Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Fossdal R"'
Autor:
Laaksonen, M. *, Jonasdottir, A., Fossdal, R., Ruutiainen, J., Sawcer, S., Compston, A., Benediktsson, K., Thorlacius, T., Gulcher, J., Ilonen, J.
Publikováno v:
In Journal of Neuroimmunology 2003 143(1):70-73
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:
Stefansson, H., Ophoff, R. A., Steinberg, S., Andreassen, O. A., Chichon, S., Rujescu, D., Werge, T., Pietilainen, O. P., Mors, O., Mortensen, P. B., Sigurdsson, E., Gustafsson, O., Nyegaard, M., Tuulio Henriksson, A., Ingason, A., Hansen, T., Suvisaari, J., Lonnqvist, J., Paunio, T., Borglum, A. D., Hartmann, A., Fink Jensen, A., Nordentoft, M., Hougaard, D., Norgaard Petersen, B., Bottcher, J., Olesen, J., Breuer, R., Moller, H. J., Giegling, I., Rasmussen, H. B., Timm, S., Mattheisen, M., Bitter, I., Rethelyi, J. M., Magnusdottir, B. B., Sigmundsson, T., Olason, P. I., Masson, G., Gulcher, J. R., Haraldsson, M., Fossdal, R., Thorgeirsson, T. E., Thorsteinsdottir, U., Ruggeri, Mirella, Tosato, Sarah, Franke, B., Strengman, E., Kiemeney, L. A., Group, Melle, I., Djurovic, S., Abramova, I., Kaleda, V., Sanjuan, J., de Frutos, R., Bramon, E., Vassos, E., Fraser, G., Ettinger, U., Picchioni, M., Walker, N., Toulopoulou, T., Need, A. C., Ge, D., Lim Yoon, J., Shianna, K. V., Freimer, N. B., Cator, R. M., Murray, R., Kong, A., Golimbet, V., Carracedo, A., Arango, C., Costas, J., Jonsson, E. G., Terenius, L., Agartz, I., Petursson, H., Nothen, M. M., Rietschel, M., Matthews, P. M., Muglia, P., Peltonen, L., St Clair, D., Goldstein, D. B., Collier, D., Genetic, Risk, Outcome in Psychosis, Kahn, R. S., Linszen, D. H., Van Os, J., Wiersma, D., Bruggeman, R., Cahn, H., de Haan, L., Krabbendam, L., Myin Germeys, I.
Publikováno v:
Nature, 460(7256), 744-747. Nature Publishing Group
Nature; Vol
Stefansson, H, Ophoff, R A, Steinberg, S, Andreassen, O A, Rujescu, D, Werge, T, Cichon, S, Pietiläinen, O P H, Mors, O, Mortensen, P B, Sigurdsson, E, Gustafsson, O, Nyegaard, M, Tuulio-Henriksson, A, Ingason, A, Hansen, T, Suvisaari, J, Lonnqvist, J, Paunio, T, Børglum, A, Hartmann, A, Fink-Jensen, A, Nordentoft, M, Hougaard, D, Norgaard-Pedersen, B, Böttcher, Y, Olesen, J, Breuer, R, Möller, H-J, Giegling, I, Rasmussen, H B, Timm, S, Mattheisen, M, Bitter, I, Réthelyi, J M, Sigmundsson, T, Magnusdottir, B B, Olason, P, Masson, G, Gulcher, J R, Haraldsson, M, Fossdal, R, Thorgeirsson, T E, Thorsteinsdottir, U, Ruggeri, M, Tosato, S, Franke, B, Strengman, E, Group, Kiemeney, L A & Genetic Risk and Outcome in Psychosis (GROUP) 2009, ' Common variants conferring risk of schizophrenia ', Nature, vol. 460, no. 7256, pp. 744-747 . https://doi.org/10.1038/nature08186
Stefansson, H & Krabbendam, L 2009, ' Common variants conferring risk of schizophrenia ', Nature, vol. 460, pp. 744-747 . https://doi.org/10.1038/nature08186
Nature, 460, 744-7
Nature, 460, 7256, pp. 744-7
Nature, 460(7256), 744-U99. Nature Publishing Group
Nature
Nature, 460, 744-747. Nature Publishing Group
Nature; Vol
Stefansson, H, Ophoff, R A, Steinberg, S, Andreassen, O A, Rujescu, D, Werge, T, Cichon, S, Pietiläinen, O P H, Mors, O, Mortensen, P B, Sigurdsson, E, Gustafsson, O, Nyegaard, M, Tuulio-Henriksson, A, Ingason, A, Hansen, T, Suvisaari, J, Lonnqvist, J, Paunio, T, Børglum, A, Hartmann, A, Fink-Jensen, A, Nordentoft, M, Hougaard, D, Norgaard-Pedersen, B, Böttcher, Y, Olesen, J, Breuer, R, Möller, H-J, Giegling, I, Rasmussen, H B, Timm, S, Mattheisen, M, Bitter, I, Réthelyi, J M, Sigmundsson, T, Magnusdottir, B B, Olason, P, Masson, G, Gulcher, J R, Haraldsson, M, Fossdal, R, Thorgeirsson, T E, Thorsteinsdottir, U, Ruggeri, M, Tosato, S, Franke, B, Strengman, E, Group, Kiemeney, L A & Genetic Risk and Outcome in Psychosis (GROUP) 2009, ' Common variants conferring risk of schizophrenia ', Nature, vol. 460, no. 7256, pp. 744-747 . https://doi.org/10.1038/nature08186
Stefansson, H & Krabbendam, L 2009, ' Common variants conferring risk of schizophrenia ', Nature, vol. 460, pp. 744-747 . https://doi.org/10.1038/nature08186
Nature, 460, 744-7
Nature, 460, 7256, pp. 744-7
Nature, 460(7256), 744-U99. Nature Publishing Group
Nature
Nature, 460, 744-747. Nature Publishing Group
Schizophrenia is a complex disorder, caused by both genetic and environmental factors and their interactions. Research on pathogenesis has traditionally focused on neurotransmitter systems in the brain, particularly those involving dopamine. Schizoph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95156cb6cb5d1c61a3551a8389841cec
https://pure.amc.nl/en/publications/common-variants-conferring-risk-of-schizophrenia(5f90209e-c7bd-40bc-8b26-3d8a832db709).html
https://pure.amc.nl/en/publications/common-variants-conferring-risk-of-schizophrenia(5f90209e-c7bd-40bc-8b26-3d8a832db709).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
Autor:
Stefansson, H., Rujescu, D., Cichon, S., Pietilainen, O., Ingason, A., Steinberg, S., Fossdal, R., Sigurdsson, E., Sigmundsson, T., Buizer-Voskamp, J., Hansen, T., Jakobsen, K., Muglia, P., Francks, C., Matthews, P., Gylfason, A., Halldorsson, B., Gudbjartsson, D., Thorgeirsson, T., Sigurdsson, A., Jonasdottir, A., Bjornsson, A., Mattiasdottir, S., Blondal, T., Haraldsson, M., Magnusdottir, B., Giegling, I., Möller, H., Hartmann, A., Shianna, K., Ge, D., Need, A., Crombie, C., Fraser, G., Walker, N., Lonnqvist, J., Suvisaari, J., Tuulio-Henriksson, A., Paunio, T., Toulopoulou, T., Bramon, E., Forti, M., Murray, R., Ruggeri, M., Vassos, E., Tosato, S., Walshe, M., Li, T., Vasilescu, C., Muhleisen, T., Wang, A., Ullum, H., Djurovic, S., Melle, I., Olesen, J., Kiemeney, L., Franke, B., Sabatti, C., Freimer, N., Gulcher, J., Thorsteinsdottir, U., Kong, A., Andreassen, O., Ophoff, R., Georgi, A., Rietschel, M., Werge, T., Petursson, H., Goldstein, D., Nothen, M., Peltonen, L., Collier, D., St. Clair, D., Stefansson, K.
Publikováno v:
Nature
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=od______1874::cc62db8b9826b0b5a2e92315196dc1a5
https://hdl.handle.net/11858/00-001M-0000-0012-C93F-611858/00-001M-0000-0012-C93E-8
https://hdl.handle.net/11858/00-001M-0000-0012-C93F-611858/00-001M-0000-0012-C93E-8
Autor:
Peters, D. J. M., Spruit, L., Saris, J. J., Ravine, D., Sandkuijl, L. A., Fossdal, R., Boersma, J., van Eijk, R., Nørby, S., Constantinou-Deltas, Constantinos D., Pierides, Alkis M., Briessenden, J. E., Frants, R. R., van Ommen, G. -J B., Breuning, M. H.
Publikováno v:
Nature genetics
Nat.Genet.
Nat.Genet.
Autosomal dominant polycystic kidney disease (ADPKD) is a genetically heterogeneous disorder. A gene defect located on the short arm of chromosome 16 is responsible for the disease in roughly 86% of affected European families. Using highly polymorphi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33d3d71b3a117a46f8f994a4348c9f7a
http://gnosis.library.ucy.ac.cy/handle/7/53300
http://gnosis.library.ucy.ac.cy/handle/7/53300
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