Discovery of high-affinity peptide binders to BLyS by phage display by Fleming, Tony J., Sachdeva, Meena, Delic, Marko, Beltzer, James, Wescott, Charles R., Devlin, Mary, Lander, Robert C., Nixon, Andrew E., Roschke, Viktor, Hilbert, David M., Sexton, Daniel J.

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Identification of Selective Inhibitors of Cancer Stem Cells by High-Throughput Screening by Gupta, Piyush B., Onder, Tamer T., Jiang, Guozhi, Tao, Kai, Kuperwasser, Charlotte, Weinberg, Robert A., Lander, Eric S.

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Absolute quantification of somatic DNA alterations in human cancer by Carter, Scott L, Cibulskis, Kristian, Helman, Elena, McKenna, Aaron, Shen, Hui, Zack, Travis, Laird, Peter W, Onofrio, Robert C, Winckler, Wendy, Weir, Barbara A, Beroukhim, Rameen, Pellman, David, Levine, Douglas A, Lander, Eric S, Meyerson, Matthew, Getz, Gad

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Punctuated Evolution of Prostate Cancer Genomes by Baca, Sylvan C., Prandi, Davide, Lawrence, Michael S., Mosquera, Juan Miguel, Romanel, Alessandro, Drier, Yotam, Park, Kyung, Kitabayashi, Naoki, MacDonald, Theresa Y., Ghandi, Mahmoud, Van Allen, Eliezer, Kryukov, Gregory V., Sboner, Andrea, Theurillat, Jean-Philippe, Soong, T. David, Nickerson, Elizabeth, Auclair, Daniel, Tewari, Ashutosh, Beltran, Himisha, Onofrio, Robert C., Boysen, Gunther, Guiducci, Candace, Barbieri, Christopher E., Cibulskis, Kristian, Sivachenko, Andrey, Carter, Scott L., Saksena, Gordon, Voet, Douglas, Ramos, Alex H., Winckler, Wendy, Cipicchio, Michelle, Ardlie, Kristin, Kantoff, Philip W., Berger, Michael F., Gabriel, Stacey B., Golub, Todd R., Meyerson, Matthew, Lander, Eric S., Elemento, Olivier, Getz, Gad, Demichelis, Francesca, Rubin, Mark A., Garraway, Levi A.

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Current outcomes when optimizing ‘standard’ sample preparation for single‐particle cryo‐EM by CARRAGHER, B., CHENG, Y., FROST, A., GLAESER, R.M., LANDER, G.C., NOGALES, E., WANG, H.‐W.

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A Landscape of Driver Mutations in Melanoma by Hodis, Eran, Watson, Ian R., Kryukov, Gregory V., Arold, Stefan T., Imielinski, Marcin, Theurillat, Jean-Philippe, Nickerson, Elizabeth, Auclair, Daniel, Li, Liren, Place, Chelsea, DiCara, Daniel, Ramos, Alex H., Lawrence, Michael S., Cibulskis, Kristian, Sivachenko, Andrey, Voet, Douglas, Saksena, Gordon, Stransky, Nicolas, Onofrio, Robert C., Winckler, Wendy, Ardlie, Kristin, Wagle, Nikhil, Wargo, Jennifer, Chong, Kelly, Morton, Donald L., Stemke-Hale, Katherine, Chen, Guo, Noble, Michael, Meyerson, Matthew, Ladbury, John E., Davies, Michael A., Gershenwald, Jeffrey E., Wagner, Stephan N., Hoon, Dave S.B., Schadendorf, Dirk, Lander, Eric S., Gabriel, Stacey B., Getz, Gad, Garraway, Levi A., Chin, Lynda

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Genomic surveillance elucidates Ebola virus origin and transmission during the 2014 outbreak by Gire, Stephen K., Goba, Augustine, Andersen, Kristian G., Sealfon, Rachel S. G., Park, Daniel J., Kanneh, Lansana, Jalloh, Simbirie, Momoh, Mambu, Fullah, Mohamed, Dudas, Gytis, Wohl, Shirlee, Moses, Lina M., Yozwiak, Nathan L., Winnicki, Sarah, Matranga, Christian B., Malboeuf, Christine M., Qu, James, Gladden, Adrianne D., Schaffner, Stephen F., Yang, Xiao, Jiang, Pan-Pan, Nekoui, Mahan, Colubri, Andres, Coomber, Moinya Ruth, Fonnie, Mbalu, Moigboi, Alex, Gbakie, Michael, Kamara, Fatima K., Tucker, Veronica, Konuwa, Edwin, Saffa, Sidiki, Sellu, Josephine, Jalloh, Abdul Azziz, Kovoma, Alice, Koninga, James, Mustapha, Ibrahim, Kargbo, Kandeh, Foday, Momoh, Yillah, Mohamed, Kanneh, Franklyn, Robert, Willie, Massally, James L. B., Chapman, Sinéad B., Bochicchio, James, Murphy, Cheryl, Nusbaum, Chad, Young, Sarah, Birren, Bruce W., Grant, Donald S., Scheiffelin, John S., Lander, Eric S., Happi, Christian, Gevao, Sahr M., Gnirke, Andreas, Rambaut, Andrew, Garry, Robert F., Khan, S. Humarr, Sabeti, Pardis C.

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Mapping and characterization of structural variation in 17,795 human genomes by Abel, Haley J., Larson, David E., Regier, Allison A., Chiang, Colby, Das, Indraniel, Kanchi, Krishna L., Layer, Ryan M., Neale, Benjamin M., Salerno, William J., Reeves, Catherine, Buyske, Steven, Matise, Tara C., Muzny, Donna M., Zody, Michael C., Lander, Eric S., Dutcher, Susan K., Stitziel, Nathan O., Hall, Ira M.

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A comparative genomics multitool for scientific discovery and conservation by Genereux, Diane P, Serres, Aitor, Armstrong, Joel, Johnson, Jeremy, Marinescu, Voichita D, Murén, Eva, Juan, David

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Sequence analysis of mutations and translocations across breast cancer subtypes by Banerji, Shantanu, Cibulskis, Kristian, Rangel-Escareno, Claudia, Brown, Kristin K., Carter, Scott L., Frederick, Abbie M., Lawrence, Michael S., Sivachenko, Andrey Y., Sougnez, Carrie, Zou, Lihua, Cortes, Maria L., Fernandez-Lopez, Juan C., Peng, Shouyong, Ardlie, Kristin G., Auclair, Daniel, Bautista-Piña, Veronica, Duke, Fujiko, Francis, Joshua, Jung, Joonil, Maffuz-Aziz, Antonio, Onofrio, Robert C., Parkin, Melissa, Pho, Nam H., Quintanar-Jurado, Valeria, Ramos, Alex H., Rebollar-Vega, Rosa, Rodriguez-Cuevas, Sergio, Romero-Cordoba, Sandra L., Schumacher, Steven E., Stransky, Nicolas, Thompson, Kristin M., Uribe-Figueroa, Laura, Baselga, Jose, Beroukhim, Rameen, Polyak, Kornelia, Sgroi, Dennis C., Richardson, Andrea L., Jimenez-Sanchez, Gerardo, Lander, Eric S., Gabriel, Stacey B., Garraway, Levi A., Golub, Todd R., Melendez-Zajgla, Jorge, Toker, Alex, Getz, Gad, Hidalgo-Miranda, Alfredo, Meyerson, Matthew

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The Mutational Landscape of Head and Neck Squamous Cell Carcinoma by Stransky, Nicolas, Egloff, Ann Marie, Tward, Aaron D., Kostic, Aleksandar D., Cibulskis, Kristian, Sivachenko, Andrey, Kryukov, Gregory V., Lawrence, Michael S., Sougnez, Carrie, McKenna, Aaron, Shefler, Erica, Ramos, Alex H., Stojanov, Petar, Carter, Scott L., Voet, Douglas, Cortés, Maria L., Auclair, Daniel, Berger, Michael F., Saksena, Gordon, Guiducci, Candace, Onofrio, Robert C., Parkin, Melissa, Romkes, Marjorie, Weissfeld, Joel L., Seethala, Raja R., Wang, Lin, Rangel-Escareño, Claudia, Fernandez-Lopez, Juan Carlos, Hidalgo-Miranda, Alfredo, Melendez-Zajgla, Jorge, Winckler, Wendy, Ardlie, Kristin, Gabriel, Stacey B., Meyerson, Matthew, Lander, Eric S., Getz, Gad, Golub, Todd R., Garraway, Levi A., Grandis, Jennifer R.

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Integrative analysis of the melanoma transcriptome by Berger, Michael F, Levin, Joshua Z, Vijayendran, Krishna, Sivachenko, Andrey, Adiconis, Xian, Maguire, Jared, Johnson, Laura A, Robinson, James, Verhaak, Roel G, Sougnez, Carrie, Onofrio, Robert C, Ziaugra, Liuda, Cibulskis, Kristian, Laine, Elisabeth, Barretina, Jordi, Winckler, Wendy, Fisher, David E, Getz, Gad, Meyerson, Matthew, Jaffe, David B, Gabriel, Stacey B, Lander, Eric S, Dummer, Reinhard, Gnirke, Andreas, Nusbaum, Chad, Garraway, Levi A

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Structural diagenesis by Laubach, S.E., Eichhubl, P., Hilgers, C., Lander, R.H.

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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction by Do, Ron, Stitziel, Nathan O., Won, Hong-Hee, Jørgensen, Anders Berg, Duga, Stefano, Angelica Merlini, Pier, Kiezun, Adam, Farrall, Martin, Goel, Anuj, Zuk, Or, Guella, Illaria, Asselta, Rosanna, Lange, Leslie A., Peloso, Gina M., Auer, Paul L., Girelli, Domenico, Martinelli, Nicola, Farlow, Deborah N., DePristo, Mark A., Roberts, Robert, Stewart, Alexander F. R., Saleheen, Danish, Danesh, John, Epstein, Stephen E., Sivapalaratnam, Suthesh, Kees Hovingh, G., Kastelein, John J., Samani, Nilesh J., Schunkert, Heribert, Erdmann, Jeanette, Shah, Svati H., Kraus, William E., Davies, Robert, Nikpay, Majid, Johansen, Christopher T., Wang, Jian, Hegele, Robert A., Hechter, Eliana, Marz, Winfried, Kleber, Marcus E., Huang, Jie, Johnson, Andrew D., Li, Mingyao, Burke, Greg L., Gross, Myron, Liu, Yongmei, Assimes, Themistocles L., Heiss, Gerardo, Lange, Ethan M., Folsom, Aaron R., Taylor, Herman A., Olivieri, Oliviero, Hamsten, Anders, Clarke, Robert, Reilly, Dermot F., Yin, Wu, Rivas, Manuel A., Donnelly, Peter, Rossouw, Jacques E., Psaty, Bruce M., Herrington, David M., Wilson, James G., Rich, Stephen S., Bamshad, Michael J., Tracy, Russell P., Adrienne Cupples, L., Rader, Daniel J., Reilly, Muredach P., Spertus, John A., Cresci, Sharon, Hartiala, Jaana, Wilson Tang, W. H., Hazen, Stanley L., Allayee, Hooman, Reiner, Alex P., Carlson, Christopher S., Kooperberg, Charles, Jackson, Rebecca D., Boerwinkle, Eric, Lander, Eric S., Schwartz, Stephen M., Siscovick, David S., McPherson, Ruth, Tybjaerg-Hansen, Anne, Abecasis, Goncalo R., Watkins, Hugh, Nickerson, Deborah A., Ardissino, Diego, Sunyaev, Shamil R., O'Donnell, Christopher J., Altshuler, David, Gabriel, Stacey, Kathiresan, Sekar

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28-way vertebrate alignment and conservation track in the UCSC Genome Browser by Miller, Webb, Rosenbloom, Kate, Hardison, Ross C, Hou, Minmei, Taylor, James, Raney, Brian, Burhans, Richard, King, David C, Baertsch, Robert, Blankenberg, Daniel, Kosakovsky Pond, Sergei L, Nekrutenko, Anton, Giardine, Belinda, Harris, Robert S, Tyekucheva, Svitlana, Diekhans, Mark, Pringle, Thomas H, Murphy, William J, Lesk, Arthur, Weinstock, George M, Lindblad-Toh, Kerstin, Gibbs, Richard A, Lander, Eric S, Siepel, Adam, Haussler, David, Kent, W James

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Inherited causes of clonal haematopoiesis in 97,691 whole genomes by Weinstock, Joshua S., Nandakumar, Satish K., Bao, Erik L., Szeto, Mindy D., Liao, Xiaotian, Nasser, Joseph, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J., Lin, Amy E., Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D., Barnes, Kathleen C., Moscati, Arden, Redline, Susan, Psaty, Bruce M., Silverman, Edwin K., Weiss, Scott T., Palmer, Nicholette D., Vasan, Ramachandran S., Burchard, Esteban G., He, Jiang, Kaplan, Robert C., Smith, Nicholas L., Arnett, Donna K., Schwartz, David A., Guo, Xiuqing, Konkle, Barbara A., Custer, Brian, Peralta, Juan M., Gui, Hongsheng, Meyers, Deborah A., McGarvey, Stephen T., Chen, Ida Yii-Der, Shoemaker, M. Benjamin, Peyser, Patricia A., Broome, Jai G., Wang, Fei Fei, North, Kari E., Launer, Lenore J., Cade, Brian E., Bis, Joshua C., Cho, Michael H., Lasky-Su, Jessica, Bowden, Donald W., Cupples, L. Adrienne, Mak, Angel C. Y., Smith, Jennifer A., Kelly, Tanika N., Aslibekyan, Stella, Heckbert, Susan R., Tiwari, Hemant K., Yang, Ivana V., Heit, John A., Johnsen, Jill M., Curran, Joanne E., Wenzel, Sally E., Rao, Dabeeru C., Darbar, Dawood, Moon, Jee-Young, Tracy, Russell P., Buth, Erin J., Rafaels, Nicholas, Loos, Ruth J. F., Liu, Yongmei, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I., Levy, Daniel, Bielak, Lawrence F., Hixson, James E., Floyd, James S., Whitsel, Eric A., Ellinor, Patrick T., Irvin, Marguerite R., Fingerlin, Tasha E., Armasu, Sebastian M., Wheeler, Marsha M., Blangero, John, Williams, L. Keoki, Levy, Bruce D., Sheu, Wayne Huey-Herng, Roden, Dan M., Taylor, Kent D., Johnson, Andrew D., Auer, Paul L., Kooperberg, Charles, Laurie, Cathy C., Blackwell, Thomas W., Smith, Albert V., Lange, Ethan, Rotter, Jerome I., Kitzman, Jacob O., Lander, Eric S., Ebert, Benjamin L., Reiner, Alexander P., Jaiswal, Siddhartha, Kathiresan, Sekar

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Redox Potential as a Predictor of Polyethylene Branching Using Nickel α‑Diimine Catalysts by Doerr, Alicia M, Curry, Matthew R, Chapleski, Robert C, Burroughs, Justin M, Lander, Elizabeth K, Roy, Sharani, Long, Brian K

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Comparison of Echocardiographic and Catheter Mean Gradient to Assess Stenosis After Transcatheter Aortic Valve Implantation by DeSa, Travis B., Tecson, Kristen M., Lander, Stuart R., Stoler, Robert C., Vallabhan, Ravi C., Hebeler, Robert F., Henry, A. Carl, Grayburn, Paul A.

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Somatic mutations affect key pathways in lung adenocarcinoma by Meyerson, Matthew, Wilson, Richard K, Ding, Li, Getz, Gad, Wheeler, David A, Mardis, Elaine R, McLellan, Michael D, Cibulskis, Kristian, Sougnez, Carrie, Greulich, Heidi, Muzny, Donna M, Morgan, Margaret B, Fulton, Lucinda, Fulton, Robert S, Zhang, Qunyuan, Wendl, Michael C, Lawrence, Michael S, Larson, David E, Chen, Ken, Dooling, David J, Sabo, Aniko, Hawes, Alicia C, Shen, Hua, Jhangiani, Shalini N, Lewis, Lora R, Hall, Otis, Zhu, Yiming, Mathew, Tittu, Ren, Yanru, Yao, Jiqiang, Scherer, Steven E, Clerc, Kerstin, Metcalf, Ginger A, Ng, Brian, Milosavljevic, Aleksandar, Gonzalez-Garay, Manuel L, Osborne, John R, Meyer, Rick, Shi, Xiaoqi, Tang, Yuzhu, Koboldt, Daniel C, Lin, Ling, Abbott, Rachel, Miner, Tracie L, Pohl, Craig, Fewell, Ginger, Haipek, Carrie, Schmidt, Heather, Dunford-Shore, Brian H, Kraja, Aldi, Crosby, Seth D, Sawyer, Christopher S, Vickery, Tammi, Sander, Sacha, Robinson, Jody, Winckler, Wendy, Baldwin, Jennifer, Chirieac, Lucian R, Dutt, Amit, Fennell, Tim, Hanna, Megan, Johnson, Bruce E, Onofrio, Robert C, Thomas, Roman K, Tonon, Giovanni, Weir, Barbara A, Zhao, Xiaojun, Ziaugra, Liuda, Zody, Michael C, Giordano, Thomas, Orringer, Mark B, Roth, Jack A, Spitz, Margaret R, Wistuba, Ignacio I, Ozenberger, Bradley, Good, Peter J, Chang, Andrew C, Beer, David G, Watson, Mark A, Ladanyi, Marc, Broderick, Stephen, Yoshizawa, Akihiko, Travis, William D, Pao, William, Province, Michael A, Weinstock, George M, Varmus, Harold E, Gabriel, Stacey B, Lander, Eric S, Gibbs, Richard A

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Identification of a Gene Causing Human Cytochrome c Oxidase Deficiency by Integrative Genomics by Mootha, Vamsi K., Lepage, Pierre, Miller, Kathleen, Bunkenborg, Jakob, Reich, Michael, Hjerrild, Majbrit, Delmonte, Terrye, Villeneuve, Amelie, Sladek, Robert, Xu, Fenghao, Mitchell, Grant A., Morin, Charles, Mann, Matthias, Hudson, Thomas J., Robinson, Brian, Rioux, John D., Lander, Eric S.

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