Treffer 1 - 20 von 86 für Suche 'NEWTON DALE C', Suchdauer: 1,45s Treffer weiter einschränken
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    Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility von Landi, Maria Teresa, MacGregor, Stuart, Machiela, Mitchell J., Stratigos, Alexander J., Ghiorzo, Paola, Brossard, Myriam, Calista, Donato, Zhang, Tongwu, Rodolfo, Monica, Trower, Adam J., Martinez, Jacobo, Hadjisavvas, Andreas, Stefanaki, Irene, Scolyer, Richard, Yang, Rose, Pastorino, Lorenza, Cattaneo, Laura, Zawistowski, Matthew, Gimenez-Xavier, Pol, Rodriguez, Arantxa, Elefanti, Lisa, Rivoltini, Licia, Del Regno, Laura, Massi, Daniela, Mandala, Mario, Amos, Christopher I., Andresen, Per A., Avril, Marie-Françoise, Azizi, Esther, Soyer, H. Peter, Bataille, Veronique, Bowdler, Lisa M., Burdon, Kathryn P., Chen, Wei V., Craig, Jamie E., Fang, Shenying, Friedman, Eitan, Simi, Sarah, Galan, Pilar, Gillanders, Elizabeth M., Gordon, Scott, Green, Adele, Hansson, Johan, Harland, Mark, Helsing, Per, Henders, Anjali, Hočevar, Marko, Hunter, David, Ingvar, Christian, Lang, Julie, Lathrop, G. Mark, Li, Xin, Lubiński, Jan, Malvehy, Josep, Molven, Anders, Moses, Eric K., Nyholt, Dale R., Olsson, Håkan, Orr, Nicholas, Radford-Smith, Graham L., Randerson-Moor, Juliette, Rowe, Casey, Schadendorf, Dirk, Simms, Lisa A., Smithers, Mark, Song, Fengju, Visconti, Alessia, Wallace, Leanne, Wheeler, Lawrie, Sturm, Richard A., Hutchinson, Amy, Jones, Kristine, Malasky, Michael, Vogt, Aurelie, Zhou, Weiyin, Elder, David E., Han, Jiali, Hicks, Belynda, Hayward, Nicholas K., Brummett, Chad, Montgomery, Grant W., Olsen, Catherine M., Hayward, Caroline, Dunning, Alison M., Martin, Nicholas G., Mann, Graham J., Long, Georgina, Pharoah, Paul D. P., Barrett, Jennifer H., Abecasis, Goncalo, Whiteman, David C., Gogas, Helen, Tucker, Margaret A., Newton-Bishop, Julia A., Peris, Ketty, Chanock, Stephen J., Nagore, Eduardo, Shi, Jianxin, Iles, Mark M., Law, Matthew H.

    Veröffentlicht in Nature genetics

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  20. 20

    Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol von Lange, Leslie A., Schmidt, Ellen M., Bizon, Chris, Jun, Goo, Auer, Paul, Li, Kuo-ping, Locke, Adam, Rivas, Manuel A., Feitosa, Mary F., Zhang, Qunyuan, Huffman, Jennifer E., Crosby, Jacy, Robinson, Jennifer G., Crosslin, David R., Rosenthal, Elisabeth A., Tsai, Michael, Rieder, Mark J., Fox, Ervin R., van Duijn, Cornelia M., Taylor, Herman A., Loos, Ruth J.F., Ballantyne, Christie M., Reiner, Alexander P., Cupples, L. Adrienne, Kang, Hyun Min, Lettre, Guillaume, Rader, Daniel J., Reilly, Muredach P., Stoletzki, Nina, Barr, R. Graham, Benjamin, Emelia J., Carr, Jeff, Dupuis, Josée, Ellis, Jaclyn, Fornage, Myriam, Goff, David, Grody, Wayne, Heard-Costa, Nancy L., Levy, Daniel, Li, Dalin, Loria, Cay, Mackey, Rachel, Quinlan, Aaron R., Rice, Kenneth, Sanders, Jill P., Tracy, Russell P., Tsai, Michael Y., Wassel, Chrstina L., Watson, Karol, Wilson, Gregory, Wilson, James G., Zakai, Neil A., Nalls, Michael, Bamshad, Michael J., Accurso, Frank, Beaty, Terri, Caplan, Daniel, Chidekel, Aaron, Christiani, David C., De Paula, Alicia, Gutierrez, Hector, Hassoun, Paul M., Hiatt, Peter, Hummer, Laura K., Kim, Yoonhee, Lin, Xihong, Louie, Tin L., Mathias, Rasika A., McNamara, John, McNamara, Sharon, Nielson, Dennis, Orenstein, David, O’Sullivan, Brian, Passero, Mary Ann, Perkett, Elizabeth, Spencer, Terry, Tabor, Holly K., Weiss, Robert, Wigley, Fred, Wise, Robert A., Wurfel, Mark M., Eichler, Evan E., Fu, Wenqing, Smith, Joshua D., Tennessen, Jacob A., Peters, Ulrike, Brzyski, Robert, Curb, J. David, Eaton, Charles B., Heiss, Gerardo, Johnson, Karen C., Lasser, Norman, Lin, Dan-Yu, Logsdon, Benjamin A., Manson, JoAnn E., Martin, Lisa, Stein, Evan, Applebaum-Bowden, Deborah, Paltoo, Dina N., Sturcke, Anne


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