Systematic Analysis and Biomarker Study for Alzheimer’s Disease von Li, Xinzhong, Wang, Haiyan, Long, Jintao, Pan, Genhua, He, Taigang, Anichtchik, Oleg, Belshaw, Robert, Albani, Diego, Edison, Paul, Green, Elaine K, Scott, James

Volltext

P2RX7: A bipolar and unipolar disorder candidate susceptibility gene? von Green, Elaine K., Grozeva, Detelina, Raybould, Rachel, Elvidge, Gareth, Macgregor, Stuart, Craig, Ian, Farmer, Anne, McGuffin, Peter, Forty, Liz, Jones, Lisa, Jones, Ian, O'Donovan, Mick C., Owen, Mike J., Kirov, George, Craddock, Nick

Volltext

Affective temperaments across the bipolar–unipolar spectrum: Examination of the TEMPS-A in 927 patients and controls von Di Florio, Arianna, Hamshere, Marian, Forty, Liz, Green, Elaine K, Grozeva, Detelina, Jones, Ian, Caesar, Sian, Fraser, Christine, Gordon-Smith, Katherine, Jones, Lisa, Craddock, Nick, Smith, Daniel J

Volltext

Gene Ontology Analysis of GWA Study Data Sets Provides Insights into the Biology of Bipolar Disorder von Holmans, Peter, Green, Elaine K., Pahwa, Jaspreet Singh, Ferreira, Manuel A.R., Purcell, Shaun M., Sklar, Pamela, Owen, Michael J., O'Donovan, Michael C., Craddock, Nick

Volltext

Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders von Van Den Bossche, Maarten J., Strazisar, Mojca, De Bruyne, Stephan, Bervoets, Chris, Lenaerts, An-Sofie, De Zutter, Sonia, Nordin, Annelie, Norrback, Karl-Fredrik, Goossens, Dirk, De Rijk, Peter, Green, Elaine K., Grozeva, Detelina, Mendlewicz, Julien, Craddock, Nick, Sabbe, Bernard G., Adolfsson, Rolf, Souery, Daniel, Del-Favero, Jurgen

Volltext

Novel ATP2A2 mutations in a large sample of individuals with Darier disease von Green, Elaine K., Gordon-Smith, Katherine, Burge, Susan M., Grozeva, Detelina, Munro, Colin S., Tavadia, Sherine, Jones, Lisa, Craddock, Nicholoas

Volltext

Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder: Case-control study of over 3000 individuals from the UK von GREEN, ELAINE K, RAYBOULD, RACHEL, MACGREGOR, STUART, HYDE, SALLY, YOUNG, ALLAN H, O'DONOVAN, MICHAEL C, OWEN, MICHAEL J, KIROV, GEORGE, JONES, LISA, JONES, IAN, CRADDOCK, NICK

Volltext

Genome‐wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type von Green, Elaine K., Di Florio, Arianna, Forty, Liz, Gordon‐Smith, Katherine, Grozeva, Detelina, Fraser, Christine, Richards, Alexander L., Moran, Jennifer L., Purcell, Shaun, Sklar, Pamela, Kirov, George, Owen, Michael J., O'Donovan, Michael C., Craddock, Nick, Jones, Lisa, Jones, Ian R.

Volltext

Bipolar disorder and polymorphisms in the dysbindin gene ( DTNBP1) von Raybould, Rachel, Green, Elaine K., MacGregor, Stuart, Gordon-Smith, Katherine, Heron, Jess, Hyde, Sally, Caesar, Sian, Nikolov, Ivan, Williams, Nigel, Jones, Lisa, O’Donovan, Michael C., Owen, Michael J., Jones, Ian, Kirov, George, Craddock, Nick

Volltext

Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder von Green, Elaine K., Grozeva, Detelina, Moskvina, Valentina, Hamshere, Marian L., Jones, Ian R., Jones, Lisa, Forty, Liz, Caesar, Sian, Gordon-Smith, Katherine, Fraser, Christine, Russell, Ellie, St Clair, David, Young, Allan H., Ferrier, Nicol, Farmer, Anne, McGuffin, Peter, Holmans, Peter A., Owen, Michael J., O'Donovan, Michael C., Craddock, Nick

Volltext

Operation of the Schizophrenia Susceptibility Gene, Neuregulin 1, Across Traditional Diagnostic Boundaries to Increase Risk for Bipolar Disorder von Green, Elaine K, Raybould, Rachel, Macgregor, Stuart, Gordon-Smith, Katherine, Heron, Jess, Hyde, Sally, Grozeva, Detelina, Hamshere, Marian, Williams, Nigel, Owen, Michael J, O’Donovan, Michael C, Jones, Lisa, Jones, Ian, Kirov, George, Craddock, Nick

Volltext

Genome-wide association study identifies eight loci associated with blood pressure von Jackson, Anne U, Burton, Paul R, Di Gregorio, Alessandra, Mohlke, Karen L, Galan, Pilar, Syvänen, Ann-Christine, Marrugat, Jaume, Jarvelin, Marjo-Riitta, Newton-Cheh, Christopher, Meitinger, Thomas, Watkins, Hugh, Lucas, Gavin, Soranzo, Nicole, Tobin, Martin D, Wain, Louise V, Kooner, Jaspal S, Wallace, Chris, Altshuler, David, Najjar, Samer S, Zeggini, Eleftheria, Felix, Stephan B, Freimer, Nelson B, Laakso, Markku, Homuth, Georg, Ferrucci, Luigi, Brown, Morris, Snieder, Harold, Wichmann, H Erich, Orho-Melander, Marju, Chambers, John C, Valle, Timo T, van der Schouw, Yvonne T, Ernst, Florian, Strachan, David P, van der Harst, Pim, Kathiresan, Sekar, Romanazzi, Valeria, Dörr, Marcus, McArdle, Wendy L, Peden, John F, Beckmann, Jacques S, Song, Kijoung, Yuan, Xin, Melander, Olle, Coin, Lachlan, Lim, Noha, Barroso, Inês, Eyheramendy, Susana, O'Reilly, Paul F, Salomaa, Veikko, Gut, Ivo G, Tuomilehto, Jaakko, Peltonen, Leena, Morken, Mario A, Org, Elin, Luan, Jian'an, Panico, Salvatore, de Jong, Paul E, Schwartz, Stephen M, Matullo, Giuseppe, Wareham, Nicholas J, Seedorf, Udo, Laan, Maris, Uiterwaal, Cuno S, Boehnke, Michael, Farrall, Martin, Elosua, Roberto, Webster, John, Vollenweider, Peter, Reffelmann, Thorsten, Abecasis, Gonçalo R, Rettig, Rainer, Zhao, Jing Hua, Khaw, Kay-Tee, Elliott, Katherine S, Forouhi, Nita G, Voight, Benjamin F, Caulfield, Mark, Dominiczak, Anna, Munroe, Patricia B, Zhai, Guangju, Loos, Ruth JF, Sacerdote, Carlotta, Mooser, Vincent, Bergmann, Sven, Lakatta, Edward G, Bingham, Sheila A, Numans, Mattijs E, Völker, Uwe, Stringham, Heather M, Jousilahti, Pekka, Williams, Frances M, Clarke, Robert, Allione, Alessandra, Spector, Tim D, Elliott, Paul, Collins, Francis S, Lorbeer, Roberto, Sanna, Serena, Ricceri, Fulvio

Volltext

Common variants near MC4R are associated with fat mass, weight and risk of obesity von Day, Ian, Dermitzakis, Emmanouil T, Randall, Joshua C, Weedon, Michael N, Hinney, Anke, Evans, David M, Qi, Lu, Bennett, Amanda J, Munroe, Patricia B, Herrera, Blanca, Johnson, Toby, Elliott, Katherine S, Song, Kijoung, Zeggini, Eleftheria, Cauchi, Stéphane, Teichmann, Sarah A, Lindgren, Cecilia M, Brown, Morris, Sims, Matthew A, Karpe, Fredrik, O'Rahilly, Stephen, Hattersley, Andrew T, Scherag, André, Samani, Nilesh J, Keniry, Andrew, Li, Shengxu, Beckmann, Jacques S, Cooper, Cyrus, Caulfield, Mark J, Owen, Katharine R, Luben, Robert N, McGinnis, Ralph, Ghori, Jilur, Ness, Andrew R, Bochud, Murielle, Jarvelin, Marjo-Riitta, Hebebrand, Johannes, Ong, Ken K, Freathy, Rachel M, McArdle, Wendy L, Potter, Simon, Wareham, Nicholas J, Ganz Vogel, Carla I, Mooser, Vincent, Barroso, Inês, Deloukas, Panos, Waterworth, Dawn M, Bergmann, Sven, Elliott, Paul, Gwilliam, Rhian, Tobias, Jonathan H, Jolley, Jennifer D M, Morris, Andrew D, Loos, Ruth J F, Yuan, Xin, Smith, George Davey, Palmer, Colin N A, Groves, Christopher J, Dina, Christian, Syddall, Holly E, Waeber, Gerard, Zhao, Jing Hua, Sandhu, Manjinder S, Doney, Alex S F, Hunt, Sarah E, Pouta, Anneli, Speliotes, Elizabeth K, Connell, John M, Timpson, Nicholas J, Wallace, Chris, Attwood, Antony P, Hall, Alistair S, Khaw, Kay-Tee, Meyre, David, Vollenweider, Peter, Bingham, Sheila A, Berndt, Sonja I, Hadley, David, Rayner, Nigel W, Frayling, Timothy M, Sadaf Farooqi, I, Hirschhorn, Joel N, Strachan, David P, Inouye, Michael, Papadakis, Konstantinos, Ring, Susan M, Wraight, Vicki L, Willer, Cristen J, Marchini, Jonathan, Uda, Manuela, Nica, Alexandra C, Mangino, Massimo, Soranzo, Nicole, McCarthy, Mark I, De, Subhajyoti, Neville, Matthew J, Prokopenko, Inga, Wheeler, Eleanor, Heid, Iris M, Froguel, Philippe

Volltext

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls von Clayton, David G, Cardon, Lon R, Duncanson, Audrey, Ouwehand, Willem H, Todd, John A, Donnelly, Peter, Easton, Doug, Evans, David, Morris, Andrew P, Spencer, Chris C. A, Boorman, James P, Cant, Barbara, Everson, Ursula, Hussey, Judith M, Knight, Alexandra S, Nutland, Sarah, Stevens, Helen E, Watkins, Nicholas A, Jones, Richard W, Ring, Susan M, Breen, Gerome, Caesar, Sian, Green, Elaine K, Grozeva, Detelina, Jones, Ian R, Kirov, George, Moskvina, Valentina, Nikolov, Ivan, Collier, David A, Farmer, Anne, Williamson, Richard, Young, Allan H, Ball, Stephen G, Balmforth, Anthony J, Bishop, D. Timothy, Iles, Mark M, Dixon, Richard J, Stevens, Suzanne, Thompson, John R, Bredin, Francesca, Tremelling, Mark, Drummond, Hazel, Nimmo, Elaine R, Fisher, Sheila A, Forbes, Alastair, Lewis, Cathryn M, Prescott, Natalie J, Barbour, Jamie, Mohiuddin, M. Khalid, Mansfield, John C, Cummings, Fraser R, Connell, John, Dobson, Richard, Gungadoo, Johannie, Newhouse, Stephen J, Barton, Anne, Bruce, Ian N, John, Sally L, Potter, Catherine, Silman, Alan J, Symmons, Deborah P. M, Dunger, David B, Widmer, Barry, Frayling, Timothy M, Lango, Hana, Perry, John R. B, Groves, Christopher J, Rayner, Nigel W, Timpson, Nicholas J, Zeggini, Eleftheria, Newport, Melanie, Vannberg, Fredrik, Farrar, Claire, Wordsworth, Paul, Brown, Matthew A, Franklyn, Jayne A, Heward, Joanne M, Simmonds, Matthew J, Seal, Sheila, Stratton, Michael R, Ban, Maria, Conway, David, Chaney, Amy, Ghori, Mohammed J. R, Gwilliam, Rhian, Hunt, Sarah E, McGinnis, Ralph, Potter, Simon, Whittaker, Pamela, Widden, Claire, Withers, David, Hallgrimsdottir, Ingileif B, Vukcevic, Damjan, Bentley, David, Caulfield, Mark, Compston, Alistair, Farrall, Martin, Hall, Alistair S, Hattersley, Andrew T, Mathew, Christopher G

Volltext

Genome-wide and fine-resolution association analysis of malaria in West Africa von Jallow, Muminatou, Molyneux, Malcolm E, Singhasivanon, Pratap, Clark, Taane G, Donnelly, Peter, Parker, Michael, Mueller, Ivo, Pinder, Margaret, Karunaweera, Nadira, Dolo, Amagana, Fry, Andrew E, Gwilliam, Rhian, Bojang, Kalifa A, Williams, Thomas N, Amodu, Olukemi, Horstmann, Rolf D, Kokwaro, Gilbert, Rowlands, Kate, Drakeley, Chris, Auburn, Sarah, Bumpstead, Suzannah J, Doumbo, Ogobara K, Achidi, Eric Akum, Agbenyega, Tsiri, Peshu, Norbert, Somaskantharajah, Elilan, Mendy, Alieu, Marchini, Jonathan, Dunstan, Sarah, Lemnge, Martha, Teo, Yik Ying, Tall, Adama, Ibrahim, Muntaser, Deloukas, Panos, Makani, Julie, Rockett, Kirk A, Green, Angela, Jeffreys, Anna E, Sirima, Sodiomon, Koram, Kwadwo A, Campino, Susana, Morris, Andrew, Corran, Patrick, Modiano, David, Sisay-Joof, Fatou, Troye-Blomberg, Marita, Potter, Simon, Fernando, Deepika, Riley, Eleanor M, Evans, Jennifer, Sakuntabhai, Anavaj, Conway, David J, Widden, Claire, Ragoussis, Jiannis, Allen, Angela, Inouye, Michael, Hien, Tran Tinh, Palotie, Aarno, Sirugo, Giorgio, Taylor, Terrie E, Howie, Bryan, Kwiatkowski, Dominic P, Thera, Mahamadou, Kivinen, Katja, Small, Kerrin S, Puijalon, Odile, Hunt, Sarah E, Djimde, Abdoulaye, Farrar, Jeremy, Marsh, Kevin, Michon, Pascal, Reyburn, Hugh, Usen, Stanley, Wilson, Michael, Coffey, Alison, SanJoaquin, Miguel, Plowe, Christopher V, Dunham, Andrew, Rogers, Jane, Reeder, John, Whittaker, Pamela

Volltext

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders von Andlauer, Till F. M., Guzman-Parra, Jose, Streit, Fabian, Strohmaier, Jana, González, Maria José, Gil Flores, Susana, Cabaleiro Fabeiro, Francisco J., del Río Noriega, Francisco, Perez, Fermin Perez, Haro González, Jesus, Orozco Diaz, Guillermo, de Diego-Otero, Yolanda, Moreno-Küstner, Berta, Auburger, Georg, Degenhardt, Franziska, Heilmann-Heimbach, Stefanie, Herms, Stefan, Hoffmann, Per, Frank, Josef, Foo, Jerome C., Treutlein, Jens, Witt, Stephanie H., Cichon, Sven, Kogevinas, Manolis, Rivas, Fabio, Mayoral, Fermín, Müller-Myhsok, Bertram, Forstner, Andreas J., Nöthen, Markus M., Rietschel, Marcella

Volltext

Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease von Ouwehand, Willem, Keniry, Andrew, Fisher, Sheila A, Jewell, Derek P, Anderson, Carl A, Prescott, Natalie J, Deloukas, Panos, Blaszczyk, Katarzyna, Mansfield, John C, Mathew, Christopher G, Watkins, Nick, Drummond, Hazel, Cummings, Fraser R, Forbes, Alastair, Barrett, Jeffrey C, Ravindrarajah, Radhi, Sanderson, Jeremy, Inouye, Mike, Hunt, Sarah, Nimmo, Elaine R, Johnson, Christopher, Bumpstead, Suzannah, Hanson, Catherine E, Lobo, Alan, Massey, Dunecan, Cardon, Lon, Ewels, Philip, Satsangi, Jack, Tremelling, Mark, Gwilliam, Rhian, Carter, Martyn, Berzuini, Carlo, Lees, Charlie W, Onnie, Clive M, Parkes, Miles, Lewis, Cathryn M

Volltext

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder von Sklar, Pamela, Craddock, Nick, Ferreira, Manuel A R, O'Donovan, Michael C, Meng, Yan A, Jones, Ian R, Ruderfer, Douglas M, Jones, Lisa, Fan, Jinbo, Kirov, George, Perlis, Roy H, Green, Elaine K, Smoller, Jordan W, Grozeva, Detelina, Stone, Jennifer, Nikolov, Ivan, Chambert, Kimberly, Hamshere, Marian L, Nimgaonkar, Vishwajit L, Moskvina, Valentina, Thase, Michael E, Caesar, Sian, Sachs, Gary S, Franklin, Jennifer, Gordon-Smith, Katherine, Ardlie, Kristin G, Gabriel, Stacey B, Fraser, Christine, Blumenstiel, Brendan, Defelice, Matthew, Breen, Gerome, Gill, Michael, Morris, Derek W, Elkin, Amanda, Muir, Walter J, McGhee, Kevin A, Williamson, Richard, MacIntyre, Donald J, MacLean, Alan W, St Clair, David, Robinson, Michelle, Van Beck, Margaret, Pereira, Ana C P, Kandaswamy, Radhika, McQuillin, Andrew, Collier, David A, Bass, Nicholas J, Young, Allan H, Lawrence, Jacob, Nicol Ferrier, I, Anjorin, Adebayo, Farmer, Anne, Curtis, David, Scolnick, Edward M, McGuffin, Peter, Daly, Mark J, Corvin, Aiden P, Holmans, Peter A, Blackwood, Douglas H, Gurling, Hugh M, Owen, Michael J, Purcell, Shaun M

Volltext

Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases von Charney, Alexander W., Stahl, Eli A., Green, Elaine K., Chen, Chia-Yen, Moran, Jennifer L., Chambert, Kimberly, Belliveau, Richard A., Forty, Liz, Gordon-Smith, Katherine, Lee, Phil H., Bromet, Evelyn J., Buckley, Peter F., Escamilla, Michael A., Fanous, Ayman H., Fochtmann, Laura J., Lehrer, Douglas S., Malaspina, Dolores, Marder, Stephen R., Morley, Christopher P., Nicolini, Humberto, Perkins, Diana O., Rakofsky, Jeffrey J., Rapaport, Mark H., Medeiros, Helena, Sobell, Janet L., Backlund, Lena, Bergen, Sarah E., Juréus, Anders, Schalling, Martin, Lichtenstein, Paul, Knowles, James A., Burdick, Katherine E., Jones, Ian, Jones, Lisa A., Hultman, Christina M., Perlis, Roy, Purcell, Shaun M., McCarroll, Steven A., Pato, Carlos N., Pato, Michele T., Di Florio, Ariana, Craddock, Nick, Landén, Mikael, Smoller, Jordan W., Ruderfer, Douglas M., Sklar, Pamela

Volltext

Detailed mapping of a congenital heart disease gene in chromosome 3p25 von Green, Elaine K, Priestley, Matthew D, Waters, Jonathan, Maliszewska, Chris, Latif, Farida, Maher, Eamonn R

Volltext