Synonymous ABCA3 Variants Do Not Increase Risk for Neonatal Respiratory Distress Syndrome von Wambach, Jennifer A., MD, MS, Wegner, Daniel J., MS, Heins, Hillary B., BS, Druley, Todd E., MD, PhD, Mitra, Robi D., PhD, Hamvas, Aaron, MD, Cole, F. Sessions, MD

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Clonal haematopoiesis harbouring AML-associated mutations is ubiquitous in healthy adults von Young, Andrew L., Challen, Grant A., Birmann, Brenda M., Druley, Todd E.

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Clonal hematopoiesis and risk of acute myeloid leukemia von Young, Andrew L, Tong, R Spencer, Birmann, Brenda M, Druley, Todd E

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Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma von Kalish, Jennifer M, Doros, Leslie, Helman, Lee J, Hennekam, Raoul C, Kuiper, Roland P, Maas, Saskia M, Maher, Eamonn R, Nichols, Kim E, Plon, Sharon E, Porter, Christopher C, Rednam, Surya, Schultz, Kris Ann P, States, Lisa J, Tomlinson, Gail E, Zelley, Kristin, Druley, Todd E

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Role of TP53 mutations in the origin and evolution of therapy-related acute myeloid leukaemia von Wong, Terrence N., Ramsingh, Giridharan, Young, Andrew L., Miller, Christopher A., Touma, Waseem, Welch, John S., Lamprecht, Tamara L., Shen, Dong, Hundal, Jasreet, Fulton, Robert S., Heath, Sharon, Baty, Jack D., Klco, Jeffery M., Ding, Li, Mardis, Elaine R., Westervelt, Peter, DiPersio, John F., Walter, Matthew J., Graubert, Timothy A., Ley, Timothy J., Druley, Todd E., Link, Daniel C., Wilson, Richard K.

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Integrated analysis of germline and somatic variants in ovarian cancer von Kanchi, Krishna L., Johnson, Kimberly J., Lu, Charles, McLellan, Michael D., Leiserson, Mark D. M., Wendl, Michael C., Zhang, Qunyuan, Koboldt, Daniel C., Xie, Mingchao, Kandoth, Cyriac, McMichael, Joshua F., Wyczalkowski, Matthew A., Larson, David E., Schmidt, Heather K., Miller, Christopher A., Fulton, Robert S., Spellman, Paul T., Mardis, Elaine R., Druley, Todd E., Graubert, Timothy A., Goodfellow, Paul J., Raphael, Benjamin J., Wilson, Richard K., Ding, Li

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Section Meetings von Velde, T. L. Vander, Thompson, Leonard N., Druley, M. E.

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Dnmt3a regulates T-cell development and suppresses T-ALL transformation von Kramer, A C, Kothari, A, Wilson, W C, Celik, H, Nikitas, J, Mallaney, C, Ostrander, E L, Eultgen, E, Martens, A, Valentine, M C, Young, A L, Druley, T E, Figueroa, M E, Zhang, B, Challen, G A

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Section Meetings von Mathews, C. M., Kramer, Warren A., Pleibel, Albert F., Blanchard, Kimball, Druley, M. E., Breimeister, Harry

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Section Meeting Reports von Thompson, Leonard N., Druley, M. E., Finney, J. Wiley, Kramer, Warren A., Turre, George J.

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Cancer therapy shapes the fitness landscape of clonal hematopoiesis von Bolton, Kelly L., Ptashkin, Ryan N., Gao, Teng, Braunstein, Lior, Devlin, Sean M., Kelly, Daniel, Patel, Minal, Berthon, Antonin, Syed, Aijazuddin, Yabe, Mariko, Coombs, Catherine C., Caltabellotta, Nicole M., Walsh, Mike, Offit, Kenneth, Stadler, Zsofia, Mandelker, Diana, Schulman, Jessica, Patel, Akshar, Philip, John, Bernard, Elsa, Gundem, Gunes, Ossa, Juan E. Arango, Levine, Max, Martinez, Juan S. Medina, Farnoud, Noushin, Glodzik, Dominik, Li, Sonya, Robson, Mark E., Lee, Choonsik, Pharoah, Paul D. P., Stopsack, Konrad H., Spitzer, Barbara, Mantha, Simon, Fagin, James, Boucai, Laura, Gibson, Christopher J., Ebert, Benjamin L., Young, Andrew L., Druley, Todd, Takahashi, Koichi, Gillis, Nancy, Ball, Markus, Padron, Eric, Hyman, David M., Baselga, Jose, Norton, Larry, Gardos, Stuart, Klimek, Virginia M., Scher, Howard, Bajorin, Dean, Paraiso, Eder, Benayed, Ryma, Arcila, Maria E., Ladanyi, Marc, Solit, David B., Berger, Michael F., Tallman, Martin, Garcia-Closas, Montserrat, Chatterjee, Nilanjan, Diaz, Luis A., Levine, Ross L., Morton, Lindsay M., Zehir, Ahmet, Papaemmanuil, Elli

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Section Meetings von Anderson, Irving E., Ongerth, Henry J., Roth, J. D., Pleibel, Albert F., Blanchard, Kimball, Druley, M. E., Jackson, Leslie A.

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Section Meetings von Druley, M. E., Finney, J. Wiley, Kramer, Warren A., Pedersen, H. V., Smith, Leon A., Carl, Charles E.

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The cyclic AMP pathway is a sex-specific modifier of glioma risk in type I neurofibromatosis patients von Warrington, Nicole M, Sun, Tao, Luo, Jingqin, McKinstry, Robert C, Parkin, Patricia C, Ganzhorn, Sara, Spoljaric, Debra, Albers, Anne C, Merkelson, Amanda, Stewart, Douglas R, Stevenson, David A, Viskochil, David, Druley, Todd E, Forys, Jason T, Reilly, Karlyne M, Fisher, Michael J, Tabori, Uri, Allen, Jeffrey C, Schiffman, Joshua D, Gutmann, David H, Rubin, Joshua B

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Quantification of rare allelic variants from pooled genomic DNA von Mitra, Robi D, Druley, Todd E, Vallania, Francesco L M, Wegner, Daniel J, Varley, Katherine E, Knowles, Olivia L, Bonds, Jacqueline A, Robison, Sarah W, Doniger, Scott W, Hamvas, Aaron, Cole, F Sessions, Fay, Justin C

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Novel coenzyme Q6 genetic variant increases susceptibility to pneumococcal disease von Walker, Emma C., Javati, Sarah, Todd, Elizabeth M., Matlam, John-Paul, Lin, Xue, Bryant, Michelle, Krone, Emily, Ramani, Rashmi, Chandra, Pallavi, Green, Taylor P., Anaya, Edgar P., Zhou, Julie Y., Alexander, Katherine A., Tong, R. Spencer, Yuasi, Lapule, Boluarte, Sebastian, Yang, Fan, Greenberg, Lina, Nerbonne, Jeanne M., Greenberg, Michael J., Clemens, Regina A., Philips, Jennifer A., Wilson, Leslie D., Halabi, Carmen M., DeBosch, Brian J., Blyth, Christopher C., Druley, Todd E., Kazura, James W., Pomat, William S., Morley, Sharon Celeste

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ArCH: improving the performance of clonal hematopoiesis variant calling and interpretation von Chan, Irenaeus C C, Panchot, Alex, Schmidt, Evelyn, McNulty, Samantha, Wiley, Brian J, Liu, Jie, Turner, Kimberly, Moukarzel, Lea, Wong, Wendy S W, Tran, Duc, Beeler, J Scott, Batchi-Bouyou, Armel Landry, Machiela, Mitchell J, Karyadi, Danielle M, Krajacich, Benjamin J, Zhao, Junhua, Kruglyak, Semyon, Lajoie, Bryan, Levy, Shawn, Patel, Minal, Kantoff, Philip W, Mason, Christopher E, Link, Daniel C, Druley, Todd E, Stopsack, Konrad H, Bolton, Kelly L

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Excess congenital non-synonymous variation in leukemia-associated genes in MLL− infant leukemia: a Children’s Oncology Group report von Valentine, M C, Linabery, A M, Chasnoff, S, Hughes, A E O, Mallaney, C, Sanchez, N, Giacalone, J, Heerema, N A, Hilden, J M, Spector, L G, Ross, J A, Druley, T E

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Whole-exome sequencing of familial esophageal squamous cell carcinoma identified rare pathogenic variants in new predisposition genes von Golyan, F. F., Druley, T. E., Abbaszadegan, M. R.

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Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome von Wambach, Jennifer A, Wegner, Daniel J, Depass, Kelcey, Heins, Hillary, Druley, Todd E, Mitra, Robi D, An, Ping, Zhang, Qunyuan, Nogee, Lawrence M, Cole, F Sessions, Hamvas, Aaron

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