Eric Boerwinkle

发表

Genomewide Association Studies of Stroke.

Ricardo J Komotar, E Sander Connolly, M. Fornage, 2009, Neurosurgery.

Guidelines of the National Heart, Lung, and Blood Institute Working Group on Blood Drawing, Processing, and Storage for Genetic Studies.

E. Boerwinkle, J. Ordovás, J. Lalouel, 1996, American journal of epidemiology.

Association analyses of 249 , 796 individuals reveal 18 new loci associated with body mass index

Tanya M. Teslovich, Eric, P. Elliott, 2012 .

Genome-wide association and functional follow-up reveals new loci for kidney function

Audrey Y. Chu, Jeanette S. Andrews, W. Goessling, 2012 .

Determinants of mosaic chromosomal alteration fitness

P. Scheet, M. Taub, A. Stilp, 2023, medRxiv.

Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci

M. P. Concas, Nicholette D. Palmer, M. Fornage, 2023, Frontiers in genetics.

Impact of Receiving Hospital on Out‐of‐Hospital Cardiac Arrest Outcome: Racial and Ethnic Disparities in Texas

B. Bobrow, Micah J Panczyk, R. Witkov, 2023, Journal of the American Heart Association.

Influence of lipoprotein lipase serine 447 stop polymorphism on tracking of triglycerides and HDL cholesterol from childhood to adulthood and familial risk of coronary artery disease: the Bogalusa heart study.

E. Boerwinkle, S. Srinivasan, D. Ellsworth, 2001, Atherosclerosis.

Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification

May E. Montasser, Nicholette D. Palmer, Caitlin P. McHugh, 2023, Nature Cardiovascular Research.

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Fabian J Theis, Andrew D. Johnson, Lorna M. Lopez, 2012, Nature Genetics.

Association between patterns of nucleotide variation across the three fibrinogen genes and plasma fibrinogen levels: the Coronary Artery Risk Development in Young Adults (CARDIA) study

M. Rieder, M. Fornage, C. Carty, 2006, Journal of thrombosis and haemostasis : JTH.

Population genetics of hypervariable loci: analysis of PCR based VNTR polymorphism within a population.

M. Fornage, E. Boerwinkle, R. Chakraborty, 1991, EXS.

Bias of the contribution of single-locus effects to the variance of a quantitative trait.

E. Boerwinkle, C. Sing, E Boerwinkle, 1986, American journal of human genetics.

Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance

M. Fornage, I. Deary, D. Chasman, 2024, Alzheimer's research & therapy.

Stroke genetics informs drug discovery and risk prediction across ancestries

Sebastian M. Armasu, Laurent F. Thomas, J. Danesh, 2022, Nature.

Clonal hematopoiesis of indeterminate potential is associated with acute kidney injury

C. Robinson-Cohen, D. Arking, M. Lanktree, 2024, Nature medicine.

SMIM1 absence is associated with reduced energy expenditure and excess weight.

Tanya M. Teslovich, May E. Montasser, Nicholette D. Palmer, 2024, i Medicina.

Large scale plasma proteomics identifies novel proteins and protein networks associated with heart failure development

K. Hveem, T. Omland, B. Claggett, 2024, Nature communications.

Determinants of mosaic chromosomal alteration fitness

P. Scheet, M. Taub, A. Stilp, 2024, Nature communications.

The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point Mutations

P. Scheet, S. Kardia, P. Peyser, 2024, medRxiv.

Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

Sara M. Willems, Lorna M. Lopez, Loren R. Risch, 2024, Kidney international reports.

Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application.

G. Abecasis, D. Arking, Xiuqing Guo, 2024, Mitochondrion.

Impact of adding a single allele in the 9p21 locus to traditional risk factors on reclassification of coronary heart disease risk and implications for lipid-modifying therapy in the Atherosclerosis Risk in Communities (ARIC) study

Vijay Nambi, Kim S Lawson, Chris Ballantyne, 2010 .

Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

S. Redline, K. Ardlie, P. Scheet, 2024, medRxiv.

Admixture mapping of cognitive function in diverse Hispanic and Latino adults: Results from the Hispanic Community Health Study/Study of Latinos.

X. Jian, C. Satizabal, F. Testai, 2024, Alzheimer's & dementia : the journal of the Alzheimer's Association.

TDT statistics for mapping quantitative trait loci

J Krushkal, E. Boerwinkle, J. Krushkal, 1998, Annals of human genetics.

A Large-Scale Genome-Wide Gene-Sleep Interaction Study in 732,564 Participants Identifies Lipid Loci Explaining Sleep-Associated Lipid Disturbances

Nicholette D. Palmer, Sina A. Gharib, A. Luik, 2024, medRxiv.

Edinburgh Research Explorer No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index

Lorna M. Lopez, Audrey Y. Chu, M. Fornage, 2018 .

Familial Hypercholesterolemia Variant and Cardiovascular Risk in Individuals With Elevated Cholesterol.

Matthew S. Lebo, M. Fornage, C. Willer, 2024, JAMA cardiology.

A polygenic risk score of atrial fibrillation improves prediction of lifetime risk for heart failure

A. Morrison, C. Ballantyne, T. Alkis, 2024, ESC heart failure.