Individual common variants exert weak effects on the risk for autism spectrum disorders

Anney, R.; Klei, L.; Pinto, D.; Almeida, J.; Bacchelli, E.; Baird, G.; Bolshakova, N.; Bolte, S.; Bolton, P. F.; Bourgeron, T.; Brennan, S.; Brian, J.; Casey, J.; Conroy, J.; Correia, C.; Corsello, C.; Crawford, E. L.; de Jonge, M.; Delorme, R.; Duketis, E.; Duque, F.; Estes, A.; Farrar, P.; Fernandez, B. A.; Folstein, S. E.; Fombonne, E.; Gilbert, J.; Gillberg, C.; Glessner, J. T.; Green, A.; Green, J.; Guter, S. J.; Heron, E. A.; Holt, R.; Howe, J. L.; Hughes, G.; Hus, V.; Igliozzi, R.; Jacob, S.; Kenny, G. P.; Kim, C.; Kolevzon, A.; Kustanovich, V.; Lajonchere, C. M.; Lamb, J. A.; Law-Smith, M.; Leboyer, M.; Le Couteur, A.; Leventhal, B. L.; Liu, X.-Q.; Lombard, F.; Lord, C.; Lotspeich, L.; Lund, S. C.; T. R. Magalhaes; Mantoulan, C.; McDougle, C. J.; Melhem, N. M.; Merikangas, A.; Minshew, N. J.; Mirza, G. K.; Munson, J.; Noakes, C.; Nygren, G.; Papanikolaou, K.; Pagnamenta, A. T.; Parrini, B.; Paton, T.; Pickles, A.; Posey, D. J.; Poustka, F.; Ragoussis, J.; Regan, R.; Roberts, W.; Roeder, K.; Roge, B.; Rutter, M. L.; Schlitt, S.; Shah, N.; Sheffield, V. C.; Soorya, L.; Sousa, I.; Stoppioni, V.; Sykes, N.; Tancredi, R.; Thompson, A. P.; Thomson, S.; Tryfon, A.; Tsiantis, J.; Van Engeland, H.; Vincent, J. B.; Volkmar, F.; Vorstman, J.; Wallace, S.; Wing, K.; Wittemeyer, K.; Wood, S.; Zurawiecki, D.; Zwaigenbaum, L.; Bailey, A. J.; Battaglia, A.; Cantor, R. M.; Coon, H.; Cuccaro, M. L.; Dawson, G.; Ennis, S.; Freitag, C. M.; Geschwind, D. H.; Haines, J. L.; Klauck, S. M.; McMahon, W. M.; Maestrini, E.; Miller, J.; Monaco, A. P.; Nelson, S. F.; Nurnberger, J. I.; Oliveira, G.; Parr, J. R.; Pericak-Vance, M. A.; Piven, J.; Schellenberg, G. D.; Scherer, S. W.; Vicente, A. M.; Wassink, T. H.; Wijsman, E. M.; Betancur, C.; Buxbaum, J. D.; Cook, E. H.; Gallagher, L.; Gill, M.; Hallmayer, J.; Paterson, A. D.; Sutcliffe, J. S.; Szatmari, P.; Vieland, V. J.; Hakonarson, H.; Devlin, B.

Journal Article

Title	Individual common variants exert weak effects on the risk for autism spectrum disorders
Publication Type	Journal Article
Authors	Anney, R, Klei, L, Pinto, D, Almeida, J, Bacchelli, E, Baird, G, Bolshakova, N, Bolte, S, Bolton, PF, Bourgeron, T, Brennan, S, Brian, J, Casey, J, Conroy, J, Correia, C, Corsello, C, Crawford, EL, de Jonge, M, Delorme, R, Duketis, E, Duque, F, Estes, A, Farrar, P, Fernandez, BA, Folstein, SE, Fombonne, E, Gilbert, J, Gillberg, C, Glessner, JT, Green, A, Green, J, Guter, SJ, Heron, EA, Holt, R, Howe, JL, Hughes, G, Hus, V, Igliozzi, R, Jacob, S, Kenny, GP, Kim, C, Kolevzon, A, Kustanovich, V, Lajonchere, CM, Lamb, JA, Law-Smith, M, Leboyer, M, Le Couteur, A, Leventhal, BL, Liu, X-Q, Lombard, F, Lord, C, Lotspeich, L, Lund, SC, Magalhaes, TR, Mantoulan, C, McDougle, CJ, Melhem, NM, Merikangas, A, Minshew, NJ, Mirza, GK, Munson, J, Noakes, C, Nygren, G, Papanikolaou, K, Pagnamenta, AT, Parrini, B, Paton, T, Pickles, A, Posey, DJ, Poustka, F, Ragoussis, J, Regan, R, Roberts, W, Roeder, K, Roge, B, Rutter, ML, Schlitt, S, Shah, N, Sheffield, VC, Soorya, L, Sousa, I, Stoppioni, V, Sykes, N, Tancredi, R, Thompson, AP, Thomson, S, Tryfon, A, Tsiantis, J, Van Engeland, H, Vincent, JB, Volkmar, F, Vorstman, J, Wallace, S, Wing, K, Wittemeyer, K, Wood, S, Zurawiecki, D, Zwaigenbaum, L, Bailey, AJ, Battaglia, A, Cantor, RM, Coon, H, Cuccaro, ML, Dawson, G, Ennis, S, Freitag, CM, Geschwind, DH, Haines, JL, Klauck, SM, McMahon, WM, Maestrini, E, Miller, J, Monaco, AP, Nelson, SF, Nurnberger, JI, Oliveira, G, Parr, JR, Pericak-Vance, MA, Piven, J, Schellenberg, GD, Scherer, SW, Vicente, AM, Wassink, TH, Wijsman, EM, Betancur, C, Buxbaum, JD, Cook, EH, Gallagher, L, Gill, M, Hallmayer, J, Paterson, AD, Sutcliffe, JS, Szatmari, P, Vieland, VJ, Hakonarson, H, Devlin, B
Year of Publication	2012
Journal	Human Molecular Genetics
Volume	21
Issue	21
Date Published	Jan-11-2012
Pagination	4781 - 4792
ISSN	0964-6906
URL	http://hmg.oxfordjournals.org/cgi/doi/10.1093/hmg/dds301https://academic.oup.com/hmg/article/21/21/4781/781997/Individual-common-variants-exert-weak-effects-on
DOI	10.1093/hmg/dds301
Short Title	Human Molecular Genetics

CCMAR Authors

Tiago Magalhães