Copy number variations of chromosome 16p13.1 region associated with schizophrenia

Autor: Ingason, A., Rujescu, D., Sigurdsson, E., Sigmundsson, T., Pietilainen, O.P., Buizer-Voskamp, J.E., Strengman, E., Francks, C., Muglia, P., Gylfason, A., Gustafsson, O., Olason, P.I., Steinberg, S., Hansen, T., Jakobsen, K.D., Rasmussen, H.B., Giegling, I., Moller, H.J., Hartmann, A., Crombie, C., Fraser, G., Walker, N., Lonnqvist, J., Suvisaari, J., Tuulio-Henriksson, A., Bramon, E., Kiemeney, L.A., Franke, B., Murray, R., Vassos, E., Toulopoulou, T., Muhleisen, T.W., Tosato, S., Ruggeri, M., Djurovic, S., Andreassen, O.A., Zhang, Z., Werge, T., Ophoff, R.A., Bruggeman, R., Cahn, W., de Haan, L., Kahn, R., Krabbendam, L., Linzen, D., Myin-Germeys, I., van Os, J., Wiersma, D., Rietschel, M., Nothen, M.M., Petursson, H., Stefansson, H., Peltonen, L., Collier, D., Stefansson, K., Clair, D.M.

Publikováno v: Molecular Psychiatry
Molecular Psychiatry, 16(1), 17-25. Nature Publishing Group
Molecular Psychiatry; Vol 16
Molecular Psychiatry, 16, 1, pp. 17-25
Molecular Psychiatry, 16, 17-25
Molecular Psychiatry, 16, 17-25. Nature Publishing Group
Molecular psychiatry, 16(1), 17-25. Nature Publishing Group
Ingason, A, Rujescu, D, Sigurdsson, E, Sigmundsson, T, Pietilainen, O P, Buizer-Voskamp, J E, Strengman, E, Francks, C, Muglia, P, Gylfason, A, Gustafsson, O, Olason, P I, Steinberg, S, Hansen, T, Jakobsen, K D, Rasmussen, H B, Giegling, I, Moller, H J, Hartmann, A, Crombie, C, Fraser, G, Walker, N, Lonnqvist, J, Suvisaari, J, Tuulio-Henriksson, A, Bramon, E, Kiemeney, L A, Franke, B, Murray, R, Vassos, E, Toulopoulou, T, Muhleisen, T W, Tosato, S, Ruggeri, M, Djurovic, S, Andreassen, O A, Zhang, Z, Werge, T, Ophoff, R A, Bruggeman, R, Cahn, W, de Haan, L, Kahn, R, Krabbendam, L, Linzen, D, Myin-Germeys, I, van Os, J, Wiersma, D, Rietschel, M, Nothen, M M, Petursson, H, Stefansson, H, Peltonen, L, Collier, D, Stefansson, K & Clair, D M 2011, ' Copy number variations of chromosome 16p13.1 region associated with schizophrenia ', Molecular Psychiatry, vol. 16, pp. 17-25 . https://doi.org/10.1038/mp.2009.101

Deletions and reciprocal duplications of the chromosome 16p13.1 region have recently been reported in several cases of autism and mental retardation (MR). As genomic copy number variants found in these two disorders may also associate with schizophre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5889b74398573a76813690d2cfd730e
https://hdl.handle.net/11858/00-001M-0000-0012-C925-D21.11116/0000-0003-4A54-C

Direct microdissection and microcloning of a translocation breakpoint region, t(1;11) (q42.2;q21), associated with schizophrenia.

Autor: Muir, W.J., Gosden, C.M., Brookes, A.J., Fantes, J., Evans, K.L., Maguire, S.M., Stevenson, B., Boyle, S., Blackwood, D.H.R., St Clair, D.M., Porteous, D.J., Weith, A.

Publikováno v: Cytogenetics & Cell Genetics; 1995, Vol. 70 Issue 1/2, p35-40, 6p

Twin zygosity testing for medical purposes

Autor: St. Clair, D.M, St. Clair, J.B, Swainson, O.P, Bamforth, F, Machin, G.A

Publikováno v: In Journal of Clinical Forensic Medicine 1999 6(3):168-168

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