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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

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Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C

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ITPA Polymorphism Affects Ribavirin-Induced Anemia and Outcomes of Therapy—A Genome-Wide Study of Japanese HCV Virus Patients

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Finding the missing heritability of complex diseases

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A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits

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Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data

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Genetic Mapping in Human Disease

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