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Paper Details

Associations Between Common and Rare Exonic Genetic Variants and Serum Levels of 20 Cardiovascular-Related Proteins: The Tromsø Study.
Circ Cardiovasc Genet
15
2016
Exonic Genetic Variants, F12, NTproBNP, NTproBNP precursor, cardiovascular diseases, cis-pQTLs, kallikrein, kininogen, pQTLs, proBNP, protein quantitative trait loci, rare variants, uPAR, venous thromboembolism
Author NameAffiliation
Erin N SmithUniversity of California, Rady's Children's Hospital, K.A.F.) Institute for Genomic Medicine, UiT The Arctic University of Norway and Division of Internal Medicine, University Hospital of North Norway
Tom WilsgaardUniversity of California, Rady's Children's Hospital, K.A.F.) Institute for Genomic Medicine, UiT The Arctic University of Norway and Division of Internal Medicine, University Hospital of North Norway
Inger NjølstadUniversity of California, Rady's Children's Hospital, K.A.F.) Institute for Genomic Medicine, UiT The Arctic University of Norway and Division of Internal Medicine, University Hospital of North Norway
Kelly A FrazerUniversity of California, Rady's Children's Hospital, K.A.F.) Institute for Genomic Medicine, UiT The Arctic University of Norway and Division of Internal Medicine, University Hospital of North Norway
Kelly A FrazerUniversity of California, Rady's Children's Hospital, K.A.F.) Institute for Genomic Medicine, UiT The Arctic University of Norway and Division of Internal Medicine, University Hospital of North Norway
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Release 1.2