Whole-genome sequencing reveals activation-induced cytidine deaminase signatures during indolent chronic lymphocytic leukaemia evolution von Kasar, S., Kim, J., Improgo, R., Tiao, G., Polak, P., Haradhvala, N., Lawrence, M. S., Kiezun, A., Fernandes, S. M., Bahl, S., Sougnez, C., Gabriel, S., Lander, E. S., Kim, H. T., Getz, G., Brown, J. R.

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Integrated genomic analyses of ovarian carcinoma von Cancer Genome Atlas Research Network, The, Neuvial, Pierre

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A role for MAP kinase in differentiated smooth muscle contraction evoked by alpha -adrenoceptor stimulation von Dessy, Chantal, Kim, Inkyeom, Sougnez, Carrie L, Laporte, Regent, Morgan, Kathleen G

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Diversity of Human Copy Number Variation and Multicopy Genes von Sudmant, Peter H., Kitzman, Jacob O., Antonacci, Francesca, Alkan, Can, Malig, Maika, Tsalenko, Anya, Sampas, Nick, Bruhn, Laurakay, Shendure, Jay, Eichler, Evan E.

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Whole-genome association study of bipolar disorder von Sklar, P, Smoller, J W, Fan, J, Ferreira, M A R, Perlis, R H, Chambert, K, Nimgaonkar, V L, McQueen, M B, Faraone, S V, Kirby, A, de Bakker, P I W, Ogdie, M N, Thase, M E, Sachs, G S, Todd-Brown, K, Gabriel, S B, Sougnez, C, Gates, C, Blumenstiel, B, Defelice, M, Ardlie, K G, Franklin, J, Muir, W J, McGhee, K A, MacIntyre, D J, McLean, A, VanBeck, M, McQuillin, A, Bass, N J, Robinson, M, Lawrence, J, Anjorin, A, Curtis, D, Scolnick, E M, Daly, M J, Blackwood, D H, Gurling, H M, Purcell, S M

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Evidence for involvement of the PKC-alpha isoform in myogenic contractions of the coronary microcirculation von Dessy, Chantal, Matsuda, Naruto, Hulvershorn, Justin, Sougnez, Carrie L, Sellke, Frank W, Morgan, Kathleen G

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Whole-genome sequencing reveals activation-induced cytidine deaminase signatures during indolent chronic lymphocytic leukaemia evolution von Kasar, S, Kim, J, Improgo, R, Tiao, G, Polak, P, Haradhvala, N, Lawrence, M. S, Kiezun, A, Fernandes, S. M, Bahl, S, Sougnez, C, Gabriel, S, Lander, E. S, Kim, H. T, Getz, G, Brown, J. R

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Human chromosome 11 DNA sequence and analysis including novel gene identification von Taylor, Todd D, Sakaki, Yoshiyuki, Noguchi, Hideki, Totoki, Yasushi, Toyoda, Atsushi, Kuroki, Yoko, Dewar, Ken, Lloyd, Christine, Itoh, Takehiko, Takeda, Tadayuki, Kim, Dae-Won, She, Xinwei, Barlow, Karen F, Bloom, Toby, Bruford, Elspeth, Chang, Jean L, Cuomo, Christina A, Eichler, Evan, FitzGerald, Michael G, Jaffe, David B, LaButti, Kurt, Nicol, Robert, Park, Hong-Seog, Seaman, Christopher, Sougnez, Carrie, Yang, Xiaoping, Zimmer, Andrew R, Zody, Michael C, Birren, Bruce W, Nusbaum, Chad, Fujiyama, Asao, Hattori, Masahira, Rogers, Jane, Lander, Eric S

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GE-17 ALTERATION OF THE p53 PATHWAY AND ANCESTRAL PROGENITORS ARE ASSOCIATED WITH TUMOR RECURRENCE IN GLIOBLASTOMA von Kim, H., Zheng, S., Amini, S., Virk, S., Mikkelsen, T., Brat, D., Sougnez, C., Muller, F., Hu, J., Sloan, A., Cohen, M., Van Meir, E., Scarpace, L., Lander, E., Gabriel, S., Getz, G., Meyerson, M., Chin, L., Barnholtz-Sloan, J., Verhaak, R.

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THE P53 PATHWAY AND ANCESTRAL PROGENITORS ARE ASSOCIATED WITH TUMOR RECURRENCE IN GLIOBLASTOMA von Verhaak, R. G. W., Kim, H., Zheng, S., Amini, S. S., Virk, S. M., Mikkelsen, T., Brat, D. J., Grimsby, J., Sougnez, C., Muller, F., Hu, J., Sloan, A. E., Cohen, M. L., Van Meir, E. G., Scarpace, L., Laird, P. W., Weinstein, J. N., Lander, E., Gabriel, S., Getz, G., Meyerson, M., Chin, L., Barnholtz-Sloan, J. S.

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A Functional Analysis of Mouse Models of Cardiac Disease through Metabolic Profiling von Jones, Gareth L A H, Sang, Elizabeth, Goddard, Catharine, Mortishire-Smith, Russell J, Sweatman, Brian C, Haselden, John N, Davies, Kay, Grace, Andrew A, Clarke, Kieran, Griffin, Julian L

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Integrative analysis of the melanoma transcriptome von Berger, M F, Levin, J Z, Vijayendran, K, Sivachenko, A, Adiconis, X, Maguire, J, Johnson, L A, Robinson, J, Verhaak, R G, Sougnez, C, Onofrio, R C, Ziaugra, L, Cibulskis, K, Laine, E, Barretina, J, Winckler, W, Fisher, D E, Getz, G, Meyerson, M, Jaffe, D B, Gabriel, S B, Lander, E S, Dummer, R, Gnirke, A, Nusbaum, C, Garraway, L A

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Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes von Valente, E M, Logan, C V, Mougou-Zerelli, S, Lee, J H, Silhavy, J L, Brancati, F, Iannicelli, M, Travaglini, L, Romani, S, Illi, B, Adams, M, Szymanska, K, Mazzotta, A, Lee, J E, Tolentino, J C, Swistun, D, Salpietro, C D, Fede, C, Gabriel, S, Russ, C, Cibulskis, K, Sougnez, C, Hildebrandt, F, Otto, E A, Held, S, Diplas, B H, Davis, E E, Mikula, M, Strom, C M, Ben-Zeev, B, Lev, D, Sagie, T L, Michelson, M, Yaron, Y, Krause, A, Boltshauser, E, Elkhartoufi, N, Roume, J, Shalev, S, Munnich, A, Saunier, S, Inglehearn, C, Saad, A, Alkindy, A, Thomas, S, Vekemans, M, Dallapiccola, B, Katsanis, N, Johnson, C A, Attié-Bitach, T, Gleeson, J G

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A role for MAP kinase in differentiated smooth muscle contraction evoked by α-adrenoceptor stimulation von DESSY, C, INKYEOM KIM, SOUGNEZ, C. L, LAPORTE, R, MORGAN, K. G

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Comprehensive molecular profiling of lung adenocarcinoma: The cancer genome atlas research network von Collisson, E, Campbell, J, Brooks, A, Berger, A, Lee, W, Chmielecki, J, Beer, D, Cope, L, Creighton, C, Danilova, L, Ding, L, Getz, G, Hammerman, P, Hayes, D, Hernandez, B, Herman, J, Heymach, J, Jurisica, I, Kucherlapati, R, Kwiatkowski, D, Ladanyi, M, Robertson, G, Schultz, N, Shen, R, Sinha, R, Sougnez, C, Tsao, M, Travis, W, Weinstein, J, Wigle, D, Wilkerson, M, Chu, A, Cherniack, A, Hadjipanayis, A, Rosenberg, M, Weisenberger, D, Laird, P, Radenbaugh, A, Ma, S, Stuart, J, Byers, L, Baylin, S, Govindan, R, Meyerson, M, Gabriel, S, Cibulskis, K, Kim, J, Stewart, C, Lichtenstein, L, Lander, E, Lawrence, M, Getz, E, Fulton, R, Fulton, L, McLellan, M, Wilson, R, Ye, K, Fronick, C, Maher, C, Miller, C, Wendl, M, Cabanski, C, Mardis, E, Wheeler, D, Balasundaram, M, Butterfield, Y, Carlsen, R, Chuah, E, Dhalla, N, Guin, R, Hirst, C, Lee, D, Li, H, Mayo, M, Moore, R, Mungall, A, Schein, J, Sipahimalani, P, Tam, A, Varhol, Richard, Robertson, A, Wye, N, Thiessen, N, Holt, R, Jones, S, Marra, M, Imielinski, M, Onofrio, R, Hodis, E, Zack, T, Helman, E

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Integrated genomic characterization of endometrial carcinoma von Getz, G, Gabriel, S, Cibulskis, K, Lander, E, Sivachenko, A, Sougnez, C, Lawrence, M, Kandoth, C, Dooling, D, Fulton, R, Fulton, L, Kalicki-Veizer, J, McLellan, M, O'Laughlin, M, Schmidt, H, Wilson, R, Ye, K, Li, D, Ally, A, Balasundaram, M, Birol, I, Butterfield, Y, Carlsen, R, Carter, C, Chu, A, Chuah, E, Chun, H, Dhalla, N, Guin, R, Hirst, C, Holt, R, Jones, S, Lee, D, Li, H, Marra, M, Mayo, M, Moore, R, Mungall, A, Plettner, P, Schein, J, Sipahimalani, P, Tam, A, Varhol, Richard, Gordon Robertson, A, Cherniack, A, Pashtan, I, Saksena, G, Onofrio, R, Schumacher, S, Tabak, B, Carter, S, Hernandez, B, Gentry, J, Salvesen, H, Ardlie, K, Winckler, W, Beroukhim, R, Meyerson, M, Hadjipanayis, A, Lee, S, Mahadeshwar, H, Park, P, Protopopov, A, Ren, X, Seth, S, Song, X, Tang, J, Xi, R, Yang, L, Dong, Z, Kucherlapati, R, Chin, L, Zhang, J, Todd Auman, J, Balu, S, Bodenheimer, T, Buda, E, Neil Hayes, D, Hoyle, A, Jefferys, S, Jones, C, Meng, S, Mieczkowski, P, Mose, L, Parker, J, Perou, C

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A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination von Wang, Anderson T., Kim, Taeho, Wagner, John E., Conti, Brooke A., Lach, Francis P., Huang, Athena L., Molina, Henrik, Sanborn, Erica M., Zierhut, Heather, Cornes, Belinda K., Abhyankar, Avinash, Sougnez, Carrie, Gabriel, Stacey B., Auerbach, Arleen D., Kowalczykowski, Stephen C., Smogorzewska, Agata

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Demographic history and rare allele sharing among human populations von Gravel, Simon, Henn, Brenna M, Gutenkunst, Ryan N, Indap, Amit R, Marth, Gabor T, Clark, Andrew G, Yu, Fuli, Gibbs, Richard A, Bustamante, Carlos D

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Molecular Profiling Reveals Biologically Discrete Subsets and Pathways of Progression in Diffuse Glioma von Ceccarelli, Michele, Salama, Sofie R., Manyam, Ganiraju, Zoppoli, Pietro, Grifford, Mia, Rao, Arvind, Lau, Ching C., Huse, Jason, Zheng, Siyuan, Hess, Kenneth, Rao, Ganesh, Beroukhim, Rameen, Akbani, Rehan, Wrensch, Margaret, Haussler, David, Aldape, Kenneth D., Anjum, Samreen, Balu, Saianand, Barnett, Gene, Black, Keith L., Bristow, Christopher A., Chen, Qing-Rong, Cho, Juok, Chuah, Eric, Chudamani, Sudha, Cohen, Mark L., Couce, Marta, Davidsen, Tanja, Davis, Amy, Elder, J. Bradley, Eschbacher, Jennifer M., Fehrenbach, Ashley, Ferguson, Martin, Fuller, Gregory, Fulop, Jordonna, Garofano, Luciano, Gastier-Foster, Julie M., Gehlenborg, Nils, Gerken, Mark, Gibson, William J., Hadjipanayis, Angela, Hayes, D. Neil, Hilty, Joe, Hoyle, Alan P., Jones, Corbin D., Jones, Steven J.M., Ju, Zhenlin, Kastl, Alison, Kendler, Ady, Kucherlapati, Raju, Lichtenberg, Tara M., Lin, Pei, Ljubimova, Julia Y., Lu, Yiling, Ma, Yussanne, Maglinte, Dennis T., Marra, Marco A., Meng, Shaowu, Miller, C. Ryan, Mills, Gordon B., Mose, Lisle E., Naska, Theresa, Noble, Michael S., Noss, Ardene, Palmer, Cheryl, Parfenov, Michael, Parker, Joel S., Perou, Charles M., Pihl, Todd, Protopopov, Alexei, Ramirez, Nilsa C., Saksena, Gordon, Schein, Jacqueline E., Shen, Hui, Shi, Yan, Shimmel, Kristen, Sicotte, Hugues, Sifri, Suzanne, Silva, Tiago, Singh, Rosy, Song, Xingzhi, Souza, Camila, Sun, Huandong, Sun, Charlie, Tang, Jiabin, Trevisan, Felipe Amstalden, Van Den Berg, David J., Voet, Doug, Wang, Zhining, Weinstein, John N., Weisenberger, Daniel J., Wilkerson, Matthew D., Williams, Felicia, Wise, Lisa, Xu, Andrew W., Yang, Lixing, Zack, Travis I., Zhang, Jianhua, Zhang, Wei, Zmuda, Erik

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Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia von Rickman, Kimberly A., Lach, Francis P., Abhyankar, Avinash, Donovan, Frank X., Sanborn, Erica M., Kennedy, Jennifer A., Sougnez, Carrie, Gabriel, Stacey B., Elemento, Olivier, Chandrasekharappa, Settara C., Schindler, Detlev, Auerbach, Arleen D., Smogorzewska, Agata

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