Ideal Fairness in Sport is Impossible von Petersen, Thomas S., Holmen, Sebastian J., Ryberg, Jesper

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Melanoma models for the next generation of therapies von Patton, E. Elizabeth, Mueller, Kristen L., Adams, David J., Anandasabapathy, Niroshana, Aplin, Andrew E., Bertolotto, Corine, Bosenberg, Marcus, Ceol, Craig J., Burd, Christin E., Chi, Ping, Herlyn, Meenhard, Holmen, Sheri L., Karreth, Florian A., Kaufman, Charles K., Khan, Shaheen, Kobold, Sebastian, Leucci, Eleonora, Levy, Carmit, Lombard, David B., Lund, Amanda W., Marie, Kerrie L., Marine, Jean-Christophe, Marais, Richard, McMahon, Martin, Robles-Espinoza, Carla Daniela, Ronai, Ze'ev A., Samuels, Yardena, Soengas, Maria S., Villanueva, Jessie, Weeraratna, Ashani T., White, Richard M., Yeh, Iwei, Zhu, Jiyue, Zon, Leonard I., Hurlbert, Marc S., Merlino, Glenn

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Activated BRAF induces gliomas in mice when combined with Ink4a/Arf loss or Akt activation von Robinson, J P, VanBrocklin, M W, Guilbeault, A R, Signorelli, D L, Brandner, S, Holmen, S L

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Activated MEK cooperates with Ink4a/Arf loss or Akt activation to induce gliomas in vivo von Robinson, J P, VanBrocklin, M W, Lastwika, K J, McKinney, A J, Brandner, S, Holmen, S L

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Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese von Tang, Clara S., Zhang, He, Cheung, Chloe Y. Y., Xu, Ming, Ho, Jenny C. Y., Zhou, Wei, Cherny, Stacey S., Zhang, Yan, Holmen, Oddgeir, Au, Ka-Wing, Yu, Haiyi, Xu, Lin, Jia, Jia, Porsch, Robert M., Sun, Lijie, Xu, Weixian, Zheng, Huiping, Wong, Lai-Yung, Mu, Yiming, Dou, Jingtao, Fong, Carol H. Y., Wang, Shuyu, Hong, Xueyu, Dong, Liguang, Liao, Yanhua, Wang, Jiansong, Lam, Levina S. M., Su, Xi, Yan, Hua, Yang, Min-Lee, Chen, Jin, Siu, Chung-Wah, Xie, Gaoqiang, Woo, Yu-Cho, Wu, Yangfeng, Tan, Kathryn C. B., Hveem, Kristian, Cheung, Bernard M. Y., Zöllner, Sebastian, Xu, Aimin, Eugene Chen, Y, Jiang, Chao Qiang, Zhang, Youyi, Lam, Tai-Hing, Ganesh, Santhi K., Huo, Yong, Sham, Pak C., Lam, Karen S. L., Willer, Cristen J., Tse, Hung-Fat, Gao, Wei

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Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease von Nielsen, Jonas B., Rom, Oren, Surakka, Ida, Graham, Sarah E., Zhou, Wei, Roychowdhury, Tanmoy, Fritsche, Lars G., Gagliano Taliun, Sarah A., Sidore, Carlo, Liu, Yuhao, Gabrielsen, Maiken E., Wolford, Brooke, Overton, William, Zhao, Ying, Chen, Jin, Zhang, He, Hornsby, Whitney E., Acheampong, Akua, Grooms, Austen, Schaefer, Amanda, Zajac, Gregory J. M., Villacorta, Luis, Zhang, Jifeng, Brumpton, Ben, Løset, Mari, Rai, Vivek, Lundegaard, Pia R., Olesen, Morten S., Taylor, Kent D., Palmer, Nicholette D., Chen, Yii-Der, Choi, Seung H., Lubitz, Steven A., Ellinor, Patrick T., Barnes, Kathleen C., Daya, Michelle, Rafaels, Nicholas, Weiss, Scott T., Lasky-Su, Jessica, Tracy, Russell P., Vasan, Ramachandran S., Cupples, L. Adrienne, Mathias, Rasika A., Yanek, Lisa R., Becker, Lewis C., Bielak, Lawrence F., Smith, Jennifer A., Aslibekyan, Stella, Hidalgo, Bertha A., Arnett, Donna K., Irvin, Marguerite R., Wilson, James G., Musani, Solomon K., Rich, Stephen S., Guo, Xiuqing, Rotter, Jerome I., Konkle, Barbara A., Johnsen, Jill M., Ashley-Koch, Allison E., Telen, Marilyn J., Blangero, John, Curran, Joanne E., Montgomery, Courtney, Sheu, Wayne H-H, Chung, Ren-Hua, Schwander, Karen, Nouraie, Seyed M., Gordeuk, Victor R., Zhang, Yingze, Kooperberg, Charles, Reiner, Alexander P., Jackson, Rebecca D., Bleecker, Eugene R., Meyers, Deborah A., Li, Xingnan, Das, Sayantan, Yu, Ketian, Smith, Albert, Blackwell, Tom, Taliun, Daniel, Zollner, Sebastian, Forer, Lukas, Schoenherr, Sebastian, Pandit, Anita, Zawistowski, Matthew, Kheterpal, Sachin, Brummett, Chad M., Natarajan, Pradeep, Schlessinger, David, Lee, Seunggeun, Kang, Hyun Min, Cucca, Francesco, Holmen, Oddgeir L., Åsvold, Bjørn O., Boehnke, Michael, Kathiresan, Sekar, Abecasis, Goncalo R., Chen, Y. Eugene, Willer, Cristen J., Hveem, Kristian

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Melanoma Models for the Next Generation of Therapies von Patton, Elizabeth, Mueller, Kristen, Adams, David J, Anandasabapathy, Niroshana, Aplin, Andrew E, Bertolotto, Corine, Bosemberg, Marcus, Ceol, Craig J, Ping, Chi, Herlyn, Meenhard, Holmen, Sheri L, Karreth, Florian A, Kaufman, Charles K, Shaheem, Khan, Kobold, Sebastian, Leucci, Eleonora, Levy, Carmit, Lombard, David B, LUnd, Amanda W, Marie, Kerrie L, Marine, Jean Christophe, Marais, Richard, McMahon, Martin, Robles-Espinoza, Carla Daniela, Ronai, Ze'ev A, Samuels, Yardena, Soengas, Maria S, Villanueva, Jessie, Weeraratna2, Ashani T, White, Richard M, Yeh, Iwei, Zhu, Jiyue, Zon, Leonard I, Hurlbert, Marc S

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Melanoma Models for the Next Generation of Therapies von Patton, E. Elizabeth, Mueller, Kristen L, Adams, David J, Anandasabapathy, Niroshana, Aplin, Andrew E, Bertolotto, Corine, Bosemberg, Marcus, Ceol, Craig J, Ping, Chi, Herlyn, Meenhard, Holmen, Sheri L, Karreth, Florian A, Kaufman, Charles K, Shaheem, Khan, Kobold, Sebastian, Leucci, Eleonora, Levy, Carmit, Lombard, David B, Lund, Amanda W, Marie, Kerrie L, Marine, Jean-Christophe, Marais, Richard, McMahon, Martin, Robles-Espinoza, Carla Daniela, Ronai, Ze'ev A, Samuels, Yardena, Soengas, Maria S, Villanueva, Jessie, Weeraratna, Ashani T, White, Richard M, Yeh, Iwei, Zhu, Jiyue, Zon, Leonard I, Hurlbert, Marc S, Merlino, Glenn

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A reference panel of 64,976 haplotypes for genotype imputation von McCarthy, Shane, Das, Sayantan, Kretzschmar, Warren, Delaneau, Olivier, Wood, Andrew R, Teumer, Alexander, Kang, Hyun Min, Fuchsberger, Christian, Danecek, Petr, Sharp, Kevin, Luo, Yang, Sidore, Carlo, Kwong, Alan, Timpson, Nicholas, Koskinen, Seppo, Vrieze, Scott, Scott, Laura J, Zhang, He, Mahajan, Anubha, Veldink, Jan, van Duijn, Cornelia M, Gillies, Christopher E, Gandin, Ilaria, Mezzavilla, Massimo, Gilly, Arthur, Cocca, Massimiliano, Traglia, Michela, Angius, Andrea, Barrett, Jeffrey C, Boomsma, Dorrett, Branham, Kari, Breen, Gerome, Brummett, Chad M, Busonero, Fabio, Campbell, Harry, Chan, Andrew, Chen, Sai, Chew, Emily, Corbin, Laura J, Smith, George Davey, Dedoussis, George, Dorr, Marcus, Farmaki, Aliki-Eleni, Ferrucci, Luigi, Forer, Lukas, Fraser, Ross M, Gabriel, Stacey, Levy, Shawn, Groop, Leif, Harrison, Tabitha, Hattersley, Andrew, Holmen, Oddgeir L, Hveem, Kristian, Kretzler, Matthias, Lee, James C, McGue, Matt, Meitinger, Thomas, Melzer, David, Min, Josine L, Mohlke, Karen L, Vincent, John B, Nickerson, Deborah, Palotie, Aarno, Pirastu, Nicola, McInnis, Melvin, Richards, J Brent, Sala, Cinzia, Salomaa, Veikko, Schlessinger, David, Schoenherr, Sebastian, Slagboom, P Eline, Small, Kerrin, Spector, Timothy, Stambolian, Dwight, Tuke, Marcus, Tuomilehto, Jaakko, Van Rheenen, Wouter, Volker, Uwe, Wijmenga, Cisca, Zeggini, Eleftheria, Gasparini, Paolo, Sampson, Matthew G, Frayling, Timothy, de Bakker, Paul IW, Swertz, Morris A, McCarroll, Steven, Kooperberg, Charles, Dekker, Annelot, Altshuler, David, Willer, Cristen, Ripatti, Samuli, Soranzo, Nicole, Walter, Klaudia, Swaroop, Anand, Cucca, Francesco, Myers, Richard M, Boehnke, Michael, McCarthy, Mark I, Durbin, Richard, Haplotype Reference Consortium

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Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese von Tang, Clara S, Zhang, He, Cheung, Chloe Y.Y, Xu, Ming, Ho, Jenny C.Y, Zhou, Wei, Cherny, Stacey S, Zhang, Yan, Holmen, Oddgeir, Au, Ka-Wing, Yu, Haiyi, Xu, Lin, Jia, Jia, Porsch, Robert M, Sun, Lijie, Xu, Weixian, Zheng, Huiping, Wong, Lai-Yung, Mu, Yiming, Dou, Jingtao, Fong, Carol H.Y, Wang, Shuyu, Hong, Xueyu, Dong, Liguang, Liao, Yanhua, Wang, Jiansong, Lam, Levina S.M, Su, Xi, Yan, Hua, Yang, Min-Lee, Chen, Jin, Siu, Chung-Wah, Xie, Gaoqiang, Woo, Yu-Cho, Wu, Yangfeng, Tan, Kathryn C.B, Hveem, Kristian, Cheung, Bernard M.Y, Zöllner, Sebastian, Xu, Aimin, Chen, Y. Eugene, Jiang, Chao Qiang, Zhang, Youyi, Lam, Tai-Hing, Ganesh, Santhi K, Huo, Yong, Sham, Pak C, Lam, Karen S.L, Willer, Cristen J, Tse, Hung-Fat, Gao, Wei

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