Andrew McQuillin

Active 2001–2025

76
Papers
34,961
Citations
55
h-index
73
i10-index

Citations

Citations per year for Andrew McQuillin1974: 1 citations1991: 1 citations1992: 2 citations1995: 1 citations1996: 1 citations1999: 2 citations2000: 1 citations2001: 4 citations2002: 14 citations2003: 44 citations2004: 88 citations2005: 75 citations2006: 77 citations2007: 67 citations2008: 120 citations2009: 268 citations2010: 414 citations2011: 434 citations2012: 534 citations2013: 549 citations2014: 598 citations2015: 482 citations2016: 486 citations2017: 475 citations2018: 482 citations2019: 1,364 citations2020: 1,418 citations2021: 1,360 citations2022: 1,040 citations2023: 731 citations2024: 1,013 citations2025: 424 citations2026: 15 citations1975–1990: no citations, so these years are not shown1993–1994: no citations, so these years are not shown1997–1998: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,979 citing papers, 24.5% of this breakdownUnited Kingdom: 2,144 citing papers, 10.5% of this breakdownGermany: 1,192 citing papers, 5.9% of this breakdownChina: 1,068 citing papers, 5.2% of this breakdownAustralia: 935 citing papers, 4.6% of this breakdownNetherlands: 871 citing papers, 4.3% of this breakdownCanada: 834 citing papers, 4.1% of this breakdownSweden: 698 citing papers, 3.4% of this breakdownItaly: 663 citing papers, 3.3% of this breakdownFrance: 577 citing papers, 2.8% of this breakdownSpain: 519 citing papers, 2.5% of this breakdownDenmark: 451 citing papers, 2.2% of this breakdown
0%24.5%Other 26.7%

Fields

  • Biochemistry, Genetics and Molecular Biology43.2%
  • Medicine31.1%
  • Neuroscience17.1%
  • Psychology4.5%
  • Immunology and Microbiology0.9%
  • Computer Science0.7%
  • Other2.5%

Topics

  • Genetic Associations and Epidemiology9.8%
  • Alzheimer's disease research and treatments4.8%
  • Genetics and Neurodevelopmental Disorders3.8%
  • Tryptophan and brain disorders3%
  • Schizophrenia research and treatment2.8%
  • Neuroinflammation and Neurodegeneration Mechanisms2.7%
  • Other73.1%

Coauthors

All papers

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  1. 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

  2. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David Mann, A. David Smith, Seth Love, Patrick G. Kehoe, John Hardy, Simon Mead, Nick C. Fox, Martin N. Rossor, John Collinge, Wolfgang Maier, Frank Jessen, Britta Schürmann, Reinhard Heun, Hendrik van den Bussche, Isabella Heuser, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frölich, Harald Hampel, Michael Hüll, Dan Rujescu, Alison Goate, John S.K. Kauwe, Carlos Cruchaga, Petra Nowotny, John C. Morris, Kevin H. Mayo, Kristel Sleegers, Karolien Bettens, Sebastiaan Engelborghs, Peter Paul De Deyn, Christine Van Broeckhoven, Gill Livingston, Nicholas Bass, Hugh Gurling, Andrew McQuillin, Rhian Gwilliam, Panagiotis Deloukas, Ammar Al‐Chalabi, Christopher E. Shaw, Magda Tsolaki, Andrew B. Singleton, Rita Guerreiro, Thomas W. Mühleisen, Markus M. Nöthen, Susanne Moebus, Karl‐Heinz Jöckel, Norman Klopp, H‐Erich Wichmann, Minerva M. Carrasquillo, V. Shane Pankratz, Steven G. Younkin, Peter Holmans, Michael O‘Donovan, Michael J. Owen, Julie Williams - Nature Genetics 2009 cited by 3,398

  3. Analysis of shared heritability in common disorders of the brain

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , M. Ilyas Kamboh, Eric B. Larson, Ekaterina Rogaeva, Peter St George‐Hyslop, Håkon Håkonarson, Walter A. Kukull, Lindsay A. Farrer, Lisa L. Barnes, Thomas G. Beach, F. Yesim Demirci, Elizabeth Head, Christine M. Hulette, Gregory A. Jicha, John S.K. Kauwe, Jeffrey A. Kaye, James B. Leverenz, Allan I. Levey, Andrew P. Lieberman, V. Shane Pankratz, Wayne W. Poon, Joseph F. Quinn, Andrew J. Saykin, Lon S. Schneider, Amanda Smith, Joshua A. Sonnen, Robert A. Stern, Vivianna M. Van Deerlin, Linda J. Van Eldik, Denise Harold, Giancarlo Russo, David C. Rubinsztein, Anthony Bayer, Magda Tsolaki, Petra Proitsi, Nick C. Fox, Harald Hampel, Michael J. Owen, Simon Mead, Peter Passmore, Kevin Morgan, Markus M. Nöthen, Jonathan M. Schott, Martin N. Rossor, Michelle K. Lupton, Per Hoffmann, Johannes Kornhuber, Brian Lawlor, Andrew McQuillin, Ammar Al‐Chalabi, Joshua C Bis, Agustı́n Ruiz, Merçé Boada, Sudha Seshadri, Alexa Beiser, Kenneth Rice, Sven J. van der Lee, Philip L. De Jager, Daniel H. Geschwind, Matthias Riemenschneider, Steffi G. Riedel‐Heller, Jerome I. Rotter, Gerhard Ransmayr, Bradley T. Hyman, Carlos Cruchaga, Montserrat Alegret, Bendik S. Winsvold, Priit Palta, Kai-How Farh, Ester Cuenca-León, Nicholas A. Furlotte and 477 more - Science 2018 cited by 2,050

  4. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hugh Gurling, Jennifer Stone, Kristin Ardlie, Jonathan Pimm, Stacey B. Gabriel, Robert Krasucki, Jacob Lawrence, Nicholas Bass, Derek W. Morris, Colm T. O’Dushlaine, Aiden Corvin, Finny G. Kuruvilla, Naomi R. Wray, Naomi R. Wray, Stuart MacGregor, Stuart MacGregor, Peter M. Visscher, Michael O‘Donovan, Michael O‘Donovan, Peter Holmans, Nadine Norton, Ivan Nikolov, Hywel Williams, George Kirov, Michael J. Owen, Lyudmila Georgieva, Michele T. Pato, Nick Craddock, Nigel Williams, Ayman Fanous, Patrick Sullivan, James A. Knowles, Patrick F. Sullivan, Jonathan Pimm, Jacob Lawrence, Hugh Gurling, Vinay Puri, Nicholas Bass, Andrew McQuillin, Khalid Choudhury, Robert Krasucki, Susmita Datta, Andrew McQuillin, Michael Gill, Elaine Kenny, Michael Gill - Nature 2009 cited by 5,069

  5. Genome-wide association study identifies 30 loci associated with bipolar disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nicholas Bass, Michael Bauer, Richard A. Belliveau, Sarah E. Bergen, Carsten Bøcker Pedersen, Erlend Bøen, Marco P. Boks, James Boocock, Monika Budde, William E. Bunney, Margit Burmeister, Jonas Bybjerg‐Grauholm, William Byerley, Miguel Casas, Felecia Cerrato, Pablo Cervantes, Kimberly Chambert, Alexander W. Charney, Danfeng Chen, Claire Churchhouse, Toni‐Kim Clarke, William Coryell, David W. Craig, Cristiana Cruceanu, David Curtis, Piotr M. Czerski, Anders M. Dale, Simone de Jong, Franziska Degenhardt, Jurgen Del‐Favero, J. Raymond DePaulo, Srdjan Djurovic, Amanda Dobbyn, Ashley Dumont, Torbjørn Elvsåshagen, Valentina Escott‐Price, Chun Chieh Fan, Sascha B. Fischer, Matthew Flickinger, Tatiana Foroud, Liz Forty, Josef Frank, Christine Fraser, Nelson B. Freimer, Louise Frisén, Katrin Gade, Diane Gage, Julie Garnham, Claudia Giambartolomei, Marianne Giørtz Pedersen, Jaqueline Goldstein, Scott D. Gordon, Katherine Gordon‐Smith, Elaine Green, Melissa J. Green, Tiffany A. Greenwood, Jakob Grove, Weihua Guan, José Guzmán‐Parra, Marian L. Hamshere, Martin Hautzinger, Urs Heilbronner, Stefan Herms, Maria Hipolito, Per Hoffmann, Dominic Holland, Laura M. Huckins, Stéphane Jamain, Jessica Johnson, Anders Juréus and 177 more - Nature Genetics 2019 cited by 1,627

  6. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David Craig, Bernadette McGuinness, Stephen Todd, Clive Holmes, David Mann, A. David Smith, Helen Beaumont, Donald Warden, Gordon Wilcock, Seth Love, Patrick G. Kehoe, Nigel M. Hooper, Emma Vardy, John Hardy, Simon Mead, Nick C. Fox, Martin N. Rossor, John Collinge, Wolfgang Maier, Frank Jessen, Eckart Rüther, Britta Schürmann, Reiner Heun, Heike Kölsch, Hendrik van den Bussche, Isabella Heuser, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frölich, Harald Hampel, John Gallacher, Michael Hüll, Dan Rujescu, Ina Giegling, Alison Goate, John Kauwe, Carlos Cruchaga, Petra Nowotny, John C. Morris, Kevin H. Mayo, Kristel Sleegers, Karolien Bettens, Sebastiaan Engelborghs, Peter Paul De Deyn, Christine Van Broeckhoven, Gill Livingston, Nicholas Bass, Hugh Gurling, Andrew McQuillin, Rhian Gwilliam, Panagiotis Deloukas, Ammar Al‐Chalabi, Christopher E. Shaw, Magda Tsolaki, Andrew B. Singleton, Rita Guerreiro, Thomas W. Mühleisen, Markus M. Nöthen, Susanne Moebus, Karl‐Heinz Jöckel, Norman Klopp, H‐Erich Wichmann, V. Shane Pankratz, Sigrid Botne Sando, Jan Aasly, Maria Barcikowska, Zbigniew K. Wszołek, Dennis W. Dickson, Neill R. Graff‐Radford and 73 more - Nature Genetics 2011 cited by 2,083

  7. 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

  8. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter A Holmans, Ian Jones, George K Kirov, Sarah E. Bergen, Ivan Nikolov, Michael J Owen, Peter Holmans, Stanley Zammit, Katherine Gordon‐Smith, Nicholas Craddock, Lyudmila Georgieva, John S Witte, Detelina Grozeva, Ian D. Jones, Marian L. Hamshere, Ole A Andreassen, Srdjan Djurovic, Morten Mattingsdal, Michael O‘Donovan, Michael J. Owen, Anita Thapar, Robert C Thompson, Stanley J Watson, Nicholas Craddock, Lyudmila Georgieva, Nicholas Bass, Ian D. Jones, Hugh Gurling, Radhika Kandaswamy, Michael O‘Donovan, Michael J. Owen, Anita Thapar, Michael E. Goddard, Michael E. Goddard, Richard Anney, Devin Absher, Richard M. Myers, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ole A. Andreassen, Ingrid Melle, Ingrid Agartz, Robert C. Thompson, Stanley J. Watson, Huda Akil, Fan Meng, Farooq Amin, Ole A. Andreassen, Ingrid Melle, Robert Krasucki, Adebayo Anjorin, Khalid Choudhury, Jacob Lawrence, Hugh Gurling, Jonathan Pimm, Nicholas Bass, Radhika Kandaswamy, Andrew McQuillin, Vinay Puri, Elaine Kenny, Aiden Corvin, Paul Cormican, Derek W. Morris, Richard Anney, Emma M. Quinn, Gary Donohoe, Michael Gill, Louise Gallagher, Dan E. Arking and 270 more - Nature Genetics 2013 cited by 2,353

  9. A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Pierre Deltenre, Henry Völzke, Markus M. Lerch, Julia Mayerle, Florian Eyer, Clemens Schafmayer, Sven Cichon, Markus M. Nöthen, Michael Nothnagel, David Ellinghaus, Klaus Huse, André Franke, Steffen Zopf, Claus Hellerbrand, Christophe Moreno, Denis Franchimont, Marsha Y. Morgan, Jochen Hampe - Nature Genetics 2015 cited by 559

  10. Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Neuroscience 2020 cited by 404

  11. Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Daniëlle Posthuma, Andreas Reif, Neil Risch, Catherine Schaefer, Laura J. Scott, Tarjinder Singh, Jordan W. Smoller, Matthew Solomonson, David St Clair, Eli A. Stahl, Annabel Vreeker, James Walters, Weiqing Wang, Nicholas A. Watts, Robert H. Yolken, Peter P. Zandi, Benjamin M. Neale - Nature Genetics 2022 cited by 209

  12. Genome-wide association study identifies five new schizophrenia loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Stan Zammit, Michael C O'Donovan, Dan-Yu Lin, Roel A Ophoff, Eric Strengman, Rita M Cantor, Nelson B Freimer, Ole A Andreassen, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Edward Scolnick, Shaun Purcell, Benjamin M Neale, Sven Cichon, Manuel Mattheisen, Markus M Nöthen, David St. Clair, Aiden Corvin, Paul Cormican, Gary Donohoe, Michael Gill, Elaine Kenny, Derek W Morris, Colm T O'Dushlaine, Emma M Quinn, Hugh Gurling, Nicholas Bass, Khalid Choudhury, Susmita Datta, Robert Krasucki, Jacob Lawrence, Andrew McQuillin, Jonathan Pimm, Vinay Puri, Thomas Werge, Linh Duong, Thomas Hansen, Andrés Ingason, Klaus D Jakobsen, Line Olsen, Henrik B Rasmussen, Johan H Thygesen, Dan Rujescu, Marion Friedl, Ina Giegling, Annette M Hartmann, Heike Konnerth, Bettina Konte, Douglas H R Blackwood, Alan W Maclean, Pat Malloy, Kevin A McGhee, Andrew McIntosh, Carlos N Pato, Michele T Pato, Anil K Malhotra, Todd Lencz, Frank Dudbridge, Peter M Visscher, Danielle Posthuma, Richard L Amdur, Hreinn Stefansson, Stacy Steinberg, Kari Stefansson, Bryan J Mowry, John J McGrath, Deborah A Nertney, Vera Golimbet and 96 more - Nature Genetics 2011 cited by 1,954

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  14. An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Genome biology 2016 cited by 388

  15. Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael J. Owen, James H. MacCabe, Michael O‘Donovan, James Walters, Stephan Ripke, Benjamin M. Neale, Kai-How Farh, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond C. Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Martilias S. Farrell, Lude Franke, Robert Freedman and 261 more - JAMA Psychiatry 2022 cited by 106

  16. DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael O‘Donovan, Diego Quattrone, Alexander Richards, Bart P. F. Rutten, David St Clair, Sebastian Therman, Timothea Toulopoulou, Jim van Os, John L. Waddington, Patrick Sullivan, Evangelos Vassos, Gerome Breen, David Collier, Robin Murray, Leonard C. Schalkwyk, Jonathan Mill - eLife 2021 cited by 142

  17. A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sylvie Naveau, Pascal Perney, Munir Pirmohamed, Helmut K. Seitz, Michael Soyka, Felix Stickel, Andrew Thompson, Mark Thursz, Eric Trépo, Timothy R. Morgan, Devanshi Seth - Journal of Hepatology 2021 cited by 80

  18. Prediction of disease comorbidity using explainable artificial intelligence and machine learning techniques: A systematic review

    Authors: , , , , , , - International Journal of Medical Informatics, Int. J. Medical Informatics 2023 cited by 72

  19. Genome-Wide Association Study for Alcohol-Related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Felix Stickel - Gastroenterology 2020 cited by 81

  20. The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Swapnil Awasthi, Silviu‐Alin Bacanu, Judith A. Badner, Marie Bækvad‐Hansen, Jack D. Barchas, Nicholas Bass, Michael Bauer, Aartjan T.F. Beekman, Richard A. Belliveau, Sarah E. Bergen, Tim B. Bigdeli, Elisabeth B. Binder, Erlend Bøen, Marco P. Boks, James Boocock, Monika Budde, William Bunney, Margit Burmeister, Henriette N. Buttenschøn, Jonas Bybjerg‐Grauholm, William Byerley, Na Cai, Miguel Casas, Enrique Castelao, Felecia Cerrato, Pablo Cervantes, Kimberly Chambert, Alexander W. Charney, Danfeng Chen, Jane Christensen, Claire Churchhouse, David St Clair, Toni‐Kim Clarke, Lucía Colodro‐Conde, William Coryell, Baptiste Couvy‐Duchesne, David W. Craig, Gregory E. Crawford, Cristiana Cruceanu, Piotr M. Czerski, Anders M. Dale, Gail Davies, Ian J. Deary, Franziska Degenhardt, Jurgen Del‐Favero, J. Raymond DePaulo, Eske M. Derks, Neşe Direk, Srdjan Djurovic, Amanda Dobbyn, Conor V. Dolan, Ashley Dumont, Erin C. Dunn, Thalia C. Eley, Torbjørn Elvsåshagen, Valentina Escott‐Price, Chun Chieh Fan, Hilary K. Finucane, Sascha B. Fischer, Matthew Flickinger, Jerome C. Foo, Tatiana Foroud, Liz Forty, Josef Frank, Christine Fraser, Nelson B. Freimer, Louise Frisén, Katrin Gade, Diane Gage, Julie Garnham and 684 more - Biological Psychiatry 2019 cited by 210

  21. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jarmo Körkkö, Outi Kuismin, Peter Holmans, Christina M. Hultman, Conrad Iyegbe, Jouko Lönnqvist, Minna Männikkö, Steve McCarroll, Peter McGuffin, Andrew M. McIntosh, Andrew McQuillin, Jukka S. Moilanen, Carmel Moore, Robin Murray, Ruth Newbury‐Ecob, Willem H. Ouwehand, Tiina Paunio, Elena Prigmore, Elliott Rees, David J. Roberts, Jennifer Sambrook, Pamela Sklar, David St Clair, Juha Veijola, James Walters, Hywel Williams, Patrick F. Sullivan, Matthew E. Hurles, Michael O‘Donovan, Aarno Palotie, Michael J. Owen, Jeffrey C. Barrett - Nature Neuroscience 2016 cited by 476

  22. Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Clive Holmes, David Mann, A. David Smith, Seth Love, Patrick G. Kehoe, Simon Mead, Nick C. Fox, Martin N. Rossor, John Collinge, Wolfgang Maier, Frank Jessen, Britta Schürmann, Hendrik van den Bussche, Isabella Heuser, Oliver Peters, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frölich, Harald Hampel, Michael Hüll, Dan Rujescu, Alison Goate, John Kauwe, Carlos Cruchaga, Petra Nowotny, John C. Morris, Kevin H. Mayo, Gill Livingston, Nicholas Bass, Hugh Gurling, Andrew McQuillin, Rhian Gwilliam, Panos Deloukas, Ammar Al‐Chalabi, Christopher E. Shaw, Andrew B. Singleton, Rita Guerreiro, Thomas W. Mühleisen, Markus M. Nöthen, Susanne Moebus, Karl‐Heinz Jöckel, Norman Klopp, H.‐Erich Wichmann, E. Rüther, Minerva M. Carrasquillo, V. Shane Pankratz, Steven G. Younkin, John Hardy, Michael O’Donovan, Michael J. Owen, Julie Williams - PLoS ONE 2010 cited by 614

  23. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nicholas J. Schork, Cinnamon S. Bloss, Tatiana Foroud, Daniel L. Koller, Elliot S. Gershon, Chunyu Liu, Judith A. Badner, William A. Scheftner, William Lawson, Evaristus Nwulia, Maria Hipolito, William Coryell, John Rice, William Byerley, Francis J. McMahon, Thomas G. Schulze, Wade H. Berrettini, Falk W. Lohoff, James B. Potash, Pamela B. Mahon, Melvin G. McInnis, Sebastian Zöllner, Peng Zhang, David W. Craig, Szabocls Szelinger, Thomas B. Barrett, René Breuer, Sandra Meier, Jana Strohmaier, Stephanie H. Witt, Federica Tozzi, Anne Farmer, Peter McGuffin, John S. Strauss, Wei Xu, James L Kennedy, John B. Vincent, K. Matthews, Richard Day, Manuel A. R. Ferreira, Colm Ó'Dúshláine, Roy H. Perlis, Soumya Raychaudhuri, Douglas M. Ruderfer, Phil H Lee, Jordan W. Smoller, Jun Li, Devin Absher, William E. Bunney, Jack D. Barchas, Alan F. Schatzberg, Edward G. Jones, Fan Meng, Robert C. Thompson, Stanley J. Watson, Richard M. Myers, Huda Akil, Michael Boehnke, Kim Chambert, Jennifer L. Moran, Ed Scolnick, Srdjan Djurovic, Ingrid Melle, Gunnar Morken, Michael Gill, Derek W. Morris, Emma M. Quinn, Thomas W. Mühleisen, Franziska Degenhardt, Manuel Mattheisen and 72 more - Nature Genetics 2011 cited by 1,412

  24. Rare chromosomal deletions and duplications increase risk of schizophrenia

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