Ahmed O. Houmeida

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

Screening of BRCA1/2 variants in Mauritanian breast cancer patients.

Journal: BMC cancer

Published: April 19, 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-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.

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.

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

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

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.

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.

Seroprevalence and Molecular Epidemiology of Hepatitis B and D Viruses in Mauritania: a Systematic Review and Meta-Analysis.

Seroprevalence and Molecular Epidemiology of Hepatitis B and D Viruses in Mauritania: a Systematic Review and Meta-Analysis.

Prevalence and genetic etiology of poly-cystic ovarian syndrome (PCOS) in Mauritania.

Prevalence and genetic etiology of poly-cystic ovarian syndrome (PCOS) in Mauritania.

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

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

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

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

Genomic Evidence of Multiple Introductions of SARS-CoV-2 in Mauritania.

Genomic Evidence of Multiple Introductions of SARS-CoV-2 in Mauritania.

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

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

Screening of BRCA1/2 variants in Mauritanian breast cancer patients.

Screening of BRCA1/2 variants in Mauritanian breast cancer patients.

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

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

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

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

HLA-DQB102, HLA-DRB103 alleles and HLA-DQB102-HLA-DRB103 haplotype confer a significant risk of celiac disease in the Mauritanian population.

HLA-DQB102, HLA-DRB103 alleles and HLA-DQB102-HLA-DRB103 haplotype confer a significant risk of celiac disease in the Mauritanian population.