High rate of disease-related copy number variations in childhood onset schizophrenia

Por Ahn, K, Gotay, N, Andersen, TM, Anvari, AA, Gochman, P, Lee, Y, Sanders, S, Guha, S, Darvasi, A, Glessner, JT, Hakonarson, H, Lencz, T, State, MW, Shugart, YY, Rapoport, JL
Publicado no Mol Psychiatry (2013)

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

Por Addington, AM, Gauthier, J, Piton, A, Hamdan, FF, Raymond, A, Gogtay, N, Miller, R, Tossell, J, Bakalar, J, Germain, G, Gochman, P, Long, R, Rapoport, JL, Rouleau, GA
Publicado em 2010

Segmental uniparental isodisomy on 5q32‐qter in a patient with childhood‐onset schizophrenia

Por Seal, J L, Gornick, M C, Gogtay, N, Shaw, P, Greenstein, D K, Coffey, M, Gochman, P A, Stromberg, T, Chen, Z, Merriman, B, Nelson, S F, Brooks, J, Arepalli, S, Vrièze, F Wavrant‐De, Hardy, J, Rapoport, J L, Addington, A M
Publicado em 2006

Inhibition of STEP(61) ameliorates deficits in mouse and hiPSC-based schizophrenia models

Por Xu, J, Hartley, B J, Kurup, P, Phillips, A, Topol, A, Xu, M, Ononenyi, C, Foscue, E, Ho, S-M, Baguley, T D, Carty, N, Barros, C S, Müller, U, Gupta, S, Gochman, P, Rapoport, J, Ellman, J A, Pittenger, C, Aronow, B, Nairn, A C, Nestor, M W, Lombroso, P J, Brennand, K J
Publicado no Mol Psychiatry (2018)