A CLASS OF GENERALIZED UNIFORM ASYMPTOTIC EXPANSIONS von Obi, Wilson C.

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Error Analysis of a Laplace Transform Inversion Procedure von Obi, Wilson C.

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Formulas for Spanwise Distribution of Lift on Aircraft Wings von Obi, Wilson C

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Multivariable Expansions Using Time Scales Generated from Differential Equations von Levine, Lawrence E., Obi, Wilson C.

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Quantitative Measurements of the Effects of Variations in Panel Density and Distributions for Panel Method Computer Programs von Obi, Wilson C

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The prognostic effects of somatic mutations in ER-positive breast cancer von Griffith, Obi L., Spies, Nicholas C., Anurag, Meenakshi, Griffith, Malachi, Luo, Jingqin, Tu, Dongsheng, Yeo, Belinda, Kunisaki, Jason, Miller, Christopher A, Krysiak, Kilannin, Hundal, Jasreet, Ainscough, Benjamin J, Skidmore, Zachary L., Campbell, Katie, Kumar, Runjun, Fronick, Catrina, Cook, Lisa, Snider, Jacqueline E., Davies, Sherri, Kavuri, Shyam M., Chang, Eric C., Magrini, Vincent, Larson, David E., Fulton, Robert S, Liu, Shuzhen, Leung, Samuel, Voduc, David, Bose, Ron, Dowsett, Mitch, Wilson, Richard K., Nielsen, Torsten O., Mardis, Elaine R, Ellis, Matthew J.

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DGIdb 2.0: mining clinically relevant drug-gene interactions von Wagner, Alex H, Coffman, Adam C, Ainscough, Benjamin J, Spies, Nicholas C, Skidmore, Zachary L, Campbell, Katie M, Krysiak, Kilannin, Pan, Deng, McMichael, Joshua F, Eldred, James M, Walker, Jason R, Wilson, Richard K, Mardis, Elaine R, Griffith, Malachi, Griffith, Obi L

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DoCM: a database of curated mutations in cancer von Ainscough, Benjamin J, Griffith, Malachi, Coffman, Adam C, Wagner, Alex H, Kunisaki, Jason, Choudhary, Mayank NK, McMichael, Joshua F, Fulton, Robert S, Wilson, Richard K, Griffith, Obi L, Mardis, Elaine R

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Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease von Klarin, Derek, Busenkell, Emma, Judy, Renae, Lynch, Julie, Levin, Michael, Haessler, Jeffery, Aragam, Krishna, Chaffin, Mark, Haas, Mary, Lindström, Sara, Assimes, Themistocles L., Huang, Jie, Min Lee, Kyung, Shao, Qing, Huffman, Jennifer E., Kabrhel, Christopher, Huang, Yunfeng, Sun, Yan V., Vujkovic, Marijana, Saleheen, Danish, Miller, Donald R., Reaven, Peter, DuVall, Scott, Boden, William E., Pyarajan, Saiju, Reiner, Alex P., Trégouët, David-Alexandre, Henke, Peter, Kooperberg, Charles, Gaziano, J. Michael, Concato, John, Rader, Daniel J., Cho, Kelly, Chang, Kyong-Mi, Wilson, Peter W. F., Smith, Nicholas L., O’Donnell, Christopher J., Tsao, Philip S., Kathiresan, Sekar, Obi, Andrea, Damrauer, Scott M., Natarajan, Pradeep

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DGIdb: mining the druggable genome von Griffith, Malachi, Griffith, Obi L, Coffman, Adam C, Weible, James V, McMichael, Josh F, Spies, Nicholas C, Koval, James, Das, Indraniel, Callaway, Matthew B, Eldred, James M, Miller, Christopher A, Subramanian, Janakiraman, Govindan, Ramaswamy, Kumar, Runjun D, Bose, Ron, Ding, Li, Walker, Jason R, Larson, David E, Dooling, David J, Smith, Scott M, Ley, Timothy J, Mardis, Elaine R, Wilson, Richard K

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Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancer von Wagner, Alex H., Devarakonda, Siddhartha, Skidmore, Zachary L., Krysiak, Kilannin, Ramu, Avinash, Trani, Lee, Kunisaki, Jason, Masood, Ashiq, Waqar, Saiama N., Spies, Nicholas C., Morgensztern, Daniel, Waligorski, Jason, Ponce, Jennifer, Fulton, Robert S., Maggi, Leonard B., Weber, Jason D., Watson, Mark A., O’Conor, Christopher J., Ritter, Jon H., Olsen, Rachelle R., Cheng, Haixia, Mukhopadhyay, Anandaroop, Can, Ismail, Cessna, Melissa H., Oliver, Trudy G., Mardis, Elaine R., Wilson, Richard K., Griffith, Malachi, Griffith, Obi L., Govindan, Ramaswamy

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CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer von Griffith, Malachi, Spies, Nicholas C, Krysiak, Kilannin, McMichael, Joshua F, Coffman, Adam C, Danos, Arpad M, Ainscough, Benjamin J, Ramirez, Cody A, Rieke, Damian T, Kujan, Lynzey, Barnell, Erica K, Wagner, Alex H, Skidmore, Zachary L, Wollam, Amber, Liu, Connor J, Jones, Martin R, Bilski, Rachel L, Lesurf, Robert, Feng, Yan-Yang, Shah, Nakul M, Bonakdar, Melika, Trani, Lee, Matlock, Matthew, Ramu, Avinash, Campbell, Katie M, Spies, Gregory C, Graubert, Aaron P, Gangavarapu, Karthik, Eldred, James M, Larson, David E, Walker, Jason R, Good, Benjamin M, Wu, Chunlei, Su, Andrew I, Dienstmann, Rodrigo, Margolin, Adam A, Tamborero, David, Lopez-Bigas, Nuria, Jones, Steven J M, Bose, Ron, Spencer, David H, Wartman, Lukas D, Wilson, Richard K, Mardis, Elaine R, Griffith, Obi L

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Optimizing Cancer Genome Sequencing and Analysis von Griffith, Malachi, Miller, Christopher A., Griffith, Obi L., Krysiak, Kilannin, Skidmore, Zachary L., Ramu, Avinash, Walker, Jason R., Dang, Ha X., Trani, Lee, Larson, David E., Demeter, Ryan T., Wendl, Michael C., McMichael, Joshua F., Austin, Rachel E., Magrini, Vincent, McGrath, Sean D., Ly, Amy, Kulkarni, Shashikant, Cordes, Matthew G., Fronick, Catrina C., Fulton, Robert S., Maher, Christopher A., Ding, Li, Klco, Jeffery M., Mardis, Elaine R., Ley, Timothy J., Wilson, Richard K.

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Association Between Mutation Clearance After Induction Therapy and Outcomes in Acute Myeloid Leukemia von Klco, Jeffery M, Miller, Christopher A, Griffith, Malachi, Petti, Allegra, Spencer, David H, Ketkar-Kulkarni, Shamika, Wartman, Lukas D, Christopher, Matthew, Lamprecht, Tamara L, Helton, Nicole M, Duncavage, Eric J, Payton, Jacqueline E, Baty, Jack, Heath, Sharon E, Griffith, Obi L, Shen, Dong, Hundal, Jasreet, Chang, Gue Su, Fulton, Robert, O'Laughlin, Michelle, Fronick, Catrina, Magrini, Vincent, Demeter, Ryan T, Larson, David E, Kulkarni, Shashikant, Ozenberger, Bradley A, Welch, John S, Walter, Matthew J, Graubert, Timothy A, Westervelt, Peter, Radich, Jerald P, Link, Daniel C, Mardis, Elaine R, DiPersio, John F, Wilson, Richard K, Ley, Timothy J

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Clonal architectures and driver mutations in metastatic melanomas von Ding, Li, Kim, Minjung, Kanchi, Krishna L, Dees, Nathan D, Lu, Charles, Griffith, Malachi, Fenstermacher, David, Sung, Hyeran, Miller, Christopher A, Goetz, Brian, Wendl, Michael C, Griffith, Obi, Cornelius, Lynn A, Linette, Gerald P, McMichael, Joshua F, Sondak, Vernon K, Fields, Ryan C, Ley, Timothy J, Mulé, James J, Wilson, Richard K, Weber, Jeffrey S

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Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer von Griffith, Obi L., Spies, Nicholas C., Anurag, Meenakshi, Griffith, Malachi, Luo, Jingqin, Tu, Dongsheng, Yeo, Belinda, Kunisaki, Jason, Miller, Christopher A, Krysiak, Kilannin, Hundal, Jasreet, Ainscough, Benjamin J, Skidmore, Zachary L., Campbell, Katie, Kumar, Runjun, Fronick, Catrina, Cook, Lisa, Snider, Jacqueline E., Davies, Sherri, Kavuri, Shyam M., Chang, Eric C., Magrini, Vincent, Larson, David E., Fulton, Robert S, Liu, Shuzhen, Leung, Samuel, Voduc, David, Bose, Ron, Dowsett, Mitch, Wilson, Richard K., Nielsen, Torsten O., Mardis, Elaine R, Ellis, Matthew J.

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Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemia von Griffith, Malachi, Griffith, Obi L, Krysiak, Kilannin, Skidmore, Zachary L, Christopher, Matthew J, Klco, Jeffery M, Ramu, Avinash, Lamprecht, Tamara L, Wagner, Alex H, Campbell, Katie M, Lesurf, Robert, Hundal, Jasreet, Zhang, Jin, Spies, Nicholas C, Ainscough, Benjamin J, Larson, David E, Heath, Sharon E, Fronick, Catrina, O'Laughlin, Shelly, Fulton, Robert, Magrini, Vincent, McGrath, Sean, Smith, Scott M, Miller, Christopher A, Maher, Christopher A, Payton, Jacqueline E, Walker, Jason R, Eldred, James M, Walter, Matthew J, Link, Daniel C, Graubert, Timothy A, Westervelt, Peter, Kulkarni, Shashikant, DiPersio, John F, Mardis, Elaine R, Wilson, Richard K, Ley, Timothy J

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Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers von Skidmore, Zachary L, Kunisaki, Jason, Lin, Yiing, Cotto, Kelsy C, Barnell, Erica K, Hundal, Jasreet, Krysiak, Kilannin, Magrini, Vincent, Trani, Lee, Walker, Jason R, Fulton, Robert, Brunt, Elizabeth M, Miller, Christopher A, Wilson, Richard K, Mardis, Elaine R, Griffith, Malachi, Chapman, William, Griffith, Obi L

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Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes von Zhang, Jin, Griffith, Malachi, Miller, Christopher A., Griffith, Obi L., Spencer, David H., Walker, Jason R., Magrini, Vincent, McGrath, Sean D., Ly, Amy, Helton, Nichole M., Trissal, Maria, Link, Daniel C., Dang, Ha X., Larson, David E., Kulkarni, Shashikant, Cordes, Matthew G., Fronick, Catrina C., Fulton, Robert S., Klco, Jeffery M., Mardis, Elaine R., Ley, Timothy J., Wilson, Richard K., Maher, Christopher A.

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Genome Modeling System: A Knowledge Management Platform for Genomics von Griffith, Malachi, Griffith, Obi L, Smith, Scott M, Ramu, Avinash, Callaway, Matthew B, Brummett, Anthony M, Kiwala, Michael J, Coffman, Adam C, Regier, Allison A, Oberkfell, Ben J, Sanderson, Gabriel E, Mooney, Thomas P, Nutter, Nathaniel G, Belter, Edward A, Du, Feiyu, Long, Robert L, Abbott, Travis E, Ferguson, Ian T, Morton, David L, Burnett, Mark M, Weible, James V, Peck, Joshua B, Dukes, Adam, McMichael, Joshua F, Lolofie, Justin T, Derickson, Brian R, Hundal, Jasreet, Skidmore, Zachary L, Ainscough, Benjamin J, Dees, Nathan D, Schierding, William S, Kandoth, Cyriac, Kim, Kyung H, Lu, Charles, Harris, Christopher C, Maher, Nicole, Maher, Christopher A, Magrini, Vincent J, Abbott, Benjamin S, Chen, Ken, Clark, Eric, Das, Indraniel, Fan, Xian, Hawkins, Amy E, Hepler, Todd G, Wylie, Todd N, Leonard, Shawn M, Schroeder, William E, Shi, Xiaoqi, Carmichael, Lynn K, Weil, Matthew R, Wohlstadter, Richard W, Stiehr, Gary, McLellan, Michael D, Pohl, Craig S, Miller, Christopher A, Koboldt, Daniel C, Walker, Jason R, Eldred, James M, Larson, David E, Dooling, David J, Ding, Li, Mardis, Elaine R, Wilson, Richard K

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