Canlyniadau Chwilio - Kirov, Georg

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability gan Singh, Tarjinder, Walters, James T. R., Johnstone, Mandy, Curtis, David, Suvisaari, Jaana, Torniainen, Minna, Rees, Elliott, Iyegbe, Conrad, Blackwood, Douglas, McIntosh, Andrew M., Kirov, Georg, Geschwind, Daniel, Murray, Robin M., Di Forti, Marta, Bramon, Elvira, Gandal, Michael, Hultman, Christina M., Sklar, Pamela, Palotie, Aarno, Sullivan, Patrick F., O'Donovan, Michael C., Owen, Michael J., Barrett, Jeffrey C.

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders gan Singh, Tarjinder, Kurki, Mitja I, Curtis, David, Purcell, Shaun M, Crooks, Lucy, McRae, Jeremy, Suvisaari, Jaana, Chheda, Himanshu, Blackwood, Douglas, Breen, Gerome, Pietiläinen, Olli, Gerety, Sebastian S, Ayub, Muhammad, Blyth, Moira, Cole, Trevor, Collier, David, Coomber, Eve L, Craddock, Nick, Daly, Mark J, Danesh, John, DiForti, Marta, Foster, Alison, Freimer, Nelson B, Geschwind, Daniel, Johnstone, Mandy, Joss, Shelagh, Kirov, Georg, Körkkö, Jarmo, Kuismin, Outi, Holmans, Peter, Hultman, Christina M, Iyegbe, Conrad, Lönnqvist, Jouko, Männikkö, Minna, McCarroll, Steve A, McGuffin, Peter, McIntosh, Andrew M, McQuillin, Andrew, Moilanen, Jukka S, Moore, Carmel, Murray, Robin M, Newbury-Ecob, Ruth, Ouwehand, Willem, Paunio, Tiina, Prigmore, Elena, Rees, Elliott, Roberts, David, Sambrook, Jennifer, Sklar, Pamela, St Clair, David, Veijola, Juha, Walters, James T R, Williams, Hywel, Sullivan, Patrick F, Hurles, Matthew E, O’Donovan, Michael C, Palotie, Aarno, Owen, Michael J, Barrett, Jeffrey C

Cael y testun llawn Cael y testun llawn Cael y testun llawn