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Meriame Abbassi
Affiliation : Instituts Supérieurs des Professions Infirmières et Techniques de Santé · Centre Hospitalier Universitaire Hassan II · Sidi Mohamed Ben Abdellah University
- 17Publications (affiliation in Morocco)
- 20Total publications
- 111Citations
- 5h-index
Research profile
Meriame Abbassi has 17 indexed publications (2016–2026). Their work appears mainly in “Cureus”, “Molecular Biology Reports” and “Biomedicines”. Their most cited article, “FLT3 Mutations in Acute Myeloid Leukemia: Unraveling the Molecular Mechanisms and Implications for Targeted Therapies” (2023), has been cited 26 times. 7 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers.
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Create my free profile Add my publicationsResearch areas
- Genomics and Rare Diseases
- Epilepsy research and treatment
- Genetics and Neurodevelopmental Disorders
- Ion channel regulation and function
- Multiple Myeloma Research and Treatments
Publications (17)
- Idiopathic Pulmonary Fibrosis: A Comprehensive Review of Risk Factors, Genetics, Diagnosis, and Therapeutic Approaches
- High frequency of LRRK2 p.Gly2019Ser in Moroccan Parkinson’s disease: RFLP as a reliable genotyping approach
- Next Generation Sequencing in the Diagnosis of Multiple Myeloma
- MUC5B Polymorphism and Susceptibility to Idiopathic Pulmonary Fibrosis in Morocco
- Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan Population
- Identification of novel and de novo variant in the SCN1A gene confirms Dravet syndrome in Moroccan child: a case report
- The Genetic Facets of Dravet Syndrome: Recent Insights
- FLT3 Mutations in Acute Myeloid Leukemia: Unraveling the Molecular Mechanisms and Implications for Targeted Therapies
- A Case of Severe Teratozoospermia and Infertility Due to Homozygous Mutation c.144delC in the AURKC Gene
- Influence of CYP450 Enzymes and ABCB1 Polymorphisms on Clopidogrel Response in Moroccan Patients with Acute Coronary Syndromes
- A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2
- Genetic characterization of Schuurs-Hoeijmakers syndrome in a moroccan individual with heterozygote PACS1 mutation
- Autosomal Dominant Intellectual Development Disorder-6 (MRD6) Without Seizures Linked to a De Novo Mutation in the grin2b Gene Revealed by Exome Sequencing: A Case Report of a Moroccan Child
- Next Generation Sequencing in Diagnosis of Multiple Myeloma
- Clinical and molecular characterization of Xeroderma pigmentosum in Moroccan population: a case series of 40 patients
- Impact of Deletion on Angelman Syndrome Phenotype Variability: Phenotype–Genotype Correlation in 97 Patients with Motor Developmental Delay
- Syndrome de Lynch: à propos d’un cas et revue de la litterature
Publication venues
- Cureus × 4
- Molecular Biology Reports × 2
- Biomedicines × 1
- Neurogenetics × 1
- Frontiers in Bioscience-Scholar × 1
- Audiology and Neurotology × 1
Publications per year
- 20263
- 20251
- 20243
- 20237
- 20222
- 20161
Collaborations
Partner institutions : Mohammed V University · Université Moulay Ismail de Meknes · Centre National pour la Recherche Scientifique et Technique (CNRST) · Université Mohammed VI Polytechnique · Centre Hospitalier Ibn Sina
Co-authors
- Laila Bouguenouch
- Karim Ouldim
- Hinde El Mouhi
- Mohamed Ahakoud
- Sana Chaouki
- Meryem Jalte
- Samira Nmer
- Mohammed El Azami El Idrissi
- Nadia Senhaji
- B. Amara
- Yasser Ali El Asri
- Ikram El Fazazi
Bibliographic data from OpenAlex (open database).
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