Risultati della ricerca - Kandoth, Cyriac
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Enabling transparent and collaborative computational analysis of 12 tumor types within The Cancer Genome Atlas di Omberg, Larsson, Ellrott, Kyle, Yuan, Yuan, Kandoth, Cyriac, Wong, Chris, Kellen, Michael R, Friend, Stephen H, Stuart, Josh, Liang, Han, Margolin, Adam A
Pubblicazione 2013testo -
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Comprehensive identification of mutational cancer driver genes across 12 tumor types di Tamborero, David, Gonzalez-Perez, Abel, Perez-Llamas, Christian, Deu-Pons, Jordi, Kandoth, Cyriac, Reimand, Jüri, Lawrence, Michael S., Getz, Gad, Bader, Gary D., Ding, Li, Lopez-Bigas, Nuria
Pubblicazione 2013testo -
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MuSiC: Identifying mutational significance in cancer genomes di Dees, Nathan D., Zhang, Qunyuan, Kandoth, Cyriac, Wendl, Michael C., Schierding, William, Koboldt, Daniel C., Mooney, Thomas B., Callaway, Matthew B., Dooling, David, Mardis, Elaine R., Wilson, Richard K., Ding, Li
Pubblicazione 2012testo -
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Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines di Ellrott, Kyle, Bailey, Matthew H., Saksena, Gordon, Covington, Kyle R., Kandoth, Cyriac, Stewart, Chip, Hess, Julian, Ma, Singer, McLellan, Michael, Sofia, Heidi J., Hutter, Carolyn, Getz, Gad, Wheeler, David, Ding, Li
Pubblicazione 2018testo -
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Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif di Hamilton, Mark P., Rajapakshe, Kimal, Hartig, Sean M., Reva, Boris, McLellan, Michael D., Kandoth, Cyriac, Ding, Li, Zack, Travis I., Gunaratne, Preethi H., Wheeler, David A., Coarfa, Cristian, McGuire, Sean E.
Pubblicazione 2013testo -
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BreakFusion: targeted assembly-based identification of gene fusions in whole transcriptome paired-end sequencing data di Chen, Ken, Wallis, John W., Kandoth, Cyriac, Kalicki−Veizer, Joelle M., Mungall, Karen L., Mungall, Andrew J., Jones, Steven J., Marra, Marco A., Ley, Timothy J., Mardis, Elaine R., Wilson, Richard K., Weinstein, John N., Ding, Li
Pubblicazione 2012testo -
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Genetic and epigenetic evolution as a contributor to WT1-mutant leukemogenesis di Pronier, Elodie, Bowman, Robert L., Ahn, Jihae, Glass, Jacob, Kandoth, Cyriac, Merlinsky, Tiffany R., Whitfield, Justin T., Durham, Benjamin H., Gruet, Antoine, Hanasoge Somasundara, Amritha Varshini, Rampal, Raajit, Melnick, Ari, Koche, Richard P., Taylor, Barry S., Levine, Ross L.
Pubblicazione 2018testo -
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Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma di Gutmann, David H., McLellan, Michael D., Hussain, Ibrahim, Wallis, John W., Fulton, Lucinda L., Fulton, Robert S., Magrini, Vincent, Demeter, Ryan, Wylie, Todd, Kandoth, Cyriac, Leonard, Jeffrey R., Guha, Abhijit, Miller, Christopher A., Ding, Li, Mardis, Elaine R.
Pubblicazione 2013testo -
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Recurrent Mutations in Cyclin D3 Confer Clinical Resistance to FLT3 Inhibitors in Acute Myeloid Leukemia di Smith, Catherine C., Viny, Aaron D., Massi, Evan, Kandoth, Cyriac, Socci, Nicholas D., Rapaport, Franck, Najm, Matthieu, Medina, Juan S., Papaemmanuil, Elli, Tarver, Theodore, Hsu, Henry H., Le, Mai, West, Brian, Bollag, Gideon, Taylor, Barry S., Levine, Ross L., Shah, Neil P.
Pubblicazione 2021testo -
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Recurrent DNMT3A Mutations in Patients with Myelodysplastic Syndromes di Walter, Matthew J., Ding, Li, Shen, Dong, Shao, Jin, Grillot, Marcus, McLellan, Michael, Fulton, Robert, Schmidt, Heather, Kalicki-Veizer, Joelle, O’Laughlin, Michelle, Kandoth, Cyriac, Baty, Jack, Westervelt, Peter, DiPersio, John F., Mardis, Elaine R, Wilson, Richard K., Ley, Timothy J., Graubert, Timothy A.
Pubblicazione 2011testo -
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Mutational landscape and significance across 12 major cancer types di Kandoth, Cyriac, McLellan, Michael D., Vandin, Fabio, Ye, Kai, Niu, Beifang, Lu, Charles, Xie, Mingchao, Zhang, Qunyuan, McMichael, Joshua F., Wyczalkowski, Matthew A., Leiserson, Mark D. M., Miller, Christopher A., Welch, John S., Walter, Matthew J., Wendl, Michael C., Ley, Timothy J., Wilson, Richard K., Raphael, Benjamin J., Ding, Li
Pubblicazione 2013testo -
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Integrative omics analyses broaden treatment targets in human cancer di Sengupta, Sohini, Sun, Sam Q., Huang, Kuan-lin, Oh, Clara, Bailey, Matthew H., Varghese, Rajees, Wyczalkowski, Matthew A., Ning, Jie, Tripathi, Piyush, McMichael, Joshua F., Johnson, Kimberly J., Kandoth, Cyriac, Welch, John, Ma, Cynthia, Wendl, Michael C., Payne, Samuel H., Fenyö, David, Townsend, Reid R., Dipersio, John F., Chen, Feng, Ding, Li
Pubblicazione 2018testo -
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Genome Nexus: A Comprehensive Resource for the Annotation and Interpretation of Genomic Variants in Cancer di de Bruijn, Ino, Li, Xiang, Sumer, Selcuk Onur, Gross, Benjamin, Sheridan, Robert, Ochoa, Angelica, Wilson, Manda, Wang, Avery, Zhang, Hongxin, Lisman, Aaron, Abeshouse, Adam, Zhang, Emily, Thum, Alice, Sadagopan, Ananthan, Heins, Zachary, Kandoth, Cyriac, Rodenburg, Sander, Tan, Sander, Lukasse, Pieter, van Hagen, Sjoerd, Fijneman, Remond J. A., Meijer, Gerrit A., Schultz, Nikolaus, Gao, Jianjiong
Pubblicazione 2022testo -
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Tumor evolution and drug response in patient-derived organoid models of bladder cancer di Lee, Suk Hyung, Hu, Wenhuo, Matulay, Justin T., Silva, Mark V., Owczarek, Tomasz B., Kim, Kwanghee, Chua, Chee Wai, Barlow, LaMont J., Kandoth, Cyriac, Williams, Alanna B., Bergren, Sarah K., Pietzak, Eugene J., Anderson, Christopher B., Benson, Mitchell C., Coleman, Jonathan A., Taylor, Barry S., Abate-Shen, Cory, McKiernan, James M., Al-Ahmadie, Hikmat, Solit, David B., Shen, Michael M.
Pubblicazione 2018testo -
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Regional Differences in Gallbladder Cancer Pathogenesis: Insights From a Multi-Institutional Comparison of Tumor Mutations di Narayan, Raja R., Creasy, John M., Goldman, Debra A., Gönen, Mithat, Kandoth, Cyriac, Kundra, Ritika, Solit, David B., Askan, Gokce, Klimstra, David S., Basturk, Olca, Allen, Peter J., Balachandran, Vinod P., D’Angelica, Michael I., DeMatteo, Ronald P., Drebin, Jeffrey A., Kingham, T. Peter, Simpson, Amber L., Abou-Alfa, Ghassan K., Harding, James J., O’Reilly, Eileen M., Butte, Jean M., Matsuyama, Ryusei, Endo, Itaru, Jarnagin, William R.
Pubblicazione 2018testo