Treffer 1 - 20 von 98 für Suche 'Walker, Melissa Anne', Suchdauer: 1,71s Treffer weiter einschränken
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    Genetic analyses of diverse populations improves discovery for complex traits von Wojcik, Genevieve L., Graff, Mariaelisa, Nishimura, Katherine K., Tao, Ran, Haessler, Jeffrey, Gignoux, Christopher R., Highland, Heather M., Patel, Yesha M., Sorokin, Elena P., Avery, Christy L., Belbin, Gillian M., Bien, Stephanie A., Cheng, Iona, Cullina, Sinead, Hodonsky, Chani J., Hu, Yao, Huckins, Laura M., Jeff, Janina, Justice, Anne E., Kocarnik, Jonathan M., Lim, Unhee, Lin, Bridget M., Lu, Yingchang, Nelson, Sarah C., Park, Sung-Shim L., Poisner, Hannah, Preuss, Michael H., Richard, Melissa A., Schurmann, Claudia, Setiawan, Veronica W., Sockell, Alexandra, Vahi, Karan, Verbanck, Marie, Vishnu, Abhishek, Walker, Ryan W., Young, Kristin L., Zubair, Niha, Acuña-Alonso, Victor, Ambite, Jose Luis, Barnes, Kathleen C., Boerwinkle, Eric, Bottinger, Erwin P., Bustamante, Carlos D., Caberto, Christian, Canizales-Quinteros, Samuel, Conomos, Matthew P., Deelman, Ewa, Do, Ron, Doheny, Kimberly, Fernández-Rhodes, Lindsay, Fornage, Myriam, Hailu, Benyam, Heiss, Gerardo, Henn, Brenna M., Hindorff, Lucia A., Jackson, Rebecca D., Laurie, Cecelia A., Laurie, Cathy C., Li, Yuqing, Lin, Dan-Yu, Moreno-Estrada, Andres, Nadkarni, Girish, Norman, Paul J., Pooler, Loreall C., Reiner, Alexander P., Romm, Jane, Sabatti, Chiara, Sandoval, Karla, Sheng, Xin, Stahl, Eli A., Stram, Daniel O., Thornton, Timothy A., Wassel, Christina L., Wilkens, Lynne R., Winkler, Cheryl A., Yoneyama, Sachi, Buyske, Steven, Haiman, Christopher A., Kooperberg, Charles, Le Marchand, Loic, Loos, Ruth J. F., Matise, Tara C., North, Kari E., Peters, Ulrike, Kenny, Eimear E., Carlson, Christopher S.

    Veröffentlicht in Nature (London)

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    HLA-DQA105 Carriage Associated With Development of Anti-Drug Antibodies to Infliximab and Adalimumab in Patients With Crohn’s Disease von Kennedy, Nicholas A., Moutsianas, Loukas, Heap, Graham A., Chanchlani, Neil, Walker, Gareth J., Perry, Mandy H., Lees, Charlie W., Parkes, Miles, Mansfield, John C., McGovern, Dermot, Ahmad, Tariq, Patel, Vinod, Mazhar, Zia, Colleypriest, Ben, Weaver, Sean, Preston, Cathryn, Butt, Assad, Smith, Melissa, Beale, Amanda, Langlands, Sarah, Direkze, Natalie, Torrente, Franco, De La Revella Negro, Juan, Ewen MacDonald, Chris, Evans, Stephen M, Gunasekera, Anton V J, Thakur, Alka, Elphick, David, Shenoy, Achuth, Agrawal, Anurag, Bridger, Stephen, Cooper, Sheldon C, de Silva, Shanika, Mowat, Craig, Mayhead, Phillip, Lees, Charlie, Ahmad, Tariq, Russell, Richard K, Gervais, Lisa, Dunckley, Paul, Mahmood, Tariq, Banim, Paul J R, Sonwalkar, Sunil, Ghosh, Deb, Phillips, Rosemary H, Azaz, Amer, Sebastian, Shaji, Shenderey, Richard, Armstrong, Lawrence, Bell, Claire, Hariraj, Radhakrishnan, Matthews, Helen, Jafferbhoy, Hasnain, Selinger, Christian P, Willmott, Anne, Bloom, Stuart L, Chung-Faye, Guy, Harbord, Marcus, Hart, Ailsa, Lindsay, James O, Mawdsley, Joel E, McNair, Alistair, Murray, Charles D, Paul, Thankam, Pollok, Richard, Shah, Neil, Johnson, Matt W, Modi, Anita, Dawa Kabiru, Kasamu, Baburajan, B K, Bhaduri, Bim, Adebayo Fagbemi, Andrew, Limdi, Jimmy K, Ramadas, Arvind, MacFaul, George, Mansfield, John, Morris, Mary-Anne, Tremelling, Mark, Hawkey, Chris, Charlton, Charles PJ, Rodrigues, Astor, Snook, Jonathon, De Silva, Aminda N, Smith, Mark S, Panter, Simon, Cummings, Fraser, Mahmood, Zahid, Sen, Sandip, Pigott, Anna J, Hobday, David, Wesley, Emma, Beckly, John, Vani, Deven, Ramakrishnan, Subramaniam, Chaudhary, Rakesh, Trudgill, Nigel J, Cooney, Rachel, Bell, Andy, Li, Andy, Gore, Stephen


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    Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder von C Yuen, Ryan K, Merico, Daniele, Bookman, Matt, L Howe, Jennifer, Thiruvahindrapuram, Bhooma, Patel, Rohan V, Whitney, Joe, Deflaux, Nicole, Bingham, Jonathan, Wang, Zhuozhi, Pellecchia, Giovanna, Buchanan, Janet A, Walker, Susan, Marshall, Christian R, Uddin, Mohammed, Zarrei, Mehdi, Deneault, Eric, D'Abate, Lia, Chan, Ada J S, Koyanagi, Stephanie, Paton, Tara, Pereira, Sergio L, Hoang, Ny, Engchuan, Worrawat, Higginbotham, Edward J, Ho, Karen, Lamoureux, Sylvia, Li, Weili, MacDonald, Jeffrey R, Nalpathamkalam, Thomas, Sung, Wilson W L, Tsoi, Fiona J, Wei, John, Xu, Lizhen, Tasse, Anne-Marie, Kirby, Emily, Van Etten, William, Twigger, Simon, Roberts, Wendy, Drmic, Irene, Jilderda, Sanne, Modi, Bonnie MacKinnon, Kellam, Barbara, Szego, Michael, Cytrynbaum, Cheryl, Weksberg, Rosanna, Zwaigenbaum, Lonnie, Woodbury-Smith, Marc, Brian, Jessica, Senman, Lili, Iaboni, Alana, Doyle-Thomas, Krissy, Thompson, Ann, Chrysler, Christina, Leef, Jonathan, Savion-Lemieux, Tal, Smith, Isabel M, Liu, Xudong, Nicolson, Rob, Seifer, Vicki, Fedele, Angie, Cook, Edwin H, Dager, Stephen, Estes, Annette, Gallagher, Louise, Malow, Beth A, Parr, Jeremy R, Spence, Sarah J, Vorstman, Jacob, Frey, Brendan J, Robinson, James T, Strug, Lisa J, Fernandez, Bridget A, Elsabbagh, Mayada, Carter, Melissa T, Hallmayer, Joachim, Knoppers, Bartha M, Anagnostou, Evdokia, Szatmari, Peter, Ring, Robert H, Glazer, David, Pletcher, Mathew T, Scherer, Stephen W

    Veröffentlicht in Nature neuroscience

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    Defining the role of common variation in the genomic and biological architecture of adult human height von Amin, Najaf, Croteau-Chonka, Damien C, Jackson, Anne U, Randall, Joshua C, Westra, Harm-Jan, Absher, Devin, Baron, Jeffrey, Feitosa, Mary F, Fischer, Krista, Kanoni, Stavroula, Leach, Irene Mateo, Palmer, Cameron D, Prokopenko, Inga, Ripke, Stephan, Stancáková, Alena, Sung, Yun Ju, Trompet, Stella, Blüher, Matthias, Bolton, Jennifer L, Claudi-Boehm, Simone, Cooper, Matthew, Daw, E Warwick, Dörr, Marcus, Folkersen, Lasse, Grönberg, Henrik, Hannemann, Anke, Helmer, Quinta, Hemani, Gibran, Hoffmann, Wolfgang, Holmen, Oddgeir, Kho, Abel N, Kratzer, Wolfgang, Magnusson, Patrik K E, McLaren, Paul J, Menni, Cristina, Merger, Sigrun, Milani, Lili, Nauck, Matthias, Oozageer, Laticia, Pilz, Stefan, Rayner, Nigel W, Renstrom, Frida, Scott, Robert A, Stringham, Heather M, Swertz, Morris A, Syvänen, Ann-Christine, van Dijk, Suzanne, Vonk, Judith M, Wennauer, Roman, Wilsgaard, Tom, Wong, Andrew, Wright, Alan F, Bergmann, Sven, Bornstein, Stefan R, Brambilla, Paolo, Brown, Morris J, Chakravarti, Aravinda, Danesh, John, de Faire, Ulf, Erbel, Raimund, Ferrières, Jean, Gejman, Pablo V, Heath, Andrew C, Hengstenberg, Christian, Hingorani, Aroon D, Kaprio, Jaakko, Madden, Pamela A F, Marette, André, Montgomery, Grant W, Nelis, Mari, Ong, Ken K, Peters, Annette, Qi, Lu, Rice, Treva K, Saramies, Jouko, Sebert, Sylvain, Steinthorsdottir, Valgerdur, Tardif, Jean-Claude, Tremblay, Angelo, Assimes, Themistocles L, Dedoussis, George, Franks, Paul W, Groop, Leif C, Hamsten, Anders, Kuh, Diana, Laakso, Markku, Munroe, Patricia B, Schlessinger, David, Slagboom, P Eline, Snieder, Harold, Spector, Tim D, Tuomilehto, Jaakko, Uusitupa, Matti, Walker, Mark, Thorsteinsdottir, Unnur, Barroso, Inês, Borecki, Ingrid B, McCarthy, Mark I, Visscher, Peter M, Frayling, Timothy M

    Veröffentlicht in Nature genetics

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    Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations von Rebbeck, Timothy R., Hamann, Ute, Olah, Edith, Solano, Angela R., Teo, Soo‐Hwang, Chan, TL, Couch, Fergus J., Palmero, Edenir Inêz, Park, Sue Kyung, Parsons, Michael T., Leslie, Goska, Aalfs, Cora M., Adlard, Julian, Agata, Simona, Aittomäki, Kristiina, Andrulis, Irene L., Barkardottir, Rosa B., Benitez, Javier, Blanco, Amie M., Bonadona, Valérie, Bonanni, Bernardo, Caligo, Maria A., Campbell, Ian, Chung, Wendy K., Claes, Kathleen B.M., Cook, Jackie, Davidson, Rosemarie, Leeneer, Kim, Domchek, Susan M., Dorfling, Cecilia M., Velazquez, Carolina, Easton, Douglas F., Feliubadaló, Lidia, Ferrer, Sandra Fert, Foretova, Lenka, Galvão, Henrique C. R., Garber, Judy, Gesta, Paul, Giannini, Giuseppe, Gutierrez‐Barrera, Angelica, Hogervorst, Frans B.L., Imyanitov, Evgeny N., Izquierdo, Angel, Jakubowska, Anna, James, Paul, Janavicius, Ramunas, John, Esther M., Vijai, Joseph, Karlan, Beth Y., Kast, Karin, Investigators, KConFab, Korach, Jacob, Laitman, Yael, Lasset, Christine, Lázaro, Conxi, Lee, Annette, Lee, Min Hyuk, Lester, Jenny, Liljegren, Annelie, Machackova, Eva, Mari, Véronique, Meijers‐Heijboer, Hanne E.J., Miller, Austin, Montagna, Marco, Mulligan, Anna Marie, Ngeow, Joanne, Nielsen, Henriette Roed, Nussbaum, Robert L., Offit, Kenneth, Öfverholm, Anna, Osorio, Ana, Papp, Janos, Pedersen, Inge Sokilde, Peruga, Nina, Peterlongo, Paolo, Radice, Paolo, Robson, Mark, Rodriguez, Gustavo C., Rudaitis, Vilius, Schmidt, Ane Y., Senter, Leigha, Singer, Christian F., Skytte, Anne‐Bine, Sobol, Hagay, Teixeira, Manuel R., Tischkowitz, Marc, Toland, Amanda Ewart, Topka, Sabine, Trainer, Alison H, Varesco, Liliana, Varon‐Mateeva, Raymonda, Vega, Ana, Wachenfeldt, Anna, Wang‐Gohrke, Shan, Weber, Bernhard H. F., Yannoukakos, Drakoulis, Zorn, Kristin K., Chenevix‐Trench, Georgia, Spurdle, Amanda B., Nathanson, Katherine L.

    Veröffentlicht in Human mutation

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