Brain morphological changes associated with exposure to HSV1 in first-episode schizophrenia von PRASAD, K. M. R, SHIRTS, B. H, YOLKEN, R. H, KESHAVAN, M. S, NIMGAONKAR, V. L

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Sequence specificity of aminoglycoside-induced stop codon readthrough: Potential implications for treatment of Duchenne muscular dystrophy von Howard, Michael T., Shirts, Brian H., Petros, Lorin M., Flanigan, Kevin M., Gesteland, Raymond F., Atkins, John F.

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HSV1 exposure affects prefrontal cortical structure in schizophrenia patients von Prasad, K M R, Shirts, B H, Yolken, R H, Keshavan, M S, Nimgaonkar, V L

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Changing interpretations, stable genes: responsibilities of patients, professionals, and policy makers in the clinical interpretation of complex genetic information von Shirts, Brian H., Parker, Lisa S.

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Cell culture analysis of the regulatory frameshift event required for the expression of mammalian antizymes von Howard, Michael T., Shirts, Brian H., Zhou, Jiadong, Carlson, C. Lance, Matsufuji, Senya, Gesteland, Raymond F., Weeks, Reitha S., Atkins, John F.

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Are exposure to cytomegalovirus and genetic variation on chromosome 6p joint risk factors for schizophrenia? von Kim, Jung Jin, Shirts, Brian H., Dayal, Madhulika, Bacanu, Silviu-alin, Wood, Joel, Xie, Weiting, Zhang, Xiaohua, Chowdari, Kodavali V., Yolken, Robert, Devlin, Bernie, Nimgaonkar, Vishwajit L.

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Brain morphological changes associated with exposure to HSV1 in first-episode schizophrenia von Prasad, K M R, Shirts, B H, Yolken, R H, Keshavan, M S, Nimgaonkar, V L

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A comprehensive genetic association and functional study of TNF in schizophrenia risk von Shirts, Brian H., Bamne, Mikhil, Kim, Jung Jin, Talkowski, Michael, Wood, Joel, Yolken, Robert, Nimgaonkar, Vishwajit L.

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Sequence specificity of aminoglycoside-induced stop condon readthrough: potential implications for treatment of Duchenne muscular dystrophy von Howard, M T, Shirts, B H, Petros, L M, Flanigan, K M, Gesteland, R F, Atkins, J F

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Rare loss of function variants in candidate genes and risk of colorectal cancer von Rosenthal, EA, Shirts, BH, Amendola, LM, Horike-Pyne, M, Robertson, PD, Hisama, FM, Bennett, RL, Dorschner, MO, Nickerson, DA, Stanaway, IB, Nassir, R, Vickers, KT, Li, C, Grady, WM, Peters, U, Jarvik, GP, NHLBI GO Exome Sequencing Project

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Scaling resolution of variant classification differences in ClinVar between 41 clinical laboratories through an outlier approach von Harrison, Steven M., Dolinksy, Jill S., Chen, Wenjie, Collins, Christin D., Das, Soma, Deignan, Joshua L., Garber, Kathryn B., Garcia, John, Jarinova, Olga, Knight Johnson, Amy E., Koskenvuo, Juha W., Lee, Hane, Mao, Rong, Mar‐Heyming, Rebecca, McFaddin, Andrew S., Moyer, Krista, Nagan, Narasimhan, Rentas, Stefan, Santani, Avni B., Seppälä, Eija H., Shirts, Brian H., Tidwell, Timothy, Topper, Scott, Vincent, Lisa M., Vinette, Kathy, Rehm, Heidi L.

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ClinGen guidance for use of the PP1/BS4 co-segregation and PP4 phenotype specificity criteria for sequence variant pathogenicity classification von Biesecker, Leslie G., Byrne, Alicia B., Harrison, Steven M., Pesaran, Tina, Schäffer, Alejandro A., Shirts, Brian H., Tavtigian, Sean V., Rehm, Heidi L.

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Characterization of splice-altering mutations in inherited predisposition to cancer von Casadei, Silvia, Gulsuner, Suleyman, Shirts, Brian H., Mandell, Jessica B., Kortbawi, Hannah M., Norquist, Barbara S., Swisher, Elizabeth M., Lee, Ming K., Goldberg, Yael, O’Connor, Robert, Tan, Zheng, Pritchard, Colin C., King, Mary-Claire, Walsha, Tom

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Genetic Mechanisms of Immune Evasion in Colorectal Cancer von Grasso, Catherine S, Giannakis, Marios, Wells, Daniel K, Hamada, Tsuyoshi, Mu, Xinmeng Jasmine, Quist, Michael, Nowak, Jonathan A, Nishihara, Reiko, Qian, Zhi Rong, Inamura, Kentaro, Morikawa, Teppei, Nosho, Katsuhiko, Abril-Rodriguez, Gabriel, Connolly, Charles, Escuin-Ordinas, Helena, Geybels, Milan S, Grady, William M, Hsu, Li, Hu-Lieskovan, Siwen, Huyghe, Jeroen R, Kim, Yeon Joo, Krystofinski, Paige, Leiserson, Mark D M, Montoya, Dennis J, Nadel, Brian B, Pellegrini, Matteo, Pritchard, Colin C, Puig-Saus, Cristina, Quist, Elleanor H, Raphael, Ben J, Salipante, Stephen J, Shin, Daniel Sanghoon, Shinbrot, Eve, Shirts, Brian, Shukla, Sachet, Stanford, Janet L, Sun, Wei, Tsoi, Jennifer, Upfill-Brown, Alexander, Wheeler, David A, Wu, Catherine J, Yu, Ming, Zaidi, Syed H, Zaretsky, Jesse M, Gabriel, Stacey B, Lander, Eric S, Garraway, Levi A, Hudson, Thomas J, Fuchs, Charles S, Ribas, Antoni, Ogino, Shuji, Peters, Ulrike

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Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access von Amendola, Laura M., Shuster, Elizabeth, Leo, Michael C., Dorschner, Michael O., Rolf, Bradley A., Shirts, Brian H., Gilmore, Marian J., Okuyama, Sonia, Zepp, Jamilyn M., Kauffman, Tia L., Mittendorf, Kathleen F., Bellcross, Cecilia, Jenkins, Charisma L., Joseph, Galen, Riddle, Leslie, Syngal, Sapna, Ukaegbu, Chinedu, Goddard, Katrina A.B., Wilfond, Benjamin S., Jarvik, Gail P., Allen, Jake, Amendola, Laura M., Anderson, Katherine P., Angelo, Frank, Arnold, Briana L., Bellcross, Cecelia, Bendelow, Tiffany, Biesecker, Barbara B., Breslin, Kristin D., Bulkley, Joanna E., Booker, Kristina F., Caruncho, Mikaella, Davis, James V., Deutsch, Sonia, Devine, Beth, Dorschner, Michael O., Duenas, Devan M., Eubanks, Donna J., Feigelson, Heather Spencer, Freed, Amanda S., Gilmore, Marian J., Goddard, Katrina A.B., Greaney, Clay, Gruß, Inga, Guerra, Claudia, Guo, Boya, Holup, Joan, Hunter, Jessica Ezzell, Ingphakorn, Chalinya L., Jackson, Paige, Jarvik, Gail P., Jenkins, Charisma L., Joseph, Galen, Karliner, Leah S., Kauffman, Tia L., Keast, Erin, Knerr, Sarah, Koomas, Alyssa H., Kraft, Stephanie A., Lee, Mi H., Lee, Robin, Soo-Jin Lee, Sandra, Leo, Michael C., Lewis, Hannah S., Liles, Elizabeth G., Lindberg, Nangel M., Lynch, Frances, McMullen, Carmit K., Medina, Elizabeth, Mittendorf, Kathleen F., Muessig, Kristin R., Okuyama, Sonia, Peterson, C. Samuel, Paolucci, Angela R., Perez, Rosse Rodriguez, Porter, Kathryn M., Ransom, Chelese L., Reyes, Ana, Riddle, Leslie S., Robinson, Sperry, Rolf, Bradley A., Rope, Alan F., Schield, Emily, Schneider, Jennifer L., Shipman, Kelly J., Shirts, Brian H., Shuster, Elizabeth, Syngal, Sapna, Torgrimson-Ojerio, Britta N., Ukaegbu, Chinedu, Vandermeer, Meredith L., Varga, Alexandra M., Veenstra, David L., Whitebirch, W. Chris, Lee White, Larissa, Wilfond, Benjamin S., Zepp, Jamilyn M.

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Genomic data in the All of Us Research Program von Bick, Alexander G., Metcalf, Ginger A., Mayo, Kelsey R., Lichtenstein, Lee, Rura, Shimon, Carroll, Robert J., Musick, Anjene, Linder, Jodell E., Jordan, I. King, Nagar, Shashwat Deepali, Sharma, Shivam, Meller, Robert, Basford, Melissa, Boerwinkle, Eric, Cicek, Mine S., Doheny, Kimberly F., Eichler, Evan E., Gabriel, Stacey, Gibbs, Richard A., Glazer, David, Harris, Paul A., Jarvik, Gail P., Philippakis, Anthony, Rehm, Heidi L., Roden, Dan M., Thibodeau, Stephen N., Topper, Scott, Blegen, Ashley L., Wirkus, Samantha J., Wagner, Victoria A., Meyer, Jeffrey G., Muzny, Donna M., Venner, Eric, Mawhinney, Michelle Z., Griffith, Sean M. L., Hsu, Elvin, Ling, Hua, Adams, Marcia K., Walker, Kimberly, Hu, Jianhong, Doddapaneni, Harsha, Kovar, Christie L., Murugan, Mullai, Dugan, Shannon, Khan, Ziad, Lennon, Niall J., Austin-Tse, Christina, Banks, Eric, Gatzen, Michael, Gupta, Namrata, Henricks, Emma, Larsson, Katie, McDonough, Sheli, Harrison, Steven M., Kachulis, Christopher, Lebo, Matthew S., Neben, Cynthia L., Steeves, Marcie, Zhou, Alicia Y., Smith, Joshua D., Frazar, Christian D., Davis, Colleen P., Patterson, Karynne E., Wheeler, Marsha M., McGee, Sean, Lockwood, Christina M., Shirts, Brian H., Pritchard, Colin C., Murray, Mitzi L., Vasta, Valeria, Leistritz, Dru, Richardson, Matthew A., Buchan, Jillian G., Radhakrishnan, Aparna, Krumm, Niklas, Ehmen, Brenna W., Schwartz, Sophie, Aster, M. Morgan T., Cibulskis, Kristian, Haessly, Andrea, Asch, Rebecca, Cremer, Aurora, Degatano, Kylee, Shergill, Akum, Gauthier, Laura D., Lee, Samuel K., Hatcher, Aaron, Grant, George B., Brandt, Genevieve R., Covarrubias, Miguel, Able, Ashley, Green, Ashley E., Zhang, Jennifer, Condon, Henry R., Wang, Yuanyuan, Dillon, Moira K., Albach, C. H., Baalawi, Wail, Choi, Seung Hoan, Wang, Xin

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A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories von O’Daniel, Julianne M., McLaughlin, Heather M., Amendola, Laura M., Bale, Sherri J., Berg, Jonathan S., Bick, David, Bowling, Kevin M., Chao, Elizabeth C., Chung, Wendy K., Conlin, Laura K., Cooper, Gregory M., Das, Soma, Deignan, Joshua L., Dorschner, Michael O., Evans, James P., Ghazani, Arezou A., Goddard, Katrina A., Gornick, Michele, Farwell Hagman, Kelly D., Hambuch, Tina, Hegde, Madhuri, Hindorff, Lucia A., Holm, Ingrid A., Jarvik, Gail P., Knight Johnson, Amy, Mighion, Lindsey, Morra, Massimo, Plon, Sharon E., Punj, Sumit, Richards, C. Sue, Santani, Avni, Shirts, Brian H., Spinner, Nancy B., Tang, Sha, Weck, Karen E., Wolf, Susan M., Yang, Yaping, Rehm, Heidi L.

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The FamilyTalk randomized controlled trial: patient-reported outcomes in clinical genetic sequencing for colorectal cancer von Makhnoon, Sukh, Bowen, Deborah J., Shirts, Brian H., Fullerton, Stephanie M., Larson, Eric B., Ralston, James D., Leppig, Kathleen A., Crosslin, David R., Veenstra, David, Jarvik, Gail P.

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CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record von Shirts, Brian H, Salama, Joseph S, Aronson, Samuel J, Chung, Wendy K, Gray, Stacy W, Hindorff, Lucia A, Jarvik, Gail P, Plon, Sharon E, Stoffel, Elena M, Tarczy-Hornoch, Peter Z, Van Allen, Eliezer M, Weck, Karen E, Chute, Christopher G, Freimuth, Robert R, Grundmeier, Robert W, Hartzler, Andrea L, Li, Rongling, Peissig, Peggy L, Peterson, Josh F, Rasmussen, Luke V, Starren, Justin B, Williams, Marc S, Overby, Casey L

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Antibodies to cytomegalovirus and Herpes Simplex Virus 1 associated with cognitive function in schizophrenia von Shirts, Brian H, Prasad, Konasale M, Pogue-Geile, Michael F, Dickerson, Faith, Yolken, Robert H, Nimgaonkar, Vishwajit L

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