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Meriame Abbassi

Human genome meeting 2016: Houston, TX, USA. 28 February - 2 March 2016
2016 · GUSTO study group, A. K. Srivastava, et al. · Human Genomics · 42
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FLT3 Mutations in Acute Myeloid Leukemia: Unraveling the Molecular Mechanisms and Implications for Targeted Therapies
2023 · Meryem Jalte, Meriame Abbassi, et al. · Cureus · 32
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Idiopathic Pulmonary Fibrosis: A Comprehensive Review of Risk Factors, Genetics, Diagnosis, and Therapeutic Approaches
2026 · Lamiyae Senhaji, Nadia Senhaji, et al. · Biomedicines · 14
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Influence of CYP450 Enzymes and ABCB1 Polymorphisms on Clopidogrel Response in Moroccan Patients with Acute Coronary Syndromes
2023 · Ismail Mouhrach, Laila Bouguenouch, et al. · Pharmacogenomics and Personalized Medicine · 9
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A Case of Severe Teratozoospermia and Infertility Due to Homozygous Mutation c.144delC in the AURKC Gene
2023 · Meriame Abbassi, Hanane Sayel, et al. · Cureus · 6
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Genetic characterization of Schuurs-Hoeijmakers syndrome in a moroccan individual with heterozygote PACS1 mutation
2023 · Meriame Abbassi, Abdelhamid Bourmtane, et al. · Molecular Biology Reports · 4
A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2
2023 · Khawla El Fizazi, Abdelhamid Bouramtane, et al. · American Journal of Medical Genetics Part A · 4
The Genetic Facets of Dravet Syndrome: Recent Insights
2024 · Hinde El Mouhi, Meriame Abbassi, et al. · Annals of Child Neurology · 3
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Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan Population
2024 · Khawla El Fizazi, Meriame Abbassi, et al. · Audiology and Neurotology · 3
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
2023 · Hinde El Mouhi, Meriame Abbassi, et al. · Cureus · 3
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Clinical and molecular characterization of Xeroderma pigmentosum in Moroccan population: a case series of 40 patients
2022 · Meriame Abbassi, Hanane Sayel, et al. · Egyptian Journal of Medical Human Genetics · 3
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Syndrome de Lynch: à propos d’un cas et revue de la litterature
2016 · Laila Bouguenouch, Imane Samri, et al. · Pan African Medical Journal · 3
Identification of novel and de novo variant in the SCN1A gene confirms Dravet syndrome in Moroccan child: a case report
2024 · Hinde El Mouhi, Nada Amllal, et al. · Molecular Biology Reports · 2
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Next Generation Sequencing in Diagnosis of Multiple Myeloma
2023 · Ikram El Fazazi, Hajar Ihlal, et al. · Preprints.org · 1
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Impact of Deletion on Angelman Syndrome Phenotype Variability: Phenotype–Genotype Correlation in 97 Patients with Motor Developmental Delay
2022 · Hanae Daha Belghiti, Meriame Abbassi, et al. · Journal of Pediatric Genetics · 1
Next Generation Sequencing in the Diagnosis of Multiple Myeloma
2026 · Ikram EL Fazazi, Hajar Ihlal, et al. · Frontiers in Bioscience-Scholar
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High frequency of LRRK2 p.Gly2019Ser in Moroccan Parkinson’s disease: RFLP as a reliable genotyping approach
2026 · Sanae EL Bardai, Ghita Aboulem, et al. · Neurogenetics
MUC5B Polymorphism and Susceptibility to Idiopathic Pulmonary Fibrosis in Morocco
2025 · Lamiyae Senhaji, Meriame Abbassi, et al. · Cureus
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Spinal extramedullary haematopoiesis revealing β-thalassaemia major
2024 · I. Khoussar, N. Oubelkacem, et al. · Cahiers Santé Médecine thérapeutique
Works count: 20
Citation count: 130
H-index: 5
I10-index: 3
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