Amale Bousfiha

Casablanca, 20100, Morocco

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 17 publications

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

Genetic diversity of Usher syndrome in Moroccan patients.

Genetic diversity of Usher syndrome in Moroccan patients.

Journal: Human genetics
Published: November 20, 2024

Genetic diversity and genomic epidemiology of SARS-CoV-2 during the first 3 years of the pandemic in Morocco: comprehensive sequence analysis, including the unique lineage B.1.528 in Morocco.

Genetic diversity and genomic epidemiology of SARS-CoV-2 during the first 3 years of the pandemic in Morocco: comprehensive sequence analysis, including the unique lineage B.1.528 in Morocco.

Journal: Access microbiology
Published: May 22, 2024

Cytogenetic and epidemiological profile of chronic myeloid leukemia in Morocco.

Cytogenetic and epidemiological profile of chronic myeloid leukemia in Morocco.

Journal: Annals of hematology
Published: November 07, 2023

Impact and prevalence of comorbidities and complications on the severity of COVID-19 in association with age, gender, obesity, and pre-existing smoking: A meta-analysis.

Impact and prevalence of comorbidities and complications on the severity of COVID-19 in association with age, gender, obesity, and pre-existing smoking: A meta-analysis.

Journal: BioMedicine
Published: July 27, 2023

Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.

Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.

Journal: Biochemical genetics
Published: May 02, 2023

Evaluation of SARS-CoV-2 infection risks after primary vaccination with BNT162b2, BBIBP-CorV, or ChAdOx1-nCOV-19 and after homologous and heterologous booster vaccinations with these vaccines and evaluation of SARS-CoV-2 reinfection profiles.

Evaluation of SARS-CoV-2 infection risks after primary vaccination with BNT162b2, BBIBP-CorV, or ChAdOx1-nCOV-19 and after homologous and heterologous booster vaccinations with these vaccines and evaluation of SARS-CoV-2 reinfection profiles.

Journal: BioMedicine
Published: December 22, 2022

Epidemiology, clinical characteristics and risk factors of coronavirus disease 2019 (COVID-19) in Casablanca.

Epidemiology, clinical characteristics and risk factors of coronavirus disease 2019 (COVID-19) in Casablanca.

Journal: Access microbiology
Published: November 18, 2021

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco.

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco.

Journal: Molecular biology reports
Published: August 23, 2021

Chromosome Abnormalities Related to Reproductive and Sexual Development Disorders: A 5-Year Retrospective Study.

Chromosome Abnormalities Related to Reproductive and Sexual Development Disorders: A 5-Year Retrospective Study.

Journal: BioMed research international
Published: September 01, 2020

A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family.

A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family.

Journal: International journal of pediatric otorhinolaryngology
Published: June 20, 2020

Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.

Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.

Journal: Human heredity
Published: July 02, 2019
Showing 1-12 of 17

Last Updated: 09/26/2026