Walaa Kamal Eddine Ahmad Mohamed

Overview

Explore the profile of Walaa Kamal Eddine Ahmad Mohamed including associated specialties, affiliations and a list of published articles.

Snapshot

Articles 4

Citations 24

Followers 0

Related Specialties

Molecular Biology

Genetics

General Medicine

Co-Authors

Abdelaziz Tlili

Mona Mahfood

Abdullah Al Mutery

Khalid Bajou

Jihen Chouchen

Abdullah Fahd Al Mutery

Rania Harati

Hassen Hadj Kacem

Published In

Genet Test Mol Biomarkers

PLoS One

Saudi J Biol Sci

Affiliations

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Recent Articles

Whole exome sequencing, in silico and functional studies confirm the association of the mutation p.Cys169Tyr with deafness and suggest a role for the gene in the hearing process

Mahfood M, Chouchen J, Kamal Eddine Ahmad Mohamed W, Mutery A, Harati R, Tlili A

Saudi J Biol Sci . 2021 Aug; 28(8):4421-4429. PMID: 34354426

The development of next generation sequencing techniques has facilitated the detection of mutations at an unprecedented rate. These efficient tools have been particularly beneficial for extremely heterogeneous disorders such as...

Clinical Exome Sequencing Identifies a Frameshift Mutation Within the STRC Gene in a United Arab Emirates Family with Profound Nonsyndromic Hearing Loss

Mahfood M, Kamal Eddine Ahmad Mohamed W, Mutery A, Tlili A

Genet Test Mol Biomarkers . 2019 Feb; 23(3):204-208. PMID: 30758234

Aims: Autosomal recessive nonsyndromic hearing loss (ARNSHL) is the most common form of hereditary deafness. Despite its frequency, the diagnosis of this disorder continues to be a challenging task given...

Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss

Tlili A, Mutery A, Kamal Eddine Ahmad Mohamed W, Mahfood M, Hadj Kacem H

Genet Test Mol Biomarkers . 2017 Oct; 21(11):686-691. PMID: 29016196

Aim: Mutations in the gap junction protein beta 2 (GJB2) gene are responsible for more cases of nonsyndromic recessive hearing loss than any other gene. The purpose of our study...

Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation

Tlili A, Al Mutery A, Mahfood M, Kamal Eddine Ahmad Mohamed W, Bajou K

PLoS One . 2017 Sep; 12(9):e0185281. PMID: 28945813

Autosomal recessive non-syndromic hearing loss is one of the most common monogenic diseases. It is characterized by high allelic and locus heterogeneities that make a precise diagnosis difficult. In this...