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Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
