Showing 1 - 7 results of 7 for search 'Vieland, V', query time: 0.04s
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Reports of the Death of the Epistasis Model Are Greatly Exaggerated [2] (multiple letters) by Farrall, M, Vieland, V, Huang, J
Published 2003Journal article -
2
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. by Vieland, V, Hallmayer, J, Huang, Y, Pagnamenta, A, Pinto, D, Khan, H, Monaco, A, Paterson, A, Scherer, S, Sutcliffe, J, Szatmari, P
Published 2011Journal article -
3
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism by Vieland, V, Hallmayer, J, Huang, Y, Pagnamenta, A, Pinto, D, Khan, H, Monaco, A, Paterson, A, Scherer, S, Sutcliffe, J, Szatmari, P
Published 2011Journal article -
4
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. by Pagnamenta, A, Khan, H, Walker, S, Gerrelli, D, Wing, K, Bonaglia, M, Giorda, R, Berney, T, Mani, E, Molteni, M, Pinto, D, Le Couteur, A, Hallmayer, J, Sutcliffe, J, Szatmari, P, Paterson, A, Scherer, S, Vieland, V, Monaco, A
Published 2011Journal article -
5
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability by Pagnamenta, A, Khan, H, Walker, S, Gerrelli, D, Wing, K, Bonaglia, M, Giorda, R, Berney, T, Mani, E, Molteni, M, Pinto, D, Le Couteur, A, Hallmayer, J, Sutcliffe, J, Szatmari, P, Paterson, A, Scherer, S, Vieland, V, Monaco, A
Published 2011Journal article -
6
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
Published 2007Journal article -
7
Individual common variants exert weak effects on the risk for autism spectrum disorderspi. by Anney, R, Klei, L, Pinto, D, Almeida, J, Bacchelli, E, Baird, G, Bolshakova, N, Bölte, S, Bolton, P, Bourgeron, T, Brennan, S, Brian, J, Casey, J, Conroy, J, Correia, C, Corsello, C, Crawford, E, de Jonge, M, Delorme, R, Duketis, E, Duque, F, Estes, A, Farrar, P, Fernandez, B, Folstein, SE, Fombonne, E, Gilbert, J, Gillberg, C, Glessner, J, Green, A, Green, J, Guter, S, Heron, E, Holt, R, Howe, J, Hughes, G, Hus, V, Igliozzi, R, Jacob, S, Kenny, G, Kim, C, Kolevzon, A, Kustanovich, V, Lajonchere, C, Lamb, J, Law-Smith, M, Leboyer, M, Le Couteur, A, Leventhal, B, Liu, X, Lombard, F, Lord, C, Lotspeich, L, Lund, S, Magalhaes, T, Mantoulan, C, McDougle, C, Melhem, N, Merikangas, A, Minshew, N, Mirza, G, Munson, J, Noakes, C, Nygren, G, Papanikolaou, K, Pagnamenta, A, Parrini, B, Paton, T, Pickles, A, Posey, D, Poustka, F, Ragoussis, I, Regan, R, Roberts, W, Roeder, K, Roge, B, Rutter, M, Schlitt, S, Shah, N, Sheffield, VC, Soorya, L, Sousa, I, Stoppioni, V, Sykes, N, Tancredi, R, Thompson, A, Thomson, S, Tryfon, A, Tsiantis, J, Van Engeland, H, Vincent, J, Volkmar, F, Vorstman, J, Wallace, S, Wing, K, Wittemeyer, K, Wood, S, Zurawiecki, D, Zwaigenbaum, L, Bailey, A, Battaglia, A, Cantor, R, Coon, H, Cuccaro, M, Dawson, G, Ennis, S, Freitag, C, Geschwind, D, Haines, J, Klauck, S, McMahon, WM, Maestrini, E, Miller, J, Monaco, A, Nelson, S, Nurnberger, J, Oliveira, G, Oliveira, G, Parr, JR, Pericak-Vance, M, Piven, J, Schellenberg, G, Scherer, S, Vicente, A, Wassink, T, Wijsman, E, Betancur, C, Buxbaum, J, Cook, E, Gallagher, L, Gill, M, Hallmayer, J, Paterson, A, Sutcliffe, J, Szatmari, P, Vieland, V, Hakonarson, H, Devlin, B
Published 2012Journal article