Patrick Turley

Active 1984–2025

45
Papers
21,099
Citations
37
h-index
43
i10-index

Citations

Citations per year for Patrick Turley1992: 2 citations1995: 2 citations1996: 1 citations1998: 1 citations1999: 3 citations2000: 5 citations2001: 2 citations2002: 3 citations2003: 7 citations2004: 6 citations2005: 3 citations2006: 3 citations2007: 4 citations2008: 2 citations2009: 1 citations2010: 5 citations2011: 6 citations2013: 2 citations2014: 2 citations2015: 9 citations2016: 43 citations2017: 139 citations2018: 265 citations2019: 1,062 citations2020: 1,179 citations2021: 1,319 citations2022: 1,118 citations2023: 786 citations2024: 1,124 citations2025: 483 citations2026: 24 citations1993–1994: no citations, so these years are not shown1997: no citations, so this year is not shown2012: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,787 citing papers, 21% of this breakdownUnited Kingdom: 1,414 citing papers, 10.7% of this breakdownChina: 862 citing papers, 6.5% of this breakdownNetherlands: 742 citing papers, 5.6% of this breakdownGermany: 679 citing papers, 5.1% of this breakdownAustralia: 647 citing papers, 4.9% of this breakdownCanada: 526 citing papers, 4% of this breakdownSweden: 499 citing papers, 3.8% of this breakdownDenmark: 411 citing papers, 3.1% of this breakdownNorway: 406 citing papers, 3.1% of this breakdownItaly: 325 citing papers, 2.4% of this breakdownFrance: 324 citing papers, 2.4% of this breakdown
0%21%Other 27.4%

Fields

  • Biochemistry, Genetics and Molecular Biology44.6%
  • Medicine24.8%
  • Neuroscience16.9%
  • Psychology7.2%
  • Dentistry1.5%
  • Social Sciences1.3%
  • Other3.7%

Topics

  • Genetic Associations and Epidemiology13%
  • Genetics and Neurodevelopmental Disorders4.3%
  • Autism Spectrum Disorder Research4.2%
  • Attention Deficit Hyperactivity Disorder3%
  • Functional Brain Connectivity Studies2.4%
  • Epigenetics and DNA Methylation2.3%
  • Other70.8%

Coauthors

All papers

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  1. 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

  2. Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Joey W. Trampush, Shefali S. Verma, Yang Wu, Max Lam, Jing Hua Zhao, Zhili Zheng, Jason D. Boardman, Harry Campbell, Jeremy Freese, Kathleen Mullan Harris, Caroline Hayward, Pamela Herd, Meena Kumari, Todd Lencz, Jian’an Luan, Anil K. Malhotra, Andres Metspalu, Lili Milani, Ken K. Ong, John R. B. Perry, David J. Porteous, Marylyn D. Ritchie, Melissa Smart, Blair H. Smith, Joyce Y. Tung, Nicholas J. Wareham, James F. Wilson, Jonathan Beauchamp, Dalton Conley, Tõnu Esko, Steven F. Lehrer, Patrik K. E. Magnusson, Sven Oskarsson, Tune H. Pers, Matthew R. Robinson, Kevin Thom, Chelsea Watson, Christopher F. Chabris, Michelle N. Meyer, David Laibson, Jian Yang, Magnus Johannesson, Philipp Koellinger, Patrick Turley, Peter M. Visscher, Daniel J. Benjamin, David Cesarini - Nature Genetics 2018 cited by 2,846

  3. 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

  4. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Clement C. Zai, Esben Agerbo, María J. Arranz, Philip Asherson, Marie Bækvad‐Hansen, Gísli Baldursson, Mark A. Bellgrove, Richard A. Belliveau, Jan K. Buitelaar, Christie L. Burton, Jonas Bybjerg‐Grauholm, Miguel Casas, Felecia Cerrato, Kimberly Chambert, Claire Churchhouse, Bru Cormand, Jennifer Crosbie, Søren Dalsgaard, Ditte Demontis, Alysa E. Doyle, Ashley Dumont, Josephine Elia, Jakob Grove, Ólafur Ó. Guðmundsson, Jan Haavik, Håkon Håkonarson, Christine Søholm Hansen, Catharina A. Hartman, Ziarih Hawi, Amaia Hervás, David M. Hougaard, Daniel P. Howrigan, Hailiang Huang, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Patrick W. L. Leung, Sandra K. Loo, Joanna Martin, Alicia R. Martin, James J. McGough, Sarah E. Medland, Jennifer L. Moran, Ole Mors, Preben Bo Mortensen, Robert D. Oades, Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne G. Pedersen, Triinu Peters, Timothy Poterba, Jesper Buchhave Poulsen, Josep Antoni Ramos‐Quiroga, Andreas Reif, Marta Ribasés, Aribert Rothenberger, Paula Rovira, Cristina Sánchez‐Mora, F. Kyle Satterstrom, Russell Schachar, María Soler Artigas, Stacy Steinberg, Hreinn Stefánsson, Patrick Turley, G. Bragi Walters, Thomas Werge, Tetyana Zayats, Dan E. Arking, Francesco Bettella, Joseph D. Buxbaum and 506 more - Cell 2019 cited by 1,516

  5. Multi-trait analysis of genome-wide association summary statistics using MTAG

    Authors: , , , , , , , , , , , , , , , , , - Nature Genetics 2017 cited by 1,233

  6. 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

  7. 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

  8. Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm, Deepika Dokuru, Luke M. Evans, Eco J. C. de Geus, Sudheer Giddaluru, Scott D. Gordon, K. Paige Harden, W. David Hill, Amanda Hughes, Shona M. Kerr, Yongkang Kim, Hyeokmoon Kweon, Antti Latvala, Debbie A. Lawlor, Liming Li, Kuang Lin, Per Magnus, Patrik K. E. Magnusson, Travis T. Mallard, Pekka Martikainen, Melinda C. Mills, Pål R. Njølstad, John D. Overton, Nancy L. Pedersen, David J. Porteous, Jeffrey G. Reid, Karri Silventoinen, Melissa C. Southey, Camilla Stoltenberg, Elliot M. Tucker–Drob, Margaret J. Wright, Hyeokmoon Kweon, Philipp Koellinger, Daniel J. Benjamin, Patrick Turley, Laurence J. Howe, Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho, Geetha Chittoor, Rafael Ahlskog, Penelope A. Lind, Teemu Palviainen, Matthijs D. van der Zee, Rosa Cheesman, Massimo Mangino, Yunzhang Wang, Shuai Li, Lucija Klaric, Scott M. Ratliff, Lawrence F. Bielak, Marianne Nygaard, Alexandros Giannelis, Emily A. Willoughby, Chandra A. Reynolds, Jared V. Balbona, Ole A. Andreassen, Helga Ask, Dorret I. Boomsma, Archie Campbell, Harry Campbell, Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm and 96 more - Nature Genetics 2022 cited by 393

  9. Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gerard Muntané, Sandra Sanchez‐Roige, Frank J.A. van Rooij, Erdogan Taskesen, Yang Wu, Futao Zhang, Adam Auton, Jason D. Boardman, David W. Clark, Andrew Conlin, Conor Dolan, Urs Fischbacher, Patrick J. F. Groenen, Kathleen Mullan Harris, Gregor Hasler, Albert Hofman, M. Arfan Ikram, Sonia Jain, Robert Karlsson, Ronald C. Kessler, Maarten Kooyman, James MacKillop, Minna Männikkö, Carlos Morcillo-Suárez, Matthew B. McQueen, Klaus M. Schmidt, Melissa Smart, Matthias Sutter, Roy Thurik, André G. Uitterlinden, Jon White, Harriet de Wit, Jian Yang, Lars Bertram, Dorret I. Boomsma, Tõnu Esko, Ernst Fehr, David A. Hinds, Magnus Johannesson, Meena Kumari, David Laibson, Patrik K. E. Magnusson, Michelle N. Meyer, Arcadi Navarro, Abraham A. Palmer, Tune H. Pers, Daniëlle Posthuma, Daniel Schunk, Murray B. Stein, Rauli Svento, Henning Tiemeier, Paul R. H. J. Timmers, Patrick Turley, Robert J. Ursano, Gert G. Wagner, James F. Wilson, Jacob Gratten, James J. Lee, David Cesarini, Daniel J. Benjamin, Philipp Koellinger, Jonathan Beauchamp - Nature Genetics 2019 cited by 841

  10. Genome-wide association study identifies 74 loci associated with educational attainment

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Momoko Horikoshi, Jennifer E. Huffman, Kadri Kaasik, Ioanna Panagiota Kalafati, Robert Karlsson, Augustine Kong, Jari Lahti, Sven J. van der Lee, C. deLeeuw, Penelope A. Lind, Karl‐Oskar Lindgren, Tian Liu, Massimo Mangino, Jonathan Marten, Evelin Mihailov, Michael B. Miller, Peter J. van der Most, Christopher Oldmeadow, Antony Payton, Natalia Pervjakova, Wouter J. Peyrot, Yong Qian, Olli Raitakari, Rico Rueedi, Erika Salvi, Börge Schmidt, Katharina E. Schraut, Jianxin Shi, Albert V. Smith, Raymond A. Poot, Beaté St Pourcain, Alexander Teumer, Gudmar Thorleifsson, Niek Verweij, Dragana Vuckovic, Juergen Wellmann, Harm-Jan Westra, Jingyun Yang, Wei Zhao, Zhihong Zhu, Behrooz Z. Alizadeh, Najaf Amin, Andrew Bakshi, Sebastian E. Baumeister, Ginevra Biino, Klaus Bønnelykke, Patricia A. Boyle, Harry Campbell, Francesco P. Cappuccio, Gail Davies, Jan-Emmanuel De Neve, Panos Deloukas, Ilja Demuth, Jun Ding, Peter Eibich, Lewin Eisele, Niina Eklund, David M. Evans, Jessica D. Faul, Mary F. Feitosa, Andreas J. Forstner, Ilaria Gandin, Bjarni Gunnarsson, Bjarni V. Halldórsson, Tamara B. Harris, Andrew C. Heath, Lynne J. Hocking, Elizabeth G. Holliday, Georg Homuth, Michael A. Horan and 156 more - Nature 2016 cited by 1,502

  11. Pan-UK Biobank GWAS improves discovery, analysis of genetic architecture, and resolution into ancestry-enriched effects

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - medRxiv 2024 cited by 171

  12. Problems with Using Polygenic Scores to Select Embryos

    Authors: , , , , , , , , , , , , - New England Journal of Medicine 2021 cited by 185

  13. Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tian Liu, Lindsay Matteson, Evelin Mihailov, Michael Miller, Camelia C. Minică, Ilja M. Nolte, Dennis O. Mook‐Kanamori, Peter J. van der Most, Christopher Oldmeadow, Yong Qian, Olli Raitakari, Rajesh Rawal, Anu Realo, Rico Rueedi, Börge Schmidt, Albert V. Smith, Evie Stergiakouli, Toshiko Tanaka, Kent D. Taylor, Gudmar Thorleifsson, Juho Wedenoja, Juergen Wellmann, Harm-Jan Westra, Sara M. Willems, Wei Zhao, Najaf Amin, Andrew Bakshi, Sven Bergmann, Gyða Björnsdóttir, Patricia A. Boyle, Samantha Cherney, Simon R Cox, Gail Davies, Oliver S. P. Davis, Jun Ding, Neşe Direk, Peter Eibich, Rebecca T. Emeny, Ghazaleh Fatemifar, Jessica D. Faul, Luigi Ferrucci, Andreas J. Forstner, Christian Gieger, Richa Gupta, Tamara B Harris, Juliette Harris, Elizabeth G Holliday, Jouke-Jan Hottenga, Philip L De Jager, Marika Kaakinen, Eero Kajantie, Ville Karhunen, Ivana Kolčić, Meena Kumari, Lenore J Launer, Lude Franke, Ruifang Li‐Gao, David C. Liewald, Marisa Koini, Anu Loukola, Pedro Marques‐Vidal, Grant W. Montgomery, Miriam A. Mosing, Lavinia Paternoster, Alison Pattie, Katja Petrovic, Laura Pulkki-Råback, Lydia Quaye, Katri Räikkönen, Igor Rudan and 88 more - Nature Genetics 2016 cited by 1,129

  14. Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2024 cited by 78

  15. Mendelian imputation of parental genotypes improves estimates of direct genetic effects

    Authors: , , , , , , , , , - Nature Genetics 2022 cited by 120

  16. Resource profile and user guide of the Polygenic Index Repository

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Chao Tian, Joyce Y. Tung, Vladimir Vacic, Catherine H. Wilson, Avshalom Caspi, David L. Corcoran, Terrie E. Moffitt, Richie Poulton, Karen Sugden, Benjamin Williams, Kathleen Mullan Harris, Andrew Steptoe, Olesya Ajnakina, Lili Milani, Tõnu Esko, William G. Iacono, Matt McGue, Patrik K. E. Magnusson, Travis T. Mallard, K. Paige Harden, Elliot M. Tucker–Drob, Pamela Herd, Jeremy Freese, Alexander I. Young, Jonathan Beauchamp, Philipp Koellinger, Sven Oskarsson, Magnus Johannesson, Peter M. Visscher, Michelle N. Meyer, David Laibson, David Cesarini, Daniel J. Benjamin, Patrick Turley, Aysu Okbay - Nature Human Behaviour 2021 cited by 181

  17. Imprint of assortative mating on the human genome

    Authors: , , , , , , , , , , , , , - Nature Human Behaviour 2018 cited by 164

  18. Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2024 cited by 161

  19. Genomic analysis of diet composition finds novel loci and associations with health and lifestyle

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lifelines Cohort Study, George Davey Smith, Oscar H. Franco, Nita G. Forouhi, M. Arfan Ikram, André G. Uitterlinden, Jana V. van Vliet‐Ostaptchouk, Nick J. Wareham, David Cesarini, K. Paige Harden, James J. Lee, Daniel J. Benjamin, Carson C. Chow, Philipp Koellinger - Molecular Psychiatry 2020 cited by 154

  20. Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology

    Authors: , , , , , , , , , , , - Cell Genomics 2023 cited by 65

  21. Public views on polygenic screening of embryos

    Authors: , , , , - Science 2023 cited by 55

  22. Wrestling with Social and Behavioral Genomics: Risks, Potential Benefits, and Ethical Responsibility

    Authors: , , , , , , , , , , , , , , , , , , - The Hastings Center Report 2023 cited by 67

  23. Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries

    Authors: , , , , , , , , , , , , , , - 2022 cited by 39

  24. Family-GWAS reveals effects of environment and mating on genetic associations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , LifeLines Cohort Study, Kuang Lin, Richard Karlsson Linnér, Stefano Lombardi, Nicholas G. Martin, Matt McGue, Sarah E. Medland, Andres Metspalu, Brittany L. Mitchell, Guiyan Ni, Ilja M. Nolte, Matthew T. Oetjens, Sven Oskarsson, Teemu Palviainen, Rashmi B. Prasad, Anu Reigo, Kadri Reis, Julia Sidorenko, Karri Silventoinen, Harold Snieder, Tiinamaija Tuomi, Bjarni J. Vilhjálmsson, Robin Walters, Emily A. Willoughby, Jonathan Flint, Loic Yengo, Peter M. Visscher, Augustine Kong, Elliot M. Tucker–Drob, Richard Border, David Cesarini, Patrick Turley, Aysu Okbay, Daniel J. Benjamin, Alexander I. Young - medRxiv 2024 cited by 35