Mark J. Caulfield

Active 1988–2025

Also published as
Mark J Caulfield
187
Papers
65,461
Citations
103
h-index
180
i10-index

Citations

Citations per year for Mark J. Caulfield1980: 1 citations1989: 3 citations1993: 1 citations1994: 5 citations1995: 21 citations1996: 25 citations1997: 37 citations1998: 23 citations1999: 22 citations2000: 28 citations2001: 19 citations2002: 8 citations2003: 44 citations2004: 100 citations2005: 152 citations2006: 199 citations2007: 200 citations2008: 318 citations2009: 398 citations2010: 415 citations2011: 430 citations2012: 507 citations2013: 516 citations2014: 559 citations2015: 643 citations2016: 603 citations2017: 637 citations2018: 670 citations2019: 1,852 citations2020: 1,906 citations2021: 2,057 citations2022: 1,592 citations2023: 1,041 citations2024: 1,727 citations2025: 804 citations2026: 50 citations1981–1988: no citations, so these years are not shown1990–1992: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 6,387 citing papers, 18.7% of this breakdownUnited Kingdom: 3,690 citing papers, 10.8% of this breakdownChina: 1,893 citing papers, 5.5% of this breakdownGermany: 1,736 citing papers, 5.1% of this breakdownItaly: 1,615 citing papers, 4.7% of this breakdownNetherlands: 1,359 citing papers, 4% of this breakdownAustralia: 1,309 citing papers, 3.8% of this breakdownCanada: 1,192 citing papers, 3.5% of this breakdownFrance: 1,071 citing papers, 3.1% of this breakdownSweden: 981 citing papers, 2.9% of this breakdownSpain: 902 citing papers, 2.6% of this breakdownJapan: 818 citing papers, 2.4% of this breakdown
0%18.7%Other 32.9%

Fields

  • Medicine58.3%
  • Biochemistry, Genetics and Molecular Biology30.4%
  • Neuroscience2.1%
  • Immunology and Microbiology1.7%
  • Nursing1.4%
  • Dentistry0.8%
  • Other5.3%

Topics

  • Genetic Associations and Epidemiology5.6%
  • Blood Pressure and Hypertension Studies5%
  • Lipoproteins and Cardiovascular Health3%
  • Diabetes, Cardiovascular Risks, and Lipoproteins2.9%
  • Cardiovascular Health and Disease Prevention1.8%
  • Genomics and Rare Diseases1.7%
  • Other80%

Coauthors

All papers

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  1. Spironolactone versus placebo, bisoprolol, and doxazosin to determine the optimal treatment for drug-resistant hypertension (PATHWAY-2): a randomised, double-blind, crossover trial

    Authors: , , , , , , , , , , , , - The Lancet 2015 cited by 1,245

  2. PanelApp crowdsources expert knowledge to establish consensus diagnostic gene panels

    Authors: , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2019 cited by 594

  3. Blood pressure and incidence of twelve cardiovascular diseases: lifetime risks, healthy life-years lost, and age-specific associations in 1·25 million people

    Authors: , , , , , , , , , , , , - The Lancet 2014 cited by 1,644

  4. Genetic mechanisms of critical illness in COVID-19

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Chenqing Zheng, Graeme R. Grimes, Rupert Beale, Jonathan Millar, Barbara Shih, Seán Keating, Marie Zechner, Chris Haley, David J. Porteous, Caroline Hayward, Jian Yang, Julian C. Knight, Charlotte Summers, Manu Shankar‐Hari, Paul Klenerman, Lance Turtle, Antonia Ho, Shona C. Moore, Charles Hinds, Peter Horby, Alistair Nichol, David M. Maslove, Lowell Ling, Danny McAuley, Hugh Montgomery, Timothy Walsh, Alexandre C. Pereira, Alessandra Renieri, Xia Shen, Chris P. Ponting, Angie Fawkes, Albert Tenesa, Mark J. Caulfield, Richard H. Scott, Kathy Rowan, Lee Murphy, Peter Openshaw, Malcolm G. Semple, Andrew Law, Véronique Vitart, James F. Wilson, J. Kenneth Baillie, J. Kenneth Baillie - Nature 2020 cited by 1,509

  5. Whole-genome sequencing of patients with rare diseases in a national health system

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hugh S. Markus, Joannella Morales, Nicholas W. Morrell, Andrew Mumford, Elizabeth Ormondroyd, Stuart Rankin, Augusto Rendon, Sylvia Richardson, Irene Roberts, Noémi Roy, Moin A. Saleem, Kenneth G. C. Smith, Hannah Stark, Rhea Tan, Andreas C. Themistocleous, Adrian J. Thrasher, Hugh Watkins, Andrew R. Webster, Martin R. Wilkins, Catherine Williamson, James Whitworth, Sean Humphray, David R. Bentley, NIHR BioResource for the 100,000 Genomes Project, Stephen Abbs, Lara Abulhoul, Julian Adlard, Munaza Ahmed, Timothy J. Aitman, Hana Alachkar, David Allsup, J. P. Almeida, Philip Ancliff, Richard Antrobus, Ruth Armstrong, Gavin Arno, Sofie Ashford, William J. Astle, Anthony Attwood, Paul Aurora, Christian Babbs, Chiara Bacchelli, Tamam Bakchoul, Siddharth Banka, Tadbir K. Bariana, Julian Barwell, Joana Batista, Helen Baxendale, Phil Beales, David Bennett, David R. Bentley, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Graeme C. Black, Marta Bleda, Iulia Blesneac, Detlef Böckenhauer, Harm Jan Bogaard, Christian Bourne, Sara Boyce, John R. Bradley, Eugene Bragin, Gerome Breen, Paul Brennan, Carole Brewer, Matthew A. Brown, Andrew C. Browning, Michael J. Browning, Rachel Buchan and 412 more - Nature, Nat. 2020 cited by 582

  6. Effects of Torcetrapib in Patients at High Risk for Coronary Events

    Authors: , , , , , , , , , , , , , , , - New England Journal of Medicine 2007 cited by 3,144

  7. Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Augusto Rendon, Sue Hill, Mark J. Caulfield, Nirupa Murugaesu - Nature Medicine 2024 cited by 178

  8. Causal association between periodontitis and hypertension: evidence from Mendelian randomization and a randomized controlled trial of non-surgical periodontal therapy

    Authors: , , , , , , , , , , , , , , , , , , , - European Heart Journal 2019 cited by 347

  9. Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jonathan M Schott, Thomas T Warner, Nicholas W Wood, David Bourn, Kelly Eggleton, Robyn Labrum, Philip Twiss, Stephen Abbs, Liana Santos, Ghareesa Almheiri, Isabella Sheikh, Jana Vandrovcova, Christine Patch, Ana Lisa Taylor Tavares, Zerin Hyder, Anna Need, Helen Brittain, Emma Baple, Loukas Moutsianas, Viraj Deshpande, Denise L Perry, Subramanian S. Ajay, Aditi Chawla, Vani Rajan, Kathryn Oprych, Patrick F Chinnery, Angela Douglas, Gill Wilson, Sian Ellard, I Karen Temple, Andrew Mumford, Dom McMullan, Kikkeri Naresh, Frances A Flinter, Jenny C Taylor, Lynn Greenhalgh, William Newman, Paul Brennan, John A Sayer, F Lucy Raymond, Lyn S Chitty, Zandra C Deans, Sue Hill, Tom Fowler, Richard H Scott, John Hardy, Patrick F Chinnery, Henry Houlden, Augusto Rendon, Mark J Caulfield, Michael A Eberle, Ryan J Taft, Arianna Tucci, John C. Ambrose, Prabhu Arumugam, Marta Bleda, Freya Boardman-Pretty, Jeanne M. Boissiere, Christopher R. Boustred, Clare E.H. Craig, Anna de Burca, Andrew Devereau, Greg Elgar, Rebecca E. Foulger, Pedro Furió-Tarí, Joanne Hackett, Dina Halai, Angela Hamblin, Shirley Henderson, James Holman and 40 more - The Lancet Neurology 2022 cited by 183

  10. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thor Aspelund, Albert V. Smith, Vilmundur Guðnason, Thor Aspelund, Albert Hofman, María Soler Artigas, Nick Shrine, Louise V. Wain, Martin D. Tobin, André G. Uitterlinden, Najaf Amin, Yurii S. Aulchenko, Cornelia M. van Duijn, M. Arfan Ikram, Eric J.G. Sijbrands, John C. Chambers, Cornelia M. van Duijn, Peter Würtz, Ayşe Demirkan, Albert Hofman, Aaron Isaacs, Gonçalo R. Abecasis, Germaine C. Verwoert, André G. Uitterlinden, Eric J.G. Sijbrands, Joshua C. Bis, Bruce M. Psaty, Lenore Launer, Germaine C. Verwoert, Tamara B. Harris, M. Arfan Ikram, Jian’an Luan, Germaine C. Verwoert, André G. Uitterlinden, Simon Heath, Daniel Levy, Péter Vollenweider, Peter Würtz, Elin Org, Gudrun Veldre, John C. Chambers, Paul Elliott, Weihua Zhang, Gonçalo R. Abecasis, Jennifer L. Bragg‐Gresham, Uwe Völker, Alexander Teumer, Joshua C. Bis, Nicole L. Glazer, Bruce M. Psaty, Tamara B. Harris, Melissa N. Garcia, Lenore J. Launer, Nicole Soranzo, Jing Zhao, Ruth J. F. Loos, Nicholas J. Wareham, Mark Lathrop, Diana Zélénika, Simon Heath, Siim Sõber, Maris Laan, Gudrun Veldre, Elin Org, Halit Ongen, Anuj Goel, Afshin Parsa, Nanette Steinle, Alan R. Shuldiner, Yuri Milaneschi and 246 more - Nature 2011 cited by 2,083

  11. Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials

    Authors: , , , , , , , , , , , , , , , , - The Lancet 2015 cited by 707

  12. Prevention of coronary and stroke events with atorvastatin in hypertensive patients who have average or lower-than-average cholesterol concentrations, in the Anglo-Scandinavian Cardiac Outcomes Trial—Lipid Lowering Arm (ASCOT-LLA): a multicentre randomised controlled trial

    Authors: , , , , , , , , , , , , , - The Lancet 2003 cited by 3,792

  13. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gonçalo R. Abecasis, Katja K.H. Aben, Dewan S Alam, Sameer Alharthi, Matthew Allison, Philippe Amouyel, Folkert W. Asselbergs, Paul L. Auer, Beverley Balkau, Lia E. Bang, Inês Barroso, Lisa Bastarache, Marianne Benn, Sven Bergmann, Lawrence F. Bielak, Matthias Blüher, Michael Boehnke, Heiner Boeing, Eric Boerwinkle, Carsten A. Böger, Jette Bork‐Jensen, Michiel L. Bots, Erwin P. Böttinger, Donald W. Bowden, Ivan Brandslund, Gerome Breen, Murray H. Brilliant, Linda Broer, Marco Brumat, Amber Burt, Adam S. Butterworth, Peter T. Campbell, Stefania Cappellani, David J. Carey, Eulalia Catamo, Mark J. Caulfield, John C. Chambers, Daniel I. Chasman, Yii‐Der Ida Chen, Rajiv Chowdhury, Cramer Christensen, Audrey Y. Chu, Massimiliano Cocca, Francis S. Collins, James P. Cook, Janie Corley, Jordi Corominas Galbany, Amanda J. Cox, David S. Crosslin, Gabriel Cuéllar-Partida, Angela D’Eustacchio, John Danesh, Gail Davies, Paul I. W. de Bakker, Mark de Groot, Renée de Mutsert, Ian J. Deary, George Dedoussis, Ellen W. Demerath, Martin den Heijer, Anneke I. den Hollander, Hester M. den Ruijter, Joe Dennis, Joshua C. Denny, Emanuele Di Angelantonio, Fotios Drenos, Mengmeng Du, Marie‐Pierre Dubé, Alison M. Dunning, Douglas F. Easton and 304 more - Nature Genetics 2017 cited by 428

  14. Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes

    Authors: , , , , , , , , - Nature 2022 cited by 306

  15. Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study

    Authors: , , , , , , , , , , , , , , , , , , , , , , - 2022 cited by 140

  16. 2013 ESH/ESC Guidelines for the management of arterial hypertension

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Margus Viigimaa, Ettore Ambrosioni, Mark Caufield, António Coca, Michael Hecht Olsen, Roland E Schmieder, Costas Tsioufis, Philippe van de Borne, Jose Luis Zamorano, Stephan Achenbach, Helmut Baumgartner, Jeroen J. Bax, Héctor Bueno, Veronica Dean, Christi Deaton, Çetin Erol, Robert Fagard, Roberto Ferrari, David Hasdai, Arno W Hoes, Paulus Kirchhof, Juhani Knuuti, Philippe Kolh, Patrizio Lancellotti, Aleš Linhart, Petros Nihoyannopoulos, Massimo Piepoli, Piotr Ponikowski, Per Anton Sirnes, Juan Tamargo, Michał Tendera, Adam Torbicki, William Wijns, Stephan Windecker, Denis Clément, António Coca, Thierry Gillebert, Michał Tendera, Enrico Agabiti Rosei, Ettore Ambrosioni, Stefan D Anker, Johann Bauersachs, Jana Brguljan Hitij, Mark J. Caulfield, Marc De Buyzere, Sabina De Geest, Geneviève Dérumeaux, Serap Erdine, Csaba Farsang, Christian Funck‐Brentano, Vjekoslav Gerc, Giuseppe Germanò, Stephan Gielen, Herman Haller, Arno W Hoes, Jens Jordan, Thomas Kahan, Michel Komajda, Dragan Lović, Heiko Mahrholdt, Michael Hecht Olsen, Jan Östergren, Gianfranco Parati, Joep Perk, Jorge Polónia, Bogdan A Popescu, Zeljko Reiner, Lars Rydén, Yu.M. Sіrenko, Alice Stanton and 6 more - European Heart Journal 2013 cited by 13,677

  17. Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laura J. Scott, Jian’an Luan, Jing-Hua Zhao, Sara M. Willems, Sébastien Thériault, Nabi Shah, Christopher Oldmeadow, Peter Almgren, Ruifang Li‐Gao, Niek Verweij, Thibaud Boutin, Massimo Mangino, Ioanna Ntalla, Elena V. Feofanova, Praveen Surendran, James P. Cook, Savita Karthikeyan, Najim Lahrouchi, Chunyu Liu, Nuno Sepúlveda, Tom G. Richardson, Aldi T. Kraja, Philippe Amouyel, Martin Farrall, Neil R Poulter, Markku Laakso, Eleftheria Zeggini, Peter Sever, Robert A. Scott, Claudia Langenberg, Nicholas J. Wareham, David Conen, Colin Neil Alexander Palmer, John Attia, Daniel I. Chasman, Paul M. Ridker, Olle Melander, Dennis Owen Mook-Kanamori, Pim van der Harst, Francesco Cucca, David Schlessinger, Caroline Hayward, Tim D. Spector, Marjo-Riitta Jarvelin, Branwen J. Hennig, Nicholas J. Timpson, Wei-Qi Wei, Joshua Smith, Yaomin Xu, Michael E. Matheny, Edward D. Siew, Cecilia M. Lindgren, Karl‐Heinz Herzig, George Dedoussis, Joshua C. Denny, Bruce M. Psaty, Joanna M. M. Howson, Patricia B. Munroe, Christopher Newton‐Cheh, Mark J. Caulfield, Paul Elliott, J. Michael Gaziano, John Concato, Peter W.F. Wilson, Philip S. Tsao, Digna R. Velez Edwards, Katalin Suszták, Christopher J. O’Donnell, Adriana M. Hung, Todd L. Edwards - Nature Genetics 2018 cited by 501

  18. The 100 000 Genomes Project: bringing whole genome sequencing to the NHS

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - BMJ 2018 cited by 477

  19. Genetic Predisposition to High Blood Pressure and Lifestyle Factors

    Authors: , , , , , , , - Circulation 2017 cited by 298

  20. Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Dorothy Thompson, Emma Wakeling, Willem H. Ouwehand, Michel Michaelides, Anthony T. Moore, Andrew R. Webster, F. Lucy Raymond, Timothy J. Aitman, Hana Alachkar, Sonia Ali, Louise Allen, David Allsup, Gautum Ambegaonkar, Julie Anderson, Richard Antrobus, Ruth Armstrong, Gavin Arno, Gururaj Arumugakani, Sofie Ashford, William F. Astle, Antony Attwood, Steve Austin, Chiara Bacchelli, Tamam Bakchoul, Tadbir K. Bariana, Helen Baxendale, David Bennett, Claire Bethune, Shahnaz Bibi, Maria Bitner‐Glindzicz, Marta Bleda, Harm Boggard, Paula Bolton‐Maggs, Claire Booth, John R. Bradley, Angie Brady, Matthew A. Brown, Michael J. Browning, Christine Bryson, Siobhan O. Burns, Paul Calleja, Natalie Canham, Jenny Carmichael, Keren Carss, Mark J. Caulfield, Elizabeth Chalmers, Anita Chandra, Patrick F. Chinnery, Manali Chitre, Colin Church, Emma Clement, Emma Clement, Virginia Clowes, Gerry Coghlan, Peter Collins, Nichola Cooper, Amanda Creaser-Myers, Rosa DaCosta, Louise C. Daugherty, Sophie Davies, John S. Davis, Minka De Vries, Patrick Deegan, Sri V. V. Deevi, Charu Deshpande, Lisa Devlin, Eleanor Dewhurst, Rainer Döffinger, Natalie Dormand, Elizabeth Drewe and 211 more - The American Journal of Human Genetics 2016 cited by 484

  21. Hypertension

    Authors: , , - The Lancet 2015 cited by 667

  22. Dietary Nitrate Provides Sustained Blood Pressure Lowering in Hypertensive Patients

    Authors: , , , , - Hypertension 2014 cited by 497

  23. A systematic CRISPR screen defines mutational mechanisms underpinning signatures caused by replication errors and endogenous DNA damage

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Louise C. Daugherty, Anna de Burca, A. Devereau, Greg Elgar, Rebecca E. Foulger, Tom Fowler, Pedro Furió‐Tarí, Adam Giess, Joanne M. Hackett, Dina Halai, Angela Hamblin, Shirley Henderson, J. Holman, Tim Hubbard, Kristina Ibáñez, Robert W. Jackson, J. Louise Jones, Dalia Kasperavičiūtė, Melis Kayikci, Athanasios Kousathanas, L. Lahnstein, Kay Lawson, S. E. A. Leigh, I. U. S. Leong, Javier Ferreiros, F. Maleady-Crowe, Joanne Mason, Ellen M. McDonagh, Loukas Moutsianas, Michael Mueller, Nirupa Murugaesu, Anna C. Need, Pter O’Donovan, Chris A. Odhams, Andrea Orioli, Christine Patch, Mariana Buongermino Pereira, D. Perez-Gil, Dimitris Polychronopoulos, J. Pullinger, T. Rahim, Augusto Rendon, Pablo Riesgo-Ferreiro, Tim Rogers, Mina Ryten, K. Savage, Kushmita Sawant, Richard H. Scott, Afshan Siddiq, A. Sieghart, Damian Smedley, Katherine R. Smith, Samuel C. Smith, Alona Sosinsky, William Spooner, Helen E. Stevens, Alexander Stuckey, Răzvan Sultana, M. Tanguy, Ellen Thomas, Simon R. Thompson, Carolyn Tregidgo, Arianna Tucci, Emma Walsh, Sarah A. Watters, M. J. Welland, Eleanor Williams, Katarzyna Witkowska, S. M. Wood, Magdalena Zarowiecki and 3 more - Nature Cancer 2021 cited by 165

  24. Bayesian refinement of association signals for 14 loci in 3 common diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , John A. Todd, Dominic Kwiatkowski, Nilesh J. Samani, Stephen Gough, Mark I. McCarthy, Panagiotis Deloukas, Peter Donnelly - Nature Genetics 2012 cited by 553