Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders by D'Abate, L, Walker, S, Yuen, RKC, Tammimies, K, Buchanan, JA, Davies, RW, Thiruvahindrapuram, B, Wei, J, Brian, J, Bryson, SE, Dobkins, K, Howe, J, Landa, R, Leef, J, Messinger, D, Ozonoff, S, Smith, IM, Stone, WL, Warren, ZE, Young, G, Zwaigenbaum, L, Scherer, SW

Functional impact of global rare copy number variation in autism spectrum disorders. by Pinto, D, Pagnamenta, A, Klei, L, Anney, R, Merico, D, Regan, R, Conroy, J, Magalhaes, T, Correia, C, Abrahams, B, Almeida, J, Bacchelli, E, Bader, G, Bailey, A, Baird, G, Battaglia, A, Berney, T, Bolshakova, N, Bölte, S, Bolton, P, Bourgeron, T, Brennan, S, Brian, J, Bryson, SE, Carson, A

Mapping autism risk loci using genetic linkage and chromosomal rearrangements. by Szatmari, P, Paterson, A, Zwaigenbaum, L, Roberts, W, Brian, J, Liu, X, Vincent, J, Skaug, J, Thompson, A, Senman, L, Feuk, L, Qian, C, Bryson, SE, Jones, M, Marshall, C, Scherer, S, Vieland, V, Bartlett, C, Mangin, L, Goedken, R, Segre, A, Pericak-Vance, M, Cuccaro, M, Gilbert, JR, Wright, H