Association of maternal mRNA and phosphorylated EIF4EBP1 variants with the spindle in mouse oocytes: localized translational control supporting female meiosis in mammals by Romasko, Edward J, Amarnath, Dasari, Midic, Uros, Latham, Keith E

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Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss by Sheppard, Sarah, Biswas, Sawona, Li, Mindy H., Jayaraman, Vijayakumar, Slack, Ian, Romasko, Edward J., Sasson, Ariella, Brunton, Joshua, Rajagopalan, Ramakrishnan, Sarmady, Mahdi, Abrudan, Jenica L., Jairam, Sowmya, DeChene, Elizabeth T., Ying, Xiahoan, Choi, Jiwon, Wilkens, Alisha, Raible, Sarah E., Scarano, Maria I., Santani, Avni, Pennington, Jeffrey W., Luo, Minjie, Conlin, Laura K., Devkota, Batsal, Dulik, Matthew C., Spinner, Nancy B., Krantz, Ian D.

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Male-Specific Transcription Factor Occupancy Alone Does Not Account for Differential Methylation at Imprinted Genes in the mouse Germ Cell Lineage by Romasko, Edward J, Engel, Nora

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PCDH19-related epilepsy in a male with Klinefelter syndrome: Additional evidence supporting PCDH19 cellular interference disease mechanism by Romasko, Edward J., DeChene, Elizabeth T., Balciuniene, Jorune, Akgumus, Gozde T., Helbig, Ingo, Tarpinian, Jennifer M., Keena, Beth A., Vogiatzi, Maria G., Zackai, Elaine H., Izumi, Kosuke, Massey, Shavonne L., Tayoun, Ahmad N. Abou

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Utility and limitations of exome sequencing in the molecular diagnosis of pediatric inherited platelet disorders by Romasko, Edward J., Devkota, Batsal, Biswas, Sawona, Jayaraman, Vijayakumar, Rajagopalan, Ramakrishnan, Dulik, Matthew C., Thom, Christopher S., Choi, Jiwon, Jairam, Sowmya, Scarano, Maria I., Krantz, Ian D., Spinner, Nancy B., Conlin, Laura K., Lambert, Michele P.

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Use of a Dynamic Genetic Testing Approach for Childhood-Onset Epilepsy by Balciuniene, Jorune, DeChene, Elizabeth T, Akgumus, Gozde, Romasko, Edward J, Cao, Kajia, Dubbs, Holly A, Mulchandani, Surabhi, Spinner, Nancy B, Conlin, Laura K, Marsh, Eric D, Goldberg, Ethan, Helbig, Ingo, Sarmady, Mahdi, Abou Tayoun, Ahmad

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Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study by Hart, M Ragan, Biesecker, Barbara B, Blout, Carrie L, Christensen, Kurt D, Amendola, Laura M, Bergstrom, Katie L, Biswas, Sawona, Bowling, Kevin M, Brothers, Kyle B, Conlin, Laura K, Cooper, Greg M, Dulik, Matthew C, East, Kelly M, Everett, Jessica N, Finnila, Candice R, Ghazani, Arezou A, Gilmore, Marian J, Goddard, Katrina A B, Jarvik, Gail P, Johnston, Jennifer J, Kauffman, Tia L, Kelley, Whitley V, Krier, Joel B, Lewis, Katie L, McGuire, Amy L, McMullen, Carmit, Ou, Jeffrey, Plon, Sharon E, Rehm, Heidi L, Richards, C Sue, Romasko, Edward J, Miren Sagardia, Ane, Spinner, Nancy B, Thompson, Michelle L, Turbitt, Erin, Vassy, Jason L, Wilfond, Benjamin S, Veenstra, David L, Berg, Jonathan S, Green, Robert C, Biesecker, Leslie G, Hindorff, Lucia A

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Rethinking the "open future" argument against predictive genetic testing of children by Garrett, Jeremy R, Lantos, John D, Biesecker, Leslie G, Childerhose, Janet E, Chung, Wendy K, Holm, Ingrid A, Koenig, Barbara A, McEwen, Jean E, Wilfond, Benjamin S, Brothers, Kyle

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Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine by Goddard, Katrina A.B., Jarvik, Gail P., Amendola, Laura M., Berg, Jonathan S., Blout, Carrie L., Brothers, Kyle B., Caga-anan, Charlisse F., Clayton, Ellen W., East, Kelly, Evans, James P., Fullerton, Stephanie M., Holm, Ingrid A., Kaufman, David, Knoppers, Bartha M., McCullough, Laurence, McGuire, Amy, Myers, Richard M., Nickerson, Deborah A., Robinson, Dan, Salama, Joseph S., Scollon, Sarah, Shirts, Brian, Tabor, Holly K., Tarczy-Hornoch, Peter, Veenstra, David L., Wagle, Nikhil, Wynn, Julia, Amendola, Laura, Aronson, Samuel J., Arora, Shubhangi, Azzariti, Danielle R., Biesecker, Barbara B., Byers, Peter H., Calikoglu, Muge G., Cirino, Allison L., Conlin, Laura K., Cooper, Greg M., Crosslin, David R., Davis, James V., Dugan, Noreen P., Exe, Nicole, Fan, Zheng, Filipski, Kelly, Fishler, Kristen, Ghrundmeier, Bob, Gilmore, Marian J., Gordon, Adam S., Gornick, Michele C., Grady, William M., Gutierrez, Amanda M., Hensman, Naomi, Himes, Patricia, Hisama, Fuki M., Hull, Sara, Joffe, Steve, Karavite, Dean, Kauffman, Tia L., Kaufman, Dave, Kim, Jerry H., Klein, William, Krantz, Ian, Le, Lan Q., Lebo, Matthew S., Leo, Michael C., Lewis, Katie, Lewis, Michelle, Lindeman, Neal I., Lonigro, Bob, Lose, Edward J., Lupo, Philip J., Machini, Kalotina, Marchuk, Daniel S., McMullen, Carmit, Miller, Victoria A., Moore, Elizabeth G., Ng, David, Oliver, Nelly M., Parsons, Will, Patrick, Donald L., Plon, Sharon, Powell, Bradford C., Breitkopf, Carmen Radecki, Raskind, Wendy H., Rini, Christine, Robertson, Peggy D., Salama, Joseph, Shirts, Brian H., Siddiqui, Javed, Silverman, Elian, Simmons, Shirley, Simons, Janae V., Stoffel, Elena, Tilley, Christian R., Tomlinson, Ashley, Trinidad, Susan, Ubel, Peter, Walsh, Rebecca C., Wilfond, Ben, Wilhelmsen, Kirk C., Young, Carol

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Utility of Whole Exome Sequencing in Diagnosis of Pediatric Platelet Disorders: A Subanalysis of the Pediseq Study by Romasko, Edward J, Biswas, Sawona, Devkota, Batsal, Vijayakumar, Jayaraman, Jairam, Sowmyra, Thom, Christopher S, Dulik, Matthew C, Conlin, Laura K, Spinner, Nancy B., Krantz, Ian D, Lambert, Michele P.

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Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study by Hart, M. Ragan, Biesecker, Barbara B., Blout, Carrie L., Christensen, Kurt D., Amendola, Laura M., Bergstrom, Katie L., Biswas, Sawona, Bowling, Kevin M., Brothers, Kyle B., Conlin, Laura K., Cooper, Greg M., Dulik, Matthew C., East, Kelly M., Everett, Jessica N., Finnila, Candice R., Ghazani, Arezou A., Gilmore, Marian J., Goddard, Katrina A. B, Jarvik, Gail P., Johnston, Jennifer J., Kauffman, Tia L., Kelley, Whitley V., Krier, Joel B., Lewis, Katie L., McGuire, Amy L., McMullen, Carmit, Ou, Jeffrey, Plon, Sharon E., Rehm, Heidi L., Richards, C. Sue, Romasko, Edward J., Miren Sagardia, Ane, Spinner, Nancy B., Thompson, Michelle L., Turbitt, Erin, Vassy, Jason L., Wilfond, Benjamin S., Veenstra, David L., Berg, Jonathan S., Green, Robert C., Biesecker, Leslie G., Hindorff, Lucia A.

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10. Comprehensive genomic characterization of pediatric B-ALL by Luo, Minjie, Lin, Fumin, Zhao, Xiaonan, Tang, Junxia, Akgumus, Gozde T., Gallo, Daniel J., Romasko, Edward, Gleason, Adam G., Surrey, Lea F., Wertheim, Gerald, Li, Marilyn M.

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26. Uncovering the genetic etiology of inherited bone marrow failure syndromes using a custom-designed NGS panel by Lin, Fumin, Chang, Fengqi, Cao, Kajia, Hartung, Helge, Lambert, Michele, Surrey, Lea, Luo, Minjie, Paessler, Michele, Zelley, Kristin, Gallo, Daniel, Denenberg, Elizabeth, Romasko, Edward, Zhao, Xiaonan, Olson, Tim, Li, Marilyn

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Secondary findings from clinical genomic sequencing: Prevalence, patient perspectives, family history assessment, and healthcare costs from a multi-site study by Hart, M. Ragan, Biesecker, Barbara B., Blout, Carrie L., Christensen, Kurt D., Amendola, Laura M., Bergstrom, Katie L., Biswas, Sawona, Bowling, Kevin M., Brothers, Kyle B., Conlin, Laura K., Cooper, Greg M., Dulik, Matthew C., East, Kelly M., Everett, Jessica N., Finnila, Candice R., Ghazani, Arezou A., Gilmore, Marian J., Goddard, Katrina AB, Jarvik, Gail P., Johnston, Jennifer J., Kauffman, Tia L., Kelley, Whitley V., Krier, Joel B., Lewis, Katie L., McGuire, Amy L., Mullen, Carmit Mc, Ou, Jeffrey, Plon, Sharon E., Rehm, Heidi L., Richards, C. Sue, Romasko, Edward J., Sagardia, Ane Miren, Spinner, Nancy B., Thompson, Michelle L., Turbitt, Erin, Vassy, Jason L., Wilfond, Benjamin S., Veenstra, David L., Berg, Jonathan S., Green, Robert C., Biesecker, Leslie G., Hindorff, Lucia A.

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Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study by Hart, M Ragan, Biesecker, Barbara B, Blout, Carrie L, Christensen, Kurt D, Amendola, Laura M, Bergstrom, Katie L, Biswas, Sawona, Bowling, Kevin M, Brothers, Kyle B, Conlin, Laura K, Cooper, Greg M, Dulik, Matthew C, East, Kelly M, Everett, Jessica N, Finnila, Candice R, Ghazani, Arezou A, Gilmore, Marian J, Goddard, Katrina A B, Jarvik, Gail P, Johnston, Jennifer J, Kauffman, Tia L, Kelley, Whitley V, Krier, Joel B, Lewis, Katie L, McGuire, Amy L, McMullen, Carmit, Ou, Jeffrey, Plon, Sharon E, Rehm, Heidi L, Richards, C Sue, Romasko, Edward J, Sagardia, Ane Miren, Spinner, Nancy B, Thompson, Michelle L, Turbitt, Erin, Vassy, Jason L, Wilfond, Benjamin S, Veenstra, David L, Berg, Jonathan S, Green, Robert C, Biesecker, Leslie G, Hindorff, Lucia A

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Abstract 16899: Exome Sequencing for Genetic Etiology in Families With Sudden Cardiac Death or Arrest by Vetter, Victoria L, Dugan, Noreen P, Biswas, Sawona, Li, Mindy, Dulik, Matthew C, Jayaraman, Vijayakumar, Conlin, Laura K, Devkota, Basal, Romasko, Edward J, Abrudan, Jenica, Spinner, Nancy B, Krantz, Ian D

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AVHRR-based mapping of fires in Russia: New products for fire management and carbon cycle studies by Sukhinin, Anatoly I., French, Nancy H.F., Kasischke, Eric S., Hewson, Jenny H., Soja, Amber J., Csiszar, Ivan A., Hyer, Edward J., Loboda, Tatiana, Conrad, Susan G., Romasko, Victor I., Pavlichenko, Eugene A., Miskiv, Sergey I., Slinkina, Olga A.

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Corrigendum to “AVHRR-based mapping of fires in Russia: New products for fire management and carbon cycle studies” [Remote Sensing of Environment, 93, 546–564] by Sukhinin, Anatoly I., French, Nancy H.F., Kasischke, Eric S., Hewson, Jenny H., SoJa, Amber J., Csiszar, Ivan A., Hyer, Edward J., Loboda, Tatiana, Conard, Susan G., Romasko, Victor I., Pavlichenko, Eugene A., Miskiv, Sergey I., Slinkina, Olga A.

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