Accueil › Annuaire des chercheurs › Majida Charif
Majida Charif
Affiliation : Mohamed I University
- 70Publications (affiliation marocaine)
- 113Publications au total
- 1618Citations
- 23Indice h
Profil de recherche
Majida Charif compte 70 publications référencées (2010–2026). Ses travaux paraissent principalement dans « Molecular Biology Reports », « PLoS ONE » et « Brain Communications ». Son article le plus cité, « Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies » (2015), a été cité 75 fois. 21 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, Singapour.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Hereditary Neurological Disorders
- Mitochondrial Function and Pathology
- Genomics and Rare Diseases
- Retinal Development and Disorders
- Metabolism and Genetic Disorders
Publications (70)
- Identification of Novel and Known Variants in Epigenetic Genes Associated with Syndromic 46,XY Differences of Sex Development among Moroccan Patients
- Genetic diversity of Usher syndrome in Moroccan patients
- Clinical and Genetic Spectrum of ACO2 -Linked Dominant Optic Atrophy
- Hairy root-derived metabolites from Pelargonium graveolens L′Hér.: Phytochemical insights and cosmeceutical properties
- Phenotypic Variations in a Large Family with Dominant Optic Atrophy Related to a Novel OPA1 Deletion
- Identification of a novel homozygous RAB3GAP1 variant associated with Warburg micro syndrome type 1 in a Moroccan patient and a literature review
- Additional file 1 of Identification of a novel homozygous RAB3GAP1 variant associated with Warburg micro syndrome type 1 in a Moroccan patient and a literature review
- Identification of a novel homozygous RAB3GAP1 variant associated with Warburg micro syndrome type 1 in a Moroccan patient and a literature review
- Integrated exome and mitochondrial genome sequencing reveals the genetic landscape of primary mitochondrial diseases: findings from a large Tunisian cohort
- Pathophysiological insights into ACO2-related inherited disorders through combined functional and multi-omic analyses of ACO2 patient-derived fibroblasts
- Two Cases of ROSAH-Like Syndrome Restricted to the Ophthalmologic Presentation
- Clinical and Molecular Spectrum of Wilson Disease in the Arab World: A Systematic Review
- Novel splice variants implicated in inherited retinal dystrophies in two Moroccan families
- Environmental and genetic interactions underlying the morphological and genetic variability of the red juniper (Juniperus turbinata Guss.) in northeastern Morocco: implications for conservation
- Identification of the Genetic Causes of Inherited Diseases in a North African Biobank: Implications for Genetic Diagnosis
- The human OPA1delTTAG mutation induces adult onset and progressive auditory neuropathy in mice
- First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array
- Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairment
- Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing
- JAK2 mutational status and the contribution of TERT and JAK2 polymorphisms to the occurrence of myeloproliferative neoplasms in Eastern Morocco
- Carrier frequency and molecular basis of hemoglobinopathies among blood donors in eastern Morocco: Implications for blood donation and genetic diagnosis
- Autosomal recessive Leber hereditary optic neuropathy, a new neuro-ophthalmo-genetic paradigm
- Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders
- Population structure and genetic diversity of Moroccan cannabis (Cannabis sativa L.) germplasm through simple sequence repeat (SSR) analysis
- Triple-A Syndrome in Morocco: Founder Effect, Age Estimation of the AAAS c.1331+1G>A Variant, and Implications for Genetic Diagnosis
- Vitamin B1 deficiency leads to high oxidative stress and mtDNA depletion caused by SLC19A3 mutation in consanguineous family with Leigh syndrome
- A novel variant in BMPR1B causes acromesomelic dysplasia Grebe type in a consanguineous Moroccan family: Expanding the phenotypic and mutational spectrum of acromesomelic dysplasias
- A case report of two Moroccan patients with hereditary neurological disorders and molecular modeling study on the S72L de novo PMP22 variant
- GNE Myopathy and Duchenne Muscular Dystrophy in Two Moroccans Families
- Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families
- Genetic structure and diversity of cannabis (Cannabis sativa L.) populations from northern Morocco through genomic SSR analysis
- Novel variant in Moroccan patient with hereditary spastic paraplegia type 35
- The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probands
- Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies
- A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability
- Molecular heterogeneity of β‐thalassemia variants in the Eastern region of Morocco
- Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
- Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy
- First characterization of LTBP3 variants in two Moroccan families with hypoplastic amelogenesis imperfecta
- Syndromic Hearing Loss in Moroccan families is associated to homozygous missense variants in COL4A3 and MASP1
- DominantACO2mutations are a frequent cause of isolated optic atrophy
- Pathogenic NR2F1 variants cause a developmental ocular phenotype recapitulated in a mutant mouse model
- Use of Next-Generation Sequencing for the Molecular Diagnosis of 1,102 Patients With a Autosomal Optic Neuropathy
- Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathy
- Characterization of SSBP1-related optic atrophy and foveopathy
- Clinical and genetic investigations of three Moroccan families with retinitis pigmentosa phenotypes.
- ACO2 clinicobiological dataset with extensive phenotype ontology annotation
- Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy
- Morocco’s First Biobank: Establishment, Ethical Issues, Biomedical Research Opportunities, and Challenges
- A ROD–CONE DYSTROPHY IS SYSTEMATICALLY ASSOCIATED TO THE RTN4IP1 RECESSIVE OPTIC ATROPHY
- A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family
- Mutations in aARS genes revealed by targeted next-generation sequencing in patients with mitochondrial diseases
- First characterization of LHON pedigrees in North Africa
- Next generation sequencing in family with MNGIE syndrome associated to optic atrophy: Novel homozygous POLG mutation in the C-terminal sub-domain leading to mtDNA depletion
- Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families
- Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family
- Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss
- Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss
- Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies
- Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees
- A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
- 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
- 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
- Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss
- Maternal Effect and Familial Aggregation in a Type 2 Diabetic Moroccan Population
- Mutations in TPRN Cause a Progressive Form of Autosomal-Recessive Nonsyndromic Hearing Loss
- Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss
Revues de publication
- Molecular Biology Reports × 4
- PLoS ONE × 4
- Brain Communications × 3
- International Journal of Pediatric Otorhinolaryngology × 3
- Figshare × 2
- Scientific Reports × 2
Publications par année
- 202610
- 20255
- 20246
- 202311
- 20228
- 20217
- 20206
- 20181
- 20173
- 20161
Collaborations
Établissements partenaires : Inserm · Institut Pasteur du Maroc · Centre National de la Recherche Scientifique · Mitochondrial and Cardiovascular Physiopathology · Université d'Angers
Pays des co-auteurs : France · Singapour
Co-auteurs
- Abdelhamid Barakat
- Redouane Boulouiz
- Mohammed Bellaoui
- Saida Lhousni
- Hassan Rouba
- Ghita Amalou
- Meryem Ouarzane
- Halima Nahili
- Mostafa Kandil
- Mounia Elidrissi Errahhali
- Manal Elidrissi Errahhali
- Hicham Charoute
Données bibliographiques issues d’OpenAlex (base ouverte).
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