Association of maternal mRNA and phosphorylated EIF4EBP1 variants with the spindle in mouse oocytes: localized translational control supporting female meiosis in mammals von 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 von 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 von 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 von 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 von 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 von 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 von 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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The spectrum of RAF1 fusion positive solid tumors in children and young adults von Chen, Jiani, Wu, Jinhua, Schubert, Jeff, Lin, Fumin, Denenberg, Elizabeth H., Muir, Alison, Romasko, Edward J., Fanning, Elizabeth A., Bhatti, Tricia R., Cole, Kristina Ann, Kreiger, Portia A., Mattei, Peter, Luo, Minjie, Zhong, Yiming, Resnick, Adam C, Storm, Phillip B, Santi, Mariarita, Surrey, Lea F., Li, Marilyn M.

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Rethinking the “open future” argument against predictive genetic testing of children von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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] von 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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