Peter S. Braund

Active 2004–2025

Also published as
Peter S Braund
66
Papers
30,819
Citations
52
h-index
63
i10-index

Citations

Citations per year for Peter S. Braund1971: 1 citations1975: 1 citations1979: 1 citations1988: 1 citations1994: 1 citations1998: 3 citations2002: 1 citations2004: 1 citations2005: 6 citations2006: 9 citations2007: 108 citations2008: 557 citations2009: 592 citations2010: 573 citations2011: 534 citations2012: 467 citations2013: 443 citations2014: 395 citations2015: 393 citations2016: 377 citations2017: 366 citations2018: 337 citations2019: 803 citations2020: 764 citations2021: 752 citations2022: 569 citations2023: 482 citations2024: 706 citations2025: 322 citations2026: 26 citations1972–1974: no citations, so these years are not shown1976–1978: no citations, so these years are not shown1980–1987: no citations, so these years are not shown1989–1993: no citations, so these years are not shown1995–1997: no citations, so these years are not shown1999–2001: no citations, so these years are not shown2003: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,045 citing papers, 21.5% of this breakdownUnited Kingdom: 2,215 citing papers, 11.8% of this breakdownGermany: 1,087 citing papers, 5.8% of this breakdownChina: 1,075 citing papers, 5.7% of this breakdownNetherlands: 818 citing papers, 4.4% of this breakdownAustralia: 738 citing papers, 3.9% of this breakdownCanada: 702 citing papers, 3.7% of this breakdownItaly: 661 citing papers, 3.5% of this breakdownSweden: 617 citing papers, 3.3% of this breakdownFrance: 550 citing papers, 2.9% of this breakdownFinland: 425 citing papers, 2.3% of this breakdownDenmark: 411 citing papers, 2.2% of this breakdown
0%21.5%Other 29%

Fields

  • Biochemistry, Genetics and Molecular Biology49.2%
  • Medicine39.2%
  • Immunology and Microbiology5.1%
  • Neuroscience1.8%
  • Computer Science0.9%
  • Nursing0.7%
  • Other3.1%

Topics

  • Genetic Associations and Epidemiology12%
  • Genetic Mapping and Diversity in Plants and Animals2.7%
  • Bioinformatics and Genomic Networks2.5%
  • Lipoproteins and Cardiovascular Health2.3%
  • Genetic and phenotypic traits in livestock1.9%
  • Genomics and Rare Diseases1.8%
  • Other76.8%

Coauthors

All papers

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  1. A saturated map of common genetic variants associated with human height

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tarunveer S. Ahluwalia, Masato Akiyama, Matthew Allison, Marcus Alvarez, Mette K. Andersen, Alireza Ani, Vivek Appadurai, Liubov Arbeeva, Seema Bhaskar, Lawrence F. Bielak, Sailalitha Bollepalli, Lori L. Bonnycastle, Jette Bork‐Jensen, Jonathan P. Bradfield, Yuki Bradford, Peter S. Braund, Jennifer A. Brody, Kristoffer Sølvsten Burgdorf, Brian E. Cade, Hui Cai, Qiuyin Cai, Archie Campbell, Marisa Cañadas‐Garre, Eulalia Catamo, Jin Fang Chai, Xiaoran Chai, Li-Ching Chang, Yi‐Cheng Chang, Chien-Hsiun Chen, Alessandra Chesi, Seung Hoan Choi, Ren‐Hua Chung, Massimiliano Cocca, Maria Pina Concas, Christian Couture, Gabriel Cuéllar-Partida, Rebecca Danning, E. Warwick Daw, Frauke Degenhard, Graciela E. Delgado, Alessandro Delitala, Ayşe Demirkan, Xuan Deng, Poornima Devineni, Alexander Dietl, Maria Dimitriou, Latchezar Dimitrov, Rajkumar Dorajoo, Arif B. Ekici, Jorgen Engmann, Zammy Fairhurst-Hunter, Aliki‐Eleni Farmaki, Jessica D. Faul, Juan-Carlos Fernandez-Lopez, Lukas Forer, Margherita Francescatto, Sandra Freitag‐Wolf, Christian Fuchsberger, Tessel E. Galesloot, Yan Gao, Zishan Gao, Frank Geller, Olga Giannakopoulou, Franco Giulianini, Anette P. Gjesing, Anuj Goel, Scott D. Gordon, Mathias Gorski, Jakob Grove, Xiuqing Guo and 532 more - Nature 2022 cited by 921

  2. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jun Ding, Franco Giulianini, Elizabeth Holliday, Anne Jackson, Ruifang Li‐Gao, Wei‐Yu Lin, Jian’an Luan, Massimo Mangino, Christopher Oldmeadow, Bram P. Prins, Yong Qian, Muralidharan Sargurupremraj, Nabi Shah, Praveen Surendran, Sébastien Thériault, Niek Verweij, Sara M. Willems, Jing-Hua Zhao, Philippe Amouyel, John Connell, Renée de Mutsert, Alex S. F. Doney, Martin Farrall, Cristina Menni, Andrew D. Morris, Raymond Noordam, Guillaume Paré, Neil R Poulter, Denis C. Shields, Alice Stanton, Simon Thom, Gonçalo Abecasis, Najaf Amin, Dan E. Arking, Kristin L. Ayers, Caterina Barbieri, Chiara Batini, Joshua C. Bis, Tineka Blake, Murielle Bochud, Michael Boehnke, Eric Boerwinkle, Dorret I. Boomsma, Erwin P. Böttinger, Peter S. Braund, Marco Brumat, Archie Campbell, Harry Campbell, Aravinda Chakravarti, John C. Chambers, Ganesh Chauhan, Marina Ciullo, Massimiliano Cocca, Francis S. Collins, Heather J. Cordell, Gail Davies, Martin H. de Borst, Eco J. C. de Geus, Ian J. Deary, Joris Deelen, Fabiola Del Greco M, Cumhur Yusuf Demirkale, Marcus Dörr, Georg Ehret, Roberto Elosúa, Stefan Enroth, A. Mesut Erzurumluoglu, Teresa Ferreira, Mattias Frånberg, Oscar H. Franco and 181 more - Nature Genetics 2018 cited by 1,500

  3. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jennifer D. Jolley, Alexandra S. Knight, Kerstin Koch, Elizabeth Meech, Sarah Nutland, C V Prowse, Helen E. Stevens, Niall Taylor, Graham R. Walters, Neil M. Walker, Nicholas A. Watkins, Thilo Winzer, John A. Todd, Willem H. Ouwehand, 1958 Birth Cohort Controls, Richard W. Jones, Wendy L. McArdle, Susan M. Ring, David P. Strachan, Marcus Pembrey, Bipolar Disorder, Gerome Breen, David St Clair, Sian Caesar, Katherine Gordon‐Smith, Lisa Jones, Christine Fraser, Elaine Green, Detelina Grozeva, Marian L. Hamshere, Peter Holmans, Ian Jones, George Kirov, Valentina Moskvina, Ivan Nikolov, Michael O‘Donovan, Michael J. Owen, Nick Craddock, David Collier, Amanda Elkin, Anne Farmer, Richard Williamson, Peter McGuffin, Allan H. Young, I. Nicol Ferrier, Coronary Artery Disease, Stephen G. Ball, Anthony J. Balmforth, Jennifer H. Barrett, D. Timothy Bishop, Mark M. Iles, Azhar Maqbool, Nadira Yuldasheva, Alistair S. Hall, Peter S. Braund, Paul R. Burton, Richard J. Dixon, Massimo Mangino, Suzanne Stevens, Martin D. Tobin, J. Thompson, Nilesh J. Samani, Crohn’s Disease, Francesca Bredin, Mark Tremelling, Miles Parkes, Hazel E. Drummond, Charles W. Lees, Elaine R. Nimmo, Jack Satsangi and 176 more - Nature 2007 cited by 9,690

  4. Large-scale association analysis identifies new risk loci for coronary artery disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Suzanne Rafelt, Dmitry Shungin, Rona J. Strawbridge, Guðmar Þorleifsson, Emmi Tikkanen, Natalie Van Zuydam, Benjamin F. Voight, Lindsay L. Waite, Weihua Zhang, Andreas Ziegler, Devin Absher, David Altshuler, Anthony J. Balmforth, Inês Barroso, Peter S. Braund, Christof Burgdorf, Simone Claudi-Boehm, David Cox, Maria Dimitriou, Ron Do, Alex S. F. Doney, NourEddine El Mokhtari, Per Eriksson, Krista Fischer, Pierre Fontanillas, Anders Franco‐Cereceda, Bruna Gigante, Leif Groop, Stefan Gustafsson, Jörg Hager, Göran Hallmans, Bok-Ghee Han, Sarah Hunt, Hyun Min Kang, Thomas Illig, Thorsten Kessler, Joshua W Knowles, Genovefa Kolovou, Johanna Kuusisto, Claudia Langenberg, Cordelia Langford, Karin Leander, Marja‐Liisa Lokki, Anders Lundmark, Mark I. McCarthy, Christa Meisinger, Olle Melander, Evelin Mihailov, Seraya Maouche, Andrew D. Morris, Martina Müller‐Nurasyid, Kjell Nikus, John F. Peden, Nigel W. Rayner, Asif Rasheed, Silke Rosinger, Deborah C. Rubin, Moritz Rumpf, Arne Schäfer, Mohan U. Sivananthan, Ci Song, Alexandre F.R. Stewart, Sian-Tsung Tan, Guðmundur Þorgeirsson, C. Ellen van der Schoot, Peter J. Wagner, George A. Wells, Philipp S. Wild, Tsun-Po Yang, Philippe Amouyel and 83 more - Nature Genetics 2012 cited by 1,669

  5. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mary Susan Burnett, Ian Buysschaert, John F. Carlquist, Li Chen, Sven Cichon, Veryan Codd, R. W. Davies, George Dedoussis, Abbas Dehghan, Serkalem Demissie, Joseph M. Devaney, Patrick Diemert, Ron Do, Angela Doering, Sandra Eifert, Nour Eddine El Mokhtari, Stephen G. Ellis, Roberto Elosúa, James C. Engert, Stephen E. Epstein, Ulf dé Fairé, Marcus Fischer, Aaron R. Folsom, Jennifer Freyer, Bruna Gigante, Domenico Girelli, Sólveig Grétarsdóttir, Vilmundur Guðnason, Jeffrey R. Gulcher, Eran Halperin, Naomi Hammond, Stanley L. Hazen, Albert Hofman, Benjamin D. Horne, Thomas Illig, Carlos Iribarren, Gregory T. Jones, J. Wouter Jukema, Michael Kaiser, Lee M. Kaplan, John J.P. Kastelein, Kay‐Tee Khaw, Joshua W. Knowles, Genovefa Kolovou, Augustine Kong, Reijo Laaksonen, Diether Lambrechts, Karin Leander, Guillaume Lettre, Mingyao Li, Wolfgang Lieb, Christina Loley, Andrew Lotery, Pier Mannuccio Mannucci, Seraya Maouche, Nicola Martinelli, Pascal McKeown, Christa Meisinger, Thomas Meitinger, Olle Melander, Pier Angelica Merlini, Vincent Mooser, Thomas M. Morgan, Thomas W Mühleisen, Joseph B. Muhlestein, Thomas Münzel, Kiran Musunuru, Janja Nahrstaedt, Christopher P. Nelson, Markus M. Nöthen and 67 more - Nature Genetics 2011 cited by 1,951

  6. Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Åsa Johansson, Anja Moltke Jørgensen, Marika Kaakinen, Robert Karlsson, Kathleen F. Kerr, Boram Kim, Chantal M. Koolhaas, Zoltán Kutalik, Vasiliki Lagou, Penelope A. Lind, Mattias Lorentzon, Leo‐Pekka Lyytikäinen, Massimo Mangino, Christoph Metzendorf, Kristine R. Monroe, Alexander Pacolet, Louis Përusse, René Pool, Rebecca C. Richmond, Natalia V. Rivera, Sébastien Robiou-du-Pont, Katharina E. Schraut, Christina‐Alexandra Schulz, Heather M. Stringham, Toshiko Tanaka, Alexander Teumer, Constance Turman, Peter J. van der Most, Mathias Vanmunster, Frank J.A. van Rooij, Jana V. van Vliet‐Ostaptchouk, Xiaoshuai Zhang, Jinghua Zhao, Wei Zhao, Zhanna Balkhiyarova, Marie Balslev‐Harder, Sebastian E. Baumeister, John Beilby, John Blangero, Dorret I. Boomsma, Søren Brage, Peter S. Braund, Jennifer A. Brody, Marcel Bruinenberg, Ulf Ekelund, Ching‐Ti Liu, John W. Cole, Francis S. Collins, L. Adrienne Cupples, Tõnu Esko, Stefan Enroth, Jessica D. Faul, Lindsay Fernández‐Rhodes, Alison E. Fohner, Oscar H. Franco, Tessel E. Galesloot, Scott D. Gordon, Niels Grarup, Catharina A. Hartman, Gerardo Heiss, Jennie Hui, Thomas Illig, Russell Jago, Alan James, Peter K. Joshi, Taeyeong Jung, Mika Kähönen, Tuomas O. Kilpeläinen, Woon‐Puay Koh, Ivana Kolčić and 128 more - Nature Genetics 2022 cited by 236

  7. Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David Melzer, David Reich, Bruce M. Psaty, Marcus E. Kleber, Demosthenes B. Panagiotakos, Johann Willeit, Patrik Wennberg, Mark Woodward, Svetlana Adamovic, Eric B. Rimm, Tom Meade, Richard F. Gillum, Jonathan A. Shaffer, Albert Hofman, Altan Onat, Johan Sundström, Sylvia Wassertheil‐Smoller, Dan Mellström, John Gallacher, Mary Cushman, Russell P. Tracy, Jussi Kauhanen, Magnus K. Karlsson, Jukka T. Salonen, Lars Wilhelmsen, Philippe Amouyel, Bernard Cantin, Lyle G. Best, Yoav Ben‐Shlomo, JoAnn E. Manson, Paul I W de Bakker, Paul I. W. de Bakker, Christopher J. O’Donnell, Anthony G Wilson, Anthony G. Wilson, Themistocles L. Assimes, John-Olov Jansson, Claes Ohlsson, Åsa Tivesten, Östen Ljunggren, Muredach P. Reilly, Anders Hamsten, Erik Ingelsson, François Cambien, Joseph Hung, G. Neil Thomas, Michael Boehnke, Heribert Schunkert, Folkert W. Asselbergs, John J.P. Kastelein, Vilmundur Guðnason, Veikko Salomaa, Tamara B. Harris, Jaspal S. Kooner, Kristine H. Allin, Jemma C Hopewell, Jemma C. Hopewell, Alison H. Goodall, Paul M. Ridker, Hilma Hólm, Hugh Watkins, Willem H. Ouwehand, N. J. Samani, Stephen Kaptoge, Emanuele Di Angelantonio, Olivier Harari - The Lancet 2012 cited by 824

  8. Identification of seven loci affecting mean telomere length and their association with disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Konstantinos Douroudis, Dubinina Ev, Johan G. Eriksson, K. Garlaschelli, Dehuang Guo, Anna‐Liisa Hartikainen, Anjali K. Henders, Jeanine J. Houwing‐Duistermaat, Laura Kananen, Lennart C. Karssen, Johannes Kettunen, Norman Klopp, Vasiliki Lagou, Elisabeth M van Leeuwen, Pamela A. F. Madden, Reedik Mägi, Patrik K. E. Magnusson, Satu Männistö, Mark I. McCarthy, Sarah E. Medland, Evelin Mihailov, Grant W. Montgomery, Ben A. Oostra, Aarno Palotie, Annette Peters, Helen Perlstein Pollard, Anneli Pouta, Inga Prokopenko, Samuli Ripatti, Veikko Salomaa, H. Eka D. Suchiman, Ana M. Valdes, Niek Verweij, Ana Viñuela, Xiaoling Wang, H‐Erich Wichmann, Elisabeth Widén, Gonneke Willemsen, Margaret J. Wright, Kai Xia, Xiangjun Xiao, Dirk J. van Veldhuisen, Alberico L. Catapano, Martin D. Tobin, Alistair S. Hall, Alexandra I. F. Blakemore, Wiek H. van Gilst, Haidong Zhu, Jeanette Erdmann, Muredach P. Reilly, Sekar Kathiresan, Heribert Schunkert, Philippa J. Talmud, Nancy L. Pedersen, Markus Perola, Willem H. Ouwehand, Jaakko Kaprio, Nicholas G. Martin, Cornelia M. van Duijn, Iiris Hovatta, Christian Gieger, Andres Metspalu, Dorret I. Boomsma, Marjo‐Riitta Järvelin, P. Eline Slagboom, John R. Thompson, Tim D. Spector, Pim van der Harst, Nilesh J. Samani - Nature Genetics 2013 cited by 962

  9. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jessica D. Faul, Eric B. Fauman, Cristiano Fava, Teresa Ferreira, Christopher N. Foley, Nora Franceschini, He Gao, Olga Giannakopoulou, Franco Giulianini, Daníel F. Guðbjartsson, Xiuqing Guo, Sarah E. Harris, Aki S. Havulinna, Anna Helgadóttir, Jennifer E. Huffman, Shih‐Jen Hwang, Stavroula Kanoni, Jukka Kontto, Martin G. Larson, Ruifang Li‐Gao, Jaana Lindström, Luca A. Lotta, Yingchang Lu, Jian’an Luan, Anubha Mahajan, Giovanni Malerba, Nicholas G. D. Masca, Hao Mei, Cristina Menni, Dennis O. Mook‐Kanamori, David Mosén-Ansorena, Martina Müller‐Nurasyid, Guillaume Paré, Dirk S. Paul, Markus Perola, Alaitz Poveda, Rainer Rauramaa, Melissa A. Richard, Tom G. Richardson, Nuno Sepúlveda, Xueling Sim, Albert V. Smith, Jennifer A. Smith, James R Staley, Alena Stanáková, Patrick Sulem, Sébastien Thériault, Unnur Þorsteinsdóttir, Stella Trompet, Tibor V. Varga, Digna R. Velez Edwards, Giovanni Veronesi, Stefan Weiß, Sara M. Willems, Jie Yao, Robin Young, Bing Yu, Weihua Zhang, Jinghua Zhao, Wei Zhao, Wei Zhao, Εvangelos Εvangelou, Stefanie Aeschbacher, Eralda Asllanaj, Stefan Blankenberg, Lori L. Bonnycastle, Jette Bork‐Jensen, Ivan Brandslund, Peter S. Braund, Stephen Burgess and 212 more - Nature Genetics 2020 cited by 239

  10. Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Roberto Elosúa, Ruth McPherson, Martin Farrall, Hugh Watkins, Eric S. Lander, Daniel J. Rader, John Danesh, Diego Ardissino, Stacey Gabriel, Cristen J. Willer, Gonçalo R. Abecasis, Danish Saleheen, Frederick E. Dewey, Sekar Kathiresan - JAMA 2017 cited by 204

  11. Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ramachandran S. Vasan, Eric S. Lander, Daniel J. Rader, John Danesh, Diego Ardissino, Stacey Gabriel, Danish Saleheen, Sekar Kathiresan - Journal of the American College of Cardiology 2016 cited by 250

  12. Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Stephanie Hesselson, Keerat Junday, Stavroula Kanoni, Krishna G. Aragam, Adam S. Butterworth, CARDIoGRAMPlusC4D, MEGASTROKE, Mark K. Bakker, Ynte M. Ruigrok, Marysia S. Tweet, Rajiv Gulati, Nicolas Combaret, DISCO register, Daniella Kadian‐Dodov, Jonathan M. Kalman, Diane Fatkin, Aroon D. Hingorani, Jacqueline Saw, Tom R. Webb, Sharonne N. Hayes, Xia Yang, Santhi K. Ganesh, Timothy M. Olson, Jason C. Kovacic, Robert M. Graham, N. J. Samani, Nabila Bouatia‐Naji - Nature Genetics 2023 cited by 89

  13. Genomewide Association Analysis of Coronary Artery Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Martin D. Tobin, Andreas Ziegler, John R. Thompson, Heribert Schunkert - New England Journal of Medicine 2007 cited by 2,050

  14. VariantASGR1Associated with a Reduced Risk of Coronary Artery Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael Williams, André M. van Rij, Gregory T. Jones, Riyaz Patel, Allan I. Levey, Salim S. Hayek, Svati H. Shah, Muredach P. Reilly, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ísleifur Ólafsson, Lambertus A. Kiemeney, Arshed A. Quyyumi, Daniel J. Rader, William E. Kraus, Nilesh J. Samani, Oluf Pedersen, Guðmundur Þorgeirsson, Gísli Másson, Hilma Hólm, Daníel F. Guðbjartsson, Patrick Sulem, Unnur Þorsteinsdóttir, Kāri Stefánsson - New England Journal of Medicine 2016 cited by 191

  15. Elucidation of the genetic causes of bicuspid aortic valve disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Yannick Haas, Matthias Karck, Uwe Mehlhorn, Lars O. Conzelmann, Ingo Breitenbach, Corinna Lebherz, Paul P. Urbanski, Won‐Keun Kim, Joscha Kandels, David Ellinghaus, Ulrike Nowak-Goettl, Per Hoffmann, Felix Wirth, S. Doppler, Harald Lahm, Martina Dreßen, Moritz von Scheidt, Katharina Knoll, Thorsten Kessler, Christian Hengstenberg, Heribert Schunkert, Georg Nickenig, Markus M. Nöthen, Aidan P. Bolger, Salim Abdelilah‐Seyfried, Nilesh J. Samani, Jeanette Erdmann, Teresa Trenkwalder, Johannes Schumacher - Cardiovascular Research 2022 cited by 48

  16. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Joel N. Hirschhorn, Peter S Braund, Steven A. McCarroll, Stacey B. Gabriel, Leena Peltonen, Sekar Kathiresan, Anika Grosshennig, Daniel B. Mirel, Muredach P Reilly, Aarti Surti, David M Nathan, William Matthai, Atif Qasim, Mark Daly, David Altshuler, James B Meigs, Calum A. MacRae, Domenico Girelli, Nicola Martinelli, Oliviero Olivieri, Roberto Corrocher, Gordon Williams, Chris C Patterson, David S Siscovick, Stephen M Schwartz, Benjamin F. Voight, David Siscovick, Steven A. McCarroll, Joshua M. Korn, Gavin Lucas, Shaun Purcell, Panos Deloukas, Veikko Salomaa, Diego Ardissino, Olle Melander, Flora Peyvandi, Marta Spreafico, Pier M Mannucci, Pier M Mannucci, Changchun Xie, Sonia Anand, Sonia Anand, James C. Engert, James C. Engert, Peter S. Braund, Nilesh J Samani, Nilesh J Samani, Nilesh J Samani, Pietro Zonzin, Anika Grosshennig, Heribert Schunkert, Heribert Schunkert, Patrick Linsel‐Nitschke, Michael Preuß, Wolfgang Lieb, Jeanette Erdmann, John R Thompson, Benjamin J Wright, Anthony J Balmforth, Stephen G Ball, Alistair S Hall, Andreas Ziegler, William Matthai, Christian Hengstenberg, Atif Qasim, Klaus Stark, H-Erich Wichmann, Stefan Schreiber, Willem Ouwehand, Michael Scholz and 23 more - Nature Genetics 2009 cited by 1,096

  17. Polygenic risk score adds to a clinical risk score in the prediction of cardiovascular disease in a clinical setting

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - European Heart Journal 2024 cited by 70

  18. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Adrian V. S. Hill, Cecilia M. Lindgren, Kirk A. Rockett, Mohammed JR Ghori, Nick Craddock, David Withers, Mohammed J. R. Ghori, Panos Deloukas, Andrew Keniry, Rathi Ravindrarajah, Amy Chaney, Claire Widden, Panos Deloukas, Claire Widden, Andrew Keniry, David Bentley, Ralph McGinnis, A Keniry, Simon Potter, Suzannah J. Bumpstead, Panos Deloukas, Sarah Hunt, Rhian Gwilliam, Emma King, Ralph McGinnis, Michael Inouye, Pamela Whittaker, David Bentley, Audrey Duncanson, Mark I. McCarthy, Kate Elliott, Eleftheria Zeggini, Christopher J. Groves, Massimo Mangino, Mark I. McCarthy, Dan Davison, Cecilia M. Lindgren, Jonathan L Marchini, Niall Taylor, Kerstin Koch, Teresa Ferreira, Nicholas A. Watkins, Thilo Winzer, Bryan N Howie, Zhan Su, Jennifer D. Jolley, Doug Easton, Barbara Cant, Alexandra S. Knight, Elizabeth Meech, Christopher V Prowse, Nicholas A. Watkins, Richard W Jones, Wendy L McArdle, Susan M Ring, Richard J. Dixon, Nilesh J. Samani, Massimo Mangino, David St Clair, Suzanne Stevens, Peter S. Braund, Peter Donnelly, Niall J. Cardin, Chris C. A. Spencer, Damjan Vukcevic, Jonathan Marchini, Joanne Pereira-Gale, Dan Davison, George Kirov, Yik Ying Teo and 115 more - Nature Genetics 2007 cited by 1,375

  19. Polygenic basis and biomedical consequences of telomere length variation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2021 cited by 371

  20. Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Emmanuelle Filippi, Louis Le Bivic, Brahim Harbaoui, Hakim Benamer, Guillaume Cayla, Olivier Varenne, Stephane Peggy Manzo-Silberman, Johanne Silvain, Christian Spaulding, Christophe Caussin, Édouard Gerbaud, Yann Valy, René Köning, Thibault Lhermusier, Stanislas Champin, Emmanuel Salengro, Arnaud Fluttaz, A. Zabalawi, Yves Cottin, Emmanuel Teíger, Christophe Saint‐Etienne, Grégory Ducrocq, Stéphanie Marlière, Emmanuel Boiffard, Pierre Aubry, Jean Georges, Hakim Benamer, Didier Bresson, F. De Poli, Gaëtan Karrillon, Vincent Roule, Laurent Bali, Mathieu Valla, Antoine Gerbay, David Houpe, Olivier Dubreuil, Arsène Monnier, Norbert Mayaud, Aurélie Manchuelle, Philippe Commeau, Marc Bédossa, Claire Mei Yi Wong, Eleni Giannoulatou, Michael Sweeting, David W.M. Muller, Alice Wood, Lucy McGrath‐Cadell, Diane Fatkin, Sally L. Dunwoodie, Richard P. Harvey, Cameron Holloway, Jean-Philippe Empana, Xavier Jouven, Majid Nikpay, Anuj Goel, Hong‐Hee Won, Leanne M. Hall, Christina Willenborg, Stavroula Kanoni, Danish Saleheen, Theodosios Kyriakou, Christopher P. Nelson, Jemma C. Hopewell, Tom R. Webb, Lingyao Zeng, Abbas Dehghan, Maris Alver, Sebastian M. Armasu, Kirsi Auro, Andrew Bjonnes and 142 more - Journal of the American College of Cardiology 2019 cited by 189

  21. Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Angelo Scuteri, Anne Jackson, Karen L. Mohlke, Jaako Tuomilehto, Robert Roberts, Alexandre F.R. Stewart, Y. Antero Kesäniemi, Robert W. Mahley, Scott M. Grundy, Wendy L. McArdle, Lon R. Cardon, Gérard Waeber, Péter Vollenweider, John C. Chambers, Michael Boehnke, Gonçalo R. Abecasis, Veikko Salomaa, Marjo‐Riitta Järvelin, Aimo Ruokonen, Inês Barroso, Stephen E. Epstein, Håkon Håkonarson, Daniel J. Rader, Muredach P. Reilly, Jacqueline C.M. Witteman, Alistair S. Hall, Nilesh J. Samani, David P. Strachan, Philip J. Barter, Cornelia M. van Duijn, Jaspal S. Kooner, Leena Peltonen, Nicholas J. Wareham, Ruth McPherson, Vincent Mooser, Manjinder S. Sandhu - Arteriosclerosis Thrombosis and Vascular Biology 2010 cited by 408

  22. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

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