Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies von Cowley, Glenn S, Weir, Barbara A, Vazquez, Francisca, Tamayo, Pablo, Scott, Justine A, Rusin, Scott, East-Seletsky, Alexandra, Ali, Levi D, Gerath, William FJ, Pantel, Sarah E, Lizotte, Patrick H, Jiang, Guozhi, Hsiao, Jessica, Tsherniak, Aviad, Dwinell, Elizabeth, Aoyama, Simon, Okamoto, Michael, Harrington, William, Gelfand, Ellen, Green, Thomas M, Tomko, Mark J, Gopal, Shuba, Wong, Terence C, Li, Hubo, Howell, Sara, Stransky, Nicolas, Liefeld, Ted, Jang, Dongkeun, Bistline, Jonathan, Hill Meyers, Barbara, Armstrong, Scott A, Anderson, Ken C, Stegmaier, Kimberly, Reich, Michael, Pellman, David, Boehm, Jesse S, Mesirov, Jill P, Golub, Todd R, Root, David E, Hahn, William C

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MAPK Pathway Suppression Unmasks Latent DNA Repair Defects and Confers a Chemical Synthetic Vulnerability in BRAF-, NRAS -, and NF1 -Mutant Melanomas von Maertens, Ophélia, Kuzmickas, Ryan, Manchester, Haley E, Emerson, Chloe E, Gavin, Alessandra G, Guild, Caroline J, Wong, Terence C, De Raedt, Thomas, Bowman-Colin, Christian, Hatchi, Elodie, Garraway, Levi A, Flaherty, Keith T, Pathania, Shailja, Elledge, Stephen J, Cichowski, Karen

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Systematic investigation of genetic vulnerabilities across cancer cell lines reveals lineage-specific dependencies in ovarian cancer von Cheung, Hiu Wing, Cowley, Glenn S, Weir, Barbara A, Boehm, Jesse S, Rusin, Scott, Scott, Justine A, East, Alexandra, Ali, Levi D, Lizotte, Patrick H, Wong, Terence C, Jiang, Guozhi, Hsiao, Jessica, Mermel, Craig H, Getz, Gad, Barretina, Jordi, Gopal, Shuba, Tamayo, Pablo, Gould, Joshua, Tsherniak, Aviad, Stransky, Nicolas, Luo, Biao, Ren, Yin, Drapkin, Ronny, Bhatia, Sangeeta N, Mesirov, Jill P, Garraway, Levi A, Meyerson, Matthew, Lander, Eric S, Root, David E, Hahn, William C

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Functional Precision Medicine Identifies New Therapeutic Candidates for Medulloblastoma von Rusert, Jessica M, Juarez, Edwin F, Brabetz, Sebastian, Jensen, James, Garancher, Alexandra, Chau, Lianne Q, Tacheva-Grigorova, Silvia K, Wahab, Sameerah, Udaka, Yoko T, Finlay, Darren, Seker-Cin, Huriye, Reardon, Brendan, Gröbner, Susanne, Serrano, Jonathan, Ecker, Jonas, Qi, Lin, Kogiso, Mari, Du, Yuchen, Baxter, Patricia A, Henderson, Jacob J, Berens, Michael E, Vuori, Kristiina, Milde, Till, Cho, Yoon-Jae, Li, Xiao-Nan, Olson, James M, Reyes, Iris, Snuderl, Matija, Wong, Terence C, Dimmock, David P, Nahas, Shareef A, Malicki, Denise, Crawford, John R, Levy, Michael L, Van Allen, Eliezer M, Pfister, Stefan M, Tamayo, Pablo, Kool, Marcel, Mesirov, Jill P, Wechsler-Reya, Robert J

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The genomic landscape of familial glioma von Choi, Dong-Joo, Armstrong, Georgina, Lozzi, Brittney, Vijayaraghavan, Prashanth, Plon, Sharon E, Wong, Terence C, Boerwinkle, Eric, Muzny, Donna M, Chen, Hsiao-Chi, Gibbs, Richard A, Ostrom, Quinn T, Melin, Beatrice, Deneen, Benjamin, Bondy, Melissa L, Bainbridge, Matthew N, Amos, Christopher I, Barnholtz-Sloan, Jill S, Bernstein, Jonine L, Claus, Elizabeth B, Houlston, Richard S, Il'yasova, Dora, Jenkins, Robert B, Johansen, Christoffer, Lachance, Daniel, Lai, Rose, Melin, Beatrice S, Merrell, Ryan T, Olson, Sara H, Sadetzki, Siegal, Schildkraut, Joellen, Shete, Sanjay, Ambrose, J C, Arumugam, P, Bevers, R, Bleda, M, Boardman-Pretty, F, Boustred, C R, Brittain, H, Brown, M A, Caulfield, M J, Chan, G C, Giess, A, Griffin, J N, Hamblin, A, Henderson, S, Hubbard, T J P, Jackson, R, Jones, L J, Kasperaviciute, D, Kayikci, M, Kousathanas, A, Lahnstein, L, Lakey, A, Leigh, S E A, Leong, I U S, Lopez, F J, Maleady-Crowe, F, McEntagart, M, Minneci, F, Mitchell, J, Moutsianas, L, Mueller, M, Murugaesu, N, Need, A C, O'Donovan, P, Odhams, C A, Patch, C, Perez-Gil, D, Pereira, M B, Pullinger, J, Rahim, T, Rendon, A, Rogers, T, Savage, K, Sawant, K, Scott, R H, Siddiq, A, Sieghart, A, Smith, S C, Sosinsky, A, Stuckey, A, Tanguy, M, Taylor Tavares, A L, Thomas, E R A, Thompson, S R, Tucci, A, Welland, M J, Williams, E, Witkowska, K, Wood, S M, Zarowiecki, M

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A Green, Enantioselective Synthesis of Warfarin for the Undergraduate Organic Laboratory von Wong, Terence C, Sultana, Camille M, Vosburg, David A

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Transcriptional repression by the proximal exonic region at the human TERT gene von Wong, Terence C., Sokol, Ethan S., Schep, Alicia N., Punjiya, Meera, Tran, Diana A., Allan, Divina, Drewell, Robert A.

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Auditory Brainstem Implantation in Chinese Patients With Neurofibromatosis Type II: The Hong Kong Experience von Thong, Jiun Fong, Sung, John K.K, Wong, Terence K.C, Tong, Michael C.F

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Characterization of an ultra-conserved putative cis-regulatory module at the mammalian telomerase reverse transcriptase gene von Tran, Diana A, Wong, Terence C, Schep, Alicia N, Drewell, Robert A

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Age and Outcome of Cochlear Implantation for Patients with Bilateral Congenital Deafness in a Cantonese-Speaking Population von Tong, Michael C. F, Leung, Eric K. S, Au, Albert, Lee, William, Yue, Virgil, Lee, Kathy Y. S, Chan, Vanessa S. W, Wong, Terence K. C, Cheung, Dilys M. C, van Hasselt, C Andrew

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Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies von Cowley, Glenn S, Weir, Barbara A, Vazquez, Francisca, Tamayo, Pablo, Scott, Justine A, Rusin, Scott, East-seletsky, Alexandra, Ali, Levi D, Gerath, William Fj, Pantel, Sarah E, Lizotte, Patrick H, Jiang, Guozhi, Hsiao, Jessica, Tsherniak, Aviad, Dwinell, Elizabeth, Aoyama, Simon, Okamoto, Michael, Harrington, William, Gelfand, Ellen, Green, Thomas M, Tomko, Mark J, Gopal, Shuba, Wong, Terence C, Li, Hubo, Howell, Sara, Stransky, Nicolas, Liefeld, Ted, Jang, Dongkeun, Bistline, Jonathan, Meyers, Barbara Hill, Armstrong, Scott A, Anderson, Ken C, Stegmaier, Kimberly, Reich, Michael, Pellman, David, Boehm, Jesse S, Mesirov, Jill P, Golub, Todd R, Root, David E, Hahn, William C

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Abstract B33: Integration of genome-wide datasets identifies SOX10 as a lineage-specific genetic dependency in melanoma von Wong, Terence C., Johannessen, Cory M., Garraway, Levi A.

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Syndromic Microphthalmia 9: Role of rapid genome sequencing and novel mutations in STRA6 gene von Saini, Ashish, Almasarweh, Saleem, Acosta, Stephanie, Jayakar, Parul, Janvier, Michelin, Wong, Terence C., Salyakina, Daria, Sasaki, Jun

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Artificial Intelligence in the Genetic Diagnosis of Rare Disease von James, Kiely N., Phadke, Sujal, Wong, Terence C., Chowdhury, Shimul

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The BAHA hearing system for hearing-impaired postirradiated nasopharyngeal cancer patients: a new indication von Soo, Gordon, Tong, Michael C F, Tsang, Willis S S, Wong, Terence K C, To, Ka-fai, Leung, Sing-fai, van Hasselt, C Andrew

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Systematic investigation of genetic vulnerabilities across cancer cell lines reveals lineage-specific dependencies in ovarian cancer von Cheung, Hiu Wing, Cowley, Glenn S, Weir, Barbara A, Boehm, Jesse S, Rusin, Scott, Scott, Justine A, East, Alexandra, Ali, Levi D, Lizotte, Patrick H, Wong, Terence C, Jiang, Guozhi, Hsiao, Jessica, Mermel, Craig H, Getz, Gad, Barretina, Jordi, Gopal, Shuba, Tamayo, Pablo, Gould, Joshua, Tsherniak, Aviad, Stransky, Nicolas, Luo, Biao, Ren, Yin, Drapkin, Ronny, Bhatia, Sangeeta N, Mesirov, Jill P, Garraway, Levi A, Meyerson, Matthew, Lander, Eric S, Root, David E, Hahn, William C

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Contemporary solutions for patients with microtia and congenital aural atresia – Hong Kong experience von Tsang, Willis S.S., Tong, Michael C.F., Ku, Peter K.M., Bhatia, Kunwar S.S., Yu, Joannie K.Y., Wong, Terence K.C., van Hasselt, C. Andrew

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Erratum: Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies von Cowley, Glenn S, Weir, Barbara A, Vazquez, Francisca, Tamayo, Pablo, Scott, Justine A, Rusin, Scott, East-Seletsky, Alexandra, Ali, Levi D, Gerath, William F.J, Pantel, Sarah E, Lizotte, Patrick H, Jiang, Guozhi, Hsiao, Jessica, Tsherniak, Aviad, Dwinell, Elizabeth, Aoyama, Simon, Okamoto, Michael, Harrington, William, Gelfand, Ellen, Green, Thomas M, Tomko, Mark J, Gopal, Shuba, Wong, Terence C, Li, Hubo, Howell, Sara, Stransky, Nicolas, Liefeld, Ted, Jang, Dongkeun, Bistline, Jonathan, Meyers, Barbara Hill, Armstrong, Scott A, Anderson, Ken C, Stegmaier, Kimberly, Reich, Michael, Pellman, David, Boehm, Jesse S, Mesirov, Jill P, Golub, Todd R, Root, David E, Hahn, William C

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Parallel genome-scale loss of function screens in 216 cancer cell lines for the identification of context-specific genetic dependencies von Cowley, Glenn S, Weir, Barbara A, Vazquez, Francisca, Tamayo, Pablo, Scott, Justine A, Rusin, Scott, East-Seletsky, Alexandra, Ali, Levi D, Gerath, William FJ, Pantel, Sarah E, Lizotte, Patrick H, Jiang, Guozhi, Hsiao, Jessica, Tsherniak, Aviad, Dwinell, Elizabeth, Aoyama, Simon, Okamoto, Michael, Harrington, William, Gelfand, Ellen, Green, Thomas M, Tomko, Mark J, Gopal, Shuba, Wong, Terence C, Li, Hubo, Howell, Sara, Stransky, Nicolas, Liefeld, Ted, Jang, Dongkeun, Bistline, Jonathan, Hill Meyers, Barbara, Armstrong, Scott A, Anderson, Ken C, Stegmaier, Kimberly, Reich, Michael, Pellman, David, Boehm, Jesse S, Mesirov, Jill P, Golub, Todd R, Root, David E, Hahn, William C

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Vibrant Soundbridge System: round window stimulation with the vibroplasty technique von Tsang, Willis S S, Wong, Terence K C, Tong, Michael C F

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