Draft Whole-Genome Sequence of Lactobacillus fermentum LfQi6, Derived from the Human Microbiome by Subhadra, Bobban, Krier, Jill, Hofstee, Karina, Monsul, Nicholas, Berkes, Eva

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Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project by 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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The BabySeq project: implementing genomic sequencing in newborns by 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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Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project by 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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Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine by Goddard, Katrina A.B., Bernhardt, Barbara A., Biswas, Sawona, Bowling, Kevin M., Caga-anan, Charlisse F., Chinnaiyan, Arul M., Clayton, Ellen W., East, Kelly, Garraway, Levi A., Garrett, Jeremy R., Gray, Stacy W., Hindorff, Lucia A., Lewis, Michelle Huckaby, Hutter, Carolyn M., Janne, Pasi A., Knoppers, Bartha M., Krantz, Ian D., Manolio, Teri A., Nickerson, Deborah A., Ou, Jeffrey, Parsons, Donald W., Petersen, Gloria M., Plon, Sharon E., Rehm, Heidi L., Robinson, Dan, Salama, Joseph S., Scollon, Sarah, Shirts, Brian, Tabor, Holly K., Tarczy-Hornoch, Peter, Appelbaum, Paul S., Arora, Shubhangi, Brothers, Kyle B., Brown, Brian L., Caga-anan, Charlisse F., Calikoglu, Muge G., Christensen, Kurt D., Cirino, Allison L., Conlin, Laura K., Crosslin, David R., Davis, James V., Dorschner, Michael O., Dugan, Noreen P., Exe, Nicole, Fishler, Kristen, Ghrundmeier, Bob, Gordon, Adam S., Gray, David E., Gray, Stacy W., Gutierrez, Amanda M., Hensman, Naomi, Hiatt, Susan M., Himes, Patricia, Horike-Pyne, Martha J., Hull, Sara, Jensen, Brian C., Joffe, Steve, Kaufman, Dave, Kim, Jerry H., Klein, William, Lambert, Michele P., Leo, Michael C., Lewis, Katie, Lonigro, Bob, Machini, Kalotina, Manolio, Teri A., McCullough, Laurence, McMullen, Carmit, Mooney, Sean D., Moore, Elizabeth G., Muzny, Donna, Ng, David, Nickerson, Deborah A., Oliver, Nelly M., Parsons, Will, Plon, Sharon, Powell, Bradford C., Raesz-Martinez, Robin A., Raskind, Wendy H., Rehm, Heidi L., Reiss, Jacob A., Robertson, Peggy D., Robinson, Dan, Salama, Joseph, Scarano, Maria I., Sholl, Lynette M., Silverman, Elian, Simmons, Shirley, Spinner, Nancy B., Stoffel, Elena, Tilley, Christian R., Trinidad, Susan, Ubel, Peter, Vassy, Jason L., Vries, Raymond D., Weck, Karen, Wolf, Susan M., Wynn, Julia, Yu, Joon-Ho, Zikmund-Fisher, Brian J.

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

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Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing by Reuter, Chloe M., Kohler, Jennefer N., Bonner, Devon, Zastrow, Diane, Fernandez, Liliana, Dries, Annika, Marwaha, Shruti, Davidson, Jean, Brokamp, Elly, Herzog, Matthew, Hong, Joyce, Macnamara, Ellen, Rosenfeld, Jill A., Schoch, Kelly, Spillmann, Rebecca, Loscalzo, Joseph, Krier, Joel, Stoler, Joan, Sweetser, David, Palmer, Christina G.S., Phillips, John A., Shashi, Vandana, Adams, David A., Yang, Yaping, Ashley, Euan A., Fisher, Paul G., Mulvihill, John J., Bernstein, Jonathan A., Wheeler, Matthew T.

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Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study by 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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Automated typing of red blood cell and platelet antigens from whole exome sequences by Lane, William J., Vege, Sunitha, Mah, Helen H., Lomas‐Francis, Christine, Aguad, Maria, Smeland‐Wagman, Robin, Koch, Christopher, Killian, Jacqueline M., Gardner, Cubby L., De Castro, Mauricio, Lebo, Matthew S., Kaufman, Richard M., Green, Robert C., Westhoff, Connie M.

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The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine by 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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Comprehensive red blood cell and platelet antigen prediction from whole genome sequencing: proof of principle by 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 by VanNoy, Grace E, Genetti, Casie A, McGuire, Amy L, Green, Robert C, Beggs, Alan H, Holm, Ingrid A

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Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing by Mackay, Zoë P., Dukhovny, Dmitry, Phillips, Kathryn A., Beggs, Alan H., Green, Robert C., Parad, Richard B., Christensen, Kurt D., Agrawal, Pankaj B., Ceyhan-Birsoy, Ozge, Fayer, Shawn, Frankel, Leslie A., Genetti, Casie A., Gutierrez, Amanda M., Harden, Maegan, Holm, Ingrid A., Krier, Joel B., Lebo, Matthew S., Machini, Kalotina, McGuire, Amy L., Naik, Medha, Nguyen, Tiffany T., Pereira, Stacey, Ramanathan, Vivek, Rehm, Heidi L., Roberts, Amy, Robinson, Jill O., Roumiantsev, Sergei, Schwartz, Talia S., Truong, Tina K., VanNoy, Grace E., Waisbren, Susan E., Yu, Timothy W.

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A systematic approach to the reporting of medically relevant findings from whole genome sequencing by 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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A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xg a by Lane, William J, Aguad, Maria, Smeland-Wagman, Robin, Vege, Sunitha, Mah, Helen H, Joseph, Abigail, Blout, Carrie L, Nguyen, Tiffany T, Lebo, Matthew S, Sidhu, Manpreet, Lomas-Francis, Christine, Kaufman, Richard M, Green, Robert C, Westhoff, Connie M

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A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xga by Lane, William J., Aguad, Maria, Smeland‐Wagman, Robin, Vege, Sunitha, Mah, Helen H., Joseph, Abigail, Blout, Carrie L., Nguyen, Tiffany T., Lebo, Matthew S., Sidhu, Manpreet, Lomas‐Francis, Christine, Kaufman, Richard M., Green, Robert C., Westhoff, Connie M., Bates, David W., Blout, Carrie, Christensen, Kurt D., Cirino, Allison L., Green, Robert C., Ho, Carolyn Y., Krier, Joel B., Lane, William J., 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, Lebo, Matthew S., Machini, Kalotina, McLaughlin, Heather M., Azzariti, Danielle R., Rehm, Heidi L., 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, Scott Roberts, J., Garber, Judy E., Hambuch, Tina, Murray, Michael F., Kohane, Isaac, Kong, Sek Won

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Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report by Murry, Jaclyn B, Machini, Kalotina, Ceyhan-Birsoy, Ozge, Kritzer, Amy, Krier, Joel B, Lebo, Matthew S, Fayer, Shawn, Genetti, Casie A, VanNoy, Grace E, Yu, Timothy W, Agrawal, Pankaj B, Parad, Richard B, Holm, Ingrid A, McGuire, Amy L, Green, Robert C, Beggs, Alan H, Rehm, Heidi L

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Whole genome sequencing reveals novel IGHMBP2 variant leading to unique cryptic splice‐site and Charcot‐Marie‐Tooth phenotype with early onset symptoms by Cassini, Thomas A., Rives, Lynette C., Newman, John H., Koziura, Mary E., Hamid, Rizwan, Adams, Christopher, Adams, David, Alejandro, Mercedes, Allard, Patrick, Ashley, Euan, Bacino, Carlos, Balasubramanyam, Ashok, Barseghyan, Hayk, Bellen, Hugo, Boone, Braden, Bostwick, Bret, Briere, Lauren, Burke, Elizabeth, Burrage, Lindsay, Chao, Katherine, Clark, Gary, Dhar, Shweta, Donnell‐Fink, Laurel, Eckstein, David, Frisby, Trevor, Gartner, Valerie, Godfrey, Rena, Goheen, Mitchell, Golas, Gretchen, Goldstein, David, Gordon, Mary, Gould, Sarah, Gourdine, Jean‐Philippe, Hanchard, Neil, Handley, Lori, Herzog, Matthew, Holm, Ingrid, Howerton, Ellen, Jacob, Howard, Jain, Mahim, Jiang, Yong‐hui, Johnston, Jean, Jones, Angela, Koehler, Alanna, Kohler, Jennefer, Krier, Joel, Lalani, Seema, Latour, Yvonne, Lee, Brendan, Lee, Hane, Lee, Paul, Levy, Shawn, Lewis, Richard, Lincoln, Sharyn, Loscalzo, Joseph, Maas, Richard, MacRae, Calum, Malicdan, May Christine, Mamounas, Laura, McCarty, Alexandra, McCray, Alexa, Might, Matthew, Mulvihill, John, Murphy, Jennifer, Muzny, Donna, Nehrebecky, Michele, Nelson, Stan, Novacic, Donna, Carl Pallais, J, Posey, Jennifer, Potocki, Lorraine, Ramoni, Rachel, Rodan, Lance, Rosenfeld, Jill, Samson, Susan, Schaffer, Katherine, Sharma, Prashant, Shashi, Vandana, Silverman, Edwin, Soldatos, Ariane, Spillmann, Rebecca, Splinter, Kimberly, Stoler, Joan, Stong, Nicholas, Strong, Kimberly, Sullivan, Jennifer, Tifft, Cynthia, Vilain, Eric, Vogel, Tiphanie, Waggott, Daryl, Wahl, Colleen, Waters, Katrina, Webb‐Robertson, Bobbie‐Jo, Westerfield, Monte, Wheeler, Matthew, Wise, Anastasia, Wolfe, Lynne, Worthey, Elizabeth, Yamamoto, Shinya, Yang, Yaping

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Pharmacogenomics in the U.S. Air Force: Development of a Tailored Panel for the MilSeq Project by Maxwell,Megan D, Robinson,Jill O, Gardner,Cubby, De Castro,Mauricio, Lebo,Matt, Blout,Carrie, Vassy,Jason, Christensen,Kurt, Krier,Joel, Pereira,Stacey, McGuire,Amy, Mehlman,Maxwell J, Parasidis,Efthimios, Brenner,Ruth, Green,Robert C

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The coexistence of elations and homologies by Krier, Nicholas, Yaqub, Jill C. D. S.

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