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, Mahmoud Abeidah et al.|Gene Therapy|2021Cited by 53
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
A founder <scp>RAB27A</scp> variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari familiesReem Alsulaiman, Tawfeg Ben‐Omran, Amna Othman et al.|American Journal of Medical Genetics Part A|2020Cited by 18