Tumor Sequencing and Patient-Derived Xenografts in the Neoadjuvant Treatment of Breast Cancer by Goetz, Matthew P, Kalari, Krishna R, Suman, Vera J, Moyer, Ann M, Yu, Jia, Visscher, Daniel W, Dockter, Travis J, Vedell, Peter T, Sinnwell, Jason P, Tang, Xiaojia, Thompson, Kevin J, McLaughlin, Sarah A, Moreno-Aspitia, Alvaro, Copland, John A, Northfelt, Donald W, Gray, Richard J, Hunt, Katie, Conners, Amy, Sicotte, Hugues, Eckel-Passow, Jeanette E, Kocher, Jean-Pierre, Ingle, James N, Ellingson, Marissa S, McDonough, Michelle, Wieben, Eric D, Weinshilboum, Richard, Wang, Liewei, Boughey, Judy C

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Determining the frequency of pathogenic germline variants from exome sequencing in patients with castrate-resistant prostate cancer by Hart, Steven N, Ellingson, Marissa S, Schahl, Kim, Vedell, Peter T, Carlson, Rachel E, Sinnwell, Jason P, Barman, Poulami, Sicotte, Hugues, Eckel-Passow, Jeanette E, Wang, Liguo, Kalari, Krishna R, Qin, Rui, Kruisselbrink, Teresa M, Jimenez, Rafael E, Bryce, Alan H, Tan, Winston, Weinshilboum, Richard, Wang, Liewei, Kohli, Manish

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WDR37 syndrome: identification of a distinct new cluster of disease-associated variants and functional analyses of mutant proteins by Sorokina, Elena A., Reis, Linda M., Thompson, Samuel, Agre, Katherine, Babovic-Vuksanovic, Dusica, Ellingson, Marissa S., Hasadsri, Linda, van Bever, Yolande, Semina, Elena V.

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Development of a flipped learning course to deliver and scale molecular variant evaluation education: A quality improvement initiative by Balcom, Jessica R., Ellingson, Marissa S., Bowler, Carrie A., Richardson, Darcy M., Kruisselbrink, Teresa, Thomas, Brittany C.

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Exome sequencing reveals frequent deleterious germline variants in cancer susceptibility genes in women with invasive breast cancer undergoing neoadjuvant chemotherapy by Ellingson, Marissa S., Hart, Steven N., Kalari, Krishna R., Suman, Vera, Schahl, Kimberly A., Dockter, Travis J., Felten, Sara J., Sinnwell, Jason P., Thompson, Kevin J., Tang, Xiaojia, Vedell, Peter T., Barman, Poulami, Sicotte, Hugues, Eckel-Passow, Jeanette E., Northfelt, Donald W., Gray, Richard J., McLaughlin, Sarah A., Moreno-Aspitia, Alvaro, Ingle, James N., Moyer, Ann M., Visscher, Daniel W., Jones, Katie, Conners, Amy, McDonough, Michelle, Wieben, Eric D., Wang, Liewei, Weinshilboum, Richard, Boughey, Judy C., Goetz, Matthew P.

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RNA‐Seq detects a SAMD12‐EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromas by Oliver, Gavin R., Blackburn, Patrick R., Ellingson, Marissa S., Conboy, Erin, Pinto e Vairo, Filippo, Webley, Matthew, Thorland, Erik, Ferber, Matthew, Van Hul, Els, Werf, Ilse M., Wuyts, Wim, Babovic‐Vuksanovic, Dusica, Klee, Eric W.

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CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity by Ernst, Michelle E., Baugh, Evan H., Thomas, Amanda, Bier, Louise, Lippa, Natalie, Stong, Nicholas, Mulhern, Maureen S., Kushary, Sulagna, Akman, Cigdem I., Heinzen, Erin L., Yeh, Raymond, Bi, Weimin, Hanchard, Neil A., Burrage, Lindsay C., Leduc, Magalie S., Chong, Josephine S. C., Bend, Renee, Lyons, Michael J., Lee, Jennifer A., Suwannarat, Pim, Brilstra, Eva, Simon, Marleen, Koopmans, Marije, Binsbergen, Ellen, Groepper, Daniel, Fleischer, Julie, Nava, Caroline, Keren, Boris, Mignot, Cyril, Mathieu, Sophie, Mancini, Grazia M. S., Madan‐Khetarpal, Suneeta, Infante, Elena M., Bluvstein, Judith, Seeley, Andrea, Bachman, Kristine, Klee, Eric W., Schultz‐Rogers, Laura E., Hasadsri, Linda, Barnett, Sarah, Ellingson, Marissa S., Ferber, Matthew J., Narayanan, Vinodh, Ramsey, Keri, Rauch, Anita, Joset, Pascal, Steindl, Katharina, Sheehan, Theodore, Poduri, Annapurna, Vasquez, Alejandra, Ruivenkamp, Claudia, White, Susan M., Pais, Lynn, Monaghan, Kristin G., Goldstein, David B., Sands, Tristan T., Aggarwal, Vimla

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Pregnancy in an individual with mild Smith-Lemli-Opitz syndrome by Ellingson, M.S., Wick, M.J., White, W.M., Raymond, K.M., Saenger, A.K., Pichurin, P.N., Wassif, C.A., Porter, F.D., Babovic-Vuksanovic, D.

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P897: DEIJ advancement in the genomics laboratory through GC-driven advocacy: A process improvement review of sex/gender verification SOPs by Essendrup, Anna, Brunker, Sarah, Ellingson, Marissa, Bortnova, Jessica, Salsbery, Kyle, Hasadsri, Linda, Niu, Zhiyv

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