Rare chromosomal deletions and duplications increase risk of schizophrenia
Year: 2008
Type: article
Study design: Observational Study
Authors: Craddock, N. J., Gill, M., Hultman, C. M., Lichtenstein, P., McQuillin, A., Pato, Carlos N., Ruderfer, D. M., Owen, M. J., St Clair, David, Sullivan, P. F., Sklar, P., Purcell, S. M., Stone, J. L, Korn, Joshua, Macgregor, S., Morris, D. W., O'Dushlaine, C. T., Daly, M. J., Visscher, P. M., Holmans, P. A., Scolnick, E: M., Williams, N. M., Georgieva, L., Nikolov, I., Norton, N., Williams, H., Toncheva, D., Milanova, V., Thelander, Emma F., Sullivan, P. F., Kenny, E., Waddington, John L., Choudhury, K., Datta, S., Pimm, J., Thirumalai, S., Puri, V., Krasucki, R., Lawrence, J., Quested, D., Bass, N., Curtis, David, Gurling, H., Crombie, C., Fraser, G., Kwan, Soh Leh, Walker, N., Muir, W. J., McGhee, K. A., Pickard, B., Malloy, P., Maclean, A. W., Van Beck, Margaret, Visscher, P. M., Pato, Michele T., Medeiros, Helena, Middleton, Frank A., Carvalho, Célia, Morley, C., Fanous, Ayman H., Conti, D., Knowles, James A., Ferreira, Carlos Paz, Macedo, António, Azevedo, Maria H., McCarroll, Steve A., Daly, M. J., Chambert, Kimberly, Gates, Casey
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W7014852833