Medical record digest von Sanchez, Jr., Mario, Howard, Gregory G, Krier, Robert W, Zahora, Kevin M, Goutmann, Peter G, Mears, Gregory D, Forester, Frederick W, Freeman, Gary A

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MEDICAL RECORD DIGEST von Howard, Gregory G, Krier, Robert W, Zahora, Kevin M, Goutmann, Peter G, Sanchez, JR., Mario, Mears, Gregory D, Forester, Frederick W, Freeman, Gary A

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The BabySeq project: implementing genomic sequencing in newborns von Holm, Ingrid A, Agrawal, Pankaj B, Ceyhan-Birsoy, Ozge, Christensen, Kurt D, Fayer, Shawn, Frankel, Leslie A, Genetti, Casie A, Krier, Joel B, LaMay, Rebecca C, Levy, Harvey L, McGuire, Amy L, Parad, Richard B, Park, Peter J, Pereira, Stacey, Rehm, Heidi L, Schwartz, Talia S, Waisbren, Susan E, Yu, Timothy W, Green, Robert C, Beggs, Alan H

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Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project von Ceyhan-Birsoy, Ozge, Murry, Jaclyn B., Machini, Kalotina, Lebo, Matthew S., Yu, Timothy W., Fayer, Shawn, Genetti, Casie A., Schwartz, Talia S., Agrawal, Pankaj B., Parad, Richard B., Holm, Ingrid A., McGuire, Amy L., Green, Robert C., Rehm, Heidi L., Beggs, Alan H., Agrawal, Pankaj B., Beggs, Alan H., Betting, Wendi N., Ceyhan-Birsoy, Ozge, Christensen, Kurt D., Dukhovny, Dmitry, Fayer, Shawn, Frankel, Leslie A., Genetti, Casie A., Graham, Chet, Green, Robert C., Guiterrez, Amanda M., Harden, Maegan, Holm, Ingrid A., Krier, Joel B., Lebo, Matthew S., Levy, Harvey L., Lu, Xingquan, Machini, Kalotina, McGuire, Amy L., Murry, Jaclyn B., Naik, Medha, Nguyen, Tiffany T., Parad, Richard B., Peoples, Hayley A., Pereira, Stacey, Petersen, Devan, Ramamurthy, Uma, Ramanathan, Vivek, Rehm, Heidi L., Roberts, Amy, Robinson, Jill O., Roumiantsev, Serguei, Schwartz, Talia S., Truong, Tina K., VanNoy, Grace E., Waisbren, Susan E., Yu, Timothy W.

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A randomized multicenter trial on a lung ultrasound–guided treatment strategy in patients on chronic hemodialysis with high cardiovascular risk von Zoccali, Carmine, Torino, Claudia, Mallamaci, Francesca, Sarafidis, Pantelis, Papagianni, Aikaterini, Ekart, Robert, Hojs, Radovan, Klinger, Marian, Letachowicz, Krzysztof, Fliser, Danilo, Seiler-Mußler, Sarah, Lizzi, Fabio, Wiecek, Andrzej, Miskiewicz, Agata, Siamopoulos, Kostas, Balafa, Olga, Slotki, Itzchak, Shavit, Linda, Stavroulopoulos, Aristeidis, Covic, Adrian, Siriopol, Dimitrie, Massy, Ziad A., Seidowsky, Alexandre, Battaglia, Yuri, Martinez-Castelao, Alberto, Polo-Torcal, Carolina, Coudert-Krier, Marie-Jeanne, Rossignol, Patrick, Fiaccadori, Enrico, Regolisti, Giuseppe, Hannedouche, Thierry, Bachelet, Thomas, Jager, Kitty J., Dekker, Friedo W., Tripepi, Rocco, Tripepi, Giovanni, Gargani, Luna, Sicari, Rosa, Picano, Eugenio, London, Gérard Michel

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ClinGen — The Clinical Genome Resource von Rehm, Heidi L, Berg, Jonathan S, Brooks, Lisa D, Bustamante, Carlos D, Evans, James P, Landrum, Melissa J, Ledbetter, David H, Maglott, Donna R, Martin, Christa Lese, Nussbaum, Robert L, Plon, Sharon E, Ramos, Erin M, Sherry, Stephen T, Watson, Michael S

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Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project von Genetti, Casie A., Schwartz, Talia S., Robinson, Jill O., VanNoy, Grace E., Petersen, Devan, Pereira, Stacey, Fayer, Shawn, Peoples, Hayley A., Agrawal, Pankaj B., Betting, Wendi N., Holm, Ingrid A., McGuire, Amy L., Waisbren, Susan E., Yu, Timothy W., Green, Robert C., Beggs, Alan H., Parad, Richard B.

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Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization von Blout Zawatsky, Carrie L., Shah, Nidhi, Machini, Kalotina, Perez, Emma, Christensen, Kurt D., Zouk, Hana, Steeves, Marcie, Koch, Christopher, Uveges, Melissa, Shea, Janelle, Gold, Nina, Krier, Joel, Boutin, Natalie, Mahanta, Lisa, Rehm, Heidi L., Weiss, Scott T., Karlson, Elizabeth W., Smoller, Jordan W., Lebo, Matthew S., Green, Robert C.

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Relationship of gene expression and chromosomal abnormalities in colorectal cancer von TSAFRIR, Dafna, BACOLOD, Manny, G ERALD, William L, PATY, Philip B, DOMANY, Eytan, NOTTERMAN, Daniel A, SELVANAYAGAM, Zachariah, TSAFRIR, Ilan, JINRU SHIA, ZHAOSHI ZENG, HAO LIU, KRIER, Curtis, STENGEL, Robert F, BARANY, Francis

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Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project von Wojcik, Monica H., Zhang, Tian, Ceyhan-Birsoy, Ozge, Genetti, Casie A., Lebo, Matthew S., Yu, Timothy W., Parad, Richard B., Holm, Ingrid A., Rehm, Heidi L., Beggs, Alan H., Green, Robert C., Agrawal, Pankaj B., Agrawal, Pankaj B., Betting, Wendi N., Christensen, Kurt D., Dukhovny, Dmitry, Fayer, Shawn, Frankel, Leslie A., Graham, Chet, Guiterrez, Amanda M., Harden, Maegan, Krier, Joel B., Levy, Harvey L., Lu, Xingquan, Machini, Kalotina, McGuire, Amy L., Murry, Jaclyn B., Naik, Medha, Nguyen, Tiffany T., Peoples, Hayley A., Pereira, Stacey, Petersen, Devan, Ramamurthy, Uma, Ramanathan, Vivek, Roberts, Amy, Robinson, Jill O., Roumiantsev, Serguei, Schwartz, Talia S., Truong, Tina K., VanNoy, Grace E., Waisbren, Susan E.

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Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project von Pereira, Stacey, Robinson, Jill Oliver, Gutierrez, Amanda M, Petersen, Devan K, Hsu, Rebecca L, Lee, Caroline H, Schwartz, Talia S, Holm, Ingrid A, Beggs, Alan H, Green, Robert C, McGuire, Amy L

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Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project von Holm, Ingrid A, McGuire, Amy, Pereira, Stacey, Rehm, Heidi, Green, Robert C, Beggs, Alan H

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Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder von Yoon, Wan Hee, Jangam, Sharayu, Davidson, Jean M., Grove, Megan E., Kohler, Jennefer N., Holmes, Matthew, Zhao, Chunli, Contrepois, Kévin, Heyman, Heino M., Webb-Robertson, Bobbie-Jo M., Alejandro, Mercedes E., Allard, Patrick, Balasubramanyam, Ashok, Barseghyan, Hayk, Bican, Anna, Birch, Camille L., Bostwick, Bret L., Briere, Lauren C., Brown, Donna M., Brush, Matthew, Burke, Elizabeth A., Burrage, Lindsay C., Cooper, Cynthia M., Cope, Heidi, Craigen, William J., D’Souza, Precilla, Dayal, Jyoti G., Dell’Angelica, Esteban C., Dorset, Daniel C., Draper, David D., Eckstein, David J., Emrick, Lisa T., Esteves, Cecilia, Estwick, Tyra, Ferreira, Carlos, Glanton, Emily, Godfrey, Rena A., Goldstein, David B., Gould, Sarah E., Gourdine, Jean-Philippe F., Hanchard, Neil A., Herzog, Matthew R., Hom, Jason, Howerton, Ellen M., Huang, Yong, Jacob, Howard J., Jiang, Yong-hui, Johnston, Jean M., Jones, Angela L., Kohane, Isaac S., Krier, Joel B., Lazar, Jozef, Lee, Hane, Levy, Shawn E., Lincoln, Sharyn A., Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Majcherska, Marta M., Mamounas, Laura A., Manolio, Teri A., Markello, Thomas C., Marom, Ronit, May, Thomas, McConkie-Rosell, Allyn, McCray, Alexa T., Moretti, Paolo M., Novacic, Donna, Orange, Jordan S., Palmer, Christina G.S., Potocki, Lorraine, Pusey, Barbara N., Robertson, Amy K., Rodan, Lance H., Rosenfeld, Jill A., Samson, Susan L., Schoch, Kelly, Schroeder, Molly C., Shashi, Vandana, Silverman, Edwin K., Sinsheimer, Janet S., Spillmann, Rebecca C., Stong, Nicholas, Tifft, Cynthia J., Tran, Alyssa A., Valivullah, Zaheer M., Ward, Patricia A., Yamamoto, Shinya, Snyder, Michael, Merker, Jason D., Fisher, Paul G., Mayr, Johannes A., Morris, Andrew A., Schelley, Susan, Friederich, Marisa W., Yamamoto, Shinya, Wangler, Michael F., Taylor, Robert W., Bernstein, Jonathan A.

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Family genetic risk communication and reverse cascade testing in the BabySeq project von Uveges, Melissa K., Smith, Hadley Stevens, Pereira, Stacey, Genetti, Casie, McGuire, Amy L., Beggs, Alan H., Green, Robert C., Holm, Ingrid A., Agrawal, Pankaj B., Beggs, Alan H., Betting, Wendi N., Ceyhan-Birsoy, Ozge, Christensen, Kurt D., Dukhovny, Dmitry, Fayer, Shawn, Frankel, Leslie A., Genetti, Casie A., Graham, Chet, Green, Robert C., Gutierrez, Amanda M., Harden, Maegan, Holm, Ingrid A., Krier, Joel B., Lebo, Matthew S., Lee, Kaitlyn B., Levy, Harvey L., Lu, Xingquan, Machini, Kalotina, McGuire, Amy L., Murry, Jaclyn B., Naik, Medha, Nguyen Dolphyn, Tiffany T., Parad, Richard B., Peoples, Hayley A., Pereira, Stacey, Petersen, Devan, Ramamurthy, Uma, Ramanathan, Vivek, Rehm, Heidi L., Roberts, Amy, Robinson, Jill Oliver, Roumiantsev, Sergei, Schwartz, Talia S., Smith, Hadley Stevens, Truong, Tina K., VanNoy, Grace E., Waisbren, Susan E., Yu, Timothy W., Blout Zawatsky, Carrie L., Zettler, Bethany

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The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine von Vassy, Jason L, Lautenbach, Denise M, McLaughlin, Heather M, Kong, Sek Won, Christensen, Kurt D, Krier, Joel, Kohane, Isaac S, Feuerman, Lindsay Z, Blumenthal-Barby, Jennifer, Roberts, J Scott, Lehmann, Lisa Soleymani, Ho, Carolyn Y, Ubel, Peter A, MacRae, Calum A, Seidman, Christine E, Murray, Michael F, McGuire, Amy L, Rehm, Heidi L, Green, Robert C

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Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study von Armstrong, Brittan, Christensen, Kurt D, Genetti, Casie A, Parad, Richard B, Robinson, Jill Oliver, Blout Zawatsky, Carrie L, Zettler, Bethany, Beggs, Alan H, Holm, Ingrid A, Green, Robert C, McGuire, Amy L, Smith, Hadley Stevens, Pereira, Stacey

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Comprehensive red blood cell and platelet antigen prediction from whole genome sequencing: proof of principle von Lane, William J., Westhoff, Connie M., Uy, Jon Michael, Aguad, Maria, Smeland-Wagman, Robin, Kaufman, Richard M., Rehm, Heidi L., Green, Robert C., Silberstein, Leslie E.

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Challenging the Current Recommendations for Carrier Testing in Children von VanNoy, Grace E, Genetti, Casie A, McGuire, Amy L, Green, Robert C, Beggs, Alan H, Holm, Ingrid A

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A systematic approach to the reporting of medically relevant findings from whole genome sequencing von McLaughlin, Heather M, Ceyhan-Birsoy, Ozge, Christensen, Kurt D, Kohane, Isaac S, Krier, Joel, Lane, William J, Lautenbach, Denise, Lebo, Matthew S, Machini, Kalotina, MacRae, Calum A, Azzariti, Danielle R, Murray, Michael F, Seidman, Christine E, Vassy, Jason L, Green, Robert C, Rehm, Heidi L

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Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study von Lane, William J, Westhoff, Connie M, Gleadall, Nicholas S, Aguad, Maria, Smeland-Wagman, Robin, Vege, Sunitha, Simmons, Daimon P, Mah, Helen H, Lebo, Matthew S, Walter, Klaudia, Soranzo, Nicole, Di Angelantonio, Emanuele, Danesh, John, Roberts, David J, Watkins, Nick A, Ouwehand, Willem H, Butterworth, Adam S, Kaufman, Richard M, Rehm, Heidi L, Silberstein, Leslie E, Green, Robert C, Bates, David W., Blout, Carrie, Christensen, Kurt D., Cirino, Allison L., Ho, Carolyn Y., Krier, Joel B., Lehmann, Lisa S., MacRae, Calum A., Morton, Cynthia C., Perry, Denise L., Seidman, Christine E., Sunyaev, Shamil R., Vassy, Jason L., Schonman, Erica, Nguyen, Tiffany, Steffens, Eleanor, Betting, Wendi Nicole, Aronson, Samuel J., Ceyhan-Birsoy, Ozge, Machini, Kalotina, McLaughlin, Heather M., Azzariti, Danielle R., Tsai, Ellen A., Blumenthal-Barby, Jennifer, Feuerman, Lindsay Z., McGuire, Amy L., Lee, Kaitlyn, Robinson, Jill O., Slashinski, Melody J., Diamond, Pamela M., Davis, Kelly, Ubel, Peter A., Kraft, Peter, Roberts, J. Scott, Garber, Judy E., Hambuch, Tina, Murray, Michael F., Kohane, Isaac, Kong, Sek Won

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