Mona Mahfood
Overview
Explore the profile of Mona Mahfood including associated specialties, affiliations and a list of published articles.
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16
Citations
95
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Recent Articles
1.
Tlili A, Mahfood M, Mutery A, Chouchen J
Hum Genomics
. 2024 Jun;
18(1):59.
PMID: 38844983
Background: Hereditary hearing loss is a rare hereditary condition that has a significant presence in consanguineous populations. Despite its prevalence, hearing loss is marked by substantial genetic diversity, which poses...
2.
Asaad M, Mahfood M, Mutery A, Tlili A
Hum Genomics
. 2023 May;
17(1):42.
PMID: 37189200
Background: Hearing loss is a rare hereditary deficit that is rather common among consanguineous populations. Autosomal recessive non-syndromic hearing loss is the predominant form of hearing loss worldwide. Although prevalent,...
3.
Mutery A, Mohamed W, Mahfood M, Chouchen J, Tlili A
Saudi J Biol Sci
. 2022 Dec;
30(2):103520.
PMID: 36568409
Hearing loss (HL) is the most prevalent sensory disorder whose etiology comes from environmental and/or genetic factors. Approximately 60 % of HL cases are due to mutations in genes responsible...
4.
Hammash D, Mahfood M, Khoder G, Ahmed M, Tlili A, Hamoudi R, et al.
Breast Cancer (Dove Med Press)
. 2022 Aug;
14:187-198.
PMID: 35936987
Background: Most breast cancer-related deaths result from metastasis. Understanding the molecular basis of metastasis is needed for the development of effective targeted and preventive strategies. Matrix metalloproteinase-1 (MMP1) plays an...
5.
Harati R, Hammad S, Tlili A, Mahfood M, Mabondzo A, Hamoudi R
PLoS One
. 2022 Jan;
17(1):e0262152.
PMID: 35025943
Background: The brain endothelial barrier permeability is governed by tight and adherens junction protein complexes that restrict paracellular permeability at the blood-brain barrier (BBB). Dysfunction of the inter-endothelial junctions has...
6.
Moalla M, Safi W, Babiker Mansour M, Hadj Kacem M, Mahfood M, Abid M, et al.
Front Endocrinol (Lausanne)
. 2021 Aug;
12:684018.
PMID: 34393998
Introduction/aims: Maturity-Onset Diabetes of the Young (MODY) is a monogenic non-autoimmune diabetes with 14 different genetic forms. MODY-related mutations are rarely found in the Tunisian population. Here, we explored MODY...
7.
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...
8.
Mutery A, Mahfood M, Chouchen J, Tlili A
Hum Genet
. 2021 Aug;
141(3-4):595-605.
PMID: 34338889
The past 30 years have seen an exponential growth concerning the identification of genes and variants responsible for hereditary hearing loss (HL) worldwide. This has led to a huge gain...
9.
Harati R, Mabondzo A, Tlili A, Khoder G, Mahfood M, Hamoudi R
Breast Cancer Res Treat
. 2021 May;
187(3):695-713.
PMID: 34041621
Purpose: Extravasation of triple-negative (TN) metastatic breast cancer (BC) cells through the brain endothelium (BE) is a critical step in brain metastasis (BM). During extravasation, metastatic cells induce alteration in...
10.
Chouchen J, Mahfood M, Alobathani M, Mohamed W, Tlili A
Int J Pediatr Otorhinolaryngol
. 2020 Nov;
140:110467.
PMID: 33199029
Background: The development of next generation sequencing-based techniques showed an important progress in the identification of pathogenic variants related to monogenetic diseases with genetic and phenotypic heterogeneities. Hereditary hearing loss...