Exome Sequencing Identifies Potential Risk Variants for Mendelian Disorders at High Prevalence in Qatar

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Exome Sequencing of Only Seven Qataris Identifies Potentially Deleterious Variants in the Qatari Population

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Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families

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Genetics in geographically structured populations: defining, estimating and interpreting FST

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Null mutations in human and mouse orthologs frequently result in different phenotypes

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Role of CYP1B1 in Glaucoma

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