SLC35A2‐CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported IndividualsBobby G. Ng, María J. Guillen Sacoto, Paulina Sosicka et al.|Human Mutation|2019Cited by 67
Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophyShenela Lakhani, Tawfeg Ben‐Omran, Ryan N. Doan et al.|European Journal of Medical Genetics|2017Cited by 28
Cono‐spondylar dysplasia: Clinical, radiographic, and molecular findings of a previously unreported disorderTawfeg Ben‐Omran, Sheila Unger, Shenela Lakhani et al.|American Journal of Medical Genetics Part A|2014Cited by 0
Consanguinity in Qatar: A unique opportunity for international collaborative researchTawfeg Ben‐Omran, Zafar Nawaz, Shenela Lakhani et al.|Qatar Foundation Annual Research Forum Volume 2012 Issue 1|2012Cited by 0
High diagnostic yield of clinical exome sequencing in Middle updated versionTarunashree Yavarna, Tawfeg Ben‐Omran, Fatma Al‐Mesaifri et al.|Unknown|2015Cited by 0