المؤلفون: Stahl E. A., Breen G., Forstner A. J., McQuillin A., Ripke S., Trubetskoy V., Mattheisen M., Wang Y., Coleman J. R. I., Gaspar H. A., de Leeuw C. A., Steinberg S., Pavlides J. M. W., Trzaskowski M., Byrne E. M., Pers T. H., Holmans P. A., Richards A. L., Abbott L., Agerbo E., Akil H., Albani D., Alliey-Rodriguez N., Als T. D., Anjorin A., Antilla V., Awasthi S., Badner J. A., Baekvad-Hansen M., Barchas J. D., Bass N., Bauer M., Belliveau R., Bergen S. E., Pedersen C. B., Boen E., Boks M. P., Boocock J., Budde M., Bunney W., Burmeister M., Bybjerg-Grauholm J., Byerley W., Casas M., Cerrato F., Cervantes P., Chambert K., Charney A. W., Chen D., Churchhouse C., Clarke T. -K., Coryell W., Craig D. W., Cruceanu C., Curtis D., Czerski P. M., Dale A. M., de Jong S., Degenhardt F., Del-Favero J., DePaulo J. R., Djurovic S., Dobbyn A. L., Dumont A., Elvsashagen T., Escott-Price V., Fan C. C., Fischer S. B., Flickinger M., Foroud T. M., Forty L., Frank J., Fraser C., Freimer N. B., Frisen L., Gade K., Gage D., Garnham J., Giambartolomei C., Pedersen M. G., Goldstein J., Gordon S. D., Gordon-Smith K., Green E. K., Green M. J., Greenwood T. A., Grove J., Guan W., Guzman-Parra J., Hamshere M. L., Hautzinger M., Heilbronner U., Herms S., Hipolito M., Hoffmann P., Holland D., Huckins L., Jamain S., Johnson J. S., Jureus A., Kandaswamy R., Karlsson R., Kennedy J. L., Kittel-Schneider S., Knowles J. A., Kogevinas M., Koller A. C., Kupka R., Lavebratt C., Lawrence J., Lawson W. B., Leber M., Lee P. H., Levy S. E., Li J. Z., Liu C., Lucae S., Maaser A., MacIntyre D. J., Mahon P. B., Maier W., Martinsson L., McCarroll S., McGuffin P., McInnis M. G., McKay J. D., Medeiros H., Medland S. E., Meng F., Milani L., Montgomery G. W., Morris D. W., Muhleisen T. W., Mullins N., Nguyen H., Nievergelt C. M., Adolfsson A. N., Nwulia E. A., O'Donovan C., Loohuis L. M. O., Ori A. P. S., Oruc L., Osby U., Perlis R. H., Perry A., Pfennig A., Potash J. B., Purcell S. M., Regeer E. J., Reif A., Reinbold C. S., Rice J. P., Rivas F., Rivera M., Roussos P., Ruderfer D. M., Ryu E., Sanchez-Mora C., Schatzberg A. F., Scheftner W. A., Schork N. J., Shannon Weickert C., Shehktman T., Shilling P. D., Sigurdsson E., Slaney C., Smeland O. B., Sobell J. L., Soholm Hansen C., Spijker A. T., St Clair D., Steffens M., Strauss J. S., Streit F., Strohmaier J., Szelinger S., Thompson R. C., Thorgeirsson T. E., Treutlein J., Vedder H., Wang W., Watson S. J., Weickert T. W., Witt S. H., Xi S., Xu W., Young A. H., Zandi P., Zhang P., Zollner S., Adolfsson R., Agartz I., Alda M., Backlund L., Baune B. T., Bellivier F., Berrettini W. H., Biernacka J. M., Blackwood D. H. R., Boehnke M., Borglum A. D., Corvin A., Craddock N., Daly M. J., Dannlowski U., Esko T., Etain B., Frye M., Fullerton J. M., Gershon E. S., Gill M., Goes F., Grigoroiu-Serbanescu M., Hauser J., Hougaard D. M., Hultman C. M., Jones I., Jones L. A., Kahn R. S., Kirov G., Landen M., Leboyer M., Lewis C. M., Li Q. S., Lissowska J., Martin N. G., Mayoral F., McElroy S. L., McIntosh A. M., McMahon F. J., Melle I., Metspalu A., Mitchell P. B., Morken G., Mors O., Mortensen P. B., Muller-Myhsok B., Myers R. M., Neale B. M., Nimgaonkar V., Nordentoft M., Nothen M. M., O'Donovan M. C., Oedegaard K. J., Owen M. J., Paciga S. A., Pato C., Pato M. T., Posthuma D., Ramos-Quiroga J. A., Ribases M., Rietschel M., Rouleau G. A., Schalling M., Schofield P. R., Schulze T. G., Serretti A., Smoller J. W., Stefansson H., Stefansson K., Stordal E., Sullivan P. F., Turecki G., Vaaler A. E., Vieta E., Vincent J. B., Werge T., Nurnberger J. I., Wray N. R., Di Florio A., Edenberg H. J., Cichon S., Ophoff R. A., Scott L. J., Andreassen O. A., Kelsoe J., Sklar P.

المساهمون: Stahl E.A., Breen G., Forstner A.J., McQuillin A., Ripke S., Trubetskoy V., Mattheisen M., Wang Y., Coleman J.R.I., Gaspar H.A., de Leeuw C.A., Steinberg S., Pavlides J.M.W., Trzaskowski M., Byrne E.M., Pers T.H., Holmans P.A., Richards A.L., Abbott L., Agerbo E., Akil H., Albani D., Alliey-Rodriguez N., Als T.D., Anjorin A., Antilla V., Awasthi S., Badner J.A., Baekvad-Hansen M., Barchas J.D., Bass N., Bauer M., Belliveau R., Bergen S.E., Pedersen C.B., Boen E., Boks M.P., Boocock J., Budde M., Bunney W., Burmeister M., Bybjerg-Grauholm J., Byerley W., Casas M., Cerrato F., Cervantes P., Chambert K., Charney A.W., Chen D., Churchhouse C., Clarke T.-K., Coryell W., Craig D.W., Cruceanu C., Curtis D., Czerski P.M., Dale A.M., de Jong S., Degenhardt F., Del-Favero J., DePaulo J.R., Djurovic S., Dobbyn A.L., Dumont A., Elvsashagen T., Escott-Price V., Fan C.C., Fischer S.B., Flickinger M., Foroud T.M., Forty L., Frank J., Fraser C., Freimer N.B., Frisen L., Gade K., Gage D., Garnham J., Giambartolomei C., Pedersen M.G., Goldstein J., Gordon S.D., Gordon-Smith K., Green E.K., Green M.J., Greenwood T.A., Grove J., Guan W., Guzman-Parra J., Hamshere M.L., Hautzinger M., Heilbronner U., Herms S., Hipolito M., Hoffmann P., Holland D., Huckins L., Jamain S., Johnson J.S., Jureus A.

مصطلحات موضوعية: Bipolar Disorder, Case-Control Studie, Depressive Disorder, Major, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Human, Male, Polymorphism, Single Nucleotide, Psychotic Disorder, Schizophrenia, Systems Biology, Genetic Loci

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31043756; info:eu-repo/semantics/altIdentifier/wos/WOS:000466842000007; volume:51; issue:5; firstpage:793; lastpage:803; numberofpages:11; journal:NATURE GENETICS; http://hdl.handle.net/11585/714018Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85065180508; http://www.nature.com/ng/index.htmlTest

الإتاحة: https://doi.org/10.1038/s41588-019-0397-8Test
http://hdl.handle.net/11585/714018Test
http://www.nature.com/ng/index.htmlTest

المؤلفون: Satterstrom F. K., Kosmicki J. A., Wang J., Breen M. S., De Rubeis S., An J. -Y., Peng M., Collins R., Grove J., Klei L., Stevens C., Reichert J., Mulhern M. S., Artomov M., Gerges S., Sheppard B., Xu X., Bhaduri A., Norman U., Brand H., Schwartz G., Nguyen R., Guerrero E. E., Dias C., Aleksic B., Anney R., Barbosa M., Bishop S., Brusco A., Bybjerg-Grauholm J., Carracedo A., Chan M. C. Y., Chiocchetti A. G., Chung B. H. Y., Coon H., Cuccaro M. L., Curro A., Dalla Bernardina B., Doan R., Domenici E., Dong S., Fallerini C., Fernandez-Prieto M., Ferrero G. B., Freitag C. M., Fromer M., Gargus J. J., Geschwind D., Giorgio E., Gonzalez-Penas J., Guter S., Halpern D., Hansen-Kiss E., He X., Herman G. E., Hertz-Picciotto I., Hougaard D. M., Hultman C. M., Ionita-Laza I., Jacob S., Jamison J., Jugessur A., Kaartinen M., Knudsen G. P., Kolevzon A., Kushima I., Lee S. L., Lehtimaki T., Lim E. T., Lintas C., Lipkin W. I., Lopergolo D., Lopes F., Ludena Y., Maciel P., Magnus P., Mahjani B., Maltman N., Manoach D. S., Meiri G., Menashe I., Miller J., Minshew N., Montenegro E. M. S., Moreira D., Morrow E. M., Mors O., Mortensen P. B., Mosconi M., Muglia P., Neale B. M., Nordentoft M., Ozaki N., Palotie A., Parellada M., Passos-Bueno M. R., Pericak-Vance M., Persico A. M., Pessah I., Puura K., Reichenberg A., Renieri A., Riberi E., Robinson E. B., Samocha K. E., Sandin S., Santangelo S. L., Schellenberg G., Scherer S. W., Schlitt S., Schmidt R., Schmitt L., Silva I. M. W., Singh T., Siper P. M., Smith M., Soares G., Stoltenberg C., Suren P., Susser E., Sweeney J., Szatmari P., Tang L., Tassone F., Teufel K., Trabetti E., Trelles M. D. P., Walsh C. A., Weiss L. A., Werge T., Werling D. M., Wigdor E. M., Wilkinson E., Willsey A. J., Yu T. W., Yu M. H. C., Yuen R., Zachi E., Agerbo E., Als T. D., Appadurai V., Baekvad-Hansen M., Belliveau R., Buil A., Carey C. E., Cerrato F., Chambert K., Churchhouse C., Dalsgaard S., Demontis D., Dumont A., Goldstein J., Hansen C. S., Hauberg M. E., Hollegaard M. V., Howrigan D. P., Huang H., Maller J., Martin A. R., Martin J., Mattheisen M., Moran J., Pallesen J., Palmer D. S., Pedersen C. B., Pedersen M. G., Poterba T., Poulsen J. B., Ripke S., Schork A. J., Thompson W. K., Turley P., Walters R. K., Betancur C., Cook E. H., Gallagher L., Gill M., Sutcliffe J. S., Thurm A., Zwick M. E., Borglum A. D., State M. W., Cicek A. E., Talkowski M. E., Cutler D. J., Devlin B., Sanders S. J., Roeder K., Daly M. J., Buxbaum J. D.

المساهمون: Satterstrom, F. K., Kosmicki, J. A., Wang, J., Breen, M. S., De Rubeis, S., An, J. -Y., Peng, M., Collins, R., Grove, J., Klei, L., Stevens, C., Reichert, J., Mulhern, M. S., Artomov, M., Gerges, S., Sheppard, B., Xu, X., Bhaduri, A., Norman, U., Brand, H., Schwartz, G., Nguyen, R., Guerrero, E. E., Dias, C., Aleksic, B., Anney, R., Barbosa, M., Bishop, S., Brusco, A., Bybjerg-Grauholm, J., Carracedo, A., Chan, M. C. Y., Chiocchetti, A. G., Chung, B. H. Y., Coon, H., Cuccaro, M. L., Curro, A., Dalla Bernardina, B., Doan, R., Domenici, E., Dong, S., Fallerini, C., Fernandez-Prieto, M., Ferrero, G. B., Freitag, C. M., Fromer, M., Gargus, J. J., Geschwind, D., Giorgio, E., Gonzalez-Penas, J., Guter, S., Halpern, D., Hansen-Kiss, E., He, X., Herman, G. E., Hertz-Picciotto, I., Hougaard, D. M., Hultman, C. M., Ionita-Laza, I., Jacob, S., Jamison, J., Jugessur, A., Kaartinen, M., Knudsen, G. P., Kolevzon, A., Kushima, I., Lee, S. L., Lehtimaki, T., Lim, E. T., Lintas, C., Lipkin, W. I., Lopergolo, D., Lopes, F., Ludena, Y., Maciel, P., Magnus, P., Mahjani, B., Maltman, N., Manoach, D. S., Meiri, G., Menashe, I., Miller, J., Minshew, N., Montenegro, E. M. S., Moreira, D., Morrow, E. M., Mors, O., Mortensen, P. B., Mosconi, M., Muglia, P., Neale, B. M., Nordentoft, M., Ozaki, N., Palotie, A., Parellada, M., Passos-Bueno, M. R., Pericak-Vance, M., Persico, A. M., Pessah, I., Puura, K.

مصطلحات موضوعية: autism spectrum disorder, cell type, cytoskeleton, excitatory neuron, excitatory-inhibitory balance, exome sequencing, genetic, inhibitory neuron, liability, neurodevelopment, Autistic Disorder, Case-Control Studie, Cell Lineage, Cerebral Cortex, Cohort Studie, Exome, Female, Gene Frequency, Genetic Predisposition to Disease, Human, Male, Mutation, Missense, Neurobiology, Neuron, Phenotype, Sex Factor, Single-Cell Analysi, Whole Exome Sequencing, Gene Expression Regulation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31981491; info:eu-repo/semantics/altIdentifier/wos/WOS:000512977500012; volume:180; issue:3; firstpage:568; lastpage:584.e23; journal:CELL; http://hdl.handle.net/11365/1133708Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85078664833

الإتاحة: https://doi.org/10.1016/j.cell.2019.12.036Test
http://hdl.handle.net/11365/1133708Test

المؤلفون: Grove, J., Ripke, S., Als, T.D., Mattheisen, M., Walters, R.K., Won, H., Pallesen, J., Agerbo, E., Andreassen, O.A., Anney, R., Awashti, S., Belliveau, R., Bettella, F., Buxbaum, J.D., Bybjerg-Grauholm, J., Baekvad-Hansen, M., Cerrato, F., Chambert, K., Christensen, J.H., Churchhouse, C., Dellenvall, K., Demontis, D., Rubeis, S. de, Devlin, B., Djurovic, S., Dumont, A.L., Goldstein, J.I., Hansen, C.S., Hauberg, M.E., Hollegaard, M.V., Hope, S., Howrigan, D.P., Huang, H., Hultman, C.M., Klei, L., Maller, J., Martin, J., Martin, A.R., Moran, J.L., Nyegaard, M., Naeland, T., Palmer, D.S., Palotie, A., Pedersen, C.B., Pedersen, M.G., dPoterba, T., Poulsen, J.B., St Pourcain, B., Qvist, P., Rehnstrom, K., Reichenberg, A., Reichert, J., Robinson, E.B., Roeder, K., Roussos, P., Saemundsen, E., Sandin, S., Satterstrom, F.K., Smith, G.D., Stefansson, H., Steinberg, S., Stevens, C.R., Sullivan, P.F., Turley, P., Walters, G.B., Xu, X.Y., Stefansson, K., Geschwind, D.H., Nordentoft, M., Hougaard, D.M., Werge, T., Mors, O., Mortensen, P.B., Neale, B.M., Daly, M.J., Borglum, A.D., Wray, N.R., Trzaskowski, M., Byrne, E.M., Abdellaoui, A., Adams, M.J., Air, T.M., Andlauer, T.F.M., Bacanu, S.A., Beekman, A.T.F., Bigdeli, T.B., Binder, E.B., Blackwood, D.H.R., Bryois, J., Buttenschon, H.N., Cai, N., Castelao, E., Clarke, T.K., Coleman, J.R.I., Colodro-Conde, L., Couvy-Duchesne, B., Craddock, N., Crawford, G.E., Davies, G., Deary, I.J., Degenhardt, F., Derks, E.M., Direk, N., Dolan, C.V., Dunn, E.C., Eley, T.C., Escott-Price, V., Kiadeh, F.F.H., Finucane, H.K., Forstner, A.J., Frank, J., Gaspar, H.A., Gill, M., Goes, F.S., Gordon, S.D., Hall, L.S., Hansen, T.F., Herms, S., Hickie, I.B., Hoffmann, P., Homuth, G., Horn, C., Hottenga, J.J., Ising, M., Jansen, R., Jorgenson, E., Knowles, J.A., Kohane, I.S., Kraft, J., Kretzschmar, W.W., Krogh, J., Kutalik, Z., Li, Y., Lind, P.A., MacIntyre, D.J., MacKinnon, D.F., Maier, R.M., Maier, W., Marchini, J., Mbarek, H., McGrath, P., McGuffin, P., Medland, S.E., Mehta, D., Middeldorp, C.M., Mihailov, E., Milaneschi, Y., Milani, L., Mondimore, F.M., Montgomery, G.W., Mostafavi, S., Mullins, N., Nauck, M., Ng, B., Nivard, M.G., Nyholt, D.R., O'Reilly, P.F., Oskarsson, H., Owen, M.J., Painter, J.N., Peterson, R.E., Pettersson, E., Peyrot, W.J., Pistis, G., Posthuma, D., Quiroz, J.A., Rice, J.P., Riley, B.P., Rivera, M., Mirza, S.S., Schoevers, R., Schulte, E.C., Shen, L., Shi, J.X., Shyn, S.I., Sigurdsson, E., Sinnamon, G.C.B., Smit, J.H., Smith, D.J., Streit, F., Strohmaier, J., Tansey, K.E., Teismann, H., Teumer, A., Thompson, W., Thomson, P.A., Thorgeirsson, T.E., Traylor, M., Treutlein, J., Trubetskoy, V., Uitterlinden, A.G., Umbricht, D., Auwera, S. van der, Hemert, A.M. van, Viktorin, A., Visscher, P.M., Wang, Y.P., Webb, B.T., Weinsheimer, S.M., Wellmann, J., Willemsen, G., Witt, S.H., Wu, Y., Xi, H.S., Yang, J., Zhang, F.T., Arolt, V., Baune, B.T., Berger, K., Boomsma, D.I., Cichon, S., Dannlowski, U., Geus, E.J.C. de, DePaulo, J.R., Domenici, E., Domschke, K., Esko, T., Grabe, H.J., Hamilton, S.P., Hayward, C., Heath, A.C., Kendler, K.S., Kloiber, S., Lewis, G., Li, Q.S., Lucae, S., Madden, P.A.F., Magnusson, P.K., Martin, N.G., McIntosh, A.M., Metspalu, A., Muller-Myhsok, B., Nothen, M.M., O'Donovan, M.C., Paciga, S.A., Pedersen, N.L., Penninx, B.W.J.H., Perlis, R.H., Porteous, D.J., Potash, J.B., Preisig, M., Rietschel, M., Schaefer, C., Schulze, T.G., Smoller, J.W., Tiemeier, H., Uher, R., Volzke, H., Weissman, M.M., Lewis, C.M., Levinson, D.F., Breen, G., Agee, M., Alipanahi, B., Auton, A., Bell, R.K., Bryc, K., Elson, S.L., Fontanillas, P., Furlotte, N.A., Hromatka, B.S., Huber, K.E., Kleinman, A., Litterman, N.K., McIntyre, M.H., Mountain, J.L., Noblin, E.S., Northover, C.A.M., Pitts, S.J., Sathirapongsasuti, J.F., Sazonova, O.V., Shelton, J.F., Shringarpure, S., Tung, J.Y., Vacic, V., Wilson, C.H., Psychiat Genomics Consortium, BUPGEN, 23andMe Re

المساهمون: Biological Psychology, APH - Methodology, APH - Health Behaviors & Chronic Diseases, APH - Personalized Medicine, APH - Mental Health, Complex Trait Genetics, Amsterdam Neuroscience - Complex Trait Genetics, Adult Psychiatry, Psychiatry, Human genetics, Amsterdam Reproduction & Development (AR&D), VU University medical center, APH - Digital Health, Aarno Palotie / Principal Investigator, Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders, Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), Perceptual and Cognitive Neuroscience (PCN), Clinical Cognitive Neuropsychiatry Research Program (CCNP), Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium, BUPGEN, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Me Research Team, Epidemiology, Child and Adolescent Psychiatry / Psychology

المصدر: NATURE GENETICS
Nature Genetics, 51(3), 431-444. Nature Publishing Group
Grove, J, Ripke, S, Als, T D, Mattheisen, M, Walters, R K, Won, H, Pallesen, J, Agerbo, E, Andreassen, O A, Anney, R, Awashti, S, Belliveau, R, Bettella, F, Buxbaum, J D, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Christensen, J H, Churchhouse, C, Dellenvall, K, Demontis, D, De Rubeis, S, Devlin, B, Djurovic, S, Dumont, A L, Goldstein, J I, Hansen, C S, Hauberg, M E, Hollegaard, M V, Hope, S, Howrigan, D P, Huang, H, Hultman, C M, Klei, L, Maller, J, Martin, J, Pedersen, C B, Davey Smith, G, Pourcain, B S & the 23 and Me Research Team 2019, ' Identification of common genetic risk variants for autism spectrum disorder ', Nature Genetics, vol. 51, no. 3, pp. 431-444 . https://doi.org/10.1038/s41588-019-0344-8Test
Nature genetics, 51(3), 431-444. Nature Publishing Group
Maller, J, Martin, J, Martin, A, Moran, J, Nyegaard, M, Naerland, T, Palmer, D, Palotie, A, Bocker Perdersen, C, Giortz Pedersen, M, dPoterba, T, Buchhave Poulsen, J, St Poucain, B, Qvist, P, Rehnstrom, K, Reichenberg, A, Reichert, J, Robinson, E B, Roeder, K, Roussos, P, Saemundsen, E, Sandin, S, Satterstrom, F K, Smith, G D, Stefansson, H, Steinberg, S, Stevens, C R, Sullivan, P F, Turley, P, Walters, G B, Xu, X, Stefansson, K, Geschwind, D H, Nordentoft, M, Hougaard, D M, Werge, T, Mors, O & Mortensen, P B & Neale, B M & Daly, M J & Borglum, A D 2019, ' Identification of common genetic risk variants for autism spectrum disorder ', Nature Genetics, vol. 51, no. 3, pp. 431-+ . https://doi.org/10.1038/s41588-019-0344-8Test
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Grove, J, Abdellaoui, A, Derks, E M, Dolan, C V, Hottenga, J J, Jansen, R, Mbarek, H, Middeldorp, C M, Milaneschi, Y, Nivard, M G, Posthuma, D, Willemsen, G, Boomsma, D I, de Geus, E J C, Penninx, B W J H, Børglum, A D, Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium, BUPGEN, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium & 23Andme Research Team 2019, ' Identification of common genetic risk variants for autism spectrum disorder ', Nature Genetics, vol. 51, no. 3, pp. 431-444 . https://doi.org/10.1038/s41588-019-0344-8Test
Nature Genetics
Nature Genetics, 51(3), 431-+. Nature Publishing Group
Grove, J, Ripke, S, Als, T D, Mattheisen, M, Walters, R K, Won, H, Pallesen, J, Agerbo, E, Andreassen, O A, Anney, R, Awashti, S, Belliveau, R, Bettella, F, Buxbaum, J D, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Christensen, J H, Churchhouse, C, Dellenvall, K, Demontis, D, de Rubeis, S, Devlin, B, Djurovic, S, Dumont, A L, Goldstein, J I, Hansen, C S, Hauberg, M E, Hollegaard, M V, Beekman, A T F, Jansen, R, Middeldorp, C M, Milaneschi, Y, Peyrot, W J, Posthuma, D, Schoevers, R, Smit, J H, de Geus, E J C, Smit, J H, de Geus, E J C, Penninx, B W J H, Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium, Stefansson, K, Geschwind, D H, Nordentoft, M, Hougaard, D M, Werge, T, Mors, O, Bo Mortensen, P, Neale, B M, Daly, M J & Børglum, A D 2019, ' Identification of common genetic risk variants for autism spectrum disorder ', Nature Genetics, vol. 51, no. 3, pp. 431-444 . https://doi.org/10.1038/s41588-019-0344-8Test
Nature Genetics, 51(3), 431-+. NATURE PUBLISHING GROUP
Grove, J, Ripke, S, Als, T D, Mattheisen, M, Walters, R K, Won, H, Pallesen, J, Agerbo, E, Andreassen, O A, Anney, R, Awashti, S, Belliveau, R, Bettella, F, Buxbaum, J D, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Christensen, J H, Churchhouse, C, Dellenvall, K, Demontis, D, De Rubeis, S, Devlin, B, Djurovic, S, Dumont, A L, Goldstein, J I, Hansen, C S, Hauberg, M E, Hollegaard, M V, Hope, S, Howrigan, D P, Huang, H, Hultman, C M, Klei, L, Maller, J, Martin, J, Martin, A R, Moran, J L, Nyegaard, M, Nærland, T, Palmer, D S, Palotie, A, Pedersen, C B, Pedersen, M G, dPoterba, T, Poulsen, J B, Pourcain, B S, Qvist, P, Rehnström, K, Reichenberg, A, Reichert, J, Robinson, E B, Roeder, K, Roussos, P, Saemundsen, E, Sandin, S, Satterstrom, F K, Smith, G D, Stefansson, H, Steinberg, S, Stevens, C, Sullivan, P F, Turley, P, Walters, G B, Xu, X, Autism Spectrum Disorder Working Group of the Psychiatric Genomics Consortium, BUPGEN, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 23andMe Research Team, Stefansson, K, Geschwind, D H, Nordentoft, M, Hougaard, D M, Werge, T, Mors, O, Mortensen, P B, Neale, B M, Daly, M J & Børglum, A D 2019, ' Identification of common genetic risk variants for autism spectrum disorder ', Nature Genetics, vol. 51, no. 3, pp. 431-444 . https://doi.org/10.1038/s41588-019-0344-8Test

مصطلحات موضوعية: Male, Netherlands Twin Register (NTR), Multifactorial Inheritance, Autism Spectrum Disorder, Denmark, LD SCORE REGRESSION, LOCI, Genome-wide association study, DE-NOVO, 0302 clinical medicine, Polymorphism (computer science), Risk Factors, SYNAPTIC PLASTICITY, CELL-SURFACE, Child, Genetics, 0303 health sciences, HERITABILITY, Genetic Predisposition to Disease/genetics, 1184 Genetics, developmental biology, physiology, Polymorphism, Single Nucleotide/genetics, Phenotype, 3. Good health, Schizophrenia, Autism spectrum disorder, Child, Preschool, Genome-Wide Association Study/methods, Female, SIMONS SIMPLEX COLLECTION, Adolescent, Biology, NEURITE OUTGROWTH, Polymorphism, Single Nucleotide, behavioral disciplines and activities, Article, 03 medical and health sciences, mental disorders, medicine, Humans, Genetic Predisposition to Disease, GENOME-WIDE ASSOCIATION, SDG 2 - Zero Hunger, Multifactorial Inheritance/genetics, METAANALYSIS, 030304 developmental biology, Case-control study, Heritability, medicine.disease, Autism Spectrum Disorder/genetics, Case-Control Studies, 3111 Biomedicine, 030217 neurology & neurosurgery, Genome-Wide Association Study

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http://livrepository.liverpool.ac.uk/3045243/1/_NG-A47659R1_Borglum_Edver_1543433314_1_1543434422_1_final20181204.docxTest

المؤلفون: Demontis, D, Walters, R, Martin, J, Mattheisen, M, Als, T, Agerbo, E, Baldursson, G, Belliveau, R, Bybjerg-Grauholm, J, Baekvad-Hansen, M, Cerrato, F, Chambert, K, Churchhouse, C, Dumont, A, Eriksson, N, Gandal, M, Goldstein, J, Grasby, K, Grove, J, Gudmundsson, O, Hansen, C, Hauberg, M, Hollegaard, M, Howrigan, D, Huang, H, Maller, J, Martin, A, Martin, N, Moran, J, Pallesen, J, Palmer, D, Pedersen, C, Pedersen, M, Poterba, T, Poulsen, J, Ripke, S, Robinson, E, Satterstrom, F, Stefansson, H, Stevens, C, Turley, P, Walters, G, Won, H, Wright, M, Andreassen, O, Asherson, P, Burton, C, Boomsma, D, Cormand, B, Dalsgaard, S, Franke, B, Gelernter, J, Geschwind, D, Hakonarson, H, Haavik, J, Kranzler, H, Kuntsi, J, Langley, K, Lesch, K, Middeldorp, C, Reif, A, Rohde, L, Roussos, P, Schachar, R, Sklar, P, Sonuga-Barke, E, Sullivan, P, Thapar, A, Tung, J, Waldman, I, Medland, S, Stefansson, K, Nordentoft, M, Hougaard, D, Werge, T, Mors, O, Mortensen, P, Daly, M, Faraone, S, Borglum, A, Neale, B, Albayrak, O, Anney, R, Arranz, M, Banaschewski, T, Bau, C, Biederman, J, Buitelaar, J, Casas, M, Charach, A, Crosbie, J, Dempfle, A, Doyle, A, Ebstein, R, Elia, J, Freitag, C, Focker, M, Gill, M, Grevet, E, Hawi, Z, Hebebrand, J, Herpertz-Dahlmann, B, Hervas, A, Hinney, A, Hohmann, S, Holmans, P, Hutz, M, Ickowitz, A, Johansson, S, Kent, L, Kittel-Schneider, S, Lambregts-Rommelse, N, Lehmkuhl, G, Loo, S, McGough, J, Meyer, J, Mick, E, Middletion, F, Miranda, A, Mota, N, Mulas, F, Mulligan, A, Nelson, F, Nguyen, T, Oades, R, O'Donovan, M, Owen, M, Palmason, H, Ramos-Quiroga, J, Renner, T, Ribases, M, Rietschel, M, Rivero, O, Romanos, J, Romanos, M, Rothenberger, A, Royers, H, Sanchez-Mora, C, Scherag, A, Schimmelmann, B, Schafer, H, Sergeant, J, Sinzig, J, Smalley, S, Steinhausen, H, Thompson, M, Todorov, A, Vasquez, A, Walitza, S, Wang, Y, Warnke, A, Williams, N, Witt, S, Yang, L, Zayats, T, Zhang-James, Y, Smith, G, Davies, G, Ehli, E, Evans, D, Fedko, I, Greven, C, Groen-Blokhuis, M, Guxens, M, Hammerschlag, A, Hartman, C, Heinrich, J, Hottenga, J, Hudziak, J, Jugessur, A, Kemp, J, Krapohl, E, Murcia, M, Myhre, R, Nolte, I, Nyholt, D, Ormel, J, Ouwens, K, Pappa, I, Pennell, C, Plomin, R, Ring, S, Standl, M, Stergiakouli, E, St Pourcain, B, Stoltenberg, C, Sunyer, J, Thiering, E, Tiemeier, H, Tiesler, C, Timpson, N, Trzaskowski, M, van der Most, P, Vilor-Tejedor, N, Wang, C, Whitehouse, A, Zhao, H, Agee, M, Alipanahi, B, Auton, A, Bell, R, Bryc, K, Elson, S, Fontanillas, P, Furlotte, N, Hinds, D, Hromatka, B, Huber, K, Kleinman, A, Litterman, N, McIntyre, M, Mountain, J, Northover, C, Pitts, S, Sathirapongsasuti, J, Sazonova, O, Shelton, J, Shringarpure, S, Tian, C, Vacic, V, Wilson, C, ADHD Working Grp Psychiat Genomics, Early Lifecourse Genetic, 23andMe Res Team

المساهمون: Institute for Molecular Medicine Finland, Centre of Excellence in Complex Disease Genetics, Psychiatrie & Neuropsychologie, RS: MHeNs - R3 - Neuroscience, Psychiatry, ADHD Working Group of the Psychiatric Genomics Consortium (PGC), 23andme Research Team, University of St Andrews. Cellular Medicine Division, University of St Andrews. Institute of Behavioural and Neural Sciences, University of St Andrews. School of Medicine, Child and Adolescent Psychiatry / Psychology, Erasmus MC other, Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), Life Course Epidemiology (LCE), Clinical Neuropsychology, Biological Psychology, APH - Health Behaviors & Chronic Diseases, APH - Mental Health, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, APH - Personalized Medicine, Clinical Child and Family Studies, LEARN! - Child rearing, APH - Methodology

المصدر: Demontis, D, Walters, R K, Martin, J, Mattheisen, M, Als, T D, Agerbo, E, Baldursson, G, Belliveau, R, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Churchhouse, C, Dumont, A, Eriksson, N, Gandal, M, Goldstein, J I, Grasby, K L, Grove, J, Gudmundsson, O O, Hansen, C S, Hauberg, M E, Hollegaard, M V, Howrigan, D P, Huang, H, Maller, J B, Martin, A R, Moran, J, Martin, N G, Pallesen, J, Palmer, D S, Pedersen, C B, Pedersen, M G, Poterba, T, Poulsen, J B, Ripke, S, Robinson, E B, Satterstrom, F K, Stefansson, H, Stevens, C, Turley, P, Walters, G B, Won, H, Wright, M J, ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Steinhausen, H-C E, Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium, 23andMe Research Team, Andreassen, O A, Asherson, P, Burton, C L, Boomsma, D I, Cormand, B, Dalsgaard, S, Franke, B, Gelernter, J, Geschwind, D, Hakonarson, H, Haavik, J, Kranzler, H R, Kuntsi, J, Langley, K, Lesch, K-P, Middeldorp, C, Reif, A, Rohde, L A, Roussos, P, Schachar, R, Sklar, P, Sonuga-Barke, E J S, Sullivan, P F, Thapar, A, Tung, J Y, Waldman, I D, Medland, S E, Stefansson, K, Nordentoft, M, Hougaard, D M, Werge, T, Mors, O, Mortensen, P B, Daly, M J, Faraone, S V, Børglum, A D & Neale, B M 2019, ' Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder ', Nature Genetics, vol. 51, no. 1, pp. 63-75 . https://doi.org/10.1038/s41588-018-0269-7Test
NATURE GENETICS
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Nature genetics, vol 51, iss 1
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FISABIO. Repositorio Institucional de Producción Científica
Nature Genetics
23andMe Research Team, ADHD Working Group of the Psychiatric Genomics Consortium (PGC) & Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium 2019, ' Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder ', Nature Genetics, vol. 51, no. 1, pp. 63-75 . https://doi.org/10.1038/s41588-018-0269-7Test, https://doi.org/10.1038/s41588-018-0269-7Test
Nature Genetics, 51(1), 63-75. Nature Publishing Group
Demontis, D, Walters, R K, Martin, J, Mattheisen, M, Als, T D, Agerbo, E, Baldursson, G S, Belliveau, R, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Churchhouse, C, Dumont, A, Eriksson, N, Gandal, M, Goldstein, J I, Grasby, K L, Grove, J, Gudmundsson, O O, Hansen, C S, Hauberg, M E, Hollegaard, M V, Howrigan, D P, Huang, H, Maller, J B, Martin, A R, Martin, N G, Moran, J, Pallesen, J, Palmer, D S, Pedersen, C B C, Pedersen, M G, Poterba, T, Poulsen, J B, Ripke, S, Robinson, E B, Satterstrom, F K, Stefansson, H, Stevens, C, Turley, P, Walters, G B, Won, H, Wright, M J, Albayrak, Ö, Nguyen, T T, Evans, D M, Groen-Blokhuis, M M, Hammerschlag, A R, Middeldorp, C, ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Reif, A, Rohde, L A, Roussos, P, Schachar, R, Sonuga-Barke, E J S, Sullivan, P, Thapar, A, Tung, J Y, Waldman, I D, Medland, S E, Mors, O, Bo Mortensen, P, Daly, M J, Faraone, S V, Børglum, A D & Neale, B M 2019, ' Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder ', Nature Genetics, vol. 51, no. 1, pp. 63-75 . https://doi.org/10.1038/s41588-018-0269-7Test
ADHD Working Group of the Psychiatric Genomics Consortium (PGC) 2018, ' Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder ' Nature Genetics . https://doi.org/10.1038/s41588-018-0269-7Test
Nature Genetics, 51, 1, pp. 63-75
Demontis, D, Walters, R K, Martin, J, Mattheisen, M, Als, T D, Agerbo, E, Baldursson, G, Belliveau, R, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Churchhouse, C, Dumont, A, Eriksson, N, Gandal, M, Goldstein, J I, Grasby, K L, Grove, J, Gudmundsson, O O, Hansen, C S, Hauberg, M E, Hollegaard, M V, Howrigan, D P, Huang, H, Maller, J B, Martin, A R, Martin, N G, Moran, J, Pallesen, J, Palmer, D S, Pedersen, C B, Pedersen, M G, Poterba, T, Poulsen, J B, Ripke, S, Robinson, E B, Satterstrom, F K, Stefansson, H, Stevens, C, Turley, P, Walters, G B, Won, H, Wright, M J, ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium, 23andMe Research Team, Dalsgaard, S, Mors, O, Mortensen, P B & Børglum, A D 2019, ' Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder ', Nature Genetics, vol. 51, pp. 63–75 . https://doi.org/10.1038/s41588-018-0269-7Test
Nat Genet
Nature Genetics, 51, 63-75
Nature Genetics, 51(1), 63-+. Nature Publishing Group
Demontis, D, Walters, R K, Martin, J, Mattheisen, M, Als, T D, Agerbo, E, Baldursson, G, Belliveau, R, Bybjerg-grauholm, J, Bækvad-hansen, M, Cerrato, F, Chambert, K, Churchhouse, C, Dumont, A, Eriksson, N, Gandal, M, Goldstein, J I, Grasby, K L, Grove, J, Gudmundsson, O O, Hansen, C S, Hauberg, M E, Hollegaard, M V, Howrigan, D P, Huang, H, Maller, J B, Martin, A R, Martin, N G, Moran, J, Pallesen, J, Palmer, D S, Pedersen, C B, Pedersen, M G, Poterba, T, Poulsen, J B, Ripke, S, Robinson, E B, Satterstrom, F K, Stefansson, H, Stevens, C, Turley, P, Walters, G B, Won, H, Wright, M J, Andreassen, O A, Asherson, P, Burton, C L, Kuntsi, J, Sonuga-barke, E J S & Neale, B M & Plomin, R 2019, ' Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder ', Nature Genetics, vol. 51, no. 1, pp. 63-75 . https://doi.org/10.1038/s41588-018-0269-7Test
the 23 and Me Research Team, Demontis, D, Walters, R K, Martin, J, Mattheisen, M, Als, T D, Agerbo, E, Baldursson, G, Belliveau, R, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Churchhouse, C, Dumont, A, Eriksson, N, Gandal, M, Goldstein, J I, Grasby, K L, Grove, J, Gudmundsson, O O, Hansen, C S, Hauberg, M E, Hollegaard, M V, Howrigan, D P, Huang, H, Maller, J B, Martin, A R, Martin, N G, Moran, J, Pallesen, J, Palmer, D S, Pedersen, C B, Pedersen, M G, Poterba, T, Poulsen, J B, Ripke, S, Robinson, E B, Satterstrom, F K, Smith, G D, Davies, G E, Evans, D M, Kemp, J P, Ring, S, Stergiakouli, E, Pourcain, B S, Stoltenberg, C, Timpson, N J & Langley, K & Thapar, A & Medland, S E 2019, ' Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder ', Nature Genetics, vol. 51, no. 1, pp. 63-75 . https://doi.org/10.1038/s41588-018-0269-7Test
23andMe Research Team, ADHD Working Group of the Psychiatric Genomics Consortium (PGC) & Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium 2018, ' Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder ' Nature Genetics . https://doi.org/10.1038/s41588-018-0269-7Test
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Nature Genetics, 51(1). Nature Publishing Group

مصطلحات موضوعية: Netherlands Twin Register (NTR), Male, Trastorns per dèficit d'atenció amb hiperactivitat en els infants, LD SCORE REGRESSION, Medizin, Genome-wide association study, US CHILDREN, Genoma humà, Attention deficit disorder with hyperactivity in children, Medical and Health Sciences, Cohort Studies, 0302 clinical medicine, 2.1 Biological and endogenous factors, POLYGENIC RISK, Aetiology, Child, IDENTIFIES 11, SEXUAL-BEHAVIOR, Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium, Pediatric, 0303 health sciences, education.field_of_study, Genome, Genetic Predisposition to Disease/genetics, 1184 Genetics, developmental biology, physiology, Brain, 3rd-DAS, Single Nucleotide, Biological Sciences, Polymorphism, Single Nucleotide/genetics, 3. Good health, Mental Health, Meta-analysis, Child, Preschool, Genetic Loci/genetics, Genome-Wide Association Study/methods, Trastorns per dèficit d'atenció amb hiperactivitat en els adults, Attention Deficit Disorder (ADD), Female, Attention Deficit Disorder with Hyperactivity/genetics, RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry, SDG 4 - Quality Education, Clinical psychology, Risk, Adolescent, DEFICIT HYPERACTIVITY DISORDER, Concordance, Population, PROVIDES INSIGHTS, QH426 Genetics, Biology, Quantitative trait locus, Brain/physiology, Polymorphism, Single Nucleotide, 23andMe Research Team, behavioral disciplines and activities, Gene Expression Regulation/genetics, Article, 150 000 MR Techniques in Brain Function, GENETIC ARCHITECTURE, 03 medical and health sciences, All institutes and research themes of the Radboud University Medical Center, Clinical Research, Behavioral and Social Science, mental disorders, medicine, Genetics, Attention deficit hyperactivity disorder, Humans, Genetic Predisposition to Disease, Polymorphism, education, Preschool, QH426, 030304 developmental biology, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], ASSOCIATION METAANALYSIS, Prevention, Human Genome, Case-control study, MAJOR DEPRESSION, medicine.disease, Attention Deficit Hyperactivity Disorder (ADHD), Genetic architecture, Brain Disorders, ADHD Working Group of the Psychiatric Genomics Consortium, Gene Expression Regulation, Attention Deficit Disorder with Hyperactivity, Genetic Loci, RC0321, Attention deficit disorder with hyperactivity in adults, 3111 Biomedicine, 030217 neurology & neurosurgery, Genome-Wide Association Study, Developmental Biology

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https://vbn.aau.dk/da/publications/2ea2ba33-e51e-4b07-a628-232327647cddTest

المؤلفون: Euijung Ryu, Danfeng Chen, Allan H. Young, Olav B. Smeland, James McKay, Frank Bellivier, Qingqin S. Li, Yunpeng Wang, Tõnu Esko, Bertram Müller-Myhsok, Weiqing Wang, Thomas W. Weickert, Joanna M. Biernacka, Ralph W. Kupka, Claire O'Donovan, Josep Antoni Ramos-Quiroga, Marian L. Hamshere, Derek W. Morris, Douglas M. Ruderfer, Stephan Ripke, Nelson B. Freimer, Tatiana Foroud, Shaun Purcell, Ashley Dumont, Shawn Levy, Dominic Holland, Joanna Hauser, Anders D. Børglum, Liz Forty, Alan F. Schatzberg, Christine Fraser, Jennifer M. Whitehead Pavlides, William E. Bunney, Merete Nordentoft, Andres Metspalu, Gunnar Morken, Susanne Lucae, Roy H. Perlis, Anne T. Spijker, Richard A. Belliveau, Sarah E. Bergen, Fan Meng, Eduard Vieta, Cynthia Shannon Weickert, J. Raymond DePaulo, Martin Alda, Lina Martinsson, Melvin G. McInnis, Jacob Lawrence, Markus Leber, James A. Knowles, Franziska Degenhardt, Melissa J. Green, Jaqueline Goldstein, Amanda Dobbyn, Radhika Kandaswamy, Steve McCarroll, Katrin Gade, Jack D. Barchas, Christina M. Hultman, Sarah Kittel-Schneider, Martin Hautzinger, Maria Hipolito, Louise Frisén, Kari Stefansson, Michael Conlon O'Donovan, Markus M. Nöthen, Eline J. Regeer, Jens Treutlein, Robert Karlsson, Ian Jones, Nicholas G. Martin, William A. Scheftner, Caroline M. Nievergelt, Marta Ribasés, Simone de Jong, Szabolcs Szelinger, Thomas W. Mühleisen, Michele T. Pato, Manuel Mattheisen, Maciej Trzaskowski, Urs Heilbronner, Diane Gage, Jakob Grove, Ingrid Melle, Ole A. Andreassen, Claudia Giambartolomei, Kimberly Chambert, Arne E. Vaaler, William Coryell, Peter R. Schofield, Preben Bo Mortensen, Roel A. Ophoff, Fabian Streit, Manolis Kogevinas, Ingrid Agartz, John Strauss, James L. Kennedy, Anders M. Dale, Stefan Herms, Douglas Blackwood, Torbjørn Elvsåshagen, Bernhard T. Baune, Grant W. Montgomery, Andreas Reif, Fabio Rivas, Andrew McQuillin, Jordan W. Smoller, Chun Chieh Fan, James B. Potash, Jun Li, Ketil J. Oedegaard, David Curtis, Martin Schalling, John R. Kelsoe, Valentina Escott-Price, Sascha B. Fischer, Tatyana Shehktman, Jonathan R. I. Coleman, Stanley J. Watson, Donald J. MacIntyre, Tune H. Pers, Eystein Stordal, Richard M. Myers, Jose Guzman-Parra, Danielle Posthuma, John I. Nurnberger, William Lawson, Janet L. Sobell, Felecia Cerrato, Judith A. Badner, Elliot S. Gershon, Gerome Breen, Naomi R. Wray, Thomas Werge, Lilijana Oruc, Claire Slaney, Anil P.S. Ori, Alexander W. Charney, Marianne Giørtz Pedersen, Marie Bækvad-Hansen, Michael Boehnke, Marcella Rietschel, George Kirov, Aiden Corvin, Piotr M. Czerski, Peter Holmans, Michael Steffens, Margarita Rivera, Maria Grigoroiu-Serbanescu, René S. Kahn, Laura M. Huckins, Monika Budde, Michael Gill, Lili Milani, Christiaan de Leeuw, Peng Zhang, Nicholas Bass, Jana Strohmaier, John P. Rice, Wei Xu, Cristiana Cruceanu, Vassily Trubetskoy, Philip B. Mitchell, Helena Medeiros, Thomas Damm Als, Anna C. Koller, Huda Akil, Jessica S. Johnson, Toni-Kim Clarke, Janice M. Fullerton, Guy A. Rouleau, Fernando S. Goes, Weihua Guan, Wolfgang Maier, Pamela Sklar, Diego Albani, Laura J. Scott, Pamela B. Mahon, Anna Maaser, Katherine Gordon-Smith, Urban Ösby, Jurgen Del-Favero, Jolanta Lissowska, Howard J. Edenberg, Sven Cichon, Annelie Nordin Adolfsson, Julie Garnham, Josef Frank, Hoang T. Nguyen, Michael Bauer, Helmut Vedder, Vishwajit L. Nimgaonkar, Loes M. Olde Loohuis, Thomas G. Schulze, Cristina Sánchez-Mora, Udo Dannlowski, Rolf Adolfsson, Benjamin M. Neale, Verneri Antilla, Andrea Pfennig, John B. Vincent, Niamh Mullins, Per Hoffmann, Peter McGuffin, Erlend Bøen, Ney Alliey-Rodriguez, Adebayo Anjorin, Fermín Mayoral, Arianna Di Florio, Claire Churchhouse, David M. Hougaard, Nicholas J. Schork, Tiffany A. Greenwood, Carlos N. Pato, Thorgeir E. Thorgeirsson, Nicholas John Craddock, Stephanie H. Witt, Liam Abbott, Swapnil Awasthi, Miquel Casas, Jonas Bybjerg-Grauholm, Cathryn M. Lewis, Srdjan Djurovic, Bruno Etain, Margit Burmeister, Phil Lee, Elaine K. Green, Sara A. Paciga, Lena Backlund, Engilbert Sigurdsson, Patrick F. Sullivan, Amy Perry, Pablo Cervantes, Marco P. Boks, Catharina Lavebratt, Andrew M. McIntosh, Panos Roussos, Enda M. Byrne, Alexander Richards, Eli A. Stahl, Stéphane Jamain, Hreinn Stefansson, Ole Mors, Esben Agerbo, Susan L. McElroy, Wade H. Berrettini, Peter P. Zandi, Lisa Jones, Andreas J. Forstner, Alessandro Serretti, Céline S. Reinbold, Robert C. Thompson, Matthew Flickinger, William Byerley, Michael John Owen, Helena Gaspar, Francis J. McMahon, David St Clair, Mark A. Frye, Christine Søholm Hansen, Scott D. Gordon, Mikael Landén, Gustavo Turecki, Simon Xi, Evaristus A. Nwulia, Anders Juréus, James Boocock, Stacy Steinberg, Paul D. Shilling, David Craig, Mark J. Daly, Sarah E. Medland, Marion Leboyer, Chunyu Liu, Carsten Bøcker Pedersen, Sebastian Zöllner

المساهمون: APH - Mental Health, Psychiatry, Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D), Stahl E.A., Breen G., Forstner A.J., McQuillin A., Ripke S., Trubetskoy V., Mattheisen M., Wang Y., Coleman J.R.I., Gaspar H.A., de Leeuw C.A., Steinberg S., Pavlides J.M.W., Trzaskowski M., Byrne E.M., Pers T.H., Holmans P.A., Richards A.L., Abbott L., Agerbo E., Akil H., Albani D., Alliey-Rodriguez N., Als T.D., Anjorin A., Antilla V., Awasthi S., Badner J.A., Baekvad-Hansen M., Barchas J.D., Bass N., Bauer M., Belliveau R., Bergen S.E., Pedersen C.B., Boen E., Boks M.P., Boocock J., Budde M., Bunney W., Burmeister M., Bybjerg-Grauholm J., Byerley W., Casas M., Cerrato F., Cervantes P., Chambert K., Charney A.W., Chen D., Churchhouse C., Clarke T.-K., Coryell W., Craig D.W., Cruceanu C., Curtis D., Czerski P.M., Dale A.M., de Jong S., Degenhardt F., Del-Favero J., DePaulo J.R., Djurovic S., Dobbyn A.L., Dumont A., Elvsashagen T., Escott-Price V., Fan C.C., Fischer S.B., Flickinger M., Foroud T.M., Forty L., Frank J., Fraser C., Freimer N.B., Frisen L., Gade K., Gage D., Garnham J., Giambartolomei C., Pedersen M.G., Goldstein J., Gordon S.D., Gordon-Smith K., Green E.K., Green M.J., Greenwood T.A., Grove J., Guan W., Guzman-Parra J., Hamshere M.L., Hautzinger M., Heilbronner U., Herms S., Hipolito M., Hoffmann P., Holland D., Huckins L., Jamain S., Johnson J.S., Jureus A., Kandaswamy R., Karlsson R., Kennedy J.L., Kittel-Schneider S., Knowles J.A., Kogevinas M., Koller A.C., Kupka R., Lavebratt C., Lawrence J., Lawson W.B., Leber M., Lee P.H., Levy S.E., Li J.Z., Liu C., Lucae S., Maaser A., MacIntyre D.J., Mahon P.B., Maier W., Martinsson L., McCarroll S., McGuffin P., McInnis M.G., McKay J.D., Medeiros H., Medland S.E., Meng F., Milani L., Montgomery G.W., Morris D.W., Muhleisen T.W., Mullins N., Nguyen H., Nievergelt C.M., Adolfsson A.N., Nwulia E.A., O'Donovan C., Loohuis L.M.O., Ori A.P.S., Oruc L., Osby U., Perlis R.H., Perry A., Pfennig A., Potash J.B., Purcell S.M., Regeer E.J., Reif A., Reinbold C.S., Rice J.P., Rivas F., Rivera M., Roussos P., Ruderfer D.M., Ryu E., Sanchez-Mora C., Schatzberg A.F., Scheftner W.A., Schork N.J., Shannon Weickert C., Shehktman T., Shilling P.D., Sigurdsson E., Slaney C., Smeland O.B., Sobell J.L., Soholm Hansen C., Spijker A.T., St Clair D., Steffens M., Strauss J.S., Streit F., Strohmaier J., Szelinger S., Thompson R.C., Thorgeirsson T.E., Treutlein J., Vedder H., Wang W., Watson S.J., Weickert T.W., Witt S.H., Xi S., Xu W., Young A.H., Zandi P., Zhang P., Zollner S., Adolfsson R., Agartz I., Alda M., Backlund L., Baune B.T., Bellivier F., Berrettini W.H., Biernacka J.M., Blackwood D.H.R., Boehnke M., Borglum A.D., Corvin A., Craddock N., Daly M.J., Dannlowski U., Esko T., Etain B., Frye M., Fullerton J.M., Gershon E.S., Gill M., Goes F., Grigoroiu-Serbanescu M., Hauser J., Hougaard D.M., Hultman C.M., Jones I., Jones L.A., Kahn R.S., Kirov G., Landen M., Leboyer M., Lewis C.M., Li Q.S., Lissowska J., Martin N.G., Mayoral F., McElroy S.L., McIntosh A.M., McMahon F.J., Melle I., Metspalu A., Mitchell P.B., Morken G., Mors O., Mortensen P.B., Muller-Myhsok B., Myers R.M., Neale B.M., Nimgaonkar V., Nordentoft M., Nothen M.M., O'Donovan M.C., Oedegaard K.J., Owen M.J., Paciga S.A., Pato C., Pato M.T., Posthuma D., Ramos-Quiroga J.A., Ribases M., Rietschel M., Rouleau G.A., Schalling M., Schofield P.R., Schulze T.G., Serretti A., Smoller J.W., Stefansson H., Stefansson K., Stordal E., Sullivan P.F., Turecki G., Vaaler A.E., Vieta E., Vincent J.B., Werge T., Nurnberger J.I., Wray N.R., Di Florio A., Edenberg H.J., Cichon S., Ophoff R.A., Scott L.J., Andreassen O.A., Kelsoe J., Sklar P., eQTLGen Consortium, BIOS Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Complex Trait Genetics

المصدر: Nature Genetics
NATURE GENETICS
eQTLGen Consortium, BIOS Consortium & the Bipolar Disorder Working Group of the Psychiatric Genomics Consortium 2019, ' Genome-wide association study identifies 30 loci associated with bipolar disorder ', Nature Genetics, vol. 51, no. 5, pp. 793-803 . https://doi.org/10.1038/s41588-019-0397-8Test
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Nature Genetics, 51(5), 793-803. Nature Publishing Group
Nature genetics
Nature Genetics, 51(5), 793. Nature Publishing Group
Stahl, E A, Breen, G, Forstner, A J, McQuillin, A, Ripke, S, Trubetskoy, V, Mattheisen, M, Wang, Y, Coleman, J R I, Gaspar, H L A, de Leeuw, C A, Steinberg, S, Pavlides, J M W, Trzaskowski, M, Byrne, E M, Pers, T H, Holmans, P A, Richards, A L, Abbott, L, Agerbo, E, Akil, H, Albani, D, Alliey-Rodriguez, N, Als, T D, Anjorin, A, Antilla, V, Awasthi, S, Badner, J A, Bækvad-Hansen, M, Barchas, J D, Bass, N, Bauer, M, Belliveau, R, Bergen, S E, Pedersen, C B C, Bøen, E, Boks, M P, Boocock, J, Budde, M, Bunney, W, Burmeister, M, Bybjerg-Grauholm, J, Byerley, W, Casas, M, Cerrato, F, Cervantes, P, Chambert, K, Charney, A W, Kupka, R, Posthuma, D, Stefánsson, H, Ophoff, R A, Scott, L J, Andreassen, O A, Kelsoe, J, Sklar, P & the Bipolar Disorder Working Group of the Psychiatric Genomics Consortium 2019, ' Genome-wide association study identifies 30 loci associated with bipolar disorder ', Nature Genetics, vol. 51, no. 5, pp. 793-803 . https://doi.org/10.1038/s41588-019-0397-8Test
Stahl, E A, Breen, G, Forstner, A J, McQuillin, A, Ripke, S, Trubetskoy, V, Mattheisen, M, Wang, Y, Coleman, J R I, Gaspar, H A, de Leeuw, C A, Steinberg, S, Pavlides, J M W, Trzaskowski, M, Byrne, E M, Pers, T H, Holmans, P A, Richards, A L, Abbott, L, Agerbo, E, Akil, H, Albani, D, Alliey-Rodriguez, N, Als, T D, Anjorin, A, Antilla, V, Awasthi, S, Badner, J A, Bækvad-Hansen, M, Barchas, J D, Bass, N, Bauer, M, Belliveau, R, Bergen, S E, Pedersen, C B, Bøen, E, Boks, M P, Boocock, J, Budde, M, Bunney, W, Burmeister, M, Bybjerg-Grauholm, J, Byerley, W, Pedersen, M G, Grove, J, Xu, W, Zhang, P, Børglum, A D, Mors, O, Mortensen, P B & eQTLGen Consortium 2019, ' Genome-wide association study identifies 30 loci associated with bipolar disorder ', Nature Genetics, vol. 51, no. 5, pp. 793-803 . https://doi.org/10.1038/s41588-019-0397-8Test
Stahl, E A, Breen, G, Forstner, A J, Mcquillin, A, Ripke, S, Trubetskoy, V, Mattheisen, M, Wang, Y, Coleman, J R I, Gaspar, H A, De Leeuw, C A, Steinberg, S, Pavlides, J M W, Trzaskowski, M, Byrne, E M, Pers, T H, Holmans, P A, Richards, A L, Abbott, L, Agerbo, E, Akil, H, Albani, D, Alliey-rodriguez, N, Als, T D, Anjorin, A, Antilla, V, Awasthi, S, Badner, J A, Bækvad-hansen, M, Barchas, J D, Bass, N, Bauer, M, Belliveau, R, Bergen, S E, Pedersen, C B, Bøen, E, Boks, M P, Boocock, J, Budde, M, Bunney, W, Burmeister, M, Bybjerg-grauholm, J, Byerley, W, Casas, M, Cerrato, F, Cervantes, P, Chambert, K, Charney, A W, Chen, D, Churchhouse, C, Clarke, T, Coryell, W, Craig, D W, Cruceanu, C, Curtis, D, Czerski, P M, Dale, A M, De Jong, S, Degenhardt, F, Del-favero, J, Depaulo, J R, Djurovic, S, Dobbyn, A L, Dumont, A, Elvsåshagen, T, Escott-price, V, Fan, C C, Fischer, S B, Flickinger, M, Foroud, T M, Forty, L, Frank, J, Fraser, C, Freimer, N B, Frisén, L, Gade, K, Gage, D, Garnham, J, Giambartolomei, C, Pedersen, M G, Goldstein, J, Gordon, S D, Gordon-smith, K, Green, E K, Green, M J, Greenwood, T A, Grove, J, Guan, W, Guzman-parra, J, Hamshere, M L, Hautzinger, M, Heilbronner, U, Herms, S, Hipolito, M, Hoffmann, P, Holland, D, Huckins, L, Jamain, S, Johnson, J S, Juréus, A, Kandaswamy, R, Karlsson, R, Kennedy, J L, Kittel-schneider, S, Knowles, J A, Kogevinas, M, Koller, A C, Kupka, R, Lavebratt, C, Lawrence, J, Lawson, W B, Leber, M, Lee, P H, Levy, S E, Li, J Z, Liu, C, Lucae, S, Maaser, A, Macintyre, D J, Mahon, P B, Maier, W, Martinsson, L, Mccarroll, S, Mcguffin, P, Mcinnis, M G, Mckay, J D, Medeiros, H, Medland, S E, Meng, F, Milani, L, Montgomery, G W, Morris, D W, Mühleisen, T W, Mullins, N, Nguyen, H, Nievergelt, C M, Adolfsson, A N, Nwulia, E A, O’donovan, C, Loohuis, L M O, Ori, A P S, Oruc, L, Ösby, U, Perlis, R H, Perry, A, Pfennig, A, Potash, J B, Purcell, S M, Regeer, E J, Reif, A, Reinbold, C S, Rice, J P, Rivas, F, Rivera, M, Roussos, P, Ruderfer, D M, Ryu, E, Sánchez-mora, C, Schatzberg, A F, Scheftner, W A, Schork, N J, Shannon Weickert, C, Shehktman, T, Shilling, P D, Sigurdsson, E, Slaney, C, Smeland, O B, Sobell, J L, Søholm Hansen, C, Spijker, A T, St Clair, D, Steffens, M, Strauss, J S, Streit, F, Strohmaier, J, Szelinger, S, Thompson, R C, Thorgeirsson, T E, Treutlein, J, Vedder, H, Wang, W, Watson, S J, Weickert, T W, Witt, S H, Xi, S, Xu, W, Young, A H, Zandi, P, Zhang, P, Zöllner, S, Adolfsson, R, Agartz, I, Alda, M, Backlund, L, Baune, B T, Bellivier, F, Berrettini, W H, Biernacka, J M, Blackwood, D H R, Boehnke, M, Børglum, A D, Corvin, A, Craddock, N, Daly, M J, Dannlowski, U, Esko, T, Etain, B, Frye, M, Fullerton, J M, Gershon, E S, Gill, M, Goes, F, Grigoroiu-serbanescu, M, Hauser, J, Hougaard, D M, Hultman, C M, Jones, I, Jones, L A, Kahn, R S, Kirov, G, Landén, M, Leboyer, M, Lewis, C M, Li, Q S, Lissowska, J, Martin, N G, Mayoral, F, Mcelroy, S L, Mcintosh, A M, Mcmahon, F J, Melle, I, Metspalu, A, Mitchell, P B, Morken, G, Mors, O, Mortensen, P B, Müller-myhsok, B, Myers, R M, Neale, B M, Nimgaonkar, V, Nordentoft, M, Nöthen, M M, O’donovan, M C, Oedegaard, K J, Owen, M J, Paciga, S A, Pato, C, Pato, M T, Posthuma, D, Ramos-quiroga, J A, Ribasés, M, Rietschel, M, Rouleau, G A, Schalling, M, Schofield, P R, Schulze, T G, Serretti, A, Smoller, J W, Stefansson, H, Stefansson, K, Stordal, E, Sullivan, P F, Turecki, G, Vaaler, A E, Vieta, E, Vincent, J B, Werge, T, Nurnberger, J I, Wray, N R, Di Florio, A, Edenberg, H J, Cichon, S, Ophoff, R A, Scott, L J, Andreassen, O A, Kelsoe, J & Sklar, P 2019, ' Genome-wide association study identifies 30 loci associated with bipolar disorder ', Nature Genetics, vol. 51, no. 5, pp. 793-803 . https://doi.org/10.1038/s41588-019-0397-8Test
Online: 1546-1718
Stahl, E A, Breen, G, Forstner, A J, McQuillin, A, Ripke, S, Trubetskoy, V, Mattheisen, M, Wang, Y, Coleman, J R I, Gaspar, H A, de Leeuw, C A, Steinberg, S, Pavlides, J M W, Trzaskowski, M, Byrne, E M, Pers, T H, Holmans, P A, Richards, A L, Abbott, L, Agerbo, E, Akil, H, Albani, D, Alliey-Rodriguez, N, Als, T D, Anjorin, A, Antilla, V, Awasthi, S, Badner, J A, Bækvad-Hansen, M, Barchas, J D, Bass, N, Bauer, M, Belliveau, R, Bergen, S E, Pedersen, C B, Bøen, E, Boks, M P, Boocock, J, Budde, M, Bunney, W, Burmeister, M, Bybjerg-Grauholm, J, Byerley, W, Casas, M, de Jong, S, Kandaswamy, R, McGuffin, P, Mullins, N & Young, A H & Lewis, C M 2019, ' Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder ', Nature Genetics, vol. 51, no. 5, pp. 793-803 . https://doi.org/10.1038/s41588-019-0397-8Test

مصطلحات موضوعية: Male, Bipolar Disorder, Bipolar I disorder, Schizophrenia/genetics, LD SCORE REGRESSION, Genome-wide association study, VARIANTS, Bipolar II disorder, 0302 clinical medicine, SCHIZOPHRENIA, GWAS, Psychotic Disorders/genetics, Non-U.S. Gov't, RISK, Genetics, 0303 health sciences, HERITABILITY, Research Support, Non-U.S. Gov't, Systems Biology, Major/genetics, Single Nucleotide, 3. Good health, Schizophrenia, Major depressive disorder, Female, Case-Control Studie, Depressive Disorder, Major/genetics, Human, Psychosis, GENES, Biology, Psychotic Disorder, Research Support, Polymorphism, Single Nucleotide, Article, Bipolar Disorder/classification, N.I.H, 03 medical and health sciences, SDG 3 - Good Health and Well-being, medicine, Journal Article, POLYGENICITY, Humans, Genetic Predisposition to Disease, Bipolar disorder, Polymorphism, METAANALYSIS, 030304 developmental biology, Intramural, Depressive Disorder, Major, Depressive Disorder, Genetic heterogeneity, Research Support, N.I.H., Intramural, medicine.disease, INDIVIDUALS, Psychotic Disorders, Genetic Loci, Case-Control Studies, Human medicine, 030217 neurology & neurosurgery, Genome-Wide Association Study, Meta-Analysis

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الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a01aab7c8cdaf13b3f435a46eef431f1Test
https://doi.org/10.1038/s41588-019-0397-8Test