Treffer 1 - 20 von 38 für Suche 'Hsiao, Philip F.', Suchdauer: 1,49s Treffer weiter einschränken
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    Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types von Wang, Zhaoming, Diver, W Ryan, Dorronsoro, Miren, Dossus, Laure, Gago-Dominguez, Manuela, Mirabello, Lisa, Gaudet, Mia M, Giffen, Carol, Giles, Graham G, Goggins, Michael, Savage, Sharon A, Gorlick, Richard, Guo, Huan, He, Qincheng, Helzlsouer, Kathy, Henderson, Brian, Hjalgrim, Henrik, Hoover, Robert N, Hu, Zhibin, Huang, Ming-Shyan, Jacobs, Eric J, Jeon, Hyo-Sung, Jin, Li, Kaaks, Rudolph, Rajaraman, Preetha, Kane, Eleanor, Karagas, Margaret R, Kim, Hee Nam, Kim, Jun Suk, Kurtz, Robert C, Kweon, Sun-Seog, Lawrence, Charles, Albanes, Demetrius, Li, Haixin, Li, Jihua, Li, Yao-Jen, Li, Yuqing, Lindstrom, Sara, Liu, Chenwei, Liu, Jianjun, Lloreta, Josep, An, She-Juan, Lund, Eiluv, Malats, Nuria, Mannisto, Satu, Le Marchand, Loic, Marina, Neyssa, Andersson, Ulrika, Melbye, Mads, Monnereau, Alain, Montalvan, Rebecca, Moore, Lee E, Andriole, Gerald, North, Kari E, Pao, William, Andrulis, Irene L, Patiño-Garcia, Ana, Peeters, Petra H M, Prokunina-Olsson, Ludmila, Riboli, Elio, Riby, Jacques, Arici, Cecilia, Sesso, Howard D, Shen, Hongbing, Armstrong, Bruce K, Shiraishi, Kouya, Skibola, Christine F, Sung, Jae Sook, Austin, Melissa A, Thompson, Carrie A, Vajdic, Claire M, Villano, Danylo J, Wang, Chih-Liang, Wang, Jiu-Cun, Wei, Fusheng, Weiderpass, Elisabete, Weinstein, Stephanie, Wolpin, Brian M, Wu, Tangchun, Yoon, Ho-Il, Yu, Chong-Jen, Yu, Kai, Zhang, Xu-Chao, Zhao, Zhenhong, Berg, Christine, Ferri, Giovanni M, Hartge, Patricia, Hsiung, Chao Agnes, VanDenBerg, David, Slager, Susan L, Chanock, Stephen J, Bueno-de-Mesquita, H Bas, Carta, Angela, Chang, I-Shou, Chen, Chung-Hsing, Chen, Ying-Hsiang, Choi, Jin Eun, Conti, David, Cozen, Wendy, Crous-Bou, Marta


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    Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy von Schoch, Kelly, Kranz, Peter G., Markert, M. Louise, Arbogast, Thomas, Muraresku, Colleen, Adams, David R., Alvarez, Raquel L., Balasubramanyam, Ashok, Bamshad, Michael, Beck, Anita, Behrens, Edward, Bejerano, Gill, Bellen, Hugo J., Bohnsack, John, Bonner, Devon, Botto, Lorenzo, Brown, Gabrielle, Butte, Manish J., Byrd, William E., Carrasquillo, Olveen, Cassini, Thomas, Chanprasert, Sirisak, Chinn, Ivan, Clark, Gary D., Coggins, Matthew, Cope, Heidi, Craigen, William J., D’Souza, Precilla, Dipple, Katrina, Doherty, Daniel, Fisher, Paul G., Fogel, Brent L., Glass, Ian, Gochuico, Bernadette, Godfrey, Rena A., Hahn, Sihoun, Hamid, Rizwan, Introne, Wendy, Jamal, Fariha, Jean-Marie, Orpa, Kobren, Shilpa N., Krakow, Deborah, Krasnewich, Donna M., Kravets, Elijah, LeBlanc, Kimberly, Lee, Brendan H., Loo, Sandra K., Loscalzo, Joseph, Mahoney, Rachel, Malicdan, May Christine V., Mamounas, Laura A., Marom, Ronit, Martínez-Agosto, Julian A., McConkie-Rosell, Allyn, Merritt, J. Lawrence, Might, Matthew, Mulvihill, John, Newman, John H., Nieves-Rodriguez, Shirley, Orengo, James P., Pace, Laura, Papp, Jeanette C., Parker, Neil H., Pusey Swerdzewski, Barbara N., Quinlan, Aaron, Raper, Anna, Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Rossignol, Francis, Sampson, Jacinda B., Saporta, Mario, Schaechter, Judy, Schoch, Kelly, Scott, C. Ron, Seto, Elaine, Sinsheimer, Janet S., Solnica-Krezel, Lilianna, Spillmann, Rebecca C., Stoler, Joan M., Sullivan, Jennifer A., Sun, Angela, Sutton, Shirley, Tabor, Holly K., Tan, Queenie K.-G., Telischi, Fred, Tifft, Cynthia J., Urv, Tiina K., Wahl, Colleen E., Wang, Lee-kai, Wangler, Michael F., Wheeler, Matthew T., Worley, Kim, Xiao, Changrui, Yamamoto, Shinya, Tyndall, Amanda V., Woodward, Kristine E., Wright, Nicola A.M., Davis, Erica E.

    Veröffentlicht in Genetics in medicine

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