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Author Details

Peter S Braund
2003
79
52
PMIDPaper TitleJournal TitlePublished Year
35727948Elucidation of the genetic causes of bicuspid aortic valve disease.Cardiovasc Res2023
35363781Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.PLoS Genet2022
34611362Polygenic basis and biomedical consequences of telomere length variation.Nat Genet2021
33727701Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.Nat Genet2021
33230300Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.Nat Genet2020
32654539Association of Factor V Leiden With Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data.Circulation2020
31358974New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders.Nat Hum Behav2019
30482443Effects of the coronary artery disease associated LPA and 9p21 loci on risk of aortic valve stenosis.Int J Cardiol2019
30621952Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection.J Am Coll Cardiol2019
31221261Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals.J Am Coll Cardiol2019
31127295A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.Hum Mol Genet2019
30897348Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events.Circ Genom Precis Med2019
29455858A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.Am J Hum Genet2018
30429575Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
30224653Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
28209224Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.J Am Coll Cardiol2017
28506971Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease.Circ Res2017
28747754Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.Nat Genet2017
28739976Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.Hypertension2017
28566218Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study.Lancet Diabetes Endocrinol2017
28319091Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.Nat Genet2017
28267856Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease.JAMA2017
28279971Coronary Artery Disease-Associated Coding Variant rs1051338 Reduces Lysosomal Acid Lipase Levels and Activity in Lysosomes.Arteriosclerosis, Thrombosis, and Vascular Biology2017
28007139Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels.J Am Coll Cardiol2016
26934567Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.N Engl J Med2016
27192541Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.N Engl J Med2016
27466198Analysis with the exome array identifies multiple new independent variants in lipid loci.Hum Mol Genet2016
26166477Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages.Am J Hum Genet2015
23202125Large-scale association analysis identifies new risk loci for coronary artery disease.Nat Genet2013
23824655The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis.PLoS Med2013
24213632Dysfunctional nitric oxide signalling increases risk of myocardial infarction.Nature2013
23933542The 9p21 locus does not affect risk of coronary artery disease through induction of type 1 interferons.Journal of the American College of Cardiology2013
23916927Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study.J Am Coll Cardiol2013
23535734Identification of seven loci affecting mean telomere length and their association with disease.Nat Genet2013
23593153Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease.PLoS One2013
21989056Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene.Hum Mol Genet2012
22421339Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies.Lancet2012
23063622Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.Am J Hum Genet2012
23139254Integration of genetics into a systems model of electrocardiographic traits using HumanCVD BeadChip.Circ Cardiovasc Genet2012
22100073Blood pressure loci identified with a gene-centric array.Am J Hum Genet2011
21303902Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol.Circ Cardiovasc Genet2011
21378990Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.Nat Genet2011
21283740Large-scale candidate gene analysis of HDL particle features.PLoS One2011
22006290The epithelial sodium channel γ-subunit gene and blood pressure: family based association, renal gene expression, and physiological analyses.Hypertension2011
21965548Four genetic loci influencing electrocardiographic indices of left ventricular hypertrophy.Circ Cardiovasc Genet2011
21909115Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.Nature2011
21606135A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.Circ Cardiovasc Genet2011
20139977Common variants near TERC are associated with mean telomere length.Nat Genet2010
20829508The relationship between plasma angiopoietin-like protein 4 levels, angiopoietin-like protein 4 genotype, and coronary heart disease risk.Arterioscler Thromb Vasc Biol2010
21060006Genetic architecture of ambulatory blood pressure in the general population: insights from cardiovascular gene-centric array.Hypertension2010
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William Harvey Research Institute, Queen Mary University of London
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University of Cambridge
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William Harvey Research Institute, Queen Mary University of London
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Vagelos College of Physicians and Surgeons, Columbia University
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Ludwig-Maximilians-Universitat Munchen
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Baylor College of Medicine
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Pat Macpherson Centre for Pharmacogenomics and Pharmacogenetics, University of Dundee
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London NorthWest Healthcare NHS Trust
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Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
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