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David A. van Heel

Active 2001–2025

Also published as
David A van Heel
85
Papers
18,017
Citations
64
h-index
83
i10-index

Citations

Citations per year for David A. van Heel1988: 1 citations2002: 2 citations2003: 12 citations2004: 19 citations2005: 52 citations2006: 80 citations2007: 122 citations2008: 129 citations2009: 182 citations2010: 183 citations2011: 248 citations2012: 222 citations2013: 210 citations2014: 266 citations2015: 279 citations2016: 186 citations2017: 231 citations2018: 201 citations2019: 483 citations2020: 477 citations2021: 496 citations2022: 543 citations2023: 324 citations2024: 549 citations2025: 263 citations2026: 17 citations1989–2001: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,246 citing papers, 20.7% of this breakdownUnited Kingdom: 1,245 citing papers, 11.5% of this breakdownGermany: 647 citing papers, 6% of this breakdownNetherlands: 526 citing papers, 4.8% of this breakdownItaly: 521 citing papers, 4.8% of this breakdownChina: 490 citing papers, 4.5% of this breakdownCanada: 455 citing papers, 4.2% of this breakdownAustralia: 399 citing papers, 3.7% of this breakdownFrance: 378 citing papers, 3.5% of this breakdownSpain: 330 citing papers, 3% of this breakdownSweden: 319 citing papers, 2.9% of this breakdownNorway: 238 citing papers, 2.2% of this breakdown
0%20.7%Other 28.2%

Institutions

Fields

  • Medicine47.3%
  • Biochemistry, Genetics and Molecular Biology37.5%
  • Immunology and Microbiology9.9%
  • Neuroscience2.1%
  • Agricultural and Biological Sciences0.6%
  • Environmental Science0.4%
  • Other2.2%

Topics

  • Celiac Disease Research and Management5.6%
  • Genetic Associations and Epidemiology5.4%
  • Microscopic Colitis3.5%
  • Inflammatory Bowel Disease2.5%
  • Immune Cell Function and Interaction2%
  • T-cell and B-cell Immunology1.8%
  • Other79.2%

Coauthors

All papers

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  1. Mapping the human genetic architecture of COVID-19

    Authors: COVID-19 Host Genetics Initiative, COVID-19 Host Genetics InitiativeLeadership, Mari Niemi, Juha Karjalainen, Rachel G. Liao, Benjamin M. Neale, Mark J. Daly, Andrea Ganna, Writing group, Writing group leaders, Gita A. Pathak, Shea J. Andrews, Masahiro Kanai, Writing group members, Kumar Veerapen, Israel Fernández‐Cadenas, Eva C. Schulte, Pasquale Striano, M. Marttila, Camelia C. Minică, Eirini Marouli, Mohd Anisul Karim, Frank R. Wendt, Jeanne E. Savage, Laura Sloofman, Guillaume Butler‐Laporte, Han‐Na Kim, Stavroula Kanoni, Yukinori Okada, Jinyoung Byun, Younghun Han, Mohammed Jashim Uddin, George Davey Smith, Cristen J. Willer, Joseph D. Buxbaum, Analysis group, Manuscript analyses team leader, Manuscript analyses team member: meta-analysis, Juha Mehtonen, Manuscript analyses team member: heritability, methods and supplements, Manuscript analyses team member: PHEWAS, Manuscript analyses team member: Mendelian randomization, Manuscript analyses team member: PC projection and gene prioritization, Manuscript analyses team member: gene prioritization, Hilary K. Finucane, Manuscript analyses team member: sensitivity analysis, Mattia Cordioli, Manuscript analyses team members: PC projection, Alicia R. Martin, Wei Zhou, In silico analysis team members, Bogdan Paşaniuc, Hanna Julienne, Hugues Aschard, Huwenbo Shi, Loïc Yengo, Renato Polimanti, Maya Ghoussaini, Jeremy Schwartzentruber, Ian Dunham, Project management group, Project management leader, Project management support, Karolina Chwiałkowska, Margherita Francescatto, Amy Trankiem, Mary K. Balaconis, Phenotype steering group, Lea K. Davis, Sulggi A. Lee, James R. Priest, Alessandra Renieri, Vijay G. Sankaran, David A. van Heel, Patrick Deelen, J. Brent Richards, Tomoko Nakanishi, Les Biesecker, V. Eric Kerchberger, J. Kenneth Baillie, Data dictionary, Francesca Mari, Anna Bernasconi, J. Kenneth Baillie, Arif Canakoglu, Scientific communication group, Scientific communication leaders, Brooke Wolford, Scientific communication members, Annika Faucon, Atanu Kumar Dutta, Claudia Schurmann, Emi N. Harry, Ewan Birney, Huy Nguyen, Jamal Nasir, Mari Kaunisto, Matthew Solomonson, Nicole Dueker, Nirmal Vadgama and 3,796 more - Nature 2021 cited by 1,127

  2. A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease

    Authors: Aniruddh P. Patel, Minxian Wang, Yunfeng Ruan, Satoshi Koyama, Shoa L. Clarke, Xiong Yang, Catherine Tcheandjieu, Saaket Agrawal, Akl C. Fahed, Patrick T. Ellinor, Philip S. Tsao, Yan V. Sun, Kelly Cho, Peter W.F. Wilson, Themistocles L. Assimes, David A. van Heel, Adam S. Butterworth, Krishna G. Aragam, Pradeep Natarajan, Amit V. Khera - Nature Medicine 2023 cited by 263

  3. Multiple common variants for celiac disease influencing immune gene expression

    Authors: P Dubois, Gosia Trynka, Lude Franke, Karen A. Hunt, Jihane Romanos, Alessandra Curtotti, Alexandra Zhernakova, Graham Heap, Róza Ádány, Arpo Aromaa, Maria Teresa Bardella, Leonard H. van den Berg, Nicholas Bockett, Emilio G. de la Concha, Bárbara Dema, Rudolf S.N. Fehrmann, Miguel Fernández‐Arquero, Szilvia Fiatal, Elvira Grandone, Peter M. Green, Harry J.M. Groen, Rhian Gwilliam, Roderick H.J. Houwen, Sarah Hunt, Katri Kaukinen, Dermot Kelleher, Ilma R. Korponay‐Szabó, Kalle Kurppa, Padraic MacMathúna, Markku Mäki, Maria Cristina Mazzilli, Owen T McCann, M. Luisa Mearin, Charles A. Mein, Muddassar M. Mirza, Vanisha Mistry, Barbara Mora, Katherine I. Morley, Chris J. Mulder, Joseph A. Murray, Concepción Núñez, Elvira Oosterom, Roel A. Ophoff, Isabel Polanco, Leena Peltonen, Mathieu Platteel, Anna Rybak, Veikko Salomaa, Joachim J. Schweizer, Maria Pia Sperandeo, Greetje J. Tack, Graham Turner, Jan H. Veldink, Wieke H.M. Verbeek, Rinse K. Weersma, Victorien M. Wolters, Elena Urcelay, Božena Cukrowská, Luigi Greco, Susan L. Neuhausen, Ross McManus, Donatella Barisani, Panos Deloukas, Jeffrey C. Barrett, Päivi Saavalainen, Cisca Wijmenga, David A. van Heel - Nature Genetics 2010 cited by 1,052

  4. Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference

    Authors: Xiangrui Meng, Georgina Navoly, Olga Giannakopoulou, Daniel F. Levey, Dóra Koller, Gita A. Pathak, Nastassja Koen, Kuang Lin, Mark J. Adams, Miguel E. Rentería, Yanzhe Feng, J. Michael Gaziano, Dan J. Stein, Heather J. Zar, Megan L. Campbell, David A. van Heel, Bhavi Trivedi, Sarah Finer, Andrew McQuillin, Nick Bass, V. Kartik Chundru, Hilary C. Martin, Qin Qin Huang, Maria Valkovskaya, C. C. Chu, Susan Kanjira, Po‐Hsiu Kuo, Hsi‐Chung Chen, Shih‐Jen Tsai, Yu‐Li Liu, Kenneth S. Kendler, Roseann E. Peterson, Na Cai, Yu Fang, Srijan Sen, Laura J. Scott, Margit Burmeister, Ruth J. F. Loos, Michael Preuß, Ky’Era V. Actkins, Lea K. Davis, Monica Uddin, Agaz H. Wani, Derek E. Wildman, Allison E. Aiello, Robert J. Ursano, Ronald C. Kessler, Masahiro Kanai, Yukinori Okada, Saori Sakaue, Jill A. Rabinowitz, Brion S. Maher, George R. Uhl, William W. Eaton, Carlos S. Cruz-Fuentes, Gabriela Ariadna Martínez-Levy, Adrián I. Campos, Iona Y. Millwood, Zhengming Chen, Liming Li, Sylvia Wassertheil‐Smoller, Yunxuan Jiang, Chao Tian, Nicholas G. Martin, Brittany L. Mitchell, Enda M. Byrne, Swapnil Awasthi, Jonathan R. I. Coleman, Stephan Ripke, PGC-MDD Working Group, China Kadoorie Biobank Collaborative Group, BioBank Japan Project, Tamar Sofer, Robin Walters, Andrew M. McIntosh, Renato Polimanti, Erin C. Dunn, Murray B. Stein, Joel Gelernter, Cathryn M. Lewis, Karoline Kuchenbaecker - Nature Genetics 2024 cited by 170

  5. Diagnosis and management of adult coeliac disease: guidelines from the British Society of Gastroenterology

    Authors: Jonas F. Ludvigsson, Julio C. Bai, Federico Biagi, Tim Card, Carolina Ciacci, Paul J. Ciclitira, Peter H.R. Green, Marios Hadjivassiliou, Anne Holdoway, David A. van Heel, Katri Kaukinen, Daniel A. Leffler, Jonathan N. Leonard, Knut E. A. Lundin, Norma McGough, Mike Davidson, Joseph A. Murray, G L Swift, Marjorie M. Walker, Fabiana Zingone, David S. Sanders, Authors of the BSG Coeliac Disease Guidelines Development Group - Gut 2014 cited by 1,110

  6. Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

    Authors: Gosia Trynka, PreventCD Study Group, Karen A. Hunt, Nicholas Bockett, Jihane Romanos, Vanisha Mistry, Agata Szperl, Sjoerd F. Bakker, Maria Teresa Bardella, Leena Bhaw, Gemma Castillejo, Emilio G. de la Concha, Rodrigo Coutinho de Almeida, Kerith‐Rae Dias, Cleo C. van Diemen, P Dubois, Richard H. Duerr, Sarah Edkins, Lude Franke, Karin Fransén, Javier Cuesta, Graham Heap, Barbara Hrdličková, Sarah Hunt, Leticia Plaza Izurieta, Valentina Izzo, Leo A. B. Joosten, Cordelia Langford, Maria Cristina Mazzilli, Charles A. Mein, Vandana Midah, Mitja Mitrovič, Barbara Mora, Marinita Morelli, Sarah Nutland, Concepción Núñez, Suna Önengüt-Gümüşcü, Kerra Pearce, Mathieu Platteel, Isabel Polanco, Simon Potter, Carmen Ribes‐Koninckx, Isis Ricaño-Ponce, Stephen S. Rich, Anna Rybak, José Luis Santiago, Sabyasachi Senapati, Ajit Sood, Hania Szajewska, Riccardo Troncone, Jezabel Varadé, Chris Wallace, Victorien M. Wolters, Alexandra Zhernakova, B.K. Thelma, Božena Cukrowská, Elena Urcelay, José Ramón Bilbao, M. L. Mearin, Donatella Barisani, Jeffrey C. Barrett, Vincent Plagnol, Panos Deloukas, Cisca Wijmenga, David A. van Heel - Nature Genetics 2011 cited by 864

  7. Polygenic prediction of preeclampsia and gestational hypertension

    Authors: Michael C. Honigberg, Buu Truong, Raiyan R. Khan, Brenda Xiao, Laxmi Bhatta, Ha My T. Vy, Rafael F. Guerrero, Art Schuermans, Margaret Sunitha Selvaraj, Aniruddh P. Patel, Satoshi Koyama, So Mi Jemma Cho, Shamsudheen Karuthedath Vellarikkal, Mark Trinder, Sarah Urbut, Kathryn J. Gray, Ben Brumpton, Snehal Patil, Sebastian Zöllner, Mariah C. Antopia, Richa Saxena, Girish N. Nadkarni, Ron Do, Qi Yan, Itsik Pe’er, Shefali S. Verma, Rajat M. Gupta, David M. Haas, Hilary C. Martin, David A. van Heel, Triin Laisk, Pradeep Natarajan - Nature Medicine 2023 cited by 120

  8. MC3R links nutritional state to childhood growth and the timing of puberty

    Authors: Brian Lam, Alice Williamson, Sarah Finer, Felix R. Day, John A. Tadross, Ana Gonçalves Soares, Kaitlin H. Wade, Patrick Sweeney, M. N. Bedenbaugh, Danielle T. Porter, Audrey Melvin, Kate L. J. Ellacott, R. N. Lippert, Sophie Buller, Joana Rosmaninho‐Salgado, G. K. C. Dowsett, K. E. Ridley, Zhi Ming Xu, Irène Cimino, Debra Rimmington, Kara Rainbow, Katie Duckett, Staffan Holmqvist, Ahsan Khan, Xiaoyang Dai, E. G. Bochukova, Richard C. Trembath, Hilary C. Martin, Anthony P. Coll, David H. Rowitch, Nicholas J. Wareham, David A. van Heel, Nicholas J. Timpson, Richard B. Simerly, Ken K. Ong, Roger D. Cone, Claudia Langenberg, John R. B. Perry, Giles S.H. Yeo, Stephen O’Rahilly - Nature 2021 cited by 142

  9. Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

    Authors: Stefan Gräf, Matthias Haimel, Marta Bleda, Charaka Hadinnapola, Laura Southgate, Wei Li, Joshua Hodgson, Bin Liu, Richard M. Salmon, Mark Southwood, Rajiv D. Machado, Jennifer M. Martin, Carmen Treacy, Katherine Yates, Louise C. Daugherty, Olga Shamardina, Deborah Whitehorn, Simon Holden, Micheala A. Aldred, Harm Jan Bogaard, Colin Church, Gerry Coghlan, Robin Condliffe, Paul A. Corris, Cesare Danesino, Mélanie Eyries, Henning Gall, Stefano Ghio, Hossein-Ardeschir Ghofrani, J. Simon R. Gibbs, Barbara Girerd, Arjan C. Houweling, Luke Howard, Marc Humbert, David G. Kiely, Gábor Kovács, Robert V. MacKenzie Ross, Shahin Moledina, David Montani, Michael Newnham, Andrea Olschewski, Horst Olschewski, Andrew J. Peacock, Joanna Pepke‐Żaba, Inga Prokopenko, Christopher J. Rhodes, Laura Scelsi, Werner Seeger, Florent Soubrier, Dan F. Stein, Jay Suntharalingam, Emilia M. Swietlik, Mark Toshner, David A. van Heel, Anton Vonk Noordegraaf, Quinten Waisfisz, John Wharton, Stephen J. Wort, Willem H. Ouwehand, Nicole Soranzo, Allan Lawrie, Paul D. Upton, Martin R. Wilkins, Richard C. Trembath, Nicholas W. Morrell - Nature Communications 2018 cited by 384

  10. Cohort Profile: East London Genes & Health (ELGH), a community-based population genomics and health study in British Bangladeshi and British Pakistani people

    Authors: Sarah Finer, Hilary C. Martin, Ahsan Khan, Karen A. Hunt, Beverley MacLaughlin, Zaheer Ahmed, Richard Ashcroft, Ceri Durham, Daniel G. MacArthur, Mark I. McCarthy, John Robson, Bhavi Trivedi, Chris Griffiths, John Wright, Richard C. Trembath, David A. van Heel - International Journal of Epidemiology 2019 cited by 144

  11. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases

    Authors: Philip Haycock, Stephen Burgess, Aayah Nounu, Jie Zheng, George N. Okoli, Jack Bowden, Kaitlin H. Wade, Nicholas J. Timpson, David M. Evans, Peter Willeit, Abraham Aviv, Tom R. Gaunt, Gibran Hemani, Massimo Mangino, Hayley Ellis, Kathreena M. Kurian, Karen A. Pooley, Rosalind A. Eeles, Jeffrey E. Lee, Shenying Fang, Wei V. Chen, Matthew H. Law, Lisa Bowdler, Mark M. Iles, Qiong Yang, Bradford B. Worrall, Hugh S. Markus, Rayjean J. Hung, Chris Amos, Amanda B. Spurdle, Deborah J. Thompson, Tracy A. O’Mara, Brian M. Wolpin, Laufey T. Ámundadóttir, Rachael Z. Stolzenberg‐Solomon, Antonia Trichopoulou, N. Charlotte Onland‐Moret, Eiliv Lund, Eric J. Duell, Federico Canzian, Gianluca Severi, Kim Overvad, Marc J. Gunter, ­Rosario ­Tumino, Ulrika Svenson, André van Rij, Annette F. Baas, Matthew J. Bown, Nilesh J. Samani, Femke N.G. van t’Hof, Gerard Tromp, Gregory T. Jones, Helena Kuivaniemi, James R. Elmore, Mattias Johansson, James McKay, Ghislaine Scélo, Robert Carreras‐Torres, Valérie Gaborieau, Paul Brennan, Paige M. Bracci, Rachel Ε. Neale, Sara H. Olson, Steven Gallinger, Donghui Li, Gloria M. Petersen, Harvey A. Risch, Alison P. Klein, Jiali Han, Christian C. Abnet, Neal D. Freedman, Philip R. Taylor, John M. Maris, Katja K.H. Aben, Lambertus A. Kiemeney, Sita H. Vermeulen, John K. Wiencke, Kyle M. Walsh, Margaret Wrensch, Terri Rice, Clare Turnbull, Kevin Litchfield, Lavinia Paternoster, Marie Standl, Gonçalo R. Abecasis, John Paul SanGiovanni, Yong Li, Vladan Mijatovic, Yadav Sapkota, Siew‐Kee Low, Krina T. Zondervan, Grant W. Montgomery, Dale R. Nyholt, David A. van Heel, Karen A. Hunt, Dan E. Arking, Foram N. Ashar, Nona Sotoodehnia, Daniel Woo, Jonathan Rosand and 98 more - JAMA Oncology 2017 cited by 529

  12. Evaluating drug targets through human loss-of-function genetic variation

    Authors: Eric Vallabh Minikel, Konrad J. Karczewski, Hilary C. Martin, Beryl B. Cummings, Nicola Whiffin, Daniel Rhodes, Jessica Alföldi, Richard C. Trembath, David A. van Heel, Mark J. Daly, Genome Aggregation Database Production Team, Jessica Alföldi, Irina M. Armean, Eric Banks, Louis Bergelson, Kristian Cibulskis, Ryan L. Collins, Kristen M. Connolly, Miguel Covarrubias, Beryl B. Cummings, Mark J. Daly, Stacey Donnelly, Yossi Farjoun, Steven Ferriera, Laurent Francioli, Stacey Gabriel, Laura D. Gauthier, Jeff Gentry, Namrata Gupta, Thibault Jeandet, Diane Kaplan, Konrad J. Karczewski, Kristen M. Laricchia, Christopher Llanwarne, Eric V. Minikel, Ruchi Munshi, Benjamin M. Neale, Sam Novod, Anne H. O’Donnell-Luria, Nikelle Petrillo, Timothy Poterba, David Roazen, Valentin Ruano-Rubio, Andrea Saltzman, Kaitlin E. Samocha, Molly Schleicher, Cotton Seed, Matthew Solomonson, Jose Soto, Grace Tiao, Kathleen Tibbetts, Charlotte Tolonen, Christopher Vittal, Gordon Wade, Arcturus Wang, Qingbo Wang, James S. Ware, Nicholas A. Watts, Ben Weisburd, Nicola Whiffin, Carlos A. Aguilar Salinas, Tariq Ahmad, Christine M. Albert, Diego Ardissino, Gil Atzmon, John Barnard, Laurent Beaugerie, Emelia J. Benjamin, Michael Boehnke, Lori L. Bonnycastle, Erwin P. Bottinger, Donald W. Bowden, Matthew J. Bown, John C. Chambers, Juliana C. Chan, Daniel Chasman, Judy Cho, Mina K. Chung, Bruce Cohen, Adolfo Correa, Dana Dabelea, Mark J. Daly, Dawood Darbar, Ravindranath Duggirala, Josée Dupuis, Patrick T. Ellinor, Roberto Elosua, Jeanette Erdmann, Tõnu Esko, Martti Färkkilä, Jose Florez, Andre Franke, Gad Getz, Benjamin Glaser, Stephen J. Glatt, David Goldstein, Clicerio Gonzalez, Leif Groop, Christopher Haiman, Craig Hanis and 74 more - Nature 2020 cited by 181

  13. Integrating polygenic risk scores in the prediction of type 2 diabetes risk and subtypes in British Pakistanis and Bangladeshis: A population-based cohort study

    Authors: Sam Hodgson, Qin Qin Huang, Neneh Sallah, Chris Griffiths, William G. Newman, Richard C. Trembath, John Wright, R Thomas Lumbers, Karoline Kuchenbaecker, David A. van Heel, Rohini Mathur, Hilary C. Martin, Sarah Finer - PLoS Medicine 2022 cited by 71

  14. Comprehensive, Quantitative Mapping of T Cell Epitopes in Gluten in Celiac Disease

    Authors: Jason A. Tye–Din, Jessica A. Stewart, James A. Dromey, Tim Beißbarth, David A. van Heel, Arthur S. Tatham, Kate N. Henderson, Stuart I. Mannering, Carmen Gianfrani, Derek P. Jewell, Adrian V. S. Hill, James McCluskey, Jamie Rossjohn, Robert P. Anderson - Science Translational Medicine 2010 cited by 474

  15. Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study

    Authors: Bram P. Prins, Ali Abbasi, Anson Wong, Ahmad Vaez, Ilja M. Nolte, Nora Franceschini, Philip E. Stuart, Javier Guterriez Achury, Vanisha Mistry, Jonathan P. Bradfield, Ana M. Valdes, José Brás, Aleksey Shatunov, Chen Lu, Buhm Han, Soumya Raychaudhuri, Steve Bevan, Maureen D. Mayes, Lam C. Tsoi, Εvangelos Εvangelou, Rajan P. Nair, Struan F.A. Grant, Constantin Polychronakos, Timothy R. D. J. Radstake, David A. van Heel, Melanie Dunstan, Nicholas Wood, Ammar Al‐Chalabi, Abbas Dehghan, Håkon Håkonarson, Hugh S. Markus, James T. Elder, Jo Knight, Dan E. Arking, Timothy D. Spector, Bobby P. C. Koeleman, Cornelia M. van Duijn, Javier Martı́n, Andrew P. Morris, Rinse K. Weersma, Cisca Wijmenga, Patricia B. Munroe, John R. B. Perry, Jennie G. Pouget, Yalda Jamshidi, Harold Snieder, Behrooz Z. Alizadeh - PLoS Medicine 2016 cited by 206

  16. Genetic insights into common pathways and complex relationships among immune-mediated diseases

    Authors: Miles Parkes, Adrián Cortés, David A. van Heel, Matthew A. Brown - Nature Reviews Genetics 2013 cited by 531

  17. Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis

    Authors: Jimmy Z. Liu, The International PSC Study Group, Johannes R. Hov, Trine Folseraas, Eva Ellinghaus, Simon Rushbrook, Nadezhda T. Doncheva, Ole A. Andreassen, Rinse K. Weersma, Tobias J. Weismüller, Bertus Eksteen, Pietro Invernizzi, Gideon M. Hirschfield, Daniel Gotthardt, Albert Parés, David Ellinghaus, Tejas Shah, Brian D. Juran, Piotr Milkiewicz, Christian Rust, Christoph Schramm, Tobias Müller, Brijesh Srivastava, Georgios Dalekos, Markus M. Nöthen, Stefan Herms, Juliane Winkelmann, Mitja Mitrovič, Felix Braun, Cyriel Y. Ponsioen, Peter J.P. Croucher, Martina Sterneck, Andreas Teufel, Andrew L. Mason, Janna Saarela, Virpi Leppä, Ruslan Dorfman, Domenico Alvaro, Annarosa Floreani, Suna Önengüt-Gümüşcü, Stephen S. Rich, Wesley K. Thompson, Andrew J. Schork, Sigrid Næss, Ingo Thomsen, Gabriele Mayr, Inke R. König, Kristian Hveem, Isabelle Cleynen, Javier Gutierrez‐Achury, Isis Ricaño-Ponce, David A. van Heel, Einar Björnsson, Richard Sandford, Peter R. Durie, Espen Melum, Morten H. Vatn, Mark S. Silverberg, Richard H. Duerr, Leonid Padyukov, Stephan Brand, Miquel Sans, Vito Annese, Jean–Paul Achkar, Kirsten Muri Boberg, Hanns–Ulrich Marschall, Olivier Chazouillères, Christopher L. Bowlus, Cisca Wijmenga, Erik Schrumpf, Séverine Vermeire, Mario Albrecht, John D. Rioux, Graeme Alexander, Annika Bergquist, Judy H. Cho, Stefan Schreiber, Michael P. Manns, Martti Färkkilâ, Anders M. Dale, Roger W. Chapman, Konstantinos N. Lazaridis, André Franke, Carl A. Anderson, Tom H. Karlsen - Nature Genetics 2013 cited by 398

  18. Health and population effects of rare gene knockouts in adult humans with related parents

    Authors: Vagheesh M. Narasimhan, Karen A. Hunt, Dan Mason, Christopher L. Baker, Konrad J. Karczewski, Michael R. Barnes, Anthony Barnett, Chris Bates, Srikanth Bellary, Nicholas Bockett, Kristina Giorda, Chris Griffiths, Harry Hemingway, Zhilong Jia, M. A. Kelly, Hajrah Khawaja, Monkol Lek, Shane McCarthy, Rosie McEachan, Anne O’Donnell‐Luria, Kenneth Paigen, Constantinos A. Parisinos, Eamonn Sheridan, Laura Southgate, Louise Tee, Mark Thomas, Yali Xue, Michael Schnall-Levin, Petko M. Petkov, Chris Tyler‐Smith, Eamonn R. Maher, Richard C. Trembath, Daniel G. MacArthur, John Wright, Richard Durbin, David A. van Heel - Science 2016 cited by 313

  19. Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals

    Authors: Qin Qin Huang, Neneh Sallah, Diana Dunca, Bhavi Trivedi, Karen A. Hunt, Sam Hodgson, Samuel A. Lambert, Elena Arciero, John Wright, Chris Griffiths, Richard C. Trembath, Harry Hemingway, Michael Inouye, Sarah Finer, David A. van Heel, R Thomas Lumbers, Hilary C. Martin, Karoline Kuchenbaecker - Nature Communications 2022 cited by 77

  20. Genetic basis of early onset and progression of type 2 diabetes in South Asians

    Authors: Sam Hodgson, Alice Williamson, Margherita Bigossi, Daniel Stow, Benjamin M. Jacobs, Miriam Samuel, Joseph Gafton, Julia Zöllner, Marie Spreckley, Shaheen Akhtar, Ana Angel, Omar Asgar, Samina Ashraf, Saeed Bidi, Gerome Breen, James Broster, Raymond Chung, David Collier, Charles Curtis, Shabana Chaudhary, Grainne Colligan, Panos Deloukas, Ceri Durham, Faiza Durrani, Fabíola Eto, Joseph Gafton, Chris Griffiths, Joanne E. Harvey, Teng Heng, Qin Qin Huang, Karen A. Hunt, Matt Hurles, Shapna Hussain, Kamrul Islam, Vivek Iyer, Georgios Kalantzis, Ahsan Khan, Cath Lavery, Sang Hyuck Lee, Daniel G. MacArthur, Eamonn Maher, Daniel Malawsky, Sidra Malik, Hilary C. Martin, Dan Mason, Mohammed Bodrul Mazid, John McDermott, Caroline E Morton, Bill Newman, Vladimir Ovchinnikov, Elizabeth Owor, Iaroslav Popov, Asma Qureshi, Mehru Raza, Jessry Russell, Stuart Rison, Nishat Safa, Annum Salman, Michael A. Simpson, John Solly, Michael D. Taylor, Richard C. Trembath, Karen Tricker, David A. van Heel, Klaudia Walter, Jan Whalley, Caroline Winckley, S. M. Wood, John Wright, Sabina Yasmin, Ishevanhu Zengeya, Claudia Langenberg, David A. van Heel, Rohini Mathur, Moneeza K. Siddiqui, Sarah Finer - Nature Medicine 2024 cited by 38

  21. Shared and Distinct Genetic Variants in Type 1 Diabetes and Celiac Disease

    Authors: Deborah J. Smyth, Vincent Plagnol, Neil Walker, Jason D. Cooper, Kate Downes, Jennie H. M. Yang, Joanna M. M. Howson, Helen Stevens, Ross McManus, Cisca Wijmenga, Graham Heap, P Dubois, David Clayton, Karen A. Hunt, David A. van Heel, John A. Todd - New England Journal of Medicine 2008 cited by 753

  22. Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases

    Authors: Tobias L. Lenz, Aaron J. Deutsch, Buhm Han, Xinli Hu, Yukinori Okada, Stephen Eyre, Michael Knapp, Alexandra Zhernakova, T. Huizinga, Gonçalo R. Abecasis, Jessica Becker, Guy E. Boeckxstaens, Wei‐Min Chen, André Franke, Dafna D. Gladman, Ines Gockel, Javier Gutierrez‐Achury, Javier Martı́n, Rajan P. Nair, Markus M. Nöthen, Suna Önengüt-Gümüşcü, Proton Rahman, Solbritt Rantapää‐Dahlqvist, Philip E. Stuart, Lam C. Tsoi, David A. van Heel, Jane Worthington, Mira M. Wouters, Lars Klareskog, James T. Elder, Peter K. Gregersen, Johannes Schumacher, Stephen S. Rich, Cisca Wijmenga, Shamil Sunyaev, Paul I. W. de Bakker, Soumya Raychaudhuri - Nature Genetics 2015 cited by 205

  23. Influence of autozygosity on common disease risk across the phenotypic spectrum

    Authors: Daniel Malawsky, Eva van Walree, Benjamin M. Jacobs, Teng Hiang Heng, Qin Huang, Ataf Sabir, Saadia Rahman, Saghira Malik Sharif, Ahsan Khan, Maša Umićević Mirkov, Hiroyuki Kuwahara, Xin Gao, Fowzan S. Alkuraya, Daniëlle Posthuma, William G. Newman, Chris Griffiths, Rohini Mathur, David A. van Heel, Sarah Finer, Jared O’Connell, Hilary C. Martin - Cell 2023 cited by 38

  24. CYP2C19 Genotype Prevalence and Association With Recurrent Myocardial Infarction in British–South Asians Treated With Clopidogrel

    Authors: Emma Magavern, Benjamin M. Jacobs, Helen R. Warren, Gherardo Finocchiaro, Sarah Finer, David A. van Heel, Damian Smedley, Mark J. Caulfield - JACC Advances 2023 cited by 38