SCIM III (Spinal Cord Independence Measure version III): reliability of assessment by interview and comparison with assessment by observation von Itzkovich, M, Shefler, H, Front, L, Gur-Pollack, R, Elkayam, K, Bluvshtein, V, Gelernter, I, Catz, A

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The Mutational Landscape of Head and Neck Squamous Cell Carcinoma von 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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Should COVID-19 vaccines be mandated in schools? - an international caregiver perspective von Baumer-Mouradian, Shannon H., Hart, Rebecca J., Bone, Jeffrey N., Seiler, Michelle, Olson, Prasra, Keitel, Kristina, Manzano, Sergio, Gualco, Gianluca, Krupik, Danna, Schroter, Stephanie, Weigert, Rachel M., Chung, SunHee, Thompson, Graham C., Muhammad, Nina, Shah, Pareen, Gaucher, Nathalie O., Lunoe, Maren M., Evers, Megan, Pharisa Rochat, Cosette, Nelson, Courtney E., Shefler Gal, Moran, Doucas, Adrianna, Goldman, Ran D.

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Somatic mutation of CDKN1B in small intestine neuroendocrine tumors von Francis, Joshua M, Kiezun, Adam, Ramos, Alex H, Serra, Stefano, Pedamallu, Chandra Sekhar, Qian, Zhi Rong, Banck, Michaela S, Kanwar, Rahul, Kulkarni, Amit A, Karpathakis, Anna, Manzo, Veronica, Contractor, Tanupriya, Philips, Juliet, Nickerson, Elizabeth, Pho, Nam, Hooshmand, Susanne M, Brais, Lauren K, Lawrence, Michael S, Pugh, Trevor, McKenna, Aaron, Sivachenko, Andrey, Cibulskis, Kristian, Carter, Scott L, Ojesina, Akinyemi I, Freeman, Samuel, Jones, Robert T, Voet, Douglas, Saksena, Gordon, Auclair, Daniel, Onofrio, Robert, Shefler, Erica, Sougnez, Carrie, Grimsby, Jonna, Green, Lisa, Lennon, Niall, Meyer, Tim, Caplin, Martyn, Chung, Daniel C, Beutler, Andreas S, Ogino, Shuji, Thirlwell, Christina, Shivdasani, Ramesh, Asa, Sylvia L, Harris, Chris R, Getz, Gad, Kulke, Matthew, Meyerson, Matthew

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Mutational heterogeneity in cancer and the search for new cancer-associated genes von Lawrence, Michael S., Stojanov, Petar, Polak, Paz, Kryukov, Gregory V., Cibulskis, Kristian, Sivachenko, Andrey, Carter, Scott L., Stewart, Chip, Mermel, Craig H., Roberts, Steven A., Kiezun, Adam, Hammerman, Peter S., McKenna, Aaron, Drier, Yotam, Zou, Lihua, Ramos, Alex H., Pugh, Trevor J., Stransky, Nicolas, Helman, Elena, Kim, Jaegil, Sougnez, Carrie, Ambrogio, Lauren, Nickerson, Elizabeth, Shefler, Erica, Cortés, Maria L., Auclair, Daniel, Saksena, Gordon, Voet, Douglas, Noble, Michael, DiCara, Daniel, Lin, Pei, Lichtenstein, Lee, Heiman, David I., Fennell, Timothy, Imielinski, Marcin, Hernandez, Bryan, Hodis, Eran, Baca, Sylvan, Dulak, Austin M., Lohr, Jens, Landau, Dan-Avi, Wu, Catherine J., Melendez-Zajgla, Jorge, Hidalgo-Miranda, Alfredo, Koren, Amnon, McCarroll, Steven A., Mora, Jaume, Lee, Ryan S., Crompton, Brian, Onofrio, Robert, Parkin, Melissa, Winckler, Wendy, Ardlie, Kristin, Gabriel, Stacey B., Roberts, Charles W. M., Biegel, Jaclyn A., Stegmaier, Kimberly, Bass, Adam J., Garraway, Levi A., Meyerson, Matthew, Golub, Todd R., Gordenin, Dmitry A., Sunyaev, Shamil, Lander, Eric S., Getz, Gad

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Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity von Dulak, Austin M, Stojanov, Petar, Peng, Shouyong, Lawrence, Michael S, Fox, Cameron, Stewart, Chip, Bandla, Santhoshi, Imamura, Yu, Schumacher, Steven E, Shefler, Erica, McKenna, Aaron, Carter, Scott L, Cibulskis, Kristian, Sivachenko, Andrey, Saksena, Gordon, Voet, Douglas, Ramos, Alex H, Auclair, Daniel, Thompson, Kristin, Sougnez, Carrie, Onofrio, Robert C, Guiducci, Candace, Beroukhim, Rameen, Zhou, Zhongren, Lin, Lin, Lin, Jules, Reddy, Rishindra, Chang, Andrew, Landrenau, Rodney, Pennathur, Arjun, Ogino, Shuji, Luketich, James D, Golub, Todd R, Gabriel, Stacey B, Lander, Eric S, Beer, David G, Godfrey, Tony E, Getz, Gad, Bass, Adam J

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Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations von Pugh, Trevor J., Weeraratne, Shyamal Dilhan, Archer, Tenley C., Pomeranz Krummel, Daniel A., Auclair, Daniel, Bochicchio, James, Carneiro, Mauricio O., Carter, Scott L., Cibulskis, Kristian, Erlich, Rachel L., Greulich, Heidi, Lawrence, Michael S., Lennon, Niall J., McKenna, Aaron, Meldrim, James, Ramos, Alex H., Ross, Michael G., Russ, Carsten, Shefler, Erica, Sivachenko, Andrey, Sogoloff, Brian, Stojanov, Petar, Tamayo, Pablo, Mesirov, Jill P., Amani, Vladimir, Teider, Natalia, Sengupta, Soma, Francois, Jessica Pierre, Northcott, Paul A., Taylor, Michael D., Yu, Furong, Crabtree, Gerald R., Kautzman, Amanda G., Gabriel, Stacey B., Getz, Gad, Jäger, Natalie, Jones, David T. W., Lichter, Peter, Pfister, Stefan M., Roberts, Thomas M., Meyerson, Matthew, Pomeroy, Scott L., Cho, Yoon-Jae

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The genetic landscape of high-risk neuroblastoma von Pugh, Trevor J, Morozova, Olena, Attiyeh, Edward F, Asgharzadeh, Shahab, Wei, Jun S, Auclair, Daniel, Carter, Scott L, Cibulskis, Kristian, Hanna, Megan, Kiezun, Adam, Kim, Jaegil, Lawrence, Michael S, Lichenstein, Lee, McKenna, Aaron, Pedamallu, Chandra Sekhar, Ramos, Alex H, Shefler, Erica, Sivachenko, Andrey, Sougnez, Carrie, Stewart, Chip, Ally, Adrian, Birol, Inanc, Chiu, Readman, Corbett, Richard D, Hirst, Martin, Jackman, Shaun D, Kamoh, Baljit, Khodabakshi, Alireza Hadj, Krzywinski, Martin, Lo, Allan, Moore, Richard A, Mungall, Karen L, Qian, Jenny, Tam, Angela, Thiessen, Nina, Zhao, Yongjun, Cole, Kristina A, Diamond, Maura, Diskin, Sharon J, Mosse, Yael P, Wood, Andrew C, Ji, Lingyun, Sposto, Richard, Badgett, Thomas, London, Wendy B, Moyer, Yvonne, Gastier-Foster, Julie M, Smith, Malcolm A, Auvil, Jaime M Guidry, Gerhard, Daniela S, Hogarty, Michael D, Jones, Steven J M, Lander, Eric S, Gabriel, Stacey B, Getz, Gad, Seeger, Robert C, Khan, Javed, Marra, Marco A, Meyerson, Matthew, Maris, John M

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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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Mapping copy number variation by population-scale genome sequencing von Mills, Ryan E., Walter, Klaudia, Stewart, Chip, Handsaker, Robert E., Chen, Ken, Alkan, Can, Abyzov, Alexej, Yoon, Seungtai Chris, Ye, Kai, Cheetham, R. Keira, Chinwalla, Asif, Conrad, Donald F., Fu, Yutao, Grubert, Fabian, Hajirasouliha, Iman, Hormozdiari, Fereydoun, Iakoucheva, Lilia M., Iqbal, Zamin, Kang, Shuli, Kidd, Jeffrey M., Konkel, Miriam K., Korn, Joshua, Khurana, Ekta, Kural, Deniz, Lam, Hugo Y. K., Leng, Jing, Li, Ruiqiang, Li, Yingrui, Lin, Chang-Yun, Luo, Ruibang, Mu, Xinmeng Jasmine, Nemesh, James, Peckham, Heather E., Rausch, Tobias, Scally, Aylwyn, Shi, Xinghua, Stromberg, Michael P., Stütz, Adrian M., Urban, Alexander Eckehart, Walker, Jerilyn A., Wu, Jiantao, Zhang, Yujun, Zhang, Zhengdong D., Batzer, Mark A., Ding, Li, Marth, Gabor T., McVean, Gil, Sebat, Jonathan, Snyder, Michael, Wang, Jun, Ye, Kenny, Eichler, Evan E., Gerstein, Mark B., Hurles, Matthew E., Lee, Charles, McCarroll, Steven A., Korbel, Jan O.

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Should COVID-19 vaccines be mandated in schools? - an international caregiver perspective von Baumer-Mouradian, Shannon H, Hart, Rebecca J, Bone, Jeffrey N, Seiler, Michelle, Olson, Prasra, Keitel, Kristina, Manzano, Sergio, Gualco, Gianluca, Krupik, Danna, Schroter, Stephanie, Weigert, Rachel M, Chung, SunHee, Thompson, Graham C, Muhammad, Nina, Shah, Pareen, Gaucher, Nathalie O, Lunoe, Maren M, Evers, Megan, Pharisa Rochat, Cosette, Nelson, Courtney E, Shefler Gal, Moran, Doucas, Adrianna, Goldman, Ran D

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Are we following a restrictive red cell transfusion practice? A multi-centre audit of paediatric transfusion practice in PICU von Wolfenden, H., Shefler, A., Stanworth, S., Dawson, M., New, H., Steele, J., Sykes, K.

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EXPERIENCED PSYCHOANALYTICALLY ORIENTED THERAPISTS' NARRATIVE ACCOUNTS OF THEIR PERSONAL THERAPY: IMPACTS ON PROFESSIONAL AND PERSONAL DEVELOPMENT von Wiseman, Hadas, Shefler, Gaby

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Psychometric properties of goal-attainment scaling in the assessment of mann's time-limited psychotherapy von Shefler, Gaby, Canetti, Laura, Wiseman, Hadas

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Mutational heterogeneity in cancer and the search for new cancer genes von Lawrence, Michael S, Stojanov, Petar, Polak, Paz, Kryukov, Gregory V, Cibulskis, Kristian, Sivachenko, Andrey, Carter, Scott L, Stewart, Chip, Mermel, Craig H, Roberts, Steven A, Kiezun, Adam, Hammerman, Peter S, McKenna, Aaron, Drier, Yotam, Zou, Lihua, Ramos, Alex H, Pugh, Trevor J, Stransky, Nicolas, Helman, Elena, Kim, Jaegil, Sougnez, Carrie, Ambrogio, Lauren, Nickerson, Elizabeth, Shefler, Erica, Cortés, Maria L, Auclair, Daniel, Saksena, Gordon, Voet, Douglas, Noble, Michael, DiCara, Daniel, Lin, Pei, Lichtenstein, Lee, Heiman, David I, Fennell, Timothy, Imielinski, Marcin, Hernandez, Bryan, Hodis, Eran, Baca, Sylvan, Dulak, Austin M, Lohr, Jens, Landau, Dan-Avi, Wu, Catherine J, Melendez-Zajgla, Jorge, Hidalgo-Miranda, Alfredo, Koren, Amnon, McCarroll, Steven A, Mora, Jaume, Crompton, Brian, Onofrio, Robert, Parkin, Melissa, Winckler, Wendy, Ardlie, Kristin, Gabriel, Stacey B, Roberts, Charles W. M, Biegel, Jaclyn A, Stegmaier, Kimberly, Bass, Adam J, Garraway, Levi A, Meyerson, Matthew, Golub, Todd R, Gordenin, Dmitry A, Sunyaev, Shamil, Lander, Eric S, Getz, Gad

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Abstract 4868: Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations within a wide spectrum of genetic heterogeneity von Pugh, Trevor J., Cho, Yoon-Jae, Archer, Tenley, Weeraratne, Dilhan, Jones, David T. W., Jaeger, Natalie, Auclair, Daniel, Cibulskis, Kristian, Lawrence, Michael S., Ramos, Alex H., Shefler, Erica, Sivachenko, Andrey, Tamayo, Pablo, Mesirov, Jill P., Gabriel, Stacey B., Getz, Gad, Pfister, Stefan M., Lichter, Peter, Meyerson, Matthew, Pomeroy, Scott L.

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Mutational heterogeneity in cancer and the search for new cancer genes von Lawrence, Michael S., Stojanov, Petar, Polak, Paz, Kryukov, Gregory V., Cibulskis, Kristian, Sivachenko, Andrey, Carter, Scott L., Stewart, Chip, Mermel, Craig H., Roberts, Steven A., Kiezun, Adam, Hammerman, Peter S., McKenna, Aaron, Drier, Yotam, Zou, Lihua, Ramos, Alex H., Pugh, Trevor J., Stransky, Nicolas, Helman, Elena, Kim, Jaegil, Sougnez, Carrie, Ambrogio, Lauren, Nickerson, Elizabeth, Shefler, Erica, Cortés, Maria L., Auclair, Daniel, Saksena, Gordon, Voet, Douglas, Noble, Michael, DiCara, Daniel, Lin, Pei, Lichtenstein, Lee, Heiman, David I., Fennell, Timothy, Imielinski, Marcin, Hernandez, Bryan, Hodis, Eran, Baca, Sylvan, Dulak, Austin M., Lohr, Jens, Landau, Dan-Avi, Wu, Catherine J., Melendez-Zajgla, Jorge, Hidalgo-Miranda, Alfredo, Koren, Amnon, McCarroll, Steven A., Mora, Jaume, Crompton, Brian, Onofrio, Robert, Parkin, Melissa, Winckler, Wendy, Ardlie, Kristin, Gabriel, Stacey B., Roberts, Charles W. M., Biegel, Jaclyn A., Stegmaier, Kimberly, Bass, Adam J., Garraway, Levi A., Meyerson, Matthew, Golub, Todd R., Gordenin, Dmitry A., Sunyaev, Shamil, Lander, Eric S., Getz, Gad

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Exome and whole genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity von Dulak, Austin M, Stojanov, Petar, Peng, Shouyong, Lawrence, Michael S, Fox, Cameron, Stewart, Chip, Bandla, Santhoshi, Imamura, Yu, Schumacher, Steven E, Shefler, Erica, McKenna, Aaron, Cibulskis, Kristian, Sivachenko, Andrey, Carter, Scott L, Saksena, Gordon, Voet, Douglas, Ramos, Alex H, Auclair, Daniel, Thompson, Kristin, Sougnez, Carrie, Onofrio, Robert C, Guiducci, Candace, Beroukhim, Rameen, Zhou, David, Lin, Lin, Lin, Jules, Reddy, Rishindra, Chang, Andrew, Luketich, James D, Pennathur, Arjun, Ogino, Shuji, Golub, Todd R, Gabriel, Stacey B, Lander, Eric S, Beer, David G, Godfrey, Tony E, Getz, Gad, Bass, Adam J

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Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations von Pugh, Trevor J, Weeraratne, Shyamal Dilhan, Archer, Tenley C, Krummel, Daniel APomeranz, Auclair, Daniel, Bochicchio, James, Carneiro, Mauricio O, Carter, Scott L, Cibulskis, Kristian, Erlich, Rachel L, Greulich, Heidi, Lawrence, Michael S, Lennon, Niall J, McKenna, Aaron, Meldrim, James, Ramos, Alex H, Ross, Michael G, Russ, Carsten, Shefler, Erica, Sivachenko, Andrey, Sogoloff, Brian, Stojanov, Petar, Tamayo, Pablo, Mesirov, Jill P, Amani, Vladimir, Teider, Natalia, Sengupta, Soma, Francois, Jessica Pierre, Northcott, Paul A, Taylor, Michael D, Yu, Furong, Crabtree, Gerald R, Kautzman, Amanda G, Gabriel, Stacey B, Getz, Gad, Jäger, Natalie, Jones, David T W, Lichter, Peter, Pfister, Stefan M, Roberts, Thomas M, Meyerson, Matthew, Pomeroy, Scott L, Cho, Yoon-Jae

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The genetic landscape of high-risk neuroblastoma von Pugh, Trevor J, Morozova, Olena, Attiyeh, Edward F, Asgharzadeh, Shahab, Wei, Jun S, Auclair, Daniel, Carter, Scott L, Cibulskis, Kristian, Hanna, Megan, Kiezun, Adam, Kim, Jaegil, Lawrence, Michael S, Lichenstein, Lee, McKenna, Aaron, Pedamallu, Chandra Sekhar, Ramos, Alex H, Shefler, Erica, Sivachenko, Andrey, Sougnez, Carrie, Stewart, Chip, Ally, Adrian, Birol, Inanc, Chiu, Readman, Corbett, Richard D, Hirst, Martin, Jackman, Shaun D, Kamoh, Baljit, Khodabakshi, Alireza Hadj, Krzywinski, Martin, Lo, Allan, Moore, Richard A, Mungall, Karen L, Qian, Jenny, Tam, Angela, Thiessen, Nina, Zhao, Yongjun, Cole, Kristina A, Diamond, Maura, Diskin, Sharon J, Mosse, Yael P, Wood, Andrew C, Ji, Lingyun, Sposto, Richard, Badgett, Thomas, London, Wendy B, Moyer, Yvonne, Gastier-Foster, Julie M, Smith, Malcolm A, Auvil, Jaime M. Guidry, Gerhard, Daniela S, Hogarty, Michael D, Jones, Steven J. M, Lander, Eric S, Gabriel, Stacey B, Getz, Gad, Seeger, Robert C, Khan, Javed, Marra, Marco A, Meyerson, Matthew, Maris, John M

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