Treffer 1 - 20 von 218 für Suche 'Case, Chris', Suchdauer: 1,47s Treffer weiter einschränken
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    Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls von Craddock, Nick, Hurles, Matthew E, Cardin, Niall, Pearson, Richard D, Plagnol, Vincent, Robson, Samuel, Vukcevic, Damjan, Barnes, Chris, Conrad, Donald F, Giannoulatou, Eleni, Holmes, Chris, Marchini, Jonathan L, Stirrups, Kathy, Tobin, Martin D, Wain, Louise V, Yau, Chris, Aerts, Jan, Ahmad, Tariq, Andrews, T Daniel, Arbury, Hazel, Attwood, Anthony, Auton, Adam, Ball, Stephen G, Balmforth, Anthony J, Barrett, Jeffrey C, Barroso, Inês, Barton, Anne, Bennett, Amanda J, Bhaskar, Sanjeev, Blaszczyk, Katarzyna, Bowes, John, Brand, Oliver J, Braund, Peter S, Bredin, Francesca, Breen, Gerome, Brown, Morris J, Bruce, Ian N, Bull, Jaswinder, Burren, Oliver S, Burton, John, Byrnes, Jake, Caesar, Sian, Clee, Chris M, Coffey, Alison J, Connell, John M C, Cooper, Jason D, Dominiczak, Anna F, Downes, Kate, Drummond, Hazel E, Dudakia, Darshna, Dunham, Andrew, Ebbs, Bernadette, Eccles, Diana, Edkins, Sarah, Edwards, Cathryn, Elliot, Anna, Emery, Paul, Evans, David M, Evans, Gareth, Eyre, Steve, Farmer, Anne, Ferrier, I Nicol, Feuk, Lars, Fitzgerald, Tomas, Flynn, Edward, Forbes, Alistair, Forty, Liz, Franklyn, Jayne A, Freathy, Rachel M, Gibbs, Polly, Gilbert, Paul, Gokumen, Omer, Gordon-Smith, Katherine, Gray, Emma, Green, Elaine, Groves, Chris J, Grozeva, Detelina, Gwilliam, Rhian, Hall, Anita, Hammond, Naomi, Hardy, Matt, Harrison, Pile, Hassanali, Neelam, Hebaishi, Husam, Hines, Sarah, Hinks, Anne, Hitman, Graham A, Hocking, Lynne, Howard, Eleanor, Howard, Philip, Howson, Joanna M M, Hughes, Debbie, Hunt, Sarah, Isaacs, John D, Jain, Mahim, Jewell, Derek P, Johnson, Toby, Jolley, Jennifer D, Jones, Ian R, Jones, Lisa A

    Veröffentlicht in Nature (London)

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    Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility von Patsopoulos, Nikolaos A., Baranzini, Sergio E., Santaniello, Adam, Shoostari, Parisa, Cotsapas, Chris, Wong, Garrett, Beecham, Ashley H., James, Tojo, Replogle, Joseph, Vlachos, Ioannis S., McCabe, Cristin, Pers, Tune H., Brandes, Aaron, White, Charles, Keenan, Brendan, Cimpean, Maria, Winn, Phoebe, Panteliadis, Ioannis-Pavlos, Robbins, Allison, Andlauer, Till F. M., Zarzycki, Onigiusz, Dubois, Bénédicte, Goris, An, Søndergaard, Helle Bach, Sellebjerg, Finn, Sorensen, Per Soelberg, Ullum, Henrik, Thørner, Lise Wegner, Saarela, Janna, Cournu-Rebeix, Isabelle, Damotte, Vincent, Fontaine, Bertrand, Guillot-Noel, Lena, Lathrop, Mark, Vukusic, Sandra, Berthele, Achim, Pongratz, Viola, Buck, Dorothea, Gasperi, Christiane, Graetz, Christiane, Grummel, Verena, Hemmer, Bernhard, Hoshi, Muni, Knier, Benjamin, Korn, Thomas, Lill, Christina M., Luessi, Felix, Mühlau, Mark, Zipp, Frauke, Dardiotis, Efthimios, Agliardi, Cristina, Amoroso, Antonio, Barizzone, Nadia, Benedetti, Maria D., Bernardinelli, Luisa, Cavalla, Paola, Clarelli, Ferdinando, Comi, Giancarlo, Cusi, Daniele, Esposito, Federica, Ferrè, Laura, Galimberti, Daniela, Guaschino, Clara, Leone, Maurizio A., Martinelli, Vittorio, Moiola, Lucia, Salvetti, Marco, Sorosina, Melissa, Vecchio, Domizia, Zauli, Andrea, Santoro, Silvia, Mancini, Nicasio, Zuccalà, Miriam, Mescheriakova, Julia, van Duijn, Cornelia, Bos, Steffan D., Celius, Elisabeth G., Spurkland, Anne, Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Bomfim, Izaura L., Gomez-Cabrero, David, Hillert, Jan, Jagodic, Maja, Lindén, Magdalena, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mirela, Baker, Amie, Ban, Maria, Hawkins, Clive, Hysi, Pirro, Kalra, Seema, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Molyneux, Paul, Neville, Matthew


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    Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke von Bellenguez, Céline, Bevan, Steve, Gschwendtner, Andreas, Spencer, Chris C A, Burgess, Annette I, Pirinen, Matti, Jackson, Caroline A, Traylor, Matthew, Strange, Amy, Su, Zhan, Band, Gavin, Syme, Paul D, Malik, Rainer, Pera, Joanna, Norrving, Bo, Lemmens, Robin, Freeman, Colin, Schanz, Renata, James, Tom, Poole, Deborah, Murphy, Lee, Segal, Helen, Cortellini, Lynelle, Cheng, Yu-Ching, Woo, Daniel, Nalls, Michael A, Müller-Myhsok, Bertram, Meisinger, Christa, Seedorf, Udo, Ross-Adams, Helen, Boonen, Steven, Wloch-Kopec, Dorota, Valant, Valerie, Slark, Julia, Furie, Karen, Delavaran, Hossein, Langford, Cordelia, Deloukas, Panos, Edkins, Sarah, Hunt, Sarah, Gray, Emma, Dronov, Serge, Peltonen, Leena, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Stefansson, Kari, Boncoraglio, Giorgio B, Parati, Eugenio A, Attia, John, Holliday, Elizabeth, Levi, Chris, Franzosi, Maria-Grazia, Goel, Anuj, Helgadottir, Anna, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz, Mathew, Christopher G, Palmer, Colin N A, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas W, Worrall, Bradford B, Kittner, Steven J, Mitchell, Braxton D, Kissela, Brett, Meschia, James F, Thijs, Vincent, Lindgren, Arne, Macleod, Mary Joan, Slowik, Agnieszka, Walters, Matthew, Rosand, Jonathan, Sharma, Pankaj, Farrall, Martin, Sudlow, Cathie L M, Rothwell, Peter M, Dichgans, Martin, Donnelly, Peter, Markus, Hugh S

    Veröffentlicht in Nature genetics

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