Schizophrenia copy number variants and associative learning

por Clifton, N E, Pocklington, A J, Scholz, B, Rees, E, Walters, J T R, Kirov, G, O'Donovan, M C, Owen, M J, Wilkinson, L S, Thomas, K L, Hall, J
Publicado 2017

Genetic risk for schizophrenia is associated with increased proportion of indirect connections in brain networks revealed by a semi-metric analysis: evidence from population sample...

por Dimitriadis, S I, Perry, G, Lancaster, T M, Tansey, K E, Singh, K D, Holmans, P, Pocklington, A, Davey Smith, G, Zammit, S, Hall, J, O’Donovan, M C, Owen, M J, Jones, D K, Linden, D E
Publicado 2022

Exome arrays capture polygenic rare variant contributions to schizophrenia

por Richards, A. L., Leonenko, G., Walters, J. T., Kavanagh, D. H., Rees, E. G., Evans, A., Chambert, K. D., Moran, J. L., Goldstein, J., Neale, B. M., McCarroll, S. A., Pocklington, A. J., Holmans, P. A., Owen, M. J., O'Donovan, M. C.
Publicado 2016

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

por Kirov, G, Pocklington, A J, Holmans, P, Ivanov, D, Ikeda, M, Ruderfer, D, Moran, J, Chambert, K, Toncheva, D, Georgieva, L, Grozeva, D, Fjodorova, M, Wollerton, R, Rees, E, Nikolov, I, van de Lagemaat, L N, Bayés, À, Fernandez, E, Olason, P I, Böttcher, Y, Komiyama, N H, Collins, M O, Choudhary, J, Stefansson, K, Stefansson, H, Grant, S G N, Purcell, S, Sklar, P, O'Donovan, M C, Owen, M J
Publicado 2012

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia

por Rees, E, Kirov, G, Walters, J T, Richards, A L, Howrigan, D, Kavanagh, D H, Pocklington, A J, Fromer, M, Ruderfer, D M, Georgieva, L, Carrera, N, Gormley, P, Palta, P, Williams, H, Dwyer, S, Johnson, J S, Roussos, P, Barker, D D, Banks, E, Milanova, V, Rose, S A, Chambert, K, Mahajan, M, Scolnick, E M, Moran, J L, Tsuang, M T, Glatt, S J, Chen, W J, Hwu, H-G, Neale, B M, Palotie, A, Sklar, P, Purcell, S M, McCarroll, S A, Holmans, P, Owen, M J, O'Donovan, M C
Publicado 2015