Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experienceNader Al‐Dewik, Tawfeg Ben‐Omran, Howaida Mohd et al.|American Journal of Medical Genetics Part A|2019Cited by 57
Gene therapy for spinal muscular atrophy: the Qatari experienceHossamaldein Gaber Ali, Tawfeg Ben‐Omran, Karen El‐Akouri et al.|Gene Therapy|2021Cited by 53
Mutations in MYLPF Cause a Novel Segmental Amyoplasia that Manifests as Distal ArthrogryposisJessica X. Chong, Michael J. Bamshad, Jared C. Talbot et al.|The American Journal of Human Genetics|2020Cited by 36
Clinical genetics and genomic medicine in QatarNader Al‐Dewik, Tawfeg Ben‐Omran, Mariam Al‐Mureikhi et al.|Molecular Genetics & Genomic Medicine|2018Cited by 26
Natural history, with clinical, biochemical, and molecular characterization of classical homocystinuria in the Qatari populationNader Al‐Dewik, Tawfeg Ben‐Omran, Alaa Ali et al.|Journal of Inherited Metabolic Disease|2019Cited by 22