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Paper Details

Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.
Open Heart
0
2023
Lp, Lp(a), PRS, cardiovascular disease, coronary atherosclerosis, genome-wide significant loci, glycated haemoglobin, ischaemic heart disease, lipoprotein(a)
Author NameAffiliation
Laura M RaffieldThe University of North Carolina at Chapel Hill
Zhe WangThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Adolfo CorreaThe University of Mississippi Medical Center
Adolfo CorreaThe University of Mississippi Medical Center
Paul S de VriesThe University of Texas Health Science Center at Houston
Xiuqing Guouniversity of california los angeles Medical Center
Jeffrey HaesslerFred Hutchinson Cancer Research Center
Yao HuFred Hutchinson Cancer Research Center
Keri L MondaCenter for Observational Research
Kari E NorthThe University of North Carolina at Chapel Hill
Ulrike PetersFred Hutchinson Cancer Research Center
Michael PreussThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Stephen S RichUniversity of Virginia School of Medicine
Jie Yaouniversity of california los angeles Medical Center
Michael Y TsaiUniversity of Minnesota
Jerome I Rotteruniversity of california los angeles Medical Center
Charles KooperbergFred Hutchinson Cancer Research Center
Ruth J F LoosThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Ruth J F LoosNovo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen
Christie M BallantyneBaylor College of Medicine
Christie M BallantyneBaylor College of Medicine
Mariaelisa GraffThe University of North Carolina at Chapel Hill
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Datasets

Release 1.2