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Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
PLoS Genet
37
2017
ADAMTS3, Arg123His, HIF3A, LCAT, LIPC, LIPG, PLTP, associated loci, dyslipidemia, genome-wide, lipid loci, men, metabolic and cardiovascular diseases, metabolic disorders, rare genetic variants, triglyceride
Author NameAffiliation
Jeroen R HuygheDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Adam E LockeDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Anne U JacksonDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Xueling SimDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Heather M StringhamDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Tanya M TeslovichDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Ryan P WelchDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Christian FuchsbergerDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Narisu NarisuNational Human Genome Research Institute, National Institutes of Health
Peter S ChinesNational Human Genome Research Institute, National Institutes of Health
Johanna KuusistoUniversity of Eastern Finland and Kuopio University Hospital
Francis S CollinsNational Human Genome Research Institute, National Institutes of Health
Francis S CollinsNational Human Genome Research Institute, National Institutes of Health
Markku LaaksoUniversity of Eastern Finland and Kuopio University Hospital
Michael BoehnkeDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan ann arbor
Karen L MohlkeUniversity of North Carolina at Chapel Hill
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