Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
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Published:2016-11-21
Issue:1
Volume:49
Page:27-35
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ISSN:1061-4036
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Container-title:Nature Genetics
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language:en
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Short-container-title:Nat Genet
Author:
Marshall Christian R, , Howrigan Daniel P, Merico Daniele, Thiruvahindrapuram Bhooma, Wu Wenting, Greer Douglas S, Antaki Danny, Shetty Aniket, Holmans Peter A, Pinto DalilaORCID, Gujral Madhusudan, Brandler William M, Malhotra Dheeraj, Wang Zhouzhi, Fajarado Karin V Fuentes, Maile Michelle S, Ripke StephanORCID, Agartz Ingrid, Albus Margot, Alexander Madeline, Amin Farooq, Atkins Joshua, Bacanu Silviu A, Belliveau Richard A, Bergen Sarah E, Bertalan Marcelo, Bevilacqua Elizabeth, Bigdeli Tim B, Black Donald W, Bruggeman Richard, Buccola Nancy G, Buckner Randy L, Bulik-Sullivan Brendan, Byerley William, Cahn Wiepke, Cai Guiqing, Cairns Murray J, Campion Dominique, Cantor Rita M, Carr Vaughan J, Carrera Noa, Catts Stanley V, Chambert Kimberley D, Cheng Wei, Cloninger C RobertORCID, Cohen David, Cormican Paul, Craddock Nick, Crespo-Facorro Benedicto, Crowley James J, Curtis David, Davidson Michael, Davis Kenneth L, Degenhardt Franziska, Del Favero Jurgen, DeLisi Lynn E, Dikeos Dimitris, Dinan Timothy, Djurovic Srdjan, Donohoe Gary, Drapeau Elodie, Duan Jubao, Dudbridge Frank, Eichhammer Peter, Eriksson Johan, Escott-Price Valentina, Essioux Laurent, Fanous Ayman H, Farh Kai-How, Farrell Martilias SORCID, Frank JosefORCID, Franke LudeORCID, Freedman Robert, Freimer Nelson BORCID, Friedman Joseph I, Forstner Andreas J, Fromer Menachem, Genovese Giulio, Georgieva Lyudmila, Gershon Elliot S, Giegling Ina, Giusti-Rodríguez Paola, Godard Stephanie, Goldstein Jacqueline I, Gratten Jacob, de Haan Lieuwe, Hamshere Marian L, Hansen Mark, Hansen ThomasORCID, Haroutunian Vahram, Hartmann Annette M, Henskens Frans A, Herms Stefan, Hirschhorn Joel N, Hoffmann Per, Hofman Andrea, Huang HailiangORCID, Ikeda Masashi, Joa Inge, Kähler Anna K, Kahn René S, Kalaydjieva Luba, Karjalainen Juha, Kavanagh David, Keller Matthew C, Kelly Brian J, Kennedy James L, Kim Yunjung, Knowles James AORCID, Konte BettinaORCID, Laurent Claudine, Lee Phil, Lee S Hong, Legge Sophie E, Lerer Bernard, Levy Deborah L, Liang Kung-Yee, Lieberman Jeffrey, Lönnqvist Jouko, Loughland Carmel M, Magnusson Patrik K E, Maher Brion S, Maier Wolfgang, Mallet Jacques, Mattheisen ManuelORCID, Mattingsdal Morten, McCarley Robert W, McDonald Colm, McIntosh Andrew MORCID, Meier Sandra, Meijer Carin J, Melle Ingrid, Mesholam-Gately Raquelle I, Metspalu Andres, Michie Patricia T, Milani LiliORCID, Milanova Vihra, Mokrab Younes, Morris Derek W, Müller-Myhsok Bertram, Murphy Kieran C, Murray Robin M, Myin-Germeys Inez, Nenadic Igor, Nertney Deborah A, Nestadt Gerald, Nicodemus Kristin K, Nisenbaum Laura, Nordin Annelie, O'Callaghan Eadbhard, O'Dushlaine Colm, Oh Sang-Yun, Olincy Ann, Olsen Line, O'Neill F Anthony, Van Os Jim, Pantelis Christos, Papadimitriou George N, Parkhomenko Elena, Pato Michele T, Paunio Tiina, Perkins Diana O, Pers Tune H, Pietiläinen Olli, Pimm Jonathan, Pocklington Andrew J, Powell John, Price Alkes, Pulver Ann E, Purcell Shaun M, Quested Digby, Rasmussen Henrik B, Reichenberg Abraham, Reimers Mark A, Richards Alexander L, Roffman Joshua L, Roussos Panos, Ruderfer Douglas M, Salomaa Veikko, Sanders Alan R, Savitz Adam, Schall Ulrich, Schulze Thomas G, Schwab Sibylle G, Scolnick Edward M, Scott Rodney J, Seidman Larry J, Shi Jianxin, Silverman Jeremy M, Smoller Jordan W, Söderman Erik, Spencer Chris C A, Stahl Eli A, Strengman Eric, Strohmaier Jana, Stroup T Scott, Suvisaari Jaana, Svrakic Dragan M, Szatkiewicz Jin P, Thirumalai Srinivas, Tooney Paul A, Veijola Juha, Visscher Peter M, Waddington John, Walsh Dermot, Webb Bradley T, Weiser Mark, Wildenauer Dieter B, Williams Nigel M, Williams Stephanie, Witt Stephanie H, Wolen Aaron R, Wormley Brandon K, Wray Naomi R, Wu Jing Qin, Zai Clement C, Adolfsson Rolf, Andreassen Ole A, Blackwood Douglas H R, Bramon Elvira, Buxbaum Joseph D, Cichon Sven, Collier David A, Corvin Aiden, Daly Mark J, Darvasi Ariel, Domenici Enrico, Esko Tõnu, Gejman Pablo V, Gill Michael, Gurling Hugh, Hultman Christina M, Iwata Nakao, Jablensky Assen V, Jönsson Erik G, Kendler Kenneth S, Kirov George, Knight Jo, Levinson Douglas F, Li Qingqin S, McCarroll Steven A, McQuillin Andrew, Moran Jennifer L, Mowry Bryan J, Nöthen Markus M, Ophoff Roel A, Owen Michael J, Palotie Aarno, Pato Carlos N, Petryshen Tracey L, Posthuma Danielle, Rietschel Marcella, Riley Brien P, Rujescu Dan, Sklar Pamela, St Clair David, Walters James T R, Werge Thomas, Sullivan Patrick F, O'Donovan Michael C, Scherer Stephen W, Neale Benjamin M, Sebat JonathanORCID,
Publisher
Springer Science and Business Media LLC
Reference36 articles.
1. Malhotra, D. & Sebat, J. CNVs: harbingers of a rare variant revolution in psychiatric genetics. Cell 148, 1223–1241 (2012). 2. Walsh, T. et al. Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 320, 539–543 (2008). 3. International Schizophrenia Consortium. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455, 237–241 (2008). 4. Malhotra, D. et al. High frequencies of de novo CNVs in bipolar disorder and schizophrenia. Neuron 72, 951–963 (2011). 5. Xu, B. et al. Strong association of de novo copy number mutations with sporadic schizophrenia. Nat. Genet. 40, 880–885 (2008).
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