Christine Stevens

Active 1994–2024

55
Papers
36,747
Citations
45
h-index
54
i10-index

Citations

Citations per year for Christine Stevens1977: 1 citations1987: 1 citations1992: 2 citations1995: 1 citations1996: 1 citations1998: 1 citations2000: 2 citations2001: 1 citations2002: 1 citations2003: 1 citations2004: 2 citations2005: 2 citations2006: 2 citations2007: 2 citations2008: 15 citations2009: 32 citations2010: 39 citations2011: 55 citations2012: 132 citations2013: 233 citations2014: 292 citations2015: 322 citations2016: 400 citations2017: 631 citations2018: 700 citations2019: 2,135 citations2020: 2,034 citations2021: 1,853 citations2022: 1,535 citations2023: 1,218 citations2024: 1,647 citations2025: 704 citations2026: 30 citations1978–1986: no citations, so these years are not shown1988–1991: no citations, so these years are not shown1993–1994: no citations, so these years are not shown1997: no citations, so this year is not shown1999: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 6,435 citing papers, 24.7% of this breakdownUnited Kingdom: 2,315 citing papers, 8.9% of this breakdownGermany: 1,474 citing papers, 5.7% of this breakdownChina: 1,452 citing papers, 5.6% of this breakdownCanada: 1,185 citing papers, 4.5% of this breakdownNetherlands: 1,109 citing papers, 4.3% of this breakdownAustralia: 971 citing papers, 3.7% of this breakdownFrance: 933 citing papers, 3.6% of this breakdownItaly: 878 citing papers, 3.4% of this breakdownSweden: 654 citing papers, 2.5% of this breakdownSpain: 642 citing papers, 2.5% of this breakdownJapan: 595 citing papers, 2.3% of this breakdown
0%24.7%Other 28.3%

Fields

  • Biochemistry, Genetics and Molecular Biology52.6%
  • Medicine24%
  • Neuroscience14.8%
  • Immunology and Microbiology4%
  • Psychology1.5%
  • Agricultural and Biological Sciences0.6%
  • Other2.5%

Topics

  • Genomics and Rare Diseases5.7%
  • Genetics and Neurodevelopmental Disorders5.6%
  • Autism Spectrum Disorder Research4.4%
  • Genetic Associations and Epidemiology4.3%
  • Genomic variations and chromosomal abnormalities3.1%
  • Cancer Genomics and Diagnostics1.7%
  • Other75.2%

Coauthors

All papers

Open in search
  1. Analysis of protein-coding genetic variation in 60,706 humans

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mitja Kurki, Ami Levy Moonshine, Pradeep Natarajan, Lorena Orozco, Gina M. Peloso, Ryan Poplin, Manuel A. Rivas, Valentín Ruano-Rubio, Samuel A. Rose, Douglas M. Ruderfer, Khalid Shakir, Peter D. Stenson, Christine Stevens, Brett Thomas, Grace Tiao, Maria T. Tusie-Luna, Ben Weisburd, Hong‐Hee Won, Dongmei Yu, David Altshuler, Diego Ardissino, Michael Boehnke, John Danesh, Stacey Donnelly, Roberto Elosúa, José C. Florez, Stacey Gabriel, Gad Getz, Stephen J. Glatt, Christina M. Hultman, Sekar Kathiresan, Markku Laakso, Steven A. McCarroll, Mark I. McCarthy, Dermot McGovern, Ruth McPherson, Benjamin M. Neale, Aarno Palotie, Shaun Purcell, Danish Saleheen, Jeremiah M. Scharf, Pamela Sklar, Patrick F. Sullivan, Jaakko Tuomilehto, Ming T. Tsuang, Hugh Watkins, James G. Wilson, Mark J. Daly, Daniel G. MacArthur - Nature 2015 cited by 10,435

  2. Identification of common genetic risk variants for autism spectrum disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy dPoterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kāri Stefánsson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum - Nature Genetics 2019 cited by 2,632

  3. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ángel Carracedo, Marcus C.Y. Chan, Andreas G. Chiocchetti, Brian Hon‐Yin Chung, Hilary Coon, Michael L. Cuccaro, Aurora Currò, Bernardo Dalla Bernardina, Ryan N. Doan, Enrico Domenici, Shan Dong, Chiara Fallerini, Montse Fernández‐Prieto, Giovanni Battista Ferrero, Christine M. Freitag, Menachem Fromer, J. Jay Gargus, Daniel H. Geschwind, Elisa Giorgio, Javier González‐Peñas, Stephen J. Guter, Danielle Halpern, Emily Hansen‐Kiss, Xin He, Gail E. Herman, Irva Hertz‐Picciotto, David M. Hougaard, Christina M. Hultman, Iuliana Ionita‐Laza, Suma Jacob, Jesslyn Jamison, Astanand Jugessur, Miia Kaartinen, Gun Peggy Knudsen, A lexander Kolevzon, Itaru Kushima, So Lun Lee, Terho Lehtimäki, Elaine T. Lim, Carla Lintas, W. Ian Lipkin, Diego Lopergolo, Fátima Lopes, Yunin Ludeña, Patrı́cia Maciel, Per Magnus, Behrang Mahjani, Nell Maltman, Dara S. Manoach, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Eduarda Morgana Silva Montenegro, Danielle de Paula Moreira, Eric M. Morrow, Ole Mors, Preben Bo Mortensen, Matthew W. Mosconi, Pierandrea Muglia, Benjamin M. Neale, Merete Nordentoft, Norio Ozaki, Aarno Palotie, Mara Parellada, Maria Rita Passos‐Bueno, Margaret A. Pericak‐Vance, Antonio M. Persico, Isaac N. Pessah, Kaija Puura and 90 more - Cell 2020 cited by 2,501

  4. Intra- and Inter-cellular Rewiring of the Human Colon during Ulcerative Colitis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alex K. Shalek, Ramnik J. Xavier, Aviv Regev - Cell 2019 cited by 1,510

  5. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Stephan Ripke, Elise Robinson, F. Kyle Satterstrom, Hreinn Stefánsson, Christine Stevens, Patrick Turley, G. Bragi Walters, Hyejung Won, Margaret J. Wright, Ole A. Andreassen, Philip Asherson, Christie L. Burton, Dorret I. Boomsma, Bru Cormand, Søren Dalsgaard, Barbara Franke, Joel Gelernter, Daniel H. Geschwind, Håkon Håkonarson, Jan Haavik, Henry R. Kranzler, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Christel M. Middeldorp, Andreas Reif, Luís Augusto Rohde, Panos Roussos, Russell Schachar, Pamela Sklar, Edmund Sonuga‐Barke, Patrick F. Sullivan, Anita Thapar, Joyce Y. Tung, Irwin D. Waldman, Sarah E. Medland, Kāri Stefánsson, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Anders D. Børglum, Benjamin M. Neale - Nature Genetics 2018 cited by 2,320

  6. Rare coding variants in ten genes confer substantial risk for schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Andrea Ganna, Giulio Genovese, David C. Glahn, Jakob Grove, Mei‐Hua Hall, Eija Hämäläinen, Henrike Heyne, Matti Holi, David M. Hougaard, Daniel P. Howrigan, Hailiang Huang, Hai‐Gwo Hwu, René S. Kahn, Hyun Min Kang, Konrad J. Karczewski, George Kirov, James A. Knowles, Francis S. Lee, Douglas S. Lehrer, Francesco Lescai, Dolores Malaspina, Stephen R. Marder, Steven A. McCarroll, Andrew M. McIntosh, Helena Medeiros, Lili Milani, Christopher P. Morley, Derek W. Morris, Preben Bo Mortensen, R Myers, Merete Nordentoft, Niamh L. O’Brien, Ana Maria Olivares, Döst Öngür, Willem H. Ouwehand, Duncan S. Palmer, Tiina Paunio, Digby Quested, Mark Hyman Rapaport, Elliott Rees, Brandi Rollins, F. Kyle Satterstrom, Alan F. Schatzberg, Edward M. Scolnick, Laura J. Scott, Sally I. Sharp, Pamela Sklar, Jordan W. Smoller, Janet L. Sobell, Matthew Solomonson, Eli A. Stahl, Christine Stevens, Jaana Suvisaari, Grace Tiao, Stanley J. Watson, Nicholas A. Watts, Douglas Blackwood, Anders D. Børglum, Bruce M. Cohen, Aiden Corvin, Tõnu Esko, Nelson B. Freimer, Stephen J. Glatt, Christina M. Hultman, Andrew McQuillin, Aarno Palotie, Carlos N. Pato, Michele T. Pato, Ann E. Pulver, David St Clair and 11 more - Nature 2022 cited by 916

  7. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ángel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montse Fernández‐Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, A lexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt and 17 more - Nature Genetics 2022 cited by 617

  8. A structural variation reference for medical and population genetics

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 C. Francioli, Stacey Gabriel, Laura D. Gauthier, Jeff Gentry, Namrata Gupta, Thibault Jeandet, Diane Kaplan, Konrad J. Karczewski, Kristen M. Laricchia, Christopher Llanwarne, Eric Vallabh Minikel, Ruchi Munshi, Benjamin M. Neale, Sam Novod, Anne O’Donnell‐Luria, Nikelle Petrillo, Timothy Poterba, David Roazen, Valentin Ruano-Rubio, Andrea Saltzman, Kaitlin E. Samocha, Molly Schleicher, Cotton Seed, Matthew Solomonson, José Soto, Grace Tiao, Kathleen Tibbetts, Charlotte Tolonen, Christopher Vittal, Gordon Wade, Arcturus Wang, Qingbo S. Wang, James S. Ware, Nicholas A. Watts, Ben Weisburd, Nicola Whiffin, Carlos A. Aguilar‐Salinas, Tariq Ahmad, Christine M. Albert, Diego Ardissino, Gil Atzmon, J. A. Barnard, Laurent Beaugerie, Emelia J. Benjamin, Michael Boehnke, Lori L. Bonnycastle, Erwin P. Böttinger, Donald W. Bowden, Matthew J. Bown, John C. Chambers, Juliana C.N. Chan, Daniel I. Chasman, Judy H. Cho, Mina K. Chung, Bruce M. Cohen, Adolfo Correa and 108 more - Nature, Nat. 2020 cited by 1,190

  9. Synaptic, transcriptional and chromatin genes disrupted in autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Eftichia Duketis, Bridget A. Fernandez, Louise Gallagher, Evan Geller, Stephen J. Guter, R. Sean Hill, Iuliana Ionita‐Laza, Patricia González, Helena Kilpinen, Sabine M. Klauck, A lexander Kolevzon, Irene Lee, Jing Lei, Terho Lehtimäki, Chiao‐Feng Lin, Avi Ma’ayan, Christian R. Marshall, Alison McInnes, Benjamin M. Neale, Michael J. Owen, Norio Ozaki, Mara Parellada, Jeremy Parr, Shaun Purcell, Kaija Puura, Deepthi Rajagopalan, Karola Rehnström, Abraham Reichenberg, Aniko Sabo, Michael Sachse, Stephan Sanders, Chad Schafer, Martin Schulte‐Rüther, David Skuse, Christine Stevens, Péter Szatmári, Kristiina Tammimies, Otto Valladares, Annette Voran, Li‐San Wang, Lauren A. Weiss, A. Jeremy Willsey, Timothy W. Yu, Ryan K. C. Yuen, Edwin H. Cook, Christine M. Freitag, Michael Gill, Christina M. Hultman, Thomas Lehner, Aarno Palotie, Gerard D. Schellenberg, Pamela Sklar, Matthew W. State, James S. Sutcliffe, Christopher A. Walsh, Stephen W. Scherer, Michael E. Zwick, Jeffrey C. Barrett, David J. Cutler, Kathryn Roeder, Bernie Devlin, Mark J. Daly, Joseph D. Buxbaum - Nature 2014 cited by 2,974

  10. Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gregory E. Crawford, Pat Sullivan, Wesley K. Thompson, Preben Bo Mortensen, Esben Agerbo, Marianne Giørtz Pedersen, Carsten Bøcker Pedersen, Ole Mors, Anders D. Børglum, Merete Nordentoft, David M. Hougaard, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Alicia R. Martin, Ashley Dumont, Christine Stevens, Claire Churchhouse, Daniel P. Howrigan, Duncan S. Palmer, Elise Robinson, Kyle Satterstrom, Felecia Cerrato, Hailiang Huang, Jacqueline I. Goldstein, Jennifer L. Moran, Joanna Martin Julian, M. Alonge Kimberly, C. Seed Patrick, Patrick Turley, Raymond K. Walters, Rich Belliveau, Stephan Ripke, Timothy Poterba, Mark J. Daly, Benjamin M. Neale, Menachem Fromer, Panos Roussos, Jessica Johnson, Hardik Shah, Milind Mahajan, Eric E. Schadt, Vahram Haroutunian, Douglas M. Ruderfer, Joseph D. Buxbaum, Solveig K. Sieberts, Kristen K. Dang, Ben Logsdon, Lara M. Mangravite, Mette A. Peters, Raquel E. Gur, Chang-Gyu Hahn, Bernie Devlin, Lambertus Klei, David A. Lewis, Barbara K. Lipska, Keisuke Hirai, Hiroyoshi Toyoshiba, Enrico Domenici - Science 2018 cited by 1,177

  11. Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laura Fachal, Martti Färkkilâ, William A. Faubion, Manuel A. R. Ferreira, Denis Franchimont, Stacey Gabriel, Tian Ge, Michel Georges, Kyle Gettler, Mamta Giri, Benjamin Gläser, Siegfried Goerg, Philippe Goyette, Daniel B. Graham, Eija Hämäläinen, Talin Haritunians, Graham Heap, Mikko Hiltunen, Marc P. Hoeppner, Julie Horowitz, Peter M. Irving, Vivek Iyer, Chaim Jalas, Judith R. Kelsen, Hamed Khalili, Barbara S. Kirschner, Kimmo Kontula, Jukka Koskela, Subra Kugathasan, Juozas Kupčinskas, Christopher A Lamb, Matthias Laudes, Chloé Lévesque, Adam P. Levine, James D. Lewis, Claire Liefferinckx, Britt-Sabina Loescher, Édouard Louis, John Mansfield, Sandra May, Jacob L. McCauley, Emebet Mengesha, Myriam Mni, Paul Moayyedi, Christopher J. Moran, Rodney D. Newberry, Sirimon O’Charoen, David T. Okou, Bas Oldenburg, Harry Ostrer, Aarno Palotie, Jean Paquette, Joel Pekow, Inga Peter, Marieke Pierik, Cyriel Y. Ponsioen, Nikolas Pontikos, Natalie J. Prescott, Ann E. Pulver, Souad Rahmouni, Daniel L Rice, Päivi Saavalainen, Bruce E. Sands, R. Balfour Sartor, Elena Schiff, Stefan Schreiber, L. Philip Schumm, Anthony W. Segal, Philippe Seksik, Rasha Shawky and 33 more - Nature Genetics 2022 cited by 189

  12. A framework for the interpretation of de novo mutation in human disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2014 cited by 1,123

  13. Patterns and rates of exonic de novo mutations in autism spectrum disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lora Lewis, Yi Han, Benjamin F. Voight, Elaine T. Lim, Elizabeth J. Rossin, Andrew Kirby, Jason Flannick, Menachem Fromer, Khalid Shakir, Tim Fennell, Kiran Garimella, Eric Banks, Ryan Poplin, Stacey Gabriel, Mark A. DePristo, Jack R. Wimbish, Braden Boone, Shawn Levy, Catalina Betancur, Shamil Sunyaev, Eric Boerwinkle, Joseph D. Buxbaum, Edwin H. Cook, Bernie Devlin, Richard A. Gibbs, Kathryn Roeder, Gerard D. Schellenberg, James S. Sutcliffe, Mark J. Daly - Nature 2012 cited by 1,808

  14. Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Guillaume Lettre, André Franke, Mauro D’Amato, Dermot McGovern, Judy H. Cho, John D. Rioux, Ramnik J. Xavier, Mark J. Daly - Nature Genetics 2011 cited by 785

  15. A second update on mapping the human genetic architecture of COVID-19

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kumar Veerapen, Brooke N. Wolford, Scientific communication member, Hajar Fauzan Ahmad, Shea J. Andrews, Kathrin Aprile von Hohenstaufen Puoti, Cindy G. Boer, Palwendé Romuald Boua, Guillaume Butler‐Laporte, Carmen L. Cadilla, Karolina Chwiałkowska, Francesca Colombo, Venceslas Douillard, Nicole Dueker, Atanu Kumar Dutta, Yasser M. El‐Sherbiny, Madonna M. Eltoukhy, Sahar Esmaeeli, Annika Faucon, Marie-Julie Favé, Israel Fernández Cadenas, Margherita Francescatto, Laurent C. Francioli, Lude Franke, Macarena Fuentes, Rocío Gallego Durán, David Gómez-Cabrero, Emi N. Harry, Philip R. Jansen, József Szentpéteri, Elżbieta Kaja, Masahiro Kanai, Chloe Kirk, Athanasios Kousathanas, José Eduardo Krieger, Sanjay Patel, Audrey Lemaçon, Sophie Limou, Píetro Lió, Eirini Marouli, M. Marttila, Carolina Medina‐Gómez, Yael Michaeli, Isabelle Migeotte, Soumyajit Mondal, Andrés Moreno‐Estrada, Leire Moya, Tomoko Nakanishi, Jamal Nasir, Dorote Pasko, Nathaniel M. Pearson, Alexandre C. Pereira, James R. Priest, Vid Prijatelj, Ivana Nedeljković, Alexander Teumer, Réka Várnai, Manuel Romero-Gómez, Christina Roos, Jeffrey Rosenfeld, Ruolin Li, Eva C. Schulte, Claudia Schurmann, Bahareh Sedaghati-khayat, Doaa Shaheen, Ilangumaran Shivanathan, Csilla Sipeky, Zhou Sirui, Pasquale Striano, Yosuke Tanigawa and 3,785 more - Nature 2023 cited by 116

  16. LRRK2 Is Involved in the IFN-γ Response and Host Response to Pathogens

    Authors: , , , , , , , , , , - The Journal of Immunology 2010 cited by 417

  17. A first update on mapping the human genetic architecture of COVID-19

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Website development, Huy Nguyen, Matthew Solomonson, Scientific communication group, Scientific communication lead, Kumar Veerapen, Brooke Wolford, Analysis Team Lead, Genevieve Roberts, Data collection lead, Danny Park, Admin team lead, Catherine A. Ball, Analysis team member, Marie V. Coignet, Shannon McCurdy, Spencer C. Knight, Raghavendran Partha, Brooke Rhead, Data collection member, Miao Zhang, Nathan Berkowitz, Michael Gaddis, Keith Noto, Luong Ruiz, Miloš Pavlović, Admin team member, Eurie L. Hong, Kristin A. Rand, Ahna R. Girshick, Harendra Guturu, Asher Haug Baltzell, BelCovid, Analysis team lead, Mari Niemi, Data collection lead, Souad Rahmouni, Julien Guntz, Admin team lead, Y Beguin, Analysis team member, Mattia Cordioli, Sara Pigazzini, Lindokuhle Nkambule, Data collection member, Michel Georges, Michel Moutschen, Benoît Misset, Gilles Darcis, Julien Guiot, Samira Azarzar, Stéphanie Gofflot, Sabine Claassen, Olivier Malaise, Pascale Huynen, Christelle Meuris, Marie Thys, Jessica Jacques, Philippe Léonard, Frédéric Frippiat, Jean‐Baptiste Giot, Anne-Sophie Sauvage, Christian Von Frenckell, Yasmine Belhaj, Bernard Lambermont, Biobanque Quebec COVID-19, Analysis team lead, Tomoko Nakanishi, Data collection lead, David Morrison and 1,002 more - Nature 2022 cited by 174

  18. Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael C. Zody, Ramnik J. Xavier, Martin R. Pollak, Seth L. Alper, Kerstin Lindblad‐Toh, Stacey B. Gabriel, P. Suzanne Hart, Aviv Regev, Chad Nusbaum, Stanislav Kmoch, Anthony J. Bleyer, Eric S. Lander, Mark J. Daly - Nature Genetics 2013 cited by 316

  19. Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

    Authors: , , , , , , , , , , , , , , , , , , , , , - Nature Neuroscience 2019 cited by 228

  20. Genome-wide association identifies multiple ulcerative colitis susceptibility loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Yashoda Sharma, Mark S. Silverberg, Judy H. Cho, Jing Wu, Kathryn Roeder, Steven R. Brant, L. Philip Schumm, Richard H. Duerr, Marla C. Dubinsky, Nicole L. Glazer, Talin Haritunians, Andy Ippoliti, Gil Melmed, David S. Siscovick, Eric A. Vasiliauskas, Stephan R. Targan, Vito Annese, Cisca Wijmenga, Sven Pettersson, Jerome I. Rotter, Ramnik J. Xavier, Mark J. Daly, John D. Rioux, Mark Seielstad - Nature Genetics 2010 cited by 680

  21. Using Whole-Exome Sequencing to Identify Inherited Causes of Autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Annapurna Poduri, Özgür Öner, Samira Al-Saad, S A Al-Awadi, Lailá Bastaki, Tawfeg Ben‐Omran, Ahmad S. Teebi, Lihadh Al‐Gazali, Valsamma Eapen, Christine Stevens, Leonard Rappaport, Stacey Gabriel, Kyriacos Markianos, Matthew W. State, Michael E. Greenberg, Hisaaki Taniguchi, Nancy Braverman, Eric M. Morrow, Christopher A. Walsh - Neuron 2013 cited by 459

  22. Host genetic variation and its microbiome interactions within the Human Microbiome Project

    Authors: , , , , , , , , - Genome Medicine 2018 cited by 192

  23. Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kelly L. Gilmore, Bradford C. Powell, Alicia Brandt, Francesco Vetrini, Michelle DiVito, Stephan Sanders, Daniel G. MacArthur, Jennelle C. Hodge, Anne O’Donnell‐Luria, Heidi L. Rehm, Neeta L. Vora, Brynn Levy, Harrison Brand, Ronald J. Wapner, Michael E. Talkowski - The American Journal of Human Genetics 2023 cited by 54

  24. Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis

    Authors: , , , , , , , - PLoS Genetics 2008 cited by 603