Transgenic Mice Lacking NMDAR-Dependent LTD Exhibit Deficits in Behavioral Flexibility von Nicholls, Russell E., Alarcon, Juan Marcos, Malleret, Gaël, Carroll, Reed C., Grody, Michael, Vronskaya, Svetlana, Kandel, Eric R.

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Inducible Enhancement of Memory Storage and Synaptic Plasticity in Transgenic Mice Expressing an Inhibitor of ATF4 (CREB-2) and C/EBP Proteins von Chen, Amy, Muzzio, Isabel A, Malleret, Gaël, Bartsch, Dusan, Verbitsky, Miguel, Pavlidis, Paul, Yonan, Amanda L, Vronskaya, Svetlana, Grody, Michael B, Cepeda, Ivan, Gilliam, T.Conrad, Kandel, Eric R

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Presentation and treatment of acute psychosis in an adolescent girl with cerebral palsy von Grody, Michael B, Coffey, Barbara J

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Article: Transgenic Mice Lacking NMDAR-Dependent LTD Exhibit Deficits in Behavioral Flexibility von Nicholls, Russell E, Alarcon, Juan Marcos, Malleret, Gael, Carroll, Reed C, Grody, Michael, Vronskaya, Svetlana, Kandel, Eric R

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Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders von Lee, Hane, Deignan, Joshua L, Dorrani, Naghmeh, Strom, Samuel P, Kantarci, Sibel, Quintero-Rivera, Fabiola, Das, Kingshuk, Toy, Traci, Harry, Bret, Yourshaw, Michael, Fox, Michelle, Fogel, Brent L, Martinez-Agosto, Julian A, Wong, Derek A, Chang, Vivian Y, Shieh, Perry B, Palmer, Christina G. S, Dipple, Katrina M, Grody, Wayne W, Vilain, Eric, Nelson, Stanley F

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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing von Green, Robert C., Berg, Jonathan S., Grody, Wayne W., Kalia, Sarah S., Korf, Bruce R., Martin, Christa L., McGuire, Amy L., Nussbaum, Robert L., O’Daniel, Julianne M., Ormond, Kelly E., Rehm, Heidi L., Watson, Michael S., Williams, Marc S., Biesecker, Leslie G.

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Massively parallel base editing to map variant effects in human hematopoiesis von Martin-Rufino, Jorge D., Castano, Nicole, Pang, Michael, Grody, Emanuelle I., Joubran, Samantha, Caulier, Alexis, Wahlster, Lara, Li, Tongqing, Qiu, Xiaojie, Riera-Escandell, Anna Maria, Newby, Gregory A., Al’Khafaji, Aziz, Chaudhary, Santosh, Black, Susan, Weng, Chen, Munson, Glen, Liu, David R., Wlodarski, Marcin W., Sims, Kacie, Oakley, Jamie H., Fasano, Ross M., Xavier, Ramnik J., Lander, Eric S., Klein, Daryl E., Sankaran, Vijay G.

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Exploring concordance and discordance for return of incidental findings from clinical sequencing von Green, Robert C., Berg, Jonathan S., Berry, Gerard T., Biesecker, Leslie G., Dimmock, David P., Evans, James P., Grody, Wayne W., Hegde, Madhuri R., Kalia, Sarah, Korf, Bruce R., Krantz, Ian, McGuire, Amy L., Miller, David T., Murray, Michael F., Nussbaum, Robert L., Plon, Sharon E., Rehm, Heidi L., Jacob, Howard J.

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A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders von Ngo, Kathie J., Rexach, Jessica E., Lee, Hane, Petty, Lauren E., Perlman, Susan, Valera, Juliana M., Deignan, Joshua L., Mao, Yuanming, Aker, Mamdouh, Posey, Jennifer E., Jhangiani, Shalini N., Coban‐Akdemir, Zeynep H., Boerwinkle, Eric, Muzny, Donna, Nelson, Alexandra B., Hassin‐Baer, Sharon, Poke, Gemma, Neas, Katherine, Geschwind, Michael D., Grody, Wayne W., Gibbs, Richard, Geschwind, Daniel H., Lupski, James R., Below, Jennifer E., Nelson, Stanley F., Fogel, Brent L.

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Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG) von Deignan, Joshua L., Gregg, Anthony R., Grody, Wayne W., Guo, Michael H., Kearney, Hutton, Monaghan, Kristin G., Raraigh, Karen S., Taylor, Jennifer, Zepeda-Mendoza, Cinthya J., Ziats, Catherine

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Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel von Watson, Michael S., Cutting, Garry R., Desnick, Robert J., Driscoll, Deborah A., Klinger, Katherine, Mennuti, Michael, Palomaki, Glenn E., Popovich, Bradley W., Pratt, Victoria M., Rohlfs, Elizabeth M., Strom, Charles M., Richards, C. Sue, Witt, David R., Grody, Wayne W.

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Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participants von Saeidian, Amir Hossein, March, Michael E., Youssefian, Leila, Watson, Deborah J., Bhandari, Esha, Wang, Xiang, Zhao, Xiaonan, Owen, Nichole Marie, Strong, Alanna, Harr, Margaret H., Aliazami, Farnoush, Ribeiro Carneiro, Thaise Nayane, Akbarzadeh, Mahdi, Kazemioula, Golnesa, Saeidian, Amir Hesam, Palizban, Fahimeh, Biglari, Sajjad, Coleman, David, Snyder, James, Wang, Fengxiang, Billings, Jonathan, Terek, Shannon, Mentch, Frank, Regan-Fendt, Kelly, Tsoi, Lam C., Dorrani, Naghmeh, Bhoj, Elizabeth, Zackai, Elaine, Vahidnezhad, Hassan, Gudjonsson, Johann E., Cederbaum, Stephen D., Deignan, Joshua L., Glessner, Joseph, Grody, Wayne W., Hakonarson, Hakon

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Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants von Fu, Wenqing, O’Connor, Timothy D., Jun, Goo, Kang, Hyun Min, Abecasis, Goncalo, Leal, Suzanne M., Gabriel, Stacey, Rieder, Mark J., Altshuler, David, Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., NHLBI Exome Sequencing Project, Akey, Joshua M.

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Collagen content of nonsupport tissue in pelvic organ prolapse and stress urinary incontinence von Wong, Michael Y, Harmanli, Ozgur H, Agar, Mehmet, Dandolu, Vani, Grody, M.H.Terry

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A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders von Ngo, Kathie J., Rexach, Jessica E., Lee, Hane, Petty, Lauren E., Perlman, Susan, Valera, Juliana M., Deignan, Joshua L., Mao, Yuanming, Aker, Mamdouh, Posey, Jennifer E., Jhangiani, Shalini N., Coban‐Akdemir, Zeynep H., Boerwinkle, Eric, Muzny, Donna, Nelson, Alexandra B., Hassin‐Baer, Sharon, Poke, Gemma, Neas, Katherine, Geschwind, Michael D., Grody, Wayne W., Gibbs, Richard, Geschwind, Daniel H., Lupski, James R., Below, Jennifer E., Nelson, Stanley F., Fogel, Brent L.

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Laboratory standards and guidelines for population-based cystic fibrosis carrier screening von Grody, Wayne W, Cutting, Garry R, Klinger, Katherine W, Richards, Carolyn Sue, Watson, Michael S, Desnick, Robert J

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Electric Field–Induced Release and Measurement Liquid Biopsy for Noninvasive Early Lung Cancer Assessment von Wei, Fang, Strom, Charles M., Cheng, Jordan, Lin, Chien-Chung, Hsu, Ching-Yun, Soo Hoo, Guy W., Chia, David, Kim, Yong, Li, Feng, Elashoff, David, Grognan, Tristan, Tu, Michael, Liao, Wei, Xian, Rena, Grody, Wayne W., Su, Wu-Chou, Wong, David T.W.

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Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol von Lange, Leslie A., Schmidt, Ellen M., Bizon, Chris, Jun, Goo, Auer, Paul, Li, Kuo-ping, Locke, Adam, Rivas, Manuel A., Feitosa, Mary F., Zhang, Qunyuan, Huffman, Jennifer E., Crosby, Jacy, Robinson, Jennifer G., Crosslin, David R., Rosenthal, Elisabeth A., Tsai, Michael, Rieder, Mark J., Fox, Ervin R., van Duijn, Cornelia M., Taylor, Herman A., Loos, Ruth J.F., Ballantyne, Christie M., Reiner, Alexander P., Cupples, L. Adrienne, Kang, Hyun Min, Lettre, Guillaume, Rader, Daniel J., Reilly, Muredach P., Stoletzki, Nina, Barr, R. Graham, Benjamin, Emelia J., Carr, Jeff, Dupuis, Josée, Ellis, Jaclyn, Fornage, Myriam, Goff, David, Grody, Wayne, Heard-Costa, Nancy L., Levy, Daniel, Li, Dalin, Loria, Cay, Mackey, Rachel, Quinlan, Aaron R., Rice, Kenneth, Sanders, Jill P., Tracy, Russell P., Tsai, Michael Y., Wassel, Chrstina L., Watson, Karol, Wilson, Gregory, Wilson, James G., Zakai, Neil A., Nalls, Michael, Bamshad, Michael J., Accurso, Frank, Beaty, Terri, Caplan, Daniel, Chidekel, Aaron, Christiani, David C., De Paula, Alicia, Gutierrez, Hector, Hassoun, Paul M., Hiatt, Peter, Hummer, Laura K., Kim, Yoonhee, Lin, Xihong, Louie, Tin L., Mathias, Rasika A., McNamara, John, McNamara, Sharon, Nielson, Dennis, Orenstein, David, O’Sullivan, Brian, Passero, Mary Ann, Perkett, Elizabeth, Spencer, Terry, Tabor, Holly K., Weiss, Robert, Wigley, Fred, Wise, Robert A., Wurfel, Mark M., Eichler, Evan E., Fu, Wenqing, Smith, Joshua D., Tennessen, Jacob A., Peters, Ulrike, Brzyski, Robert, Curb, J. David, Eaton, Charles B., Heiss, Gerardo, Johnson, Karen C., Lasser, Norman, Lin, Dan-Yu, Logsdon, Benjamin A., Manson, JoAnn E., Martin, Lisa, Stein, Evan, Applebaum-Bowden, Deborah, Paltoo, Dina N., Sturcke, Anne

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P672: Commercial cystic fibrosis carrier screening tests and coverage of the ACMG 100 recommended variants von Tidwell, Timothy, Gregg, Anthony, Grody, Wayne, Guo, Michael, Kearney, Hutton, Monaghan, Kristin, Taylor, Jennifer, Mendoza, Cinthya Zepeda, Ziats, Catherine, Deignan, Joshua, Raraigh, Karen

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Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results von Tabor, Holly K., Auer, Paul L., Jamal, Seema M., Chong, Jessica X., Yu, Joon-Ho, Gordon, Adam S., Graubert, Timothy A., O’Donnell, Christopher J., Rich, Stephen S., Nickerson, Deborah A., Bamshad, Michael J.

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