Výsledky vyhledávání - Hamshere, M
- Zobrazuji výsledky 1 - 16 z 16
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Genome-wide association of mood-incongruent psychotic bipolar disorder Autor Goes, F S, Hamshere, M L, Seifuddin, F, Pirooznia, M, Belmonte-Mahon, P, Breuer, R, Schulze, T, Nöthen, M, Cichon, S, Rietschel, M, Holmans, P, Zandi, P P, Craddock, N, Potash, J B
Vydáno 2012Text -
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Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes Autor Hamshere, M L, Williams, N M, Norton, N, Williams, H, Cardno, A G, Zammit, S, Jones, L A, Murphy, K C, Sanders, R D, McCarthy, G, Gray, M Y, Jones, G, Holmans, P, O'Donovan, M C, Owen, M J, Craddock, N
Vydáno 2006Text -
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The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia Autor Green, E K, Grozeva, D, Jones, I, Jones, L, Kirov, G, Caesar, S, Gordon-Smith, K, Fraser, C, Forty, L, Russell, E, Hamshere, M L, Moskvina, V, Nikolov, I, Farmer, A, McGuffin, P, Holmans, P A, Owen, M J, O'Donovan, M C, Craddock, N
Vydáno 2010Text -
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Polygenic dissection of the bipolar phenotype Autor Hamshere, M. L., O’Donovan, M. C., Jones, I. R., Jones, L., Kirov, G., Green, E. K., Moskvina, V., Grozeva, D., Bass, N., McQuillin, A., Gurling, H., St Clair, D., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Sklar, P., Purcell, S., Holmans, P. A., Owen, M. J., Craddock, N.
Vydáno 2011Text -
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A Systematic Genomewide Linkage Study in 353 Sib Pairs with Schizophrenia Autor Williams, N. M., Norton, N., Williams, H., Ekholm, B., Hamshere, M. L., Lindblom, Y., Chowdari, K. V., Cardno, A. G., Zammit, S., Jones, L. A., Murphy, K. C., Sanders, R. D., McCarthy, G., Gray, M. Y., Jones, G., Holmans, P., Nimgaonkar, V., Adolfson, R., Ösby, U., Terenius, L., Sedvall, G., O’Donovan, M. C., Owen, M. J.
Vydáno 2003Text -
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Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept Autor Hamshere, M. L., Green, E. K., Jones, I. R., Jones, L., Moskvina, V., Kirov, G., Grozeva, D., Nikolov, I., Vukcevic, D., Caesar, S., Gordon-Smith, K., Fraser, C., Russell, E., Breen, G., St Clair, D., Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Holmans, P. A., Owen, M. J., O’Donovan, M. C., Craddock, N.
Vydáno 2009Text -
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Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia Autor Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R
Vydáno 2017Text -
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Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia Autor Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R
Vydáno 2016Text -
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Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia Autor Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R
Vydáno 2017Text -
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Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2 (FGFR2) Autor O’Donovan, M.C., Norton, N., Williams, H., Peirce, T., Moskvina, V., Nikolov, I., Hamshere, M., Carroll, L., Georgieva, L., Dwyer, S, Holmans, P., Marchini, J. L., Spencer, C.C.A., Howie, B., Leung, H-T., Giegling, I., Hartmann, A.M., Möller, H.-J., Morris, D.W., Shi, Y., Feng, G., Hoffmann, P., Propping, P., Vasilescu, C., Maier, W., Rietschel, M., Zammit, S., Schumacher, J., Quinn, E.M., Schulze, T.G., Iwata, N., Ikeda, M., Darvasi, A., Shifman, S., He, L., Duan, J., Sanders, A.R., Levinson, D.F., Adolfsson, R., Ösby, U., Terenius, Lars, Jönsson, Erik G, Cichon, S., Nöthen, M. M., Gill, M., Corvin, A.P., Rujescu, D., Gejman, P.V., Kirov, G., Craddock, N., Williams, N.M., Owen, M.J.
Vydáno 2008Text -
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No consistent evidence for association between mtDNA variants and Alzheimer disease Autor Hudson, G., Sims, R., Harold, D., Chapman, J., Hollingworth, P., Gerrish, A., Russo, G., Hamshere, M., Moskvina, V., Jones, N., Thomas, C., Stretton, A., Holmans, P.A., O'Donovan, M.C., Owen, M.J., Williams, J., Chinnery, P.F., Harold, Denise, Abraham, Richard, Hollingworth, Paul, Sims, Rebecca, Gerrish, Amy, Chapman, Jade, Russo, Giancarlo, Hamshere, Marian, Pahwa, Jaspreet Singh, Moskvina, Valentina, Dowzell, Kimberley, Williams, Amy, Jones, Nicola, Thomas, Charlene, Stretton, Alexandra, Morgan, Angharad, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K, Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle, Passmore, Peter, Craig, David, McGuinness, Bernadette, Todd, Stephen, Johnston, Janet, Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Heun, Reiner, Kölsch, Heike, Schürmann, Britta, van den Bussche, Hendrik, Heuser, Isabella, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison, Kauwe, John S.K., Cruchaga, Carlos, Nowotny, Petra, Morris, John C., Mayo, Kevin, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panagiotis, Holmans, Peter, O'Donovan, Michael, Owen, Michael J., Williams, Julie
Vydáno 2012Text -
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Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia Autor Witt, S H, Streit, F, Jungkunz, M, Frank, J, Awasthi, S, Reinbold, C S, Treutlein, J, Degenhardt, F, Forstner, A J, Heilmann-Heimbach, S, Dietl, L, Schwarze, C E, Schendel, D, Strohmaier, J, Abdellaoui, A, Adolfsson, R, Air, T M, Akil, H, Alda, M, Alliey-Rodriguez, N, Andreassen, O A, Babadjanova, G, Bass, N J, Bauer, M, Baune, B T, Bellivier, F, Bergen, S, Bethell, A, Biernacka, J M, Blackwood, D H R, Boks, M P, Boomsma, D I, Børglum, A D, Borrmann-Hassenbach, M, Brennan, P, Budde, M, Buttenschøn, H N, Byrne, E M, Cervantes, P, Clarke, T-K, Craddock, N, Cruceanu, C, Curtis, D, Czerski, P M, Dannlowski, U, Davis, T, de Geus, E J C, Di Florio, A, Djurovic, S, Domenici, E, Edenberg, H J, Etain, B, Fischer, S B, Forty, L, Fraser, C, Frye, M A, Fullerton, J M, Gade, K, Gershon, E S, Giegling, I, Gordon, S D, Gordon-Smith, K, Grabe, H J, Green, E K, Greenwood, T A, Grigoroiu-Serbanescu, M, Guzman-Parra, J, Hall, L S, Hamshere, M, Hauser, J, Hautzinger, M, Heilbronner, U, Herms, S, Hitturlingappa, S, Hoffmann, P, Holmans, P, Hottenga, J-J, Jamain, S, Jones, I, Jones, L A, Juréus, A, Kahn, R S, Kammerer-Ciernioch, J, Kirov, G, Kittel-Schneider, S, Kloiber, S, Knott, S V, Kogevinas, M, Landén, M, Leber, M, Leboyer, M, Li, Q S, Lissowska, J, Lucae, S, Martin, N G, Mayoral-Cleries, F, McElroy, S L, McIntosh, A M, McKay, J D, McQuillin, A, Medland, S E, Middeldorp, C M, Milaneschi, Y, Mitchell, P B, Montgomery, G W, Morken, G, Mors, O, Mühleisen, T W, Müller-Myhsok, B, Myers, R M, Nievergelt, C M, Nurnberger, J I, O'Donovan, M C, Loohuis, L M O, Ophoff, R, Oruc, L, Owen, M J, Paciga, S A, Penninx, B W J H, Perry, A, Pfennig, A, Potash, J B, Preisig, M, Reif, A, Rivas, F, Rouleau, G A, Schofield, P R, Schulze, T G, Schwarz, M, Scott, L, Sinnamon, G C B, Stahl, E A, Strauss, J, Turecki, G, Van der Auwera, S, Vedder, H, Vincent, J B, Willemsen, G, Witt, C C, Wray, N R, Xi, H S, Tadic, A, Dahmen, N, Schott, B H, Cichon, S, Nöthen, M M, Ripke, S, Mobascher, A, Rujescu, D, Lieb, K, Roepke, S, Schmahl, C, Bohus, M, Rietschel, M
Vydáno 2017Text