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Youssef El Kadiri

Observed names: EL KADIRI, YOUSSEF, El Kadiri, Youssef, Youssef EL Kadiri, Youssef El kadiri
ORCID: 0000-0002-6033-2395
Observed ORCID: 0000-0002-6033-2395
OpenAlex ID: A5033718655
Investigation of bacterial diversity using 16S rRNA sequencing and prediction of its functionalities in Moroccan phosphate mine ecosystem
2022 · Salah Eddine Azaroual, Yassine Kasmi, et al. · Scientific Reports · 49
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Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report
2021 · Youssef El Kadiri, Ilham Ratbi, et al. · BMC Medical Genomics · 10
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Novel copy number variation of COLQ gene in a Moroccan patient with congenital myasthenic syndrome: a case report and review of the literature
2022 · Youssef El Kadiri, Ilham Ratbi, et al. · BMC Neurology · 8
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Clinical and molecular genetic analysis of early-onset myopathy with fatal cardiomyopathy: Novel biallelic M-line TTN mutation and review of the literature
2022 · Youssef El Kadiri, Ilham Ratbi, et al. · Gene Reports · 6
Molecular diagnosis of dystrophinopathies in Morocco and report of six novel mutations
2020 · Youssef EL Kadiri, Yassir Selouani, et al. · Clinica Chimica Acta · 6
Novel Splice Site Pathogenic Variant in STXBP1 Gene in a Child with Intellectual Disability, Epilepsy, and Autism Spectrum Disorder: A Case Report
2024 · Nada Amllal, Jaber Lyahyai, et al. · Molecular Syndromology · 4
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Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: a case report
2023 · Maryem Sahli, Abdelali Zrhidri, et al. · Journal of Medical Case Reports · 3
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First application of next-generation sequencing in four families with Wilson disease in Morocco
2023 · Maryem Sahli, Abdelali Zrhidri, et al. · Egyptian Journal of Medical Human Genetics · 3
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Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia
2021 · Yassamine Doubaj, Abdelali Zrhidri, et al. · Pan African Medical Journal · 2
Coding-complete genome sequence of a measles virus genotype B3 isolate from Rabat, Morocco, in 2024
2025 · Safae Elkochri, Idrissa Diawara, et al. · Microbiology Resource Announcements · 1
Molecular diagnosis of Alpha-sarcoglycanopathies by NGS in seven Moroccan families and report of two novel variants
2024 · Yasmina Rahmuni, Youssef El Kadiri, et al. · Irish Journal of Medical Science (1971 -) · 1
Clinical Exome Sequencing Reveals Novel Mutations in SPTB Gene Associated with Hereditary Spherocytosis in Patients with Suspected Congenital Hemolytic Anemia
2024 · Amal Chiguer, Jaber Lyahyai, et al. · Hemoglobin · 1
Early diagnosis of congenital muscular pathologies using next-generation sequencing: experiences from a tertiary center in Morocco
2023 · Youssef El Kadiri, Ilham Ratbi, et al. · Egyptian Journal of Medical Human Genetics · 1
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CLAVUS curated longitudinal VUS resolution dataset
2026 · El Badisy, Imad, El Kadiri, Youssef, et al. · Zenodo (CERN European Organization for Nuclear Research)
First Moroccan Experience with Digital PCR for SMN1 and SMN2 Copy Number Analysis and Clinical Severity Prediction in Patients with Spinal Muscular Atrophy
2026 · EL KADIRI, YOUSSEF, BENYAHYA, NADA, et al. · Zenodo (CERN European Organization for Nuclear Research)
A preliminary molecular snapshot of measles virus genotypes circulating in Rabat, Morocco, during 2024-2025
2025 · Othmane Jeddoub, El Mehdi Belouad, et al. · Research Square
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Unique Female Patient with de novo 6q22.31q27 Duplication and Xq28 Deletion: Case Report and Brief Literature Review
2024 · Lamiae Afif, Zhour El Amrani, et al. · OBM Genetics
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Two Moroccan Families with Emery-Dreifuss Muscular Dystrophy and Report of a Novel LMNA Pathogenic Variant
2024 · Yasmina Rahmuni, Youssef El Kadiri, et al. · Molecular Syndromology
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Works count: 22
Citation count: 95
H-index: 5
I10-index: 2
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