Resultats de la cerca - Wijsman, EM

Replication of a Rare Risk Haplotype on 1p36.33 for Autism Spectrum Disorder per Chapman, N.H., Bernier, R.A., Webb, S.J., Munson, J., Blue, E.M., Chen, D.-H., Heigham, E., Raskind, W.H., Wijsman, E.M.

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Meta-analysis of 32 genome-wide linkage studies of schizophrenia per Ng, MYM, Levinson, DF, Faraone, SV, Suarez, BK, DeLisi, LE, Arinami, T, Riley, B, Paunio, T, Pulver, AE, Irmansyah, Holmans, PA, Escamilla, M, Wildenauer, DB, Williams, NM, Laurent, C, Mowry, BJ, Brzustowicz, LM, Maziade, M, Sklar, P, Garver, DL, Abecasis, GR, Lerer, B, Fallin, MD, Gurling, HMD, Gejman, PV, Lindholm, E, Moises, HW, Byerley, W, Wijsman, EM, Forabosco, P, Tsuang, MT, Hwu, H-G, Okazaki, Y, Kendler, KS, Wormley, B, Fanous, A, Walsh, D, O’Neill, FA, Peltonen, L, Nestadt, G, Lasseter, VK, Liang, KY, Papadimitriou, GM, Dikeos, DG, Schwab, SG, Owen, MJ, O’Donovan, MC, Norton, N, Hare, E, Raventos, H, Nicolini, H, Albus, M, Maier, W, Nimgaonkar, VL, Terenius, L, Mallet, J, Jay, M, Godard, S, Nertney, D, Alexander, M, Crowe, RR, Silverman, JM, Bassett, AS, Roy, M-A, Mérette, C, Pato, CN, Pato, MT, Roos, J Louw, Kohn, Y, Amann-Zalcenstein, D, Kalsi, G, McQuillin, A, Curtis, D, Brynjolfson, J, Sigmundsson, T, Petursson, H, Sanders, AR, Duan, J, Jazin, E, Myles-Worsley, M, Karayiorgou, M, Lewis, CM

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