Publications by authors named "Omar Abidi"

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Association of gene polymorphisms with type 2 diabetes and its complications in Moroccan population.
Houda El Alami, Meryem Bouqdayr, Khaoula Errafii, Wajih Rhalem, Lahcen Wakrim, Omar Abidi

Nucleosides Nucleotides Nucleic Acids· December 2025

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Safety and effectiveness of apixaban use for stroke prevention during Ramadan fasting (the API-RAM study).
Aiman Ghrab, Rania Gargouri, Faouzi Addad, Anis Cheikhrouhou, Mariem Jabeur, Omar Abidi

Front Pharmacol· October 2025

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Unveiling the prevalence of Helicobacter pylori CagA and VacA virulence markers in Moroccan children and adolescents.
Fatima Zahra Kheir, Aicha Baalala, Omar Abidi, Abdelhak Abkari, Ghizlane Bounder

Eur J Clin Microbiol Infect Dis· September 2025

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Risk factors for hypertension in patients with type 2 diabetes mellitus in the Casablanca-Settat region, Morocco: a cross-sectional study.
Houda El Alami, Meryem Bouqdayr, Khaoula Errafii, Mustapha Lkhider, Najib Al Idrissi, Omar Abidi

Pan Afr Med J· August 2025

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Association of CpG site of gene promoter and type 2 diabetes in Moroccan population susceptibility.
Houda El Alami, Meryem Bouqdayr, Khaoula Errafii, Nouha Messaoudi, Sofia Sehli, Omar Abidi

Nucleosides Nucleotides Nucleic Acids· July 2025

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Meta-analysis of MTHFR C677T polymorphism and type 2 diabetes mellitus in MENA region.
Houda El Alami, Faissal Ouenzar, Khaoula Errafii, Najib Alidrissi, Lahcen Belyamani, Omar Abidi

Diabetes Metab Syndr· February 2024

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Association between Methylene-Tetrahydrofolate Reductase C677T Polymorphism and Human Immunodeficiency Virus Type 1 Infection in Morocco.
Hanâ Baba, Meryem Bouqdayr, Asmae Saih, Rajaa Bensghir, Ahd Ouladlahsen, Omar Abidi

Lab Med· January 2023

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Prevalence of dyslipidemia and the relationship between HbA1C and lipid profile in Moroccan patients with T2DM: a cross-sectional study.
Houda El Alami, Imane Haddou, Ghizlane Benaadi, Mustapha Lkhider, Lahcen Wakrim, Omar Abidi

Pan Afr Med J· January 2023

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Prevalence and risk factors of chronic complications among patients with type 2 diabetes mellitus in Morocco: a cross-sectional study.
Houda El Alami, Imane Haddou, Ghizlane Benaadi, Mustapha Lkhider, Driss El Habchi, Omar Abidi

Pan Afr Med J· June 2022

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Relationship between insertion/deletion (I/D) polymorphism of angiotensin converting enzyme (ACE) gene and susceptibility to type 2 diabetes mellitus in the Middle East and North Africa Region: A meta-analysis.
Houda El Alami, Hassan Ghazal, Omar Abidi, Najib Al Idrissi, Lahcen Wakrim

Diabetes Metab Syndr· January 2022

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Methylenetetrahydrofolate Reductase Gene Polymorphisms (C677T and A1298C) and Hemorrhagic Stroke in Moroccan Patients.
Omar Abidi, Mohammed Haissam, Halima Nahili, Abdessamad El Azhari, Said Hilmani

J Stroke Cerebrovasc Dis· July 2018

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TNF A -308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis.
Hajar Sefri, Houda Benrahma, Hicham Charoute, Fouzia Lakbakbi el Yaagoubi, Hassan Rouba, Omar Abidi

Mol Biol Rep· September 2014

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The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.
Hicham Charoute, Halima Nahili, Omar Abidi, Khalid Gabi, Hassan Rouba

Eur J Hum Genet· March 2014

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Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.
Majida Charif, Amina Bakhchane, Omar Abidi, Redouane Boulouiz, Abdelmajid Eloualid

Gene· July 2013

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Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.
Majida Charif, Redouane Boulouiz, Amina Bakhechane, Houda Benrahma, Halima Nahili, Omar Abidi

Indian J Hum Genet· July 2013

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Clinicopathological features and molecular analysis of primary glioblastomas in Moroccan patients.
Said Hilmani, Omar Abidi, Houda Benrahma, Mehdi Karkouri, Souha Sahraoui

J Mol Neurosci· March 2013

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c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum.
Mohamed Amine Senhaji, Omar Abidi, Sellama Nadifi, Hakima Benchikhi, Khadija Khadir

Arch Dermatol Res· January 2013

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The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.
Majida Charif, Safaa Bounaceur, Omar Abidi, Halima Nahili, Hassan Rouba

Mol Biol Rep· December 2012

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A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.
Simon von Ameln, Geng Wang, Redouane Boulouiz, Mark A Rutherford, Geoffrey M Smith, Omar Abidi

Am J Hum Genet· November 2012

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Association of the MTHFR A1298C variant with unexplained severe male infertility.
Abdelmajid Eloualid, Omar Abidi, Majida Charif, Brahim El Houate, Houda Benrahma

PLoS One· August 2012

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Association of spermatogenic failure with the b2/b3 partial AZFc deletion.
Abdelmajid Eloualid, Houria Rhaissi, Ahmed Reguig, Safaa Bounaceur, Brahim El Houate, Omar Abidi

PLoS One· August 2012

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Association of the C677T polymorphism in the human methylenetetrahydrofolate reductase (MTHFR) gene with the genetic predisposition for type 2 diabetes mellitus in a Moroccan population.
Houda Benrahma, Omar Abidi, Leila Melouk, Maria Ajjemami, Hassan Rouba

Genet Test Mol Biomarkers· May 2012

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Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.
Omar Abidi, Sara Knari, Hajar Sefri, Majida Charif, Audrey Senechal

Mol Vis· April 2012

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Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss.
Majida Charif, Omar Abidi, Redouane Boulouiz, Halima Nahili, Hassan Rouba

Biochem Biophys Res Commun· March 2012

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Maternal effect and familial aggregation in a type 2 diabetic Moroccan population.
Houda Benrahma, Imen Arfa, Majida Charif, Safaa Bounaceur, Abdelmajid Eloualid, Omar Abidi

J Community Health· December 2011

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