Abdelhamid I. Barakat

Casablanca, Morocco

Last Updated: 09/26/2026

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Found 119 publications

Identification of deleterious missense variants of serine peptidase inhibitor Kazal type 2 gene and their impact on KAZAL domain structure, stability, flexibility, and dimension.

Identification of deleterious missense variants of serine peptidase inhibitor Kazal type 2 gene and their impact on KAZAL domain structure, stability, flexibility, and dimension.

Journal: Journal of biomolecular structure & dynamics

Published: January 30, 2026

Mutational spectrum of SLC26A4 and SLC26A5 associated with hereditary hearing loss in Moroccan families.

Mutational spectrum of SLC26A4 and SLC26A5 associated with hereditary hearing loss in Moroccan families.

Journal: Human genomics

Published: January 10, 2026

Emergence of rare SARS-CoV-2 subvariant LF.7.3 obtained from Moroccan COVID-19 patients.

Emergence of rare SARS-CoV-2 subvariant LF.7.3 obtained from Moroccan COVID-19 patients.

Journal: Microbiology resource announcements

Published: January 09, 2026

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

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

Journal: Molecular biology reports

Published: December 16, 2025

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.

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

Published: December 08, 2025

In silico analysis of missense SNPs in APPL1 gene: implications on APPL1-AKT2 complex and its relation to MODY 14.

In silico analysis of missense SNPs in APPL1 gene: implications on APPL1-AKT2 complex and its relation to MODY 14.

Journal: Journal of biomolecular structure & dynamics

Published: November 27, 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.

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

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

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

Journal: Journal of biomolecular structure & dynamics

Published: September 02, 2025

Disorders of sex development associated with MPI and RSPH1 variants expand the phenotypic spectrum of CDG and PCD in Morocco.

Disorders of sex development associated with MPI and RSPH1 variants expand the phenotypic spectrum of CDG and PCD in Morocco.

Journal: Molecular biology reports

Published: August 26, 2025

Novel splice variants implicated in inherited retinal dystrophies in two Moroccan families.

Novel splice variants implicated in inherited retinal dystrophies in two Moroccan families.

Journal: Molecular biology reports

Published: June 15, 2025

Computational study of the potential impact of WHRN protein missense SNPs on WHRN-MYO15A protein complex interaction and their association with Usher syndrome.

Computational study of the potential impact of WHRN protein missense SNPs on WHRN-MYO15A protein complex interaction and their association with Usher syndrome.

Journal: Journal of biomolecular structure & dynamics

Published: May 19, 2025

Genomic surveillance in Morocco tracks SARS-CoV-2 variant shift from Alpha to Omicron sublineage JN1.

Genomic surveillance in Morocco tracks SARS-CoV-2 variant shift from Alpha to Omicron sublineage JN1.

Journal: Npj viruses

Published: May 15, 2025

Showing 1-12 of 119

Last Updated: 09/26/2026