2023 · Malak Salame, Crystel Bonnet, et al. · European Archives of Oto-Rhino-Laryngology · 2
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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
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HLA-DQB1*02, HLA-DRB1*03 alleles and HLA-DQB1*02-HLA-DRB1*03 haplotype confer a significant risk of celiac disease in the Mauritanian population
2026 · Saleck Mahfoudh Ebebecar, Malak Salame, et al. · BMC Gastroenterology
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
2026 · Saffiya Mounira Ennahoui, Abdallah Sid M’Hamed, et al. · BMC Microbiology
Parkinson’s disease in Mauritania: Epidemiological profile and contribution to the genetic analysis (the G2019S mutation)
2025 · Elhafedh El Mouhab, Sidati Mohamed Lemine, et al. · Neuroscience
Works count: 15
Citation count: 96
H-index: 6
I10-index: 4
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