Matthew A. Brown

Active 1981–2025

Also published as
Matthew A Brown
260
Papers
54,165
Citations
118
h-index
252
i10-index

Citations

Citations per year for Matthew A. Brown1926: 3 citations1977: 1 citations1980: 1 citations1981: 10 citations1982: 18 citations1983: 8 citations1984: 17 citations1985: 26 citations1986: 25 citations1987: 30 citations1988: 31 citations1989: 28 citations1990: 33 citations1991: 30 citations1992: 24 citations1993: 35 citations1994: 19 citations1995: 21 citations1996: 35 citations1997: 74 citations1998: 92 citations1999: 91 citations2000: 102 citations2001: 118 citations2002: 121 citations2003: 118 citations2004: 125 citations2005: 158 citations2006: 150 citations2007: 174 citations2008: 188 citations2009: 243 citations2010: 361 citations2011: 431 citations2012: 509 citations2013: 623 citations2014: 735 citations2015: 821 citations2016: 694 citations2017: 711 citations2018: 803 citations2019: 1,905 citations2020: 2,028 citations2021: 1,978 citations2022: 1,464 citations2023: 1,058 citations2024: 1,481 citations2025: 638 citations2026: 32 citations1927–1976: no citations, so these years are not shown1978–1979: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 6,296 citing papers, 21.2% of this breakdownUnited Kingdom: 2,988 citing papers, 10.1% of this breakdownChina: 2,630 citing papers, 8.9% of this breakdownGermany: 1,563 citing papers, 5.3% of this breakdownAustralia: 1,305 citing papers, 4.4% of this breakdownNetherlands: 1,132 citing papers, 3.8% of this breakdownCanada: 1,100 citing papers, 3.7% of this breakdownFrance: 1,081 citing papers, 3.7% of this breakdownItaly: 990 citing papers, 3.3% of this breakdownJapan: 799 citing papers, 2.7% of this breakdownSweden: 723 citing papers, 2.4% of this breakdownSpain: 690 citing papers, 2.3% of this breakdown
0%21.2%Other 28.2%

Fields

  • Medicine38.3%
  • Biochemistry, Genetics and Molecular Biology29.5%
  • Computer Science14%
  • Immunology and Microbiology6.4%
  • Engineering4.1%
  • Neuroscience3.4%
  • Other4.3%

Topics

  • Genetic Associations and Epidemiology4.5%
  • Advanced Image and Video Retrieval Techniques3.8%
  • Spondyloarthritis Studies and Treatments2.3%
  • Robotics and Sensor-Based Localization2.2%
  • Rheumatoid Arthritis Research and Therapies1.9%
  • Image Retrieval and Classification Techniques1.5%
  • Other83.8%

Coauthors

All papers

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  1. 10 Years of GWAS Discovery: Biology, Function, and Translation

    Authors: , , , , , , - The American Journal of Human Genetics 2017 cited by 4,068

  2. Genetics of rheumatoid arthritis contributes to biology and drug discovery

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Xuezhong Zhou, Namrata Gupta, Daniel B. Mirel, Eli A. Stahl, Dorothée Diogo, Jing Cui, Katherine P. Liao, Michael H. Guo, Keiko Myouzen, Takahisa Kawaguchi, Marieke J. H. Coenen, Piet L. C. M. van Riel, Mart A F J van de Laar, Henk‐Jan Guchelaar, T. Huizinga, Philippe Dieudé, Xavier Mariette, S. Louis Bridges, Alexandra Zhernakova, René E. M. Toes, Paul P. Tak, Corinne Miceli‐Richard, So‐Young Bang, Hye‐Soon Lee, Javier Martı́n, Miguel Á. González‐Gay, Luis Rodríguez‐Rodríguez, Solbritt Rantapää‐Dahlqvist, Lisbeth Ärlestig, Hyon K. Choi, Yoichiro Kamatani, Pilar Galán, Mark Lathrop, Steve Eyre, John Bowes, Anne Barton, Niek de Vries, Larry W. Moreland, Lindsey A. Criswell, Elizabeth W. Karlson, Atsuo Taniguchi, Ryo Yamada, Michiaki Kubo, Jun S. Liu, Sang‐Cheol Bae, Jane Worthington, Leonid Padyukov, Lars Klareskog, Peter K. Gregersen, Soumya Raychaudhuri, Barbara E. Stranger, Philip L. De Jager, Lude Franke, Peter M. Visscher, Matthew A. Brown, Hisashi Yamanaka, Tsuneyo Mimori, Atsushi Takahashi, Huji Xu, Timothy W. Behrens, Katherine Siminovitch, Shigeki Momohara, Fumihiko Matsuda, Kazuhiko Yamamoto, Robert M. Plenge - Nature 2013 cited by 2,499

  3. Substitution mutational signatures in whole-genome–sequenced cancers in the UK population

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , G. C. Chan, Tom Fowler, Adam Giess, Angela Hamblin, Stephen Henderson, Tim Hubbard, R. Jackson, J. Louise Jones, Dalia Kasperavičiūtė, Melis Kayikci, Athanasios Kousathanas, L. Lahnstein, S. E. A. Leigh, Ivone Leong, F. J. Lopez, F. Maleady-Crowe, Meriel McEntagart, Federico Minneci, Loukas Moutsianas, Michael Mueller, Nirupa Murugaesu, Anna C. Need, Peter O’Donovan, Chris A. Odhams, Christine Patch, D. Perez-Gil, Mariana Buongermino Pereira, J. Pullinger, T. Rahim, Augusto Rendon, T. Rogers, K. Savage, K. Sawant, Richard H. Scott, Afshan Siddiq, A. Sieghart, Sean Smith, Alona Sosinsky, Alexander Stuckey, M. Tanguy, Ana Lisa Taylor Tavares, Elaine Thomas, Simon R. Thompson, Arianna Tucci, M. J. Welland, Elena Williams, Katarzyna Witkowska, Scott Wood - Science 2022 cited by 284

  4. 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

  5. Multi-spectral SIFT for scene category recognition

    Authors: , - CVPR 2011 cited by 465

  6. Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Judith A. Badner, Marie Bækvad‐Hansen, Steven C. Bakker, Gavin Band, Jack D. Barchas, Inês Barroso, Nicholas Bass, Michael Bauer, Bernhard T. Baune, Martin Begemann, Céline Bellenguez, Richard A. Belliveau, Frank Bellivier, Stephan Bender, Judit Bene, Sarah E. Bergen, Wade H. Berrettini, Elizabeth Bevilacqua, Joanna M. Biernacka, Tim B. Bigdeli, Donald W. Black, Hannah Blackburn, Jenefer M. Blackwell, Douglas Blackwood, Carsten Bøcker Pedersen, Michael Boehnke, Marco P. Boks, Anders D. Børglum, Elvira Bramon, Gerome Breen, Matthew A. Brown, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, Monika Budde, Brendan Bulik‐Sullivan, Suzannah J. Bumpstead, William E. Bunney, Margit Burmeister, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, William Byerley, Wiepke Cahn, Guiqing Cai, Murray J. Cairns, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Juan P. Casas, Miguel Casas, Stanley V. Catts, Pablo Cervantes, Kimberley D. Chambert, Raymond C. K. Chan, Eric Chen, Ronald Y.L. Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, Toni‐Kim Clarke, C. Robert Cloninger, David Cohen, Nadine Cohen, Jonathan R. I. Coleman, David Collier, Paul Cormican, William Coryell, Nicholas Craddock, David W. Craig and 440 more - Cell 2018 cited by 821

  7. Five Years of GWAS Discovery

    Authors: , , , - The American Journal of Human Genetics 2012 cited by 2,554

  8. Ankylosing spondylitis: an autoimmune or autoinflammatory disease?

    Authors: , , , , , - Nature Reviews Rheumatology 2021 cited by 353

  9. Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Konstantinos N. Lazaridis, Søren Brunak, Anders M. Dale, Richard C. Trembath, Stephan Weidinger, Michael Weichenthal, Eva Ellinghaus, James T Elder, Jonathan N W N Barker, Ole A. Andreassen, Dermot McGovern, Tom H. Karlsen, Jeffrey C. Barrett, Miles Parkes, Matthew A. Brown, André Franke - Nature Genetics 2016 cited by 785

  10. Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Benedicte A Lie, Øystein Førre, Jaakko Tuomilehto, Kari Laiho, Lei Jiang, Yu Liu, Xin Wu, Huji Xu, Dirk Elewaut, Ruben Burgos-Vargas, Simon Stebbings, Nigil Haroon, Robert D Inman, Manuel A Ferreira, Juan Mulero, Jose Luis Fernandez-Sueiro, Miguel A Gonzalez-Gay, Carlos Lopez-Larrea, Panos Deloukas, Peter Donnelly, Karl Gafney, Hill Gaston, Dafna D Gladman, Proton Rahman, Walter P Maksymowych, J Bart A Crusius, Irene E van der Horst-Bruinsma, Chung-Tei Chou, Raphael Valle-Oñate, Consuelo Romero-Sánchez, Inger Myrnes Hansen, Fernando M Pimentel-Santos, Vibeke Videm, Javier Martin, David M Evans - Nature Genetics 2013 cited by 873

  11. 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

  12. 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

  13. GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , José Luís Callejas-Rubio, José Antonio Vargas‐Hitos, Rosa García-Portales, M T Camps, Antonio Fernández‐Nebro, Marı́a-Francisca González-Escribano, Francisco José García Hernández, María Jesús Castillo, M. Á. Aguirre, Inmaculada Gómez-Gracia, Benjamín Fernández‐Gutiérrez, Luis Rodríguez‐Rodríguez, Paloma García de la Peña, Esther Vicente, José Luís Andreu, M. Fernández Castro, Francisco Javier López-Longo, Leticia Quintanilla Martinez, Fonollosa, Alberto Guillén, Gerard Espinosa, Carlos Tolosa, A. Pros, Mónica Rodríguez‐Carballeira, Javier Narváez, Manuel Rubio‐Rivas, Ortiz-Santamaría, Ana Belén Madroñero, Miguel Á. González‐Gay, Bianca J. Diaz, Luis Trapiella, André M. M. Sousa, M. V. Egurbide, P. Fanlo-Mateo, Luís Sáez-Comet, Fidel Díez Díaz, Hernández, E. Beltrán, José Andrés Román-Ivorra, Elena Grau, Juan José Alegre Sancho, M. Freire, Francisco J. Blanco, N. Oreiro, Torsten Witte, Alexander Kreuter, G. Riemekasten, Paolo Airó, C. Magro, Alexandre E. Voskuyl, M. C. Vonk, Roger Hesselstrand, Susanna Proudman, Wendy Stevens, Mandana Nikpour, Australian Scleroderma Interest Group (ASIG), Jane Zochling, J. Sahhar, Janet Roddy, Peter Nash, Kathleen Tymms, Maureen Rischmueller, Sue Lester, Timothy J. Vyse, Ariane L. Herrick, Jane Worthington, Christopher P. Denton, Yannick Allanore, Matthew A. Brown, Timothy R. D. J. Radstake and 4 more - Nature Communications 2019 cited by 188

  14. Whole-genome sequencing of a sporadic primary immunodeficiency cohort

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David M. Sansom, Andy G. Lynch, Karyn Mégy, Eva Ellinghaus, David Ellinghaus, Silje F. Jørgensen, Tom H. Karlsen, Kathleen Stirrups, Antony J. Cutler, Dinakantha Kumararatne, Anita Chandra, David Edgar, Archana Herwadkar, Nichola Cooper, Sofia Grigoriadou, Aarnoud Huissoon, Sarah Goddard, Stephen Jolles, Catharina Schuetz, Felix Boschann, Stephen Abbs, Zoe Adhya, Julian Adlard, Maryam Afzal, Irshad Ahmed, Munaza Ahmed, Saeed Ahmed, Timothy J. Aitman, Hana Alachkar, Jayanthi Alamelu, Raza Alikhan, Carl E. Allen, Louise Allen, David Allsup, Arif Alvi, Gautam Ambegaonkar, Ariharan Anantharachagan, Philip Ancliff, Julie A. Anderson, Richard Antrobus, Ruth Armstrong, Gavin Arno, Gururaj Arumugakani, Rita Arya, Sofie Ashford, William J. Astle, Anthony Attwood, Steve Austin, Yeşim Aydınok, Waqar Ayub, Christian Babbs, Chiara Bacchelli, Trevor Baglin, Tamam Bakchoul, Tadbir K. Bariana, Jonathan Barratt, Julian Barwell, John Baski, Rachel W. Bates, Joana Batista, Helen E. Baxendale, Gareth Baynam, David Bennett, Claire Bethune, Neha Bhatnagar, Shahnaz Bibi, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Marta Bleda and 535 more - Nature 2020 cited by 242

  15. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

    Authors: , , , , , , , , , , , , , , , , , - Nature Genetics 2006 cited by 1,232

  16. Hippocampal plasticity underpins long-term cognitive gains from resistance exercise in MCI

    Authors: , , , , , , , , , , , , , , , , , , , , - NeuroImage Clinical 2020 cited by 163

  17. HLA Alleles Associated With Risk of Ankylosing Spondylitis and Rheumatoid Arthritis Influence the Gut Microbiome

    Authors: , , , , , , , , , , , - Arthritis & Rheumatology 2019 cited by 183

  18. Brief Report: Intestinal Dysbiosis in Ankylosing Spondylitis

    Authors: , , , , , , , , , - Arthritis & Rheumatology 2014 cited by 424

  19. Origins and impact of extrachromosomal DNA

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , F. Boardman-Pretty, C. R. Boustred, Helen Brittain, Matthew A. Brown, M. J. Caulfield, G. C. Chan, Adam Giess, John N. Griffin, Angela Hamblin, Seton Henderson, Tim Hubbard, Robert W. Jackson, L. J. Jones, D. Kasperaviciute, Melis Kayikci, A. Kousathanas, L. Lahnstein, A. Lakey, S. E. A. Leigh, Ivone Leong, F. J. Lopez, F. Maleady-Crowe, Meriel McEntagart, Federico Minneci, Jonathan S. Mitchell, L. Moutsianas, Melanie Mueller, Nirupa Murugaesu, Anna C. Need, Peter O’Donovan, Christopher A. Odhams, Christine Patch, D. Perez-Gil, M. B. Pereira, J. Pullinger, T. Rahim, A. Rendon, Tim Rogers, K. Savage, K. Sawant, Richard H. Scott, Afshan Siddiq, A. Sieghart, Sean Smith, A. Sosinsky, A. Stuckey, M. Tanguy, Ana Lisa Taylor Tavares, Elaine Thomas, S. R. Thompson, Arianna Tucci, M. J. Welland, Eric O. Williams, Kate Witkowska, S. M. Wood, Magdalena Zarowiecki, Adrienne M. Flanagan, Paul S. Mischel, Mariam Jamal‐Hanjani, Charles Swanton - Nature 2024 cited by 142

  20. Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , J. S. Hill Gaston, Malcolm Smith, Jácome Bruges‐Armas, Ana Rita Couto, Rosa Sorrentino, Fabiana Paladini, Manuel A. R. Ferreira, Huji Xu, Yu Liu, Lei Jiang, Carlos López‐Larrea, Roberto Díaz‐Peña, Antonio López‐Vázquez, Tetyana Zayats, Gavin Band, Céline Bellenguez, Hannah Blackburn, Jenefer M. Blackwell, Elvira Bramon, Suzannah J. Bumpstead, Juan Pablo Casas, Aiden Corvin, Nicholas Craddock, Panos Deloukas, Serge Dronov, Audrey Duncanson, Sarah Edkins, Colin Freeman, Matthew Gillman, Emma Gray, Rhian Gwilliam, Naomi Hammond, Sarah Hunt, Janusz Jankowski, Alagurevathi Jayakumar, Cordelia Langford, Jennifer Liddle, Hugh S. Markus, Christopher G. Mathew, Owen T McCann, Mark I. McCarthy, Colin N A Palmer, Leena Peltonen, Robert Plomin, Simon Potter, Anna Rautanen, Rathi Ravindrarajah, Michelle Ricketts, Nilesh J. Samani, Stephen Sawcer, Amy Strange, Richard C. Trembath, Ananth C. Viswanathan, Matthew Waller, Paul A. Weston, Pamela Whittaker, Sara Widaa, Nicholas Wood, Gil McVean, John D. Reveille, B P Wordsworth, Matthew A. Brown, Peter Donnelly - Nature Genetics 2011 cited by 907

  21. Left ventricular end-systolic volume as the major determinant of survival after recovery from myocardial infarction.

    Authors: , , , , , - Circulation 1987 cited by 2,368

  22. NAD Deficiency, Congenital Malformations, and Niacin Supplementation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Emma L. Duncan, Duncan B. Sparrow, Sally L. Dunwoodie - New England Journal of Medicine 2017 cited by 243

  23. Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responses

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ernest Turro, Simon Tavaré, Adrian J. Thrasher, Duncan I. Jodrell, Kenneth G. C. Smith, Kaan Boztuǧ, Joshua D. Milner, James Thaventhiran - The Journal of Experimental Medicine 2019 cited by 205

  24. Shotgun metagenomics reveals an enrichment of potentially cross-reactive bacterial epitopes in ankylosing spondylitis patients, as well as the effects of TNFi therapy upon microbiome composition

    Authors: , , , , , , , , , , , - Annals of the Rheumatic Diseases 2019 cited by 129