Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta SyndromeNatascia Anastasio, Loydie A. Jerome‐Majewska, Tawfeg Ben‐Omran et al.|The American Journal of Human Genetics|2010Cited by 76
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, Fatma Al‐Mesaifri et al.|Gene Therapy|2021Cited by 53
Phenotypic heterogeneity in Woodhouse–Sakati syndrome: Two new families with a mutation in the C2orf37 geneTawfeg Ben‐Omran, Ahmad S. Teebi, Rehab Ali et al.|American Journal of Medical Genetics Part A|2011Cited by 37
W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case reportLoai Elsaadany, Tawfeg Ben‐Omran, Mahmoud F. Elsaid et al.|BMC Medical Genetics|2016Cited by 27