Ole A. Andreassen

1995–2026 年に発表

別表記
Ole A Andreassen
707
論文数
106,415
被引用数
140
h 指数
650
i10 指数

被引用数

Ole A. Andreassen の年別被引用数1939 年: 被引用 1 件1972 年: 被引用 2 件1976 年: 被引用 1 件1992 年: 被引用 5 件1994 年: 被引用 6 件1995 年: 被引用 2 件1996 年: 被引用 10 件1997 年: 被引用 4 件1998 年: 被引用 6 件1999 年: 被引用 22 件2000 年: 被引用 74 件2001 年: 被引用 129 件2002 年: 被引用 143 件2003 年: 被引用 189 件2004 年: 被引用 137 件2005 年: 被引用 128 件2006 年: 被引用 114 件2007 年: 被引用 115 件2008 年: 被引用 168 件2009 年: 被引用 284 件2010 年: 被引用 352 件2011 年: 被引用 419 件2012 年: 被引用 533 件2013 年: 被引用 681 件2014 年: 被引用 769 件2015 年: 被引用 891 件2016 年: 被引用 989 件2017 年: 被引用 1,197 件2018 年: 被引用 1,259 件2019 年: 被引用 3,973 件2020 年: 被引用 4,720 件2021 年: 被引用 5,113 件2022 年: 被引用 4,351 件2023 年: 被引用 3,325 件2024 年: 被引用 5,184 件2025 年: 被引用 2,473 件2026 年: 被引用 102 件1940〜1971 年は被引用が無いため表示していません1973〜1975 年は被引用が無いため表示していません1977〜1991 年は被引用が無いため表示していません1993 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 11,710 件、この内訳の 22.9%イギリス: 引用元論文 4,916 件、この内訳の 9.6%中国: 引用元論文 3,618 件、この内訳の 7.1%ドイツ: 引用元論文 3,018 件、この内訳の 5.9%カナダ: 引用元論文 2,346 件、この内訳の 4.6%オーストラリア: 引用元論文 2,127 件、この内訳の 4.2%オランダ: 引用元論文 2,034 件、この内訳の 4%イタリア: 引用元論文 1,731 件、この内訳の 3.4%スウェーデン: 引用元論文 1,527 件、この内訳の 3%スペイン: 引用元論文 1,446 件、この内訳の 2.8%フランス: 引用元論文 1,415 件、この内訳の 2.8%ノルウェー: 引用元論文 1,364 件、この内訳の 2.7%
0%22.9%その他 27%

分野

  • Medicine33.9%
  • Biochemistry, Genetics and Molecular Biology27%
  • Neuroscience26.7%
  • Psychology6.5%
  • Computer Science1.1%
  • Immunology and Microbiology1.1%
  • その他3.7%

トピック

  • 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%
  • その他77.9%

共著者

全論文

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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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 170 名 - The Lancet Neurology 2019 被引用: 2,541

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 2,632

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 2,526

  4. Biological insights from 108 schizophrenia-associated genetic loci

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 197 名 - Nature 2014 被引用: 8,166

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2012 被引用: 2,620

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 2,320

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

    著者: , , , , , , , , , - Nature Genetics 2019 被引用: 1,463

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 760

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 111 名 - Nature Genetics 2019 被引用: 1,181

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 17 名 - Nature Genetics 2018 被引用: 1,418

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 70 名 - Translational Psychiatry 2020 被引用: 685

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 92 名 - Biological Psychiatry 2018 被引用: 990

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 1,186

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

    著者: , , , , , , , , , , , - Nature Communications 2019 被引用: 443

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 79 名 - Nature Communications 2019 被引用: 678

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2012 被引用: 1,745

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

    著者: , , , , , , , , , , , , , - JAMA Psychiatry 2018 被引用: 530

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 96 名 - Nature Genetics 2022 被引用: 393

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

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