Common polygenic variation contributes to risk of schizophrenia and bipolardisorder
Autor(a) principal: | |
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Data de Publicação: | 2009 |
Outros Autores: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.3/3997 |
Resumo: | Schizophrenia is a severe mental disorder with a lifetime risk of about 1%, characterized by hallucinations, delusions and cognitive deficits, with heritability estimated at up to 80%. We performed a genome-wide association study of 3,322 European individuals with schizophrenia and 3,587 controls. Here we show, using two analytic approaches, the extent to which common genetic variation underlies the risk of schizophrenia. First, we implicate the major histocompatibility complex. Second, we provide molecular genetic evidence for a substantial polygenic component to the risk of schizophrenia involving thousands of common alleles of very small effect. We show that this component also contributes to the risk of bipolar disorder, but not to several non-psychiatric diseases. |
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Common polygenic variation contributes to risk of schizophrenia and bipolardisorderSchizophreniaPsychiatric DisorderGenome ScansSchizophrenia is a severe mental disorder with a lifetime risk of about 1%, characterized by hallucinations, delusions and cognitive deficits, with heritability estimated at up to 80%. We performed a genome-wide association study of 3,322 European individuals with schizophrenia and 3,587 controls. Here we show, using two analytic approaches, the extent to which common genetic variation underlies the risk of schizophrenia. First, we implicate the major histocompatibility complex. Second, we provide molecular genetic evidence for a substantial polygenic component to the risk of schizophrenia involving thousands of common alleles of very small effect. We show that this component also contributes to the risk of bipolar disorder, but not to several non-psychiatric diseases.Nature Publishing GroupRepositório da Universidade dos AçoresPurcell, S. M.Wray, N. R.Stone, J. L.Visscher, P. M.O'Donovan, M. C.Sullivan, P. F.Sklar, P.Leader, S. M.Ruderfer, D. M.McQuillin, A.Morris, D. W.O'Dushlaine, C. T.Corvin, A.Holmans, P. A.Macgregor, S.Gurling, H.Blackwood, D. H.Craddock, N. J.Gill, M.Hultman, C. M.Kirov, G. K.Lichtenstein, P.Muir, W. J.Owen, M. J.Pato, Carlos N.Scolnick, E. M.St Clair, D.Williams, N. M.Georgieva, L.Nikolov, I.Norton, N.Williams, H.Toncheva, D.Milanova, V.Helander, E. F.Kenny, E.Quinn, E. M.Choudhury, K.Datta, S.Pimm, J.Thirumalai, S.Puri, V.Krasucki, R.Lawrence, J.Quested, D.Bass, N.Crombie, C.Fraser, G.Leh, K. S.Walker, N.Black-wood, D. H.McGhee, K. A.Pickard, B.Malloy, P.Maclean, A. W.Van Beck, M.Pato, Michele T.Medeiros, HelenaMiddleton, Frank A.Carvalho, CéliaMorley, C.Fanous, Ayman H.Conti, D.Knowles, James A.Ferreira, Carlos PazMacedo, AntónioKirby, A. N.Ferreira, M. A.Daly, M. J.Cham-bert, K.Kuruvilla, F.Gabriel, S. B.Ardlie, K.Moran, J. L.2017-02-24T18:21:46Z20092009-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.3/3997engPurcell, S.M., Wray, N.R., Stone, J.L., Visscher, P.M., O'Donovan, M.C., Sullivan, P.F., Sklar, P., Purcell., Leader, S.M., Ruderfer, D.M., McQuillin, A., Morris, D.W., O'Dushlaine, C.T., Corvin, A., Holmans, P.A., Macgregor, S., Gurling, H., Blackwood, D.H., Craddock, N.J., Gill, M., Hultman, C.M., Kirov, G.K., Lichtenstein, P., Muir, W.J., Owen, M.J., Pato, C.N., Scolnick, E.M., St Clair, D, Williams, N.M., Georgieva, L., Nikolov, I., Norton, N., Williams, H., Toncheva, D., Milanova, V., Thelander, E.F., Kenny ,E., Quinn, E.M., Choudhury, K., Datta, S., Pimm, J., Thirumalai, S., Puri, V., Krasucki, R., Lawrence, J., Quested, D., Bass, N., Crombie, C., Fraser, G., Leh, K.S., Walker, N., Black-Wood, D.H., McGhee, K.A., Pickard, B., Malloy, P., Maclean, A.W., Van Beck, M., Pato, M.T., Medeiros, H., Middleton, F., Carvalho, C., Morley, C., Fanous, A., Conti, D., Knowles, J.A., Paz, F.C., Macedo, A., Helena, A.M., Kirby, A.N., Ferreira, M.A., Daly, M.J., Cham-bert, K., Kuruvilla, F., Gabriel, S.B., Ardlie, K. & Moran, J.L. (2009). Common polygenic variation contributes to risk of schizophrenia and bipolardisorder. "Nature", 460(7256), 748-752.1476-4687 (Online)10.1038/nature08185metadata only accessinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-12-20T14:32:11Zoai:repositorio.uac.pt:10400.3/3997Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:26:30.949446Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Common polygenic variation contributes to risk of schizophrenia and bipolardisorder |
title |
Common polygenic variation contributes to risk of schizophrenia and bipolardisorder |
spellingShingle |
Common polygenic variation contributes to risk of schizophrenia and bipolardisorder Purcell, S. M. Schizophrenia Psychiatric Disorder Genome Scans |
title_short |
Common polygenic variation contributes to risk of schizophrenia and bipolardisorder |
title_full |
Common polygenic variation contributes to risk of schizophrenia and bipolardisorder |
title_fullStr |
Common polygenic variation contributes to risk of schizophrenia and bipolardisorder |
title_full_unstemmed |
Common polygenic variation contributes to risk of schizophrenia and bipolardisorder |
title_sort |
Common polygenic variation contributes to risk of schizophrenia and bipolardisorder |
author |
Purcell, S. M. |
author_facet |
Purcell, S. M. Wray, N. R. Stone, J. L. Visscher, P. M. O'Donovan, M. C. Sullivan, P. F. Sklar, P. Leader, S. M. Ruderfer, D. M. McQuillin, A. Morris, D. W. O'Dushlaine, C. T. Corvin, A. Holmans, P. A. Macgregor, S. Gurling, H. Blackwood, D. H. Craddock, N. J. Gill, M. Hultman, C. M. Kirov, G. K. Lichtenstein, P. Muir, W. J. Owen, M. J. Pato, Carlos N. Scolnick, E. M. St Clair, D. Williams, N. M. Georgieva, L. Nikolov, I. Norton, N. Williams, H. Toncheva, D. Milanova, V. Helander, E. F. Kenny, E. Quinn, E. M. Choudhury, K. Datta, S. Pimm, J. Thirumalai, S. Puri, V. Krasucki, R. Lawrence, J. Quested, D. Bass, N. Crombie, C. Fraser, G. Leh, K. S. Walker, N. Black-wood, D. H. McGhee, K. A. Pickard, B. Malloy, P. Maclean, A. W. Van Beck, 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 Kirby, A. N. Ferreira, M. A. Daly, M. J. Cham-bert, K. Kuruvilla, F. Gabriel, S. B. Ardlie, K. Moran, J. L. |
author_role |
author |
author2 |
Wray, N. R. Stone, J. L. Visscher, P. M. O'Donovan, M. C. Sullivan, P. F. Sklar, P. Leader, S. M. Ruderfer, D. M. McQuillin, A. Morris, D. W. O'Dushlaine, C. T. Corvin, A. Holmans, P. A. Macgregor, S. Gurling, H. Blackwood, D. H. Craddock, N. J. Gill, M. Hultman, C. M. Kirov, G. K. Lichtenstein, P. Muir, W. J. Owen, M. J. Pato, Carlos N. Scolnick, E. M. St Clair, D. Williams, N. M. Georgieva, L. Nikolov, I. Norton, N. Williams, H. Toncheva, D. Milanova, V. Helander, E. F. Kenny, E. Quinn, E. M. Choudhury, K. Datta, S. Pimm, J. Thirumalai, S. Puri, V. Krasucki, R. Lawrence, J. Quested, D. Bass, N. Crombie, C. Fraser, G. Leh, K. S. Walker, N. Black-wood, D. H. McGhee, K. A. Pickard, B. Malloy, P. Maclean, A. W. Van Beck, 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 Kirby, A. N. Ferreira, M. A. Daly, M. J. Cham-bert, K. Kuruvilla, F. Gabriel, S. B. Ardlie, K. Moran, J. L. |
author2_role |
author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Repositório da Universidade dos Açores |
dc.contributor.author.fl_str_mv |
Purcell, S. M. Wray, N. R. Stone, J. L. Visscher, P. M. O'Donovan, M. C. Sullivan, P. F. Sklar, P. Leader, S. M. Ruderfer, D. M. McQuillin, A. Morris, D. W. O'Dushlaine, C. T. Corvin, A. Holmans, P. A. Macgregor, S. Gurling, H. Blackwood, D. H. Craddock, N. J. Gill, M. Hultman, C. M. Kirov, G. K. Lichtenstein, P. Muir, W. J. Owen, M. J. Pato, Carlos N. Scolnick, E. M. St Clair, D. Williams, N. M. Georgieva, L. Nikolov, I. Norton, N. Williams, H. Toncheva, D. Milanova, V. Helander, E. F. Kenny, E. Quinn, E. M. Choudhury, K. Datta, S. Pimm, J. Thirumalai, S. Puri, V. Krasucki, R. Lawrence, J. Quested, D. Bass, N. Crombie, C. Fraser, G. Leh, K. S. Walker, N. Black-wood, D. H. McGhee, K. A. Pickard, B. Malloy, P. Maclean, A. W. Van Beck, 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 Kirby, A. N. Ferreira, M. A. Daly, M. J. Cham-bert, K. Kuruvilla, F. Gabriel, S. B. Ardlie, K. Moran, J. L. |
dc.subject.por.fl_str_mv |
Schizophrenia Psychiatric Disorder Genome Scans |
topic |
Schizophrenia Psychiatric Disorder Genome Scans |
description |
Schizophrenia is a severe mental disorder with a lifetime risk of about 1%, characterized by hallucinations, delusions and cognitive deficits, with heritability estimated at up to 80%. We performed a genome-wide association study of 3,322 European individuals with schizophrenia and 3,587 controls. Here we show, using two analytic approaches, the extent to which common genetic variation underlies the risk of schizophrenia. First, we implicate the major histocompatibility complex. Second, we provide molecular genetic evidence for a substantial polygenic component to the risk of schizophrenia involving thousands of common alleles of very small effect. We show that this component also contributes to the risk of bipolar disorder, but not to several non-psychiatric diseases. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009 2009-01-01T00:00:00Z 2017-02-24T18:21:46Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.3/3997 |
url |
http://hdl.handle.net/10400.3/3997 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Purcell, S.M., Wray, N.R., Stone, J.L., Visscher, P.M., O'Donovan, M.C., Sullivan, P.F., Sklar, P., Purcell., Leader, S.M., Ruderfer, D.M., McQuillin, A., Morris, D.W., O'Dushlaine, C.T., Corvin, A., Holmans, P.A., Macgregor, S., Gurling, H., Blackwood, D.H., Craddock, N.J., Gill, M., Hultman, C.M., Kirov, G.K., Lichtenstein, P., Muir, W.J., Owen, M.J., Pato, C.N., Scolnick, E.M., St Clair, D, Williams, N.M., Georgieva, L., Nikolov, I., Norton, N., Williams, H., Toncheva, D., Milanova, V., Thelander, E.F., Kenny ,E., Quinn, E.M., Choudhury, K., Datta, S., Pimm, J., Thirumalai, S., Puri, V., Krasucki, R., Lawrence, J., Quested, D., Bass, N., Crombie, C., Fraser, G., Leh, K.S., Walker, N., Black-Wood, D.H., McGhee, K.A., Pickard, B., Malloy, P., Maclean, A.W., Van Beck, M., Pato, M.T., Medeiros, H., Middleton, F., Carvalho, C., Morley, C., Fanous, A., Conti, D., Knowles, J.A., Paz, F.C., Macedo, A., Helena, A.M., Kirby, A.N., Ferreira, M.A., Daly, M.J., Cham-bert, K., Kuruvilla, F., Gabriel, S.B., Ardlie, K. & Moran, J.L. (2009). Common polygenic variation contributes to risk of schizophrenia and bipolardisorder. "Nature", 460(7256), 748-752. 1476-4687 (Online) 10.1038/nature08185 |
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metadata only access info:eu-repo/semantics/openAccess |
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metadata only access |
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openAccess |
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application/pdf |
dc.publisher.none.fl_str_mv |
Nature Publishing Group |
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Nature Publishing Group |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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