Zobrazeno 1 - 2
of 2
pro vyhledávání: '"BuizerVoskamp, JE"'
Autor:
Toulopoulou, T, Wiersma, D, Murray, R, Ruggeri, M, Tosato, S, Bonetto, C, Steinberg, S, Sigurdsson, E, Sigmundsson, T, Petursson, H, Gylfason, A, Olason, PI, Hardarsson, G, Jonsdottir, GA, Cahn, W, de Haan, L, Krabbendam, L, MyinGermeys, I, Werge, T, Kiemeney, LA, Franke, B, Pietiläinen, OPH, Picchioni, M, Vassos, E, Ettinger, U, Rietschel, M, Gustafsson, O, BuizerVoskamp, JE, Fossdal, R, Giegling, I, Sabatti, C, Ophoff, RA, Möller, HJ, Hartmann, AM, Hoffmann, P, Crombie, C, Rujescu, D, Veltman, J, Fraser, G, St Clair, D, Peltonen, L, Stefansson, K, Barnes, MR, Ingason, A, Stefansson, H, Nöthen, MM, Walker, N, Lonnqvist, J, Suvisaari, J, TuulioHenriksson, A, Djurovic, S, Collier, DA, Kahn, RS, Melle, I, Andreassen, OA, Hansen, T, Linszen, D, von Os, J, Bramon, E, Cichon, S, Bruggeman, R
Publikováno v:
Human molecular genetics, 18(5), 988-996. Oxford University Press
Human Molecular Genetics, 18, 5, pp. 988-96
Human Molecular Genetics, 18, 988-96
Human Molecular Genetics, 18(5), 988-996. Oxford University Press
Rujescu, D & Krabbendam, L 2009, ' Disruption of the neurexin 1 gene is associated with schizophrenia ', Human Molecular Genetics, vol. 18, no. 5, pp. 988-996 . https://doi.org/10.1093/hmg/ddn351
Human Molecular Genetics; Vol
Human Molecular Genetics
Human Molecular Genetics, 18, 5, pp. 988-96
Human Molecular Genetics, 18, 988-96
Human Molecular Genetics, 18(5), 988-996. Oxford University Press
Rujescu, D & Krabbendam, L 2009, ' Disruption of the neurexin 1 gene is associated with schizophrenia ', Human Molecular Genetics, vol. 18, no. 5, pp. 988-996 . https://doi.org/10.1093/hmg/ddn351
Human Molecular Genetics; Vol
Human Molecular Genetics
Deletions within the neurexin 1 gene (NRXN1; 2p16.3) are associated with autism and have also been reported in two families with schizophrenia. We examined NRXN1, and the closely related NRXN2 and NRXN3 genes, for copy number variants (CNVs) in 2977
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0e7f8bb4091edfb1f666d14a1be47e2
https://pure.amc.nl/en/publications/disruption-of-the-neurexin-1-gene-is-associated-with-schizophrenia(2abe7aac-e6ff-4386-b71c-c9bbe97a21a5).html
https://pure.amc.nl/en/publications/disruption-of-the-neurexin-1-gene-is-associated-with-schizophrenia(2abe7aac-e6ff-4386-b71c-c9bbe97a21a5).html
Autor:
Toulopoulou, T, Franke, B, Crombie, C, Fossdal, R, Sigmundsson, T, BuizerVoskamp, JE, Hansen, T, Jakobsen, KD, Muglia, P, Francks, C, Matthews, PM, Murray, R, Ruggeri, M, Sabatti, C, Gylfason, A, Halldorsson, BV, Vassos, E, Tosato, S, Walshe, M, Freimer, NB, Gulcher, JR, Gudbjartsson, D, Thorsteinsdottir, U, Kong, A, Thorgeirsson, TE, Olesen, J, Vasilescu, C, Andreassen, OA, Melle, I, Mühleisen, TW, Wang, AG, Ullum, H, Need, AC, Sigurdsson, A, Jonasdottir, A, Djurovic, S, Ophoff, RA, Georgi, A, Rietschel, M, Werge, T, Bjornsson, A, Mattiasdottir, S, Blondal, T, Haraldsson, M, Petursson, H, MyinGermeys, I, Krabbendam, L, De Haan, L, Cahn, W, Bruggeman, R, Wiersma, D, Goldstein, DB, Nöthen, MM, Peltonen, L, Van Os, J, Linszen, DH, Kahn, RS, Stefansson, K, Magnusdottir, BB, Di Forti, M, Bramon, E, Paunio, T, TuulioHenriksson, A, Giegling, I, Möller, HJ, Suvisaari, J, Hartmann, A, Shianna, KV, Ge, D, Lonnqvist, J, Collier, DA, Walker, N, Li, T, Fraser, G, Ingason, A, Steinberg, S, Sigurdsson, E, St Clair, D, Kiemeney, LA, Stefansson, H, Rujescu, D, Cichon, S, Pietiläinen, OPH
Publikováno v:
Nature, 455, 7210, pp. 232-6
Nature, 455, 232-6
Nature, 455(7210), 232-236. Nature Publishing Group
Nature, 455, 232-6
Nature, 455(7210), 232-236. Nature Publishing Group
Reduced fecundity, associated with severe mental disorders, places negative selection pressure on risk alleles and may explain, in part, why common variants have not been found that confer risk of disorders such as autism, schizophrenia and mental re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abe93dab86948eaa9355e125d23ef45b
http://hdl.handle.net/10722/141844
http://hdl.handle.net/10722/141844