Identification of common genetic risk variants for autism spectrum disorder

Grove, Jakob; Ripke, Stephan; Walters, Raymond K.; Walters, Rk K.; Mattheisen, Manuel; Naeland, T.; Won, Hyejung; St Pourcain, Beate; Baekvad-Hansen, Marie; Pallesen, Jonatan; Smith, George Davey; Buxbaum, Joseph D.; Borglum, Ad; Bybjerg-Grauholm, Jonas; Td, Als; Cerrato, Felecia; Chambert, Kimberly; Churchhouse, Claire; Dellenvall, Karin; Demontis, Ditte; Wray, Nr R.; De Rubeis, Silvia; Devlin, Bernie; Hope, Sigrun; Trzaskowski, M.; Djurovic, Srdjan; Belliveau, Rich; Huang, Hailiang; Maller, Julian; Nærland, Terje; Martin, Joanna; Klei, Lambertus; Bettella, Francesco; dPoterba, Timothy; Hollegaard, Mads V.; Nyegaard, Mette; Poulsen, Jesper Buchhave; Pourcain, Beate St; Rk, Walters; Qvist, Per; Palotie, Aarno; Howrigan, Daniel P.; Rehnström, Karola; Martin, Alicia R.; Christensen, Jane H.; Reichenberg, Abraham; Moran, Jennifer L.; Robinson, Elise B.; Reichert, Jennifer; MacIntyre, Dj J.; Roeder, Kathryn; MacKinnon, Df F.; Maier, Rm M.; Roussos, Panos; Bækvad-Hansen, Marie; Kiadeh, Ffh F. H.; Maier, W.; Marchini, J.; Hultman, Christina M.; Saemundsen, Evald; Mbarek, H.; Palmer, Duncan S.; McGrath, P.; Satterstrom, Fk Kyle; Sandin, Sven; McGuffin, P.; O’Reilly, P. F.; Medland, Se E.; Mehta, D.; Middeldorp, Cm M.; Mihailov, E.; Stevens, Christine R.; Stefansson, Hreinn; Milaneschi, Y.; Sullivan, Patrick F.; Dumont, Ashley L.; Xu, Xinyi; Milani, L.; Herms, S.; Pedersen, Carsten Bøcker; Mondimore, Fm M.; Steinberg, Stacy; Goldstein, Jacqueline I.; Montgomery, Gw W.; Mostafavi, S.; Hickie, Ib B.; Hansen, Christine S.; van Hemert, Am M.; Mullins, N.; Pedersen, Marianne Giørtz; Hoffmann, P.; Nauck, M.; Walters, Gb Bragi; Turley, Patrick; Hauberg, Mads Engel; Ng, B.; Nivard, Mg G.; Homuth, G.; Wu, Y.; Nyholt, Dr R.; Xi, Hs S.; Yang, J.; Horn, C.; Zhang, Ft; de Geus, Ejc J. C.; Oskarsson, H.; Hottenga, Jj-J.; Owen, Mj J.; Painter, Jn N.; Ising, M.; Byrne, Em M.; Peterson, Re E.; Pettersson, E.; Peyrot, Wj J.; Jansen, R.; Pistis, G.; Posthuma, D.; Bacanu, Sa-A.; Beekman, Atf T. F.; Jorgenson, E.; Quiroz, Ja A.; Wellmann, J.; Bigdeli, Tb B.; Rice, Jp P.; Willemsen, G.; Binder, Eb B.; Knowles, Ja A.; Blackwood, Dhr H. R.; Riley, Bp P.; Witt, Sh H.; Bryois, J.; Kohane, Is S.; Rivera, M.; Buttenschøn, Hn N.; Cai, N.; Mirza, Ss S.; Kraft, J.; Castelao, E.; Schulte, Ec C.; Kretzschmar, Ww W.; Clarke, Tk-K.; Coleman, Jri R. I.; Krogh, J.; Shen, L.; Colodro-Conde, L.; Couvy-Duchesne, B.; Shi, Jx; Craddock, N.; Kutalik, Z.; Crawford, Ge E.; Shyn, Si I.; Davies, G.; Li, Y.; Deary, Ij J.; Als, Thomas D.; Sigurdsson, E.; Degenhardt, F.; Derks, Em M.; Sinnamon, Gcb C. B.; Agerbo, Esben; Direk, N.; Davey Smith, George; Andreassen, Ole A.; Anney, Richard; Smit, Jh H.; Dolan, Cv; Awashti, Swapnil; Dunn, Ec C.; Smith, Dj J.; Eley, Tc C.; Streit, F.; Escott-Price,; Strohmaier, J.; Finucane, Hk K.; Consortium, Psychiat Genomics; Lind, Penelope A.; Forstner, Aj J.; Frank, J.; Tansey, Ke E.; Teismann, H.; Bupgen,; Gaspar, Ha A.; Gill, M.; Goes, Fs S.; Team, 23andMe Res; Teumer, A.; Gordon, Sd D.; Hall, Ls S.; Thompson, W.; Hansen, Tf F.; Thomson, Pa A.; Thorgeirsson, Te E.; Traylor, M.; Treutlein, J.; Trubetskoy,; O'Reilly, Pf; Uitterlinden, Ag G.; Umbricht, D.; Müller-Myhsok, B.; Van der Auwera, S.; Viktorin, A.; Abdellaoui, A.; Visscher, Pm M.; Wang, Yp; Air, Tm M.; Weissman, Mm M.; Nöthen, M. M.; Adams, Mark J.; Andlauer, Tfm F. M.; Webb, Bt T.; O’Donovan, M. C.; Schoevers, Robert; Oa, Andreassen; Weinsheimer, Shantel M.; Lucae, S.; Madden, Paf A. F.; Magnusson, Pk K.; Martin, Ng G.; Werge, Thomas; Wilson, Ch H.; McIntosh, Am M.; Metspalu, A.; Kyle Satterstrom, F.; Hayward, C.; Paciga, Sa A.; Heath, Ac C.; Pedersen, Nl L.; Kloiber, S.; Perlis, Rh H.; Lewis, G.; Porteous, Dj J.; Li, Qs S.; Stefansson, Kari; Potash, Jb B.; Baune, Bt T.; Preisig, M.; Rietschel, M.; Berger, K.; Schaefer, C.; Boomsma, Di I.; Schulze, Tg G.; Kendler, Kenneth S.; Smoller, Jw W.; Nordentoft, Merete; Cichon, S.; Tiemeier, H.; Penninx, Brenda W. J. H.; Dannlowski, U.; Uher, R.; Völzke, H.; DePaulo,; Domenici, E.; Domschke, K.; Esko, T.; Mors, Ole; Grabe, Hj J.; Hamilton, Sp P.; Arolt,; Lewis, Cm M.; Naerland, Terje; Litterman, Nk K.; Levinson, Df F.; McIntyre, Mh H.; Muller-Myhsok, B.; Mountain, Jl L.; Noblin, Es S.; Nothen, Mm; Northover, Cam A. M.; Pitts, Sj J.; O'Donovan, Mc; Sathirapongsasuti, Jf F.; Sazonova, Ov; Shelton, Jf F.; Hromatka, Bs S.; Breen, G.; Shringarpure, S.; Huber, Ke E.; Mortensen, Preben Bo; Tung, Jy Y.; Kleinman, A.; Hougaard, David M.; Vacic,; Bell, Rk K.; Bryc, K.; Neale, Benjamin M.; Elson, Sl L.; Fontanillas, P.; Furlotte, Na A.; Agee, M.; Alipanahi, B.; Geschwind, Daniel H.; Auton, A.; Bragi Walters, G.; Daly, Mark J.; Børglum, Anders D.; Ad, Børglum; Awasthi, Swapnil

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Nature Research, Nature Genetics, 3(51), p. 431-444, 2019

DOI: 10.1038/s41588-019-0344-8

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Identification of common genetic risk variants for autism spectrum disorder

Journal article published in 2019 by Jakob Grove

, Stephan Ripke, Raymond K. Walters, Rk K. Walters, Manuel Mattheisen, T. Naeland, Hyejung Won, Beate St Pourcain, Marie Baekvad-Hansen, Jonatan Pallesen, George Davey Smith, Joseph D. Buxbaum, Ad Borglum, Jonas Bybjerg-Grauholm, Als Td and other authors.

This paper is made freely available by the publisher.

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Identification of common genetic risk variants for autism spectrum disorder