Ole A. Andreassen

Active 1995–2026

Also published as
Ole A Andreassen
707
Papers
106,415
Citations
140
h-index
650
i10-index

Citations

Citations per year for Ole A. Andreassen1939: 1 citations1972: 2 citations1976: 1 citations1992: 5 citations1994: 6 citations1995: 2 citations1996: 10 citations1997: 4 citations1998: 6 citations1999: 22 citations2000: 74 citations2001: 129 citations2002: 143 citations2003: 189 citations2004: 137 citations2005: 128 citations2006: 114 citations2007: 115 citations2008: 168 citations2009: 284 citations2010: 352 citations2011: 419 citations2012: 533 citations2013: 681 citations2014: 769 citations2015: 891 citations2016: 989 citations2017: 1,197 citations2018: 1,259 citations2019: 3,973 citations2020: 4,720 citations2021: 5,113 citations2022: 4,351 citations2023: 3,325 citations2024: 5,184 citations2025: 2,473 citations2026: 102 citations1940–1971: no citations, so these years are not shown1973–1975: no citations, so these years are not shown1977–1991: no citations, so these years are not shown1993: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 11,710 citing papers, 22.9% of this breakdownUnited Kingdom: 4,916 citing papers, 9.6% of this breakdownChina: 3,618 citing papers, 7.1% of this breakdownGermany: 3,018 citing papers, 5.9% of this breakdownCanada: 2,346 citing papers, 4.6% of this breakdownAustralia: 2,127 citing papers, 4.2% of this breakdownNetherlands: 2,034 citing papers, 4% of this breakdownItaly: 1,731 citing papers, 3.4% of this breakdownSweden: 1,527 citing papers, 3% of this breakdownSpain: 1,446 citing papers, 2.8% of this breakdownFrance: 1,415 citing papers, 2.8% of this breakdownNorway: 1,364 citing papers, 2.7% of this breakdown
0%22.9%Other 27%

Fields

  • Medicine33.9%
  • Biochemistry, Genetics and Molecular Biology27%
  • Neuroscience26.7%
  • Psychology6.5%
  • Computer Science1.1%
  • Immunology and Microbiology1.1%
  • Other3.7%

Topics

  • Genetic Associations and Epidemiology5.2%
  • Functional Brain Connectivity Studies4.1%
  • Schizophrenia research and treatment3.4%
  • Alzheimer's disease research and treatments3.4%
  • Tryptophan and brain disorders3.3%
  • Neuroinflammation and Neurodegeneration Mechanisms2.7%
  • Other77.9%

Coauthors

All papers

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  1. Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lisa M. Shulman, Margaret Sutherland, Pentti J. Tienari, Kari Majamaa, Mathias Toft, Ole A. Andreassen, Tushar Bangale, Alexis Brice, Jian Yang, Ziv Gan‐Or, Thomas Gasser, Peter Heutink, Joshua Shulman, Nicholas Wood, David A. Hinds, John Hardy, Huw R Morris, Jacob Gratten, Peter M. Visscher, Robert Graham, Andrew B Singleton, Astrid Adarmes‐Gómez, Miquel Aguilar, Akbota Aitkulova, Vadim Akhmetzhanov, Roy N. Alcalay, Ignacio Álvarez, Victoria Álvarez, Sara Bandrés‐Ciga, Francisco Javier Barrero, Jesús Alberto Bergareche Yarza, Inmaculada Bernal‐Bernal, Kimberley J. Billingsley, Cornelis Blauwendraat, Marta Blazquez, Marta Bonilla‐Toribio, Juan A. Botía, María Teresa Boungiorno, José Brás, Alexis Brice, Kathrin Brockmann, Vivien J. Bubb, Dolores Buiza‐Rueda, Anna Maria Novella Càmara, Fátima Carrillo, Mario Carrión‐Claro, Debora Cerdan, Viorica Chelban, Jordi Clarimón, Carl E Clarke, Yaroslau Compta, Mark Cookson, Jean‐Christophe Corvol, David W. Craig, Fabrice Danjou, Mónica Díez-Fairén, Oriol Dols‐Icardo, J. Duarte, Raquel Durán, Francisco Escamilla‐Sevilla, Valentina Escott‐Price, Mario Ezquerra, Faraz Faghri, Cici Feliz, Manel Fernández, Rubén Fernández‐Santiago, Steven Finkbeiner, Thomas Foltynie, Ziv Gan‐Or, Ciara García and 170 more - The Lancet Neurology 2019 cited by 2,541

  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. Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Arvid Rongve, Ingvild Saltvedt, Sigrid Botne Sando, Geir Selbæk, Maryam Shoai, Nathan Skene, Jón Snædal, Eystein Stordal, Ingun Ulstein, Yunpeng Wang, Linda R. White, John Hardy, Jens Hjerling‐Leffler, Patrick F. Sullivan, Wiesje M. van der Flier, Richard Dobson, Lea K. Davis, Hreinn Stefánsson, Kāri Stefánsson, Nancy L. Pedersen, Stephan Ripke, Ole A. Andreassen, Daniëlle Posthuma - Nature Genetics 2019 cited by 2,526

  4. Biological insights from 108 schizophrenia-associated genetic loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Benjamin M. Neale, James T. R. Walters, Hailiang Huang, Noa Carrera, Alkes L. Price, Mark J. Daly, Lyudmila Georgieva, Marian L. Hamshere, Benjamin M. Neale, Jordan W. Smoller, Andrew J. Pocklington, Paul Cormican, Aiden Corvin, Michael Gill, Gary Donohoe, Michael J. Owen, Alexander Richards, David A. Collier, Michael J. Owen, Noa Carrera, Marian L. Hamshere, Nick Craddock, David Kavanagh, Morten Mattingsdal, Peter Holmans, George Kirov, Sophie E. Legge, Valentina Escott‐Price, Nigel Williams, Andrew Pocklington, Lyudmila Georgieva, James Walters, Nick Craddock, Henrik B. Rasmussen, Michael J. Owen, Peter Holmans, David Collier, Younes Mokrab, David Collier, Tune H. Pers, Farooq Amin, Silviu A. Bacanu, Tim B. Bigdeli, Erik Söderman, Brandon K. Wormley, Martin Begemann, Christian Hammer, Srdjan Djurovic, Morten Mattingsdal, Judit Bene, Ole A. Andreassen, Anna K. Kähler, Ingrid Melle, Esben Agerbo, Preben Bo Mortensen, Esben Agerbo, Preben Bo Mortensen, Preben Bo Mortensen, Randy L. Buckner, Henrik B. Rasmussen, Ditte Demontis, Esben Agerbo, Line Olsen, Eric Strengman, Roel A. Ophoff, Guiqing Cai, Thomas Folkmann Hansen, Margot Albus, Madeline Alexander, Claudine Laurent and 197 more - Nature 2014 cited by 8,166

  5. Variant of TREM2 Associated with the Risk of Alzheimer's Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2012 cited by 2,620

  6. 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

  7. A global overview of pleiotropy and genetic architecture in complex traits

    Authors: , , , , , , , , , - Nature Genetics 2019 cited by 1,463

  8. Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Daniel P. Howrigan, Sarah E. Medland, Tetyana Zayats, Veera M. Rajagopal, Alexandra Havdahl, Alysa E. Doyle, Andreas Reif, Anita Thapar, Bru Cormand, Calwing Liao, Christie L. Burton, Claiton H.D. Bau, Diego Luiz Rovaris, Edmund Sonuga‐Barke, Elizabeth C. Corfield, Eugênio H. Grevet, Henrik Larsson, Ian R. Gizer, Irwin D. Waldman, Isabell Brikell, Jan Haavik, Jennifer Crosbie, James J. McGough, Jonna Kuntsi, Joseph Glessner, K. Langley, Klaus‐Peter Lesch, Luís Augusto Rohde, Mara Helena Hutz, Marieke Klein, Mark A. Bellgrove, Martin Tesli, Michael O‘Donovan, Ole A. Andreassen, Patrick W. L. Leung, Pedro Mário Pan, Ridha Joober, Russell Schachar, Sandra K. Loo, Stephanie H. Witt, Ted Reichborn‐Kjennerud, Tobias Banaschewski, Ziarih Hawi, Mark J. Daly, Ole Mors, Merete Nordentoft, Ole Mors, David M. Hougaard, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Hreinn Stefánsson, Panos Roussos, Barbara Franke, Thomas Werge, Benjamin M. Neale, Kāri Stefánsson, Anders D. Børglum - Nature Genetics 2023 cited by 760

  9. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Maurizio Clementi, Roger D. Cone, Philippe Courtet, Scott J. Crow, James J. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Monika Dmitrzak‐Węglarz, Elisa Docampo, Laramie E. Duncan, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Anne Farmer, Angela Favaro, Fernando Fernández‐Aranda, Manfred M. Fichter, Krista Fischer, Manuel Föcker, Lenka Foretová, Andreas J. Forstner, Monica Forzan, Christopher S. Franklin, Steven Gallinger, Ina Giegling, Johanna Giuranna, Fragiskos Gonidakis, Philip Gorwood, Monica Gratacos Mayora, Sébastien Guillaume, Yiran Guo, Håkon Håkonarson, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Laura M. Huckins, James I. Hudson, Hartmut Imgart, Hidetoshi Inoko, Vladimí­r Janout, Susana Jiménez‐Múrcia, Antonio Julià, Gursharan Kalsi, Deborah Kaminská, Jaakko Kaprio, Leila Karhunen, Andreas Karwautz, Martien J. Kas, James L. Kennedy, Anna Keski‐Rahkonen, Kirsty Kiezebrink, Youl‐Ri Kim, Lars Klareskog, Kelly L. Klump, Gun Peggy Knudsen, Maria C. La Via, Stéphanie Le Hellard and 111 more - Nature Genetics 2019 cited by 1,181

  10. Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Bradley T. Webb, Tonya White, Dan E. Arking, Dimitrios Avramopoulos, Robert M. Bilder, Panos Bitsios, Katherine E. Burdick, Tyrone D. Cannon, Ornit Chiba‐Falek, Andrea Christoforou, Elizabeth T. Cirulli, Eliza Congdon, Aiden Corvin, Gail Davies, Ian J. Deary, Pamela DeRosse, Dwight Dickinson, Srdjan Djurovic, Gary Donohoe, Emily Drabant Conley, Johan G. Eriksson, Thomas Espeseth, Nelson B. Freimer, Stella G. Giakoumaki, Ina Giegling, Michael Gill, David C. Glahn, Ahmad R. Hariri, Alex Hatzimanolis, Matthew C. Keller, Emma Knowles, Deborah K. Attix, Bettina Konte, Jari Lahti, Stéphanie Le Hellard, Todd Lencz, David C. Liewald, Edythe London, Astri J. Lundervold, Anil K. Malhotra, Ingrid Melle, Derek W. Morris, Anna C. Need, William Ollier, Aarno Palotie, Antony Payton, Neil Pendleton, Russell A. Poldrack, Katri Räikkönen, Ivar Reinvang, Panos Roussos, Dan Rujescu, Fred W. Sabb, Matthew A. Scult, Olav B. Smeland, Nikolaos Smyrnis, John M. Starr, Vidar M. Steen, Nikos C. Stefanis, Richard E. Straub, Kjetil Sundet, Henning Tiemeier, Aristotle N. Voineskos, Daniel R. Weinberger, Elisabeth Widén, Jin Yu, Gonçalo R. Abecasis, Ole A. Andreassen, Gerome Breen, Lene Christiansen and 17 more - Nature Genetics 2018 cited by 1,418

  11. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laura M. Huckins, Douglas M. Ruderfer, Enrique Santiago, Pamela Sklar, Eli A. Stahl, Hyejung Won, Esben Agerbo, Thomas D. Als, Ole A. Andreassen, Marie Bækvad‐Hansen, Preben Bo Mortensen, Carsten Bøcker Pedersen, Anders D. Børglum, Jonas Bybjerg‐Grauholm, Srdjan Djurovic, Naser Durmishi, Marianne Giørtz Pedersen, В. Е. Голимбет, Jakob Grove, David M. Hougaard, Manuel Mattheisen, Espen Molden, Ole Mors, Merete Nordentoft, Milica Pejović-Milovančević, Engilbert Sigurðsson, Teimuraz Silagadze, Christine Søholm Hansen, Kāri Stefánsson, Hreinn Stefánsson, Stacy Steinberg, Sarah Tosato, Thomas Werge, David Collier, Dan Rujescu, George Kirov, Michael J. Owen, Michael O‘Donovan, James Walters - Nature Genetics 2018 cited by 1,728

  12. ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laurena Holleran, Georg Homuth, Norbert Hosten, Josselin Houenou, Iliyan Ivanov, Tianye Jia, Sinéad Kelly, Marieke Klein, Jun Soo Kwon, Max A. Laansma, Jeanne Leerssen, Ulrike Lueken, Abraham Nunes, Joseph O' Neill, Nils Opel, Fabrizio Piras, Federica Piras, Merel C. Postema, Elena Pozzi, Natalia Shatokhina, Carles Soriano‐Mas, Gianfranco Spalletta, Daqiang Sun, Alexander Teumer, Amanda K. Tilot, Leonardo Tozzi, Celia van der Merwe, Eus J.W. Van Someren, Guido van Wingen, Henry Völzke, Esther Walton, Lei Wang, Anderson M. Winkler, Katharina Wittfeld, Margaret J. Wright, Je‐Yeon Yun, Guohao Zhang, Yanli Zhang‐James, Bhim M. Adhikari, Ingrid Agartz, Moji Aghajani, André Alemán, Robert R. Althoff, André Altmann, Ole A. Andreassen, David Baron, Brenda Bartnik‐Olson, Janna Marie Bas‐Hoogendam, Arielle Baskin–Sommers, Carrie E. Bearden, Laura A. Berner, Premika S.W. Boedhoe, Rachel M. Brouwer, Jan K. Buitelaar, Karen Caeyenberghs, Charlotte A. M. Cecil, Ronald A. Cohen, James H. Cole, Patricia Conrod, Stéphane A. De Brito, Sonja M. C. de Zwarte, Emily L. Dennis, Sylvane Desrivières, Danai Dima, Stefan Ehrlich, Carrie Esopenko, Graeme Fairchild, Simon E. Fisher, Jean‐Paul Fouché, Clyde Francks and 70 more - Translational Psychiatry 2020 cited by 685

  13. Common brain disorders are associated with heritable patterns of apparent aging of the brain

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lena Flyckt, Barbara Franke, Oleksandr Frei, Beathe Haatveit, Asta K. Håberg, Hanne F. Harbo, Catharina A. Hartman, Dirk J. Heslenfeld, Pieter J. Hoekstra, Einar August Høgestøl, Terry L. Jernigan, Rune Jonassen, Erik G. Jönsson, Peter Kirsch, Iwona Kłoszewska, Knut K. Kolskår, Nils Inge Landrø, Stéphanie Le Hellard, Klaus‐Peter Lesch, Simon Lovestone, Arvid Lundervold, Astri J. Lundervold, Luigi A. Maglanoc, Ulrik Fredrik Malt, Patrizia Mecocci, Ingrid Melle, Andreas Meyer‐Lindenberg, Torgeir Moberget, Linn B. Norbom, Jan Egil Nordvik, Lars Nyberg, Jaap Oosterlaan, Marco Papalino, Andreas Papassotiropoulos, Paul Pauli, Giulio Pergola, Karin Persson, Geneviève Richard, Jaroslav Rokicki, Anne‐Marthe Sanders, Geir Selbæk, Alexey Shadrin, Olav B. Smeland, Hilkka Soininen, Piotr Sowa, Vidar M. Steen, Magda Tsolaki, Kristine M. Ulrichsen, Bruno Vellas, Lei Wang, Eric Westman, Georg Ziegler, Mathias Zink, Ole A. Andreassen, Lars T. Westlye - Nature Neuroscience 2019 cited by 617

  14. Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ingrid Melle, Lars T. Westlye, Oliver Gruber, Bernd Kraemer, Anja Richter, David Zilles‐Wegner, Vince D. Calhoun, Benedicto Crespo‐Facorro, Roberto Roiz‐Santiáñez, Diana Tordesillas‐Gutiérrez, Carmel Loughland, Vaughan J. Carr, Stanley V. Catts, Vanessa Cropley, Janice M. Fullerton, Melissa J. Green, Frans Henskens, Assen Jablensky, Rhoshel Lenroot, Bryan Mowry, Patricia T. Michie, Christos Pantelis, Yann Quidé, Ulrich Schall, Rodney J. Scott, Murray J. Cairns, Marc L. Seal, Paul A. Tooney, Paul E. Rasser, Gavin Cooper, Cynthia Shannon Weickert, Thomas W. Weickert, Derek W. Morris, Elliot Hong, Peter Kochunov, Lauren M. Beard, Raquel E. Gur, Ruben C. Gur, Theodore D. Satterthwaite, Daniel H. Wolf, Ayşenil Belger, Greg Brown, Judith M. Ford, Fabìo Macciardi, Daniel H. Mathalon, Daniel S. OʼLeary, Steven G. Potkin, Adrian Preda, James T. Voyvodic, Kelvin O. Lim, Sarah McEwen, Fude Yang, Yunlong Tan, Shuping Tan, Zhiren Wang, Fengmei Fan, Jingxu Chen, Hong Xiang, Shiyou Tang, Hua Guo, Ping Wan, Wei Dong, H. Jeremy Bockholt, Stefan Ehrlich, Rick P.F. Wolthusen, Margaret King, Jody M. Shoemaker, Scott R. Sponheim, Lieuwe de Haan, Laura Koenders and 92 more - Biological Psychiatry 2018 cited by 990

  15. Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven G. Potkin, Daniel H. Mathalon, Bryon A. Mueller, Adrian Preda, Fabìo Macciardi, Stefan Ehrlich, Esther Walton, J Hass, Vince D. Calhoun, H. Jeremy Bockholt, Scott R. Sponheim, Jody M. Shoemaker, Neeltje E.M. van Haren, Hilleke E. Hulshoff Pol, R A Ophoff, R.S. Kahn, Roberto Roiz‐Santiáñez, Benedicto Crespo‐Facorro, Lei Wang, K I Alpert, E G Jönsson, Ralica Dimitrova, C. Bois, Heather C. Whalley, Andrew M. McIntosh, Stephen M. Lawrie, R Hashimoto, Paul M. Thompson, Jessica A. Turner - Molecular Psychiatry 2015 cited by 1,186

  16. Bivariate causal mixture model quantifies polygenic overlap between complex traits beyond genetic correlation

    Authors: , , , , , , , , , , , - Nature Communications 2019 cited by 443

  17. International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laura J. Bierut, Jonathan I. Bisson, Marco P. Boks, Elizabeth Bolger, Anders D. Børglum, Bekh Bradley, Megan Brashear, Gerome Breen, Richard A. Bryant, Angela C. Bustamante, Jonas Bybjerg‐Grauholm, Joseph R. Calabrese, José Miguel Caldas‐de‐Almeida, Anders M. Dale, Mark J. Daly, Nikolaos P. Daskalakis, Jürgen Deckert, Douglas L. Delahanty, Michelle F. Dennis, Seth G. Disner, Katharina Domschke, Alma Džubur Kulenović, Christopher R. Erbes, Alexandra Evans, Lindsay A. Farrer, Norah C. Feeny, Janine D. Flory, David Forbes, Carol E. Franz, Sandro Galea, Melanie E. Garrett, Bizu Gelaye, Elbert Geuze, Charles F. Gillespie, Aferdita Goci Uka, Scott D. Gordon, Guia Guffanti, Rasha Hammamieh, Supriya Harnal, Michael A. Hauser, Andrew C. Heath, Sian Hemmings, David M. Hougaard, Miro Jakovljević, Marti Jett, Eric O. Johnson, Ian Jones, Tanja Jovanović, Xuejun Qin, Angela G. Junglen, Karen‐Inge Karstoft, Milissa L. Kaufman, Ronald C. Kessler, Alaptagin Khan, Nathan A. Kimbrel, Anthony P. King, Nastassja Koen, Henry R. Kranzler, William S. Kremen, Bruce R. Lawford, Lauren A. M. Lebois, Catrin E. Lewis, Sarah D. Linnstaedt, Adriana Lori, Božo Lugonja, Jurjen J. Luykx, Michael J. Lyons, Jessica L. Maples‐Keller, Charles R. Marmar, Alicia R. Martin and 79 more - Nature Communications 2019 cited by 678

  18. A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2012 cited by 1,745

  19. Mapping the Heterogeneous Phenotype of Schizophrenia and Bipolar Disorder Using Normative Models

    Authors: , , , , , , , , , , , , , - JAMA Psychiatry 2018 cited by 530

  20. 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

  21. Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven Crawford, Scott J. Crow, James L. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Monika Dmitrzak‐Węglarz, Elisa Docampo Martínez, Laramie E. Duncan, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Anne Farmer, Angela Favaro, Fernando Fernández‐Aranda, Manfred Fichter, Krista Fischer, Manuel Föcker, Lenka Foretová, Andreas J. Forstner, Monica Forzan, C. Franklin, Steven Gallinger, Héléna A. Gaspar, Ina Giegling, Johanna Giuranna, Paola Giusti-Rodríquez, Fragiskos Gonidakis, Scott D. Gordon, Philip Gorwood, Monica Gratacos Mayora, Jakob Grove, Sébastien Guillaume, Yiran Guo, Håkon Håkonarson, Katherine A. Halmi, Ken B. Hanscombe, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Anjali K. Henders, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Anke Hinney, L. John Horwood, Christopher Hübel, Laura M. Huckins, James I. Hudson, Hartmut Imgart, Hidetoshi Inoko, Vladimí­r Janout, Susana Jiménez‐Múrcia, Craig Johnson, Jennifer Jordan, Antonio Julià, Anders Juréus, Gursharan Kalsi, Deborah Kaminská, Allan S. Kaplan, Jaakko Kaprio and 220 more - Nature Genetics 2020 cited by 387

  22. Cortical thickness across the lifespan: Data from 17,075 healthy individuals aged 3–90 years

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