Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Consortium, GERAD1"'
Autor:
Pardiñas, Antonio F, Holmans, Peter, Han, Jun, Nothen, Markus, Goate, Alison, Cruchaga, Carlos, Nowotny, Petra, Morris, John C, Mayo, Kevin, O'Donovan, Michael, Owen, Michael, Williams, Julie, Hubbard, Leon, Achilla, Evanthia, Agerbo, Esben, Barr, Cathy L, Böttger, Theresa Wimberly, Breen, Gerome, Cohen, Dan, Collier, David A, Curran, Sarah, Dempster, Emma, Dima, Danai, Lynham, Amy, Sabes-Figuera, Ramon, Flanagan, Robert J, Frangou, Sophia, Frank, Josef, Gasse, Christiane, Gaughran, Fiona, Giegling, Ina, Grove, Jakob, Hannon, Eilis, Hartmann, Annette M, Mantripragada, Kiran, Heißerer, Barbara, Helthuis, Marinka, Horsdal, Henriette Thisted, Ingimarsson, Oddur, Jollie, Karel, Kennedy, James L, Köhler, Ole, Konte, Bettina, Lang, Maren, Legge, Sophie E, Rees, Elliott, Lewis, Cathryn, MacCabe, James, Malhotra, Anil K, McCrone, Paul, Meier, Sandra M, Mill, Jonathan, Mors, Ole, Mortensen, Preben Bo, Nöthen, Markus M, O'Donovan, Michael C, MacCabe, James H, Owen, Michael J, Pedersen, Carsten B, Rietschel, Marcella, Rujescu, Dan, Schwalber, Ameli, Sigurdsson, Engilbert, Sørensen, Holger J, Spencer, Benjamin, Stefansson, Hreinn, McCarroll, Steven A, Støvring, Henrik, Strohmaier, Jana, Sullivan, Patrick, Vassos, Evangelos, Verbelen, Moira, Walters, James T R, Werge, Thomas, Baune, Bernhard T, Byrne, Enda M, Pocklington, Andrew J, Dannlowski, Udo, Eley, Thalia C, Hayward, Caroline, Martin, Nicholas G, McIntosh, Andrew M, Plomin, Robert, Porteous, David J, Wray, Naomi R, Caballero, Armando, Geschwind, Daniel H, Escott-Price, Valentina, Huckins, Laura M, Ruderfer, Douglas M, Santiago, Enrique, Sklar, Pamela, Stahl, Eli A, Won, Hyejung, Als, Thomas D, Andreassen, Ole A, Bækvad-Hansen, Marie, Ripke, Stephan, Pedersen, Carsten Bøcker, Børglum, Anders D, Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Hougaard, David M, Carrera, Noa, Mattheisen, Manuel, Molden, Espen, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Steinberg, Stacy, Tosato, Sarah, Consortium, GERAD1, Consortium, CRESTAR, Kirov, George, Bishop, Sophie, Harold, Denise, Sims, Rebecca, Gerrish, Amy, Chapman, Jade, Abraham, Richard, Hollingworth, Paul, Pahwa, Jaspreet, Denning, Nicola, Cameron, Darren, Thomas, Charlene, Taylor, Sarah, Powell, John, Proitsi, Petroula, Lupton, Michelle, Lovestone, Simon, Passmore, Peter, Craig, David, McGuinness, Bernadette, Johnston, Janet, Hamshere, Marian L, Todd, Stephen, Maier, Wolfgang, Jessen, Frank, Heun, Reiner, Schurmann, Britta, Ramirez, Alfredo, Becker, Tim, Herold, Christine, Lacour, André, Drichel, Dmitriy
Publikováno v:
Pardiñas, A F, Holmans, P, Pocklington, A J, Escott-Price, V, Ripke, S, Carrera, N, Legge, S E, Bishop, S, Cameron, D, Hamshere, M L, Han, J, Hubbard, L, Lynham, A, Mantripragada, K, Rees, E, MacCabe, J H, McCarroll, S A, Baune, B T, Breen, G, Byrne, E M, Dannlowski, U, Eley, T C, Hayward, C, Martin, N G, McIntosh, A M, Plomin, R, Porteous, D J, Wray, N R, Caballero, A, Geschwind, D H, Huckins, L M, Ruderfer, D M, Santiago, E, Sklar, P, Stahl, E A, Won, H, Agerbo, E, Als, T D, Andreassen, O A, Bækvad-Hansen, M, Mortensen, P B, Pedersen, C B, Børglum, A D, Bybjerg-Grauholm, J, Djurovic, S, Durmishi, N, Pedersen, M G, Golimbet, V, Grove, J, Collier, D A 2018, ' Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection ', Nature Genetics, vol. 50, pp. 381–389 . https://doi.org/10.1038/s41588-018-0059-2
Nature genetics 50(3), 381-389 (2018). doi:10.1038/s41588-018-0059-2
Pardiñas, A F, Holmans, P A, Pocklington, A J, Escott-Price, V, Ripke, S, Carrera, N, Legge, S E, Bishop, S, Cameron, D, Hamshere, M L, Han, J, Hubbard, L, Lynham, A, Mantripragada, K, Rees, E, MacCabe, J H, McCarroll, S A, Baune, B T, Breen, G, Byrne, E M, Dannlowski, U, Eley, T C, Hayward, C, Martin, N G, McIntosh, A M, Plomin, R, Porteous, D J, Wray, N R, Caballero, A, Geschwind, D H, Huckins, L M, Ruderfer, D M, Santiago, E, Sklar, P, Stahl, E A, Won, H, Agerbo, E, Als, T D, Andreassen, O A, Bækvad-Hansen, M, Mortensen, P B, Pedersen, C B, Børglum, A D, Bybjerg-Grauholm, J, Djurovic, S, Durmishi, N, Pedersen, M G, Golimbet, V & Grove, J & Hougaard, D M 2018, ' Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection ', Nature Genetics . https://doi.org/10.1038/s41588-018-0059-2
GERAD1 Consortium: 2018, ' Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection ', Nature Genetics, vol. 50, no. 3, pp. 381-389 . https://doi.org/10.1038/s41588-018-0059-2
Nature genetics 50(3), 381-389 (2018). doi:10.1038/s41588-018-0059-2
Pardiñas, A F, Holmans, P A, Pocklington, A J, Escott-Price, V, Ripke, S, Carrera, N, Legge, S E, Bishop, S, Cameron, D, Hamshere, M L, Han, J, Hubbard, L, Lynham, A, Mantripragada, K, Rees, E, MacCabe, J H, McCarroll, S A, Baune, B T, Breen, G, Byrne, E M, Dannlowski, U, Eley, T C, Hayward, C, Martin, N G, McIntosh, A M, Plomin, R, Porteous, D J, Wray, N R, Caballero, A, Geschwind, D H, Huckins, L M, Ruderfer, D M, Santiago, E, Sklar, P, Stahl, E A, Won, H, Agerbo, E, Als, T D, Andreassen, O A, Bækvad-Hansen, M, Mortensen, P B, Pedersen, C B, Børglum, A D, Bybjerg-Grauholm, J, Djurovic, S, Durmishi, N, Pedersen, M G, Golimbet, V & Grove, J & Hougaard, D M 2018, ' Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection ', Nature Genetics . https://doi.org/10.1038/s41588-018-0059-2
GERAD1 Consortium: 2018, ' Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection ', Nature Genetics, vol. 50, no. 3, pp. 381-389 . https://doi.org/10.1038/s41588-018-0059-2
Schizophrenia is a debilitating psychiatric condition often associated with poor quality of life and decreased life expectancy. Lack of progress in improving treatment outcomes has been attributed to limited knowledge of the underlying biology, altho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14837d7d6a1cc02387718a4222dea866
https://kclpure.kcl.ac.uk/en/publications/771f5472-29c0-4a55-9c80-2687362a1edd
https://kclpure.kcl.ac.uk/en/publications/771f5472-29c0-4a55-9c80-2687362a1edd
Autor:
Power, Robert A, Tansey, Katherine E, Buttenschon, Henriette Normolle, Cohen-Woods, Sarah, Bigdeli, Tim, Hall, Lynsey S, Kutalik, Zoltn, Lee, S Hong, Ripke, Stephan, Steinberg, Stacy, Teumer, Alexander, Viktorin, Alexander, Wray, Naomi R, Arolt, Volker, Baune, Bernard T, Boomsma, Dorret I, Borglum, Anders D, Byrne, Enda M, Castelao, Enrique, Craddock, Nick, Craig, Ian W, Dannlowski, Udo, Deary, Ian J, Degenhardt, Franziska, Forstner, Andreas J, Gordon, Scott D, Grabe, Hans J, Grove, Jakob, Hamilton, Steven P, Hayward, Caroline, Heath, Andrew C, Hocking, Lynne J, Homuth, Georg, Hottenga, Jouke J, Kloiber, Stefan, Krogh, Jesper, Landen, Mikael, Lang, Maren, Levinson, Douglas F, Lichtenstein, Paul, Lucae, Susanne, MacIntyre, Donald J, Madden, Pamela, Magnusson, Patrik KE, Martin, Nicholas G, McIntosh, Andrew M, Middeldorp, Christel M, Milaneschi, Yuri, Montgomery, Grant W, Mors, Ole, Muller-Myhsok, Bertram, Nyholt, Dale R, Oskarsson, Hogni, Owen, Michael J, Padmanabhan, Sandosh, Penninx, Brenda WJH, Pergadia, Michele L, Porteous, David J, Potash, James B, Preisig, Martin, Rivera, Margarita, Shi, Jianxin, Shyn, Stanley I, Sigurdsson, Engilbert, Smit, Johannes H, Smith, Blair H, Stefansson, Hreinn, Stefansson, Kari, Strohmaier, Jana, Sullivan, Patrick F, Thomson, Pippa, Thorgeirsson, Thorgeir E, Van der Auwera, Sandra, Weissman, Myrna M, Breen, Gerome, Lewis, Cathryn M, Consortium, CONVERGE, Consortium, CARDIoGRAM, Consortium, GERAD1
Publikováno v:
BIOLOGICAL PSYCHIATRY
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::ad0001d2216cbb4d1c7c9ab0adb28d25
Autor:
Lupton, MK, Benyamin, B, Proitsi, P, Nyholt, DR, Ferreira, MA, Montgomery, GW, Heath, AC, Madden, PA, Medland, SE, Gordon, SD, Consortium, GERAD1, Initiative, Alzheimer’s Disease Neuroimaging, Lovestone, S, Tsolaki, M, Kloszewska, I, Soininen, H, Mecocci, P, Vellas, B, Powell, JF, Bush, AI, Wright, MJ, Martin, NG, Whitfield, JB
Publikováno v:
Lupton, M K, Benyamin, B, Proitsi, P, Nyholt, D R, Ferreira, M A, Montgomery, G W, Heath, A C, Madden, P A, Medland, S E, Gordon, S D, Lovestone, S, Tsolaki, M, Kloszewska, I, Soininen, H, Mecocci, P, Vellas, B, Powell, J F, Bush, A I, Wright, M J, Martin, N G & Whitfield, J B 2017, ' No Genetic Overlap between Circulating Iron Levels and Alzheimer's Disease ', JOURNAL OF ALZHEIMERS DISEASE, vol. 59, no. 1, pp. 85-99 . https://doi.org/10.3233/JAD-170027
Article
Iron deposition in the brain is a prominent feature of Alzheimer’s disease (AD). Recently, peripheral iron measures have also been shown to be associated with AD status. However, it is not known whether these associations are causal: d
Iron deposition in the brain is a prominent feature of Alzheimer’s disease (AD). Recently, peripheral iron measures have also been shown to be associated with AD status. However, it is not known whether these associations are causal: d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66e811d1c643b1d88b6918fddb57e9d8
https://hdl.handle.net/11541.2/130362
https://hdl.handle.net/11541.2/130362
Autor:
Power, Robert A, Tansey, Katherine E, Buttenschøn, Henriette Nørmølle, Cohen-Woods, Sarah, Bigdeli, Tim, Hall, Lynsey S, Kutalik, Zoltán, Lee, S Hong, Ripke, Stephan, Steinberg, Stacy, Teumer, Alexander, Viktorin, Alexander, Wray, Naomi R, Arolt, Volker, Baune, Bernard T, Boomsma, Dorret I, Børglum, Anders D, Byrne, Enda M, Castelao, Enrique, Craddock, Nick, Craig, Ian W, Dannlowski, Udo, Deary, Ian J, Degenhardt, Franziska, Forstner, Andreas J, Gordon, Scott D, Grabe, Hans J, Grove, Jakob, Hamilton, Steven P, Hayward, Caroline, Heath, Andrew C, Hocking, Lynne J, Homuth, Georg, Hottenga, Jouke J, Kloiber, Stefan, Krogh, Jesper, Landén, Mikael, Lang, Maren, Levinson, Douglas F, Lichtenstein, Paul, Lucae, Susanne, MacIntyre, Donald J, Madden, Pamela, Magnusson, Patrik K E, Martin, Nicholas G, McIntosh, Andrew M, Middeldorp, Christel M, Milaneschi, Yuri, Montgomery, Grant W, Mors, Ole, Müller-Myhsok, Bertram, Nyholt, Dale R, Oskarsson, Hogni, Owen, Michael J, Padmanabhan, Sandosh, Penninx, Brenda W J H, Pergadia, Michele L, Porteous, David J, Potash, James B, Preisig, Martin, Rivera, Margarita, Shi, Jianxin, Shyn, Stanley I, Sigurdsson, Engilbert, Smit, Johannes H, Smith, Blair H, Stefansson, Hreinn, Stefansson, Kari, Strohmaier, Jana, Sullivan, Patrick F, Thomson, Pippa, Thorgeirsson, Thorgeir E, Van der Auwera, Sandra, Weissman, Myrna M, CONVERGE Consortium, CARDIoGRAM Consortium, GERAD1 Consortium, Breen, Gerome, Lewis, Cathryn M
Publikováno v:
Biol. Psychiatry 81, 325-335 (2017)
BACKGROUND: Major depressive disorder (MDD) is a disabling mood disorder, and despite a known heritable component, a large meta-analysis of genome-wide association studies revealed no replicable genetic risk variants. Given prior evidence of heteroge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f836398d19f5661ca83cf22cf6576a5a
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=50868
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=50868
Autor:
Pardiñas, Antonio F, Holmans, Peter, Han, Jun, Nothen, Markus, Goate, Alison, Cruchaga, Carlos, Nowotny, Petra, Morris, John C, Mayo, Kevin, Williams, Julie, Achilla, Evanthia, Agerbo, Esben, Hubbard, Leon, Barr, Cathy L, Böttger, Theresa Wimberly, Breen, Gerome, Cohen, Dan, Collier, David A, Curran, Sarah, Dempster, Emma, Dima, Danai, Sabes-Figuera, Ramon, Flanagan, Robert J, Lynham, Amy, Frangou, Sophia, Frank, Josef, Gasse, Christiane, Gaughran, Fiona, Giegling, Ina, Grove, Jakob, Hannon, Eilis, Hartmann, Annette M, Heißerer, Barbara, Helthuis, Marinka, Mantripragada, Kiran, Horsdal, Henriette Thisted, Ingimarsson, Oddur, Jollie, Karel, Kennedy, James L, Köhler, Ole, Konte, Bettina, Lang, Maren, Legge, Sophie E, Lewis, Cathryn, MacCabe, James, Rees, Elliott, Malhotra, Anil K, McCrone, Paul, Meier, Sandra M, Mill, Jonathan, Mors, Ole, Mortensen, Preben Bo, O'Donovan, Michael C, Owen, Michael J, Pedersen, Carsten B, MacCabe, James H, Rietschel, Marcella, Rujescu, Dan, Schwalber, Ameli, Sigurdsson, Engilbert, Sørensen, Holger J, Spencer, Benjamin, Stefansson, Hreinn, Støvring, Henrik, Strohmaier, Jana, Sullivan, Patrick, McCarroll, Steven A, Vassos, Evangelos, Verbelen, Moira, Walters, James T R, Werge, Thomas, Baune, Bernhard T, Byrne, Enda M, Pocklington, Andrew J, Dannlowski, Udo, Eley, Thalia C, Hayward, Caroline, Martin, Nicholas G, McIntosh, Andrew M, Plomin, Robert, Porteous, David J, Wray, Naomi R, Caballero, Armando, Geschwind, Daniel H, Escott-Price, Valentina, Huckins, Laura M, Ruderfer, Douglas M, Santiago, Enrique, Sklar, Pamela, Stahl, Eli A, Won, Hyejung, Als, Thomas D, Andreassen, Ole A, Bækvad-Hansen, Marie, Ripke, Stephan, Pedersen, Carsten Bøcker, Børglum, Anders D, Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Hougaard, David M, Carrera, Noa, Mattheisen, Manuel, Molden, Espen, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Steinberg, Stacy, Tosato, Sarah, Consortium, GERAD1, Consortium, CRESTAR, Kirov, George, Bishop, Sophie, Harold, Denise, Sims, Rebecca, Gerrish, Amy, Chapman, Jade, Abraham, Richard, Hollingworth, Paul, Pahwa, Jaspreet, Denning, Nicola, Cameron, Darren, Thomas, Charlene, Taylor, Sarah, Powell, John, Proitsi, Petroula, Lupton, Michelle, Lovestone, Simon, Passmore, Peter, Craig, David, McGuinness, Bernadette, Johnston, Janet, Hamshere, Marian L, Todd, Stephen, Maier, Wolfgang, Jessen, Frank, Heun, Reiner, Schurmann, Britta, Ramirez, Alfredo, Becker, Tim, Herold, Christine, Lacour, Andre, Drichel, Dmitriy
Publikováno v:
GERAD1 Consortium: 2019, ' Publisher Correction : Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection ', Nature Genetics, vol. 51, no. 7, pp. 1193-1193 . https://doi.org/10.1038/s41588-019-0450-7
Nature genetics 51(7), 1193-1193 (2019). doi:10.1038/s41588-019-0450-7
Nature genetics 51(7), 1193-1193 (2019). doi:10.1038/s41588-019-0450-7
Author(s): Pardinas, Antonio F; Holmans, Peter; Pocklington, Andrew J; Escott-Price, Valentina; Ripke, Stephan; Carrera, Noa; Legge, Sophie E; Bishop, Sophie; Cameron, Darren; Hamshere, Marian L; Han, Jun; Hubbard, Leon; Lynham, Amy; Mantripragada, K
Autor:
Power, Robert A., Tansey, Katherine E., Buttenschøn, Henriette Nørmølle, Cohen-Woods, Sarah, Bigdeli, Tim, Hall, Lynsey S., Kutalik, Zoltán, Lee, S. Hong, Ripke, Stephan, Steinberg, Stacy, Teumer, Alexander, Viktorin, Alexander, Wray, Naomi R., Arolt, Volker, Baune, Bernard T., Boomsma, Dorret I., Børglum, Anders D., Byrne, Enda M., Castelao, Enrique, Craddock, Nick, Craig, Ian W., Dannlowski, Udo, Deary, Ian J., Degenhardt, Franziska, Forstner, Andreas J., Gordon, Scott D., Grabe, Hans J., Grove, Jakob, Hamilton, Steven P., Hayward, Caroline, Heath, Andrew C., Hocking, Lynne J., Homuth, Georg, Hottenga, Jouke J., Kloiber, Stefan, Krogh, Jesper, Landén, Mikael, Lang, Maren, Levinson, Douglas F., Lichtenstein, Paul, Lucae, Susanne, MacIntyre, Donald J., Madden, Pamela, Magnusson, Patrik K.E., Martin, Nicholas G., McIntosh, Andrew M., Middeldorp, Christel M., Milaneschi, Yuri, Montgomery, Grant W., Mors, Ole, Müller-Myhsok, Bertram, Nyholt, Dale R., Oskarsson, Hogni, Owen, Michael J., Padmanabhan, Sandosh, Penninx, Brenda W.J.H, Pergadia, Michele L., Porteous, David J., Potash, James B., Preisig, Martin, Rivera, Margarita, Shi, Jianxin, Shyn, Stanley I., Sigurdsson, Engilbert, Smit, Johannes H., Smith, Blair H., Stefansson, Hreinn, Stefansson, Kari, Strohmaier, Jana, Sullivan, Patrick F., Thomson, Pippa, Thorgeirsson, Thorgeir E., Van der Auwera, Sandra, Weissman, Myrna M., Breen, Gerome, Lewis, Cathryn M.
Publikováno v:
Biological psychiatry, vol. 81, no. 4, pp. 325-335
Background: \ud \ud Major depressive disorder (MDD) is a disabling mood disorder, and despite a known heritable component, a large meta-analysis of genome-wide association studies revealed no replicable genetic risk variants. Given prior evidence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::265a34f722f43bffdcb628fb445f388c
https://eprints.gla.ac.uk/123338/7/123338.pdf
https://eprints.gla.ac.uk/123338/7/123338.pdf