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Hypertension

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Copy Number Variants and Their Contribution to the Risk of Obesity

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Research on Rare Variants for Complex Diseases

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Large-scale examination of neuropsychiatric, cognitive and cardiovascular phenotypic associations with 15q11.2 BP1-BP2 deletion in ∼500,000 UK Biobank individualsPreprint

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THE NATURAL AND ORTHOGONAL INTERACTION (NOIA) MODELS FOR QUANTITATIVE TRAITS (QTs) AND COMPLEX DISEASES

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Studies on causes of multiple sclerosis : From genes to transcriptome

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Genetics of rheumatoid arthritis in black South Africans

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Pharmacogenetic studies in multiple myeloma

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Detection of susceptibility to Multiple Sclerosis from Single Nucleotide Polymorphism data

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Cost effective, computer-aided analytical performance evaluation of chromosomal microarrays for clinical laboratories

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