[HTML][HTML] Sequence Variations in PCSK9, Low LDL, and Protection against Coronary Heart Disease
JC Cohen, E Boerwinkle, TH Mosley Jr… - New England Journal …, 2006 - Mass Medical Soc
Background A low plasma level of low-density lipoprotein (LDL) cholesterol is associated
with reduced risk of coronary heart disease (CHD), but the effect of lifelong reductions in …
with reduced risk of coronary heart disease (CHD), but the effect of lifelong reductions in …
Genome-wide association study of blood pressure and hypertension
…, G Heiss, CS Fox, JCM Witteman, E Boerwinkle… - Nature …, 2009 - nature.com
Blood pressure is a major cardiovascular disease risk factor. To date, few variants associated
with interindividual blood pressure variation have been identified and replicated. Here we …
with interindividual blood pressure variation have been identified and replicated. Here we …
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
…, BD Levy, WHH Sheu, DM Roden, E Boerwinkle… - Nature, 2020 - nature.com
Age is the dominant risk factor for most chronic human diseases, but the mechanisms
through which ageing confers this risk are largely unknown 1 . The age-related acquisition of …
through which ageing confers this risk are largely unknown 1 . The age-related acquisition of …
From vulnerable plaque to vulnerable patient: a call for new definitions and risk assessment strategies: Part I
…, SM Grundy, R Mehran, A Colombo, E Boerwinkle… - Circulation, 2003 - Am Heart Assoc
Atherosclerotic cardiovascular disease results in >19 million deaths annually, and coronary
heart disease accounts for the majority of this toll. Despite major advances in treatment of …
heart disease accounts for the majority of this toll. Despite major advances in treatment of …
Multi-ethnic genome-wide association study for atrial fibrillation
…, NA Bihlmeyer, JC Bis, HL Bloom, E Boerwinkle… - Nature …, 2018 - nature.com
Atrial fibrillation (AF) affects more than 33 million individuals worldwide 1 and has a complex
heritability 2 . We conducted the largest meta-analysis of genome-wide association studies (…
heritability 2 . We conducted the largest meta-analysis of genome-wide association studies (…
Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout
…, A Köttgen, J Coresh, E Boerwinkle… - Proceedings of the …, 2009 - National Acad Sciences
Genome-wide association studies (GWAS) have successfully identified common single
nucleotide polymorphisms (SNPs) associated with a wide variety of complex diseases, but do not …
nucleotide polymorphisms (SNPs) associated with a wide variety of complex diseases, but do not …
Multiple loci associated with indices of renal function and chronic kidney disease
Chronic kidney disease (CKD) has a heritable component and is an important global public
health problem because of its high prevalence and morbidity 1 . We conducted genome-…
health problem because of its high prevalence and morbidity 1 . We conducted genome-…
Common variants in KCNN3 are associated with lone atrial fibrillation
…, A Hofman, AG Uitterlinden, D Levy, E Boerwinkle… - Nature …, 2010 - nature.com
Atrial fibrillation (AF) is the most common sustained arrhythmia. Previous studies have
identified several genetic loci associated with typical AF. We sought to identify common genetic …
identified several genetic loci associated with typical AF. We sought to identify common genetic …
[HTML][HTML] Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
Background High plasma HDL cholesterol is associated with reduced risk of myocardial
infarction, but whether this association is causal is unclear. Exploiting the fact that genotypes are …
infarction, but whether this association is causal is unclear. Exploiting the fact that genotypes are …
A global reference for human genetic variation
RA Gibbs, E Boerwinkle, H Doddapaneni, Y Han… - Nature, 2015 - cdr.lib.unc.edu
The 1000 Genomes Project set out to provide a comprehensive description of common human
genetic variation by applying whole-genome sequencing to a diverse set of individuals …
genetic variation by applying whole-genome sequencing to a diverse set of individuals …