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Publications by Tawfeg Ben-Omran
Inactivating Mutations in MFSD2A, Required for Omega-3 Fatty Acid Transport in Brain, Cause a Lethal Microcephaly Syndrome
Nature Genetics
Genetics
Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta Syndrome
American Journal of Human Genetics
Genetics
Mutations in MBOAT7 , Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features
American Journal of Human Genetics
Genetics
Bi-Allelic TMEM94 Truncating Variants Are Associated With Neurodevelopmental Delay, Congenital Heart Defects, and Distinct Facial Dysmorphism
American Journal of Human Genetics
Genetics
Clinical Application of Whole-Exome Sequencing
JAMA Neurology
Neurology
Neurodevelopmental and Cognitive Outcomes of Classical Homocystinuria: Experience From Qatar
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes