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Genetics

  • A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction

    About one of every four Caucasians carry a sequence variation at a regulatory region of chromosome 9 that confers an elevated risk of heart disease.

  • A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants

    The hereditary component of type 2 diabetes reflects the contribution of at least 10 genetic variants, each with a modest effect on risk.

  • Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels

    The hereditary component of type 2 diabetes reflects the contribution of at least 10 genetic variants, each with a modest effect on risk.

  • Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes

    The hereditary component of type 2 diabetes reflects the contribution of at least 10 genetic variants, each with a modest effect on risk.

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