Get started
Author

Maryem Sahli

Observed names: Maryem M sahli, SAHLI, MARYEM, Sahli Maryem, Sahli, Maryem
ORCID: 0000-0002-7333-2052
Observed ORCID: 0000-0002-7333-2052
OpenAlex ID: A5005565333
Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series
2019 · Maryem Sahli, Abdelali Zrhidri, et al. · Journal of Medical Case Reports · 8
PDF
Molecular diagnosis of dystrophinopathies in Morocco and report of six novel mutations
2020 · Youssef EL Kadiri, Yassir Selouani, et al. · Clinica Chimica Acta · 6
Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report
2018 · Najlae Adadi, Maryem Sahli, et al. · Journal of Medical Case Reports · 6
PDF
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
PDF
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
PDF
Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report
2023 · Zhour El Amrani, Abdelhafid Natiq, et al. · Molecular Syndromology · 2
PDF
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
PDF
A Novel Nonsense Mutation p.L9X in the SRY Gene Causes Complete Gonadal Dysgenesis in a 46,XY Female Patient
2016 · Asma Tajouri, Maryem M sahli · Journal of Genetic Syndromes & Gene Therapy · 1
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)
Implementing a Tiered Genetic Testing Strategy for Muscular Dystrophies in Morocco: From Targeted Assays to Exome Sequencing
2026 · Yasmina Rahmuni, Ilham Ratbi, et al. · Molecular Genetics & Genomic Medicine
Clinical Exome Sequencing as a Key Diagnostic Tool: A Rare de novo TRIO Variant in Dizygotic Twins
2026 · Hicham Bouchahta, Maryem Sahli, et al. · Molecular Syndromology
臨床エクソーム配列決定は,てんかんのモロッコ人患者におけるscn1aおよびscn2a遺伝子の2つの新規変異を同定する:症例シリーズ【jst・京大機械翻訳】
2019 · Sahli Maryem, Zrhidri Abdelali, et al.
Le Dermatofibrosarcome de Darier et Ferrand
2015 · Sahli Maryem · Toubkal
Works count: 16
Citation count: 30
H-index: 3
I10-index:
Year
Topic
Type