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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, Mariam Al‐Mureikhi et al.|Gene Therapy|2021Cited by 53
Glutamine supplementation in a child with inherited GS deficiency improves the clinical status and partially corrects the peripheral and central amino acid imbalanceJohannes Häberle, Tawfeg Ben‐Omran, Noora Shahbeck et al.|Orphanet Journal of Rare Diseases|2012Cited by 51
Newborn screening for remethylation disorders and vitamin B12 deficiency-evaluation of new strategies in cohorts from Qatar and GermanyGwendolyn Gramer, Jürgen G. Okun, Ghassan Abdoh et al.|World Journal of Pediatrics|2017Cited by 27