Accueil › Annuaire des chercheurs › Omar Abidi
Omar Abidi
Affiliation : Institut Supérieur des Professions Infirmières et Techniques de Santé de Casablanca
- 47Publications (affiliation marocaine)
- 50Publications au total
- 698Citations
- 16Indice h
Profil de recherche
Omar Abidi compte 47 publications référencées (2007–2026). Ses travaux paraissent principalement dans « International Journal of Pediatric Otorhinolaryngology », « Genetic Testing and Molecular Biomarkers » et « Nucleosides Nucleotides & Nucleic Acids ». Son article le plus cité, « A Mutation in PNPT1, Encoding Mitochondrial-RNA-Import Protein PNPase, Causes Hereditary Hearing Loss » (2012), a été cité 94 fois. 7 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs, notamment dans des établissements de France.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Genetic Associations and Epidemiology
- Hearing, Cochlea, Tinnitus, Genetics
- Hearing Loss and Rehabilitation
- Congenital Ear and Nasal Anomalies
- Folate and B Vitamins Research
Publications (47)
- Exploring gastric pH and Helicobacter pylori infection in relation to gastric mucosal lesions
- Genetic Diversity of the ACE2 Gene and Susceptibility to COVID-19 in Morocco Population
- Unveiling the prevalence of Helicobacter pylori CagA and VacA virulence markers in Moroccan children and adolescents
- Association of CpG site of MTHFR gene promoter and type 2 diabetes in Moroccan population susceptibility
- Risk factors for hypertension in patients with type 2 diabetes mellitus in the Casablanca-Settat region, Morocco: a cross-sectional study
- Association of MBL2 gene polymorphisms with type 2 diabetes and its complications in Moroccan population
- Meta-analysis of MTHFR C677T polymorphism and type 2 diabetes mellitus in MENA region
- In vitro and in vivo Antidiabetic Effect of the Aqueous Extract of Garlic (Allium sativum L.) Compared to Glibenclamide on Biochemical Parameters in Alloxan-induced Diabetic Mice
- Prevalence and risk factors of chronic complications among patients with type 2 diabetes mellitus in Morocco: a cross-sectional study.
- 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
- Prevalence of dyslipidemia and the relationship between HbA1C and lipid profile in Moroccan patients with T2DM: a cross-sectional study
- Association between Methylene-Tetrahydrofolate Reductase C677T Polymorphism and Human Immunodeficiency Virus Type 1 Infection in Morocco
- Lack of association between methylation status of CpG in the MCP-1 promoter and type 2 diabetes mellitus and its complications in a Moroccan population
- Corrigendum to “Lack of association between methylation status of CpG in the MCP-1 promoter and type 2 diabetes mellitus and its complications in a Moroccan population” [Gene Rep. 26 (2022) 1–5]
- Angiotensin Converting Enzyme 2 (ACE2) and COVID-19: An overview of its structure, physiologic role and its involvement in SARS-COV2 infection and therapy
- COVID-19 severityin patients with diabetes and cardiovascular diseases: A Short Review
- NUMERICAL SOLUTION OF LARGE-SCALE LYAPUNOV EQUATIONS AND MODEL REDUCTION PROBLEMS USING AN EXTENDED-RATIONAL BLOCK ARNOLDI METHOD
- Genetics of breast cancer in African populations: a literature review
- Methylenetetrahydrofolate Reductase Gene Polymorphisms (C677T and A1298C) and Hemorrhagic Stroke in Moroccan Patients
- Caractérisation microbiologique et moléculaire des candidoses vaginales résistantes aux antifongiques azoles
- TNF A −308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case–control study and meta-analysis
- Prognostic factors of survival in Moroccan patients with Glioblastoma
- The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility
- Molecular Defects in Moroccan Patients with Ataxia-Telangiectasia
- Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss
- Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss
- A Mutation in PNPT1, Encoding Mitochondrial-RNA-Import Protein PNPase, Causes Hereditary Hearing Loss
- Association of the MTHFR A1298C Variant with Unexplained Severe Male Infertility
- Association of Spermatogenic Failure with the b2/b3 Partial AZFc Deletion
- The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population
- c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum
- Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss
- Clinicopathological Features and Molecular Analysis of Primary Glioblastomas in Moroccan Patients
- Glioblastomes : les facteurs pronostics cliniques et génétiques
- 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
- Maternal Effect and Familial Aggregation in a Type 2 Diabetic Moroccan Population
- Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.
- The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population
- La part de l’hérédité dans les déficits auditifs ou surdités
- Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss
- The prevalence of resistance-associated mutations to protease and reverse transcriptase inhibitors in treatment-naïve (HIV1)-infected individuals in Casablanca, Morocco
- Carrier Frequencies of Mutations/Polymorphisms in the Connexin 26 Gene ( GJB2 ) in the Moroccan Population
- Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness
- The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population
- A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family
- AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men
- GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation
Revues de publication
- International Journal of Pediatric Otorhinolaryngology × 3
- Genetic Testing and Molecular Biomarkers × 2
- Nucleosides Nucleotides & Nucleic Acids × 2
- Pan African Medical Journal × 2
- Diabetes & Metabolic Syndrome Clinical Research & Reviews × 2
- Gene Reports × 2
Publications par année
- 20262
- 20254
- 20241
- 20231
- 20226
- 20211
- 20202
- 20182
- 20161
- 20142
Collaborations
Établissements partenaires : Institut Pasteur du Maroc · Institut Pasteur · University of Hassan II Casablanca · Chouaib Doukkali University · Centre Hospitalier Universitaire Ibn Rochd
Pays des co-auteurs : France
Co-auteurs
- Abdelhamid Barakat
- Hassan Rouba
- Redouane Boulouiz
- Lahcen Wakrim
- Halima Nahili
- Salsabil Hamdi
- Naima Khlil
- Houda El Alami
- Najib Al Idrissi
- Majida Charif
- Houda Benrahma
- Abdelaziz Chafik
Données bibliographiques issues d’OpenAlex (base ouverte).
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