Publications by authors named "Peter Braund"

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Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction.
Aeron M Small, Ta-Yu Yang, Shinsuke Itoh, Sébastien Thériault, Line Dufresne, Peter S Braund

Nat Genet· December 2025

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Polygenic prediction of body mass index and obesity through the life course and across ancestries.
Roelof A J Smit, Kaitlin H Wade, Qin Hui, Joshua D Arias, Xianyong Yin, Peter S Braund

Nat Med· September 2025

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Evaluation of current indirect methods for measuring LDL-cholesterol.
Sophia Drobnik, Hubert Scharnagl, Nilesh J Samani, Peter S Braund, Christopher P Nelson

Clin Chem Lab Med· May 2025

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Distinct Genetic Risk Profile in Aortic Stenosis Compared With Coronary Artery Disease.
Teresa Trenkwalder, Carlo Maj, Baravan Al-Kassou, Radoslaw Debiec, Stefanie A Doppler, Peter S Braund

JAMA Cardiol· February 2025

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Polygenic risk score adds to a clinical risk score in the prediction of cardiovascular disease in a clinical setting.
Nilesh J Samani, Emma Beeston, Chris Greengrass, Fernando Riveros-McKay, Radoslaw Debiec, Peter S Braund

Eur Heart J· September 2024

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Author Correction: The power of genetic diversity in genome-wide association studies of lipids.
Sarah E Graham, Shoa L Clarke, Kuan-Han H Wu, Stavroula Kanoni, Greg J M Zajac, Peter S Braund

Nature· June 2023

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Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation.
David Adlam, Takiy-Eddine Berrandou, Adrien Georges, Christopher P Nelson, Eleni Giannoulatou, Peter S Braund

Nat Genet· June 2023

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Elucidation of the genetic causes of bicuspid aortic valve disease.
Jan Gehlen, Anja Stundl, Radoslaw Debiec, Federica Fontana, Markus Krane, Peter S Braund

Cardiovasc Res· May 2023

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Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
Stavroula Kanoni, Sarah E Graham, Yuxuan Wang, Ida Surakka, Shweta Ramdas, Peter S Braund

Genome Biol· December 2022

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A saturated map of common genetic variants associated with human height.
Loïc Yengo, Sailaja Vedantam, Eirini Marouli, Julia Sidorenko, Eric Bartell, Peter S Braund

Nature· October 2022

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Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention.
Zhe Wang, Andrew Emmerich, Nicolas J Pillon, Tim Moore, Daiane Hemerich, Peter S Braund

Nat Genet· September 2022

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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
Shweta Ramdas, Jonathan Judd, Sarah E Graham, Stavroula Kanoni, Yuxuan Wang, Peter S Braund

Am J Hum Genet· August 2022

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Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.
Claudia Calabrese, Angela Pyle, Helen Griffin, Jonathan Coxhead, Rafiqul Hussain, Peter S Braund

PLoS Genet· April 2022

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The power of genetic diversity in genome-wide association studies of lipids.
Sarah E Graham, Shoa L Clarke, Kuan-Han H Wu, Stavroula Kanoni, Greg J M Zajac, Peter S Braund

Nature· December 2021

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Polygenic basis and biomedical consequences of telomere length variation.
Veryan Codd, Qingning Wang, Elias Allara, Crispin Musicha, Stephen Kaptoge, Peter S Braund

Nat Genet· October 2021

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Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Praveen Surendran, Elena V Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, Peter S Braund

Nat Genet· May 2021

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Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Praveen Surendran, Elena V Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, Peter S Braund

Nat Genet· December 2020

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Association of Factor V Leiden With Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data.
Bakhtawar K Mahmoodi, Vinicius Tragante, Marcus E Kleber, Michael V Holmes, Amand F Schmidt, Peter S Braund

Circulation· August 2020

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KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern.
Alexander Teumer, Teresa Trenkwalder, Thorsten Kessler, Yalda Jamshidi, Marten E van den Berg, Peter S Braund

JCI Insight· December 2019

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New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders.
Evangelos Evangelou, He Gao, Congying Chu, Georgios Ntritsos, Paul Blakeley, Peter S Braund

Nat Hum Behav· September 2019

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A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.
Yun Ju Sung, Lisa de las Fuentes, Thomas W Winkler, Daniel I Chasman, Amy R Bentley, Peter S Braund

Hum Mol Genet· August 2019

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Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals.
Raymond Noordam, William J Young, Reem Salman, Jørgen K Kanters, Marten E van den Berg, Peter S Braund

J Am Coll Cardiol· June 2019

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Subsequent Event Risk in Individuals With Established Coronary Heart Disease.
Riyaz S Patel, Vinicius Tragante, Amand F Schmidt, Raymond O McCubrey, Michael V Holmes, Peter S Braund

Circ Genom Precis Med· April 2019

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Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events.
Riyaz S Patel, Amand F Schmidt, Vinicius Tragante, Raymond O McCubrey, Michael V Holmes, Peter S Braund

Circ Genom Precis Med· April 2019

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Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection.
David Adlam, Timothy M Olson, Nicolas Combaret, Jason C Kovacic, Siiri E Iismaa, Peter S Braund

J Am Coll Cardiol· January 2019

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