Search Results - Schreiber, Kirsten

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    The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC) by Gerhard, Daniela S, Wagner, Lukas, Feingold, Elise A, Shenmen, Carolyn M, Grouse, Lynette H, Schuler, Greg, Klein, Steven L, Old, Susan, Rasooly, Rebekah, Good, Peter, Guyer, Mark, Peck, Allison M, Derge, Jeffery G, Lipman, David, Collins, Francis S, Jang, Wonhee, Sherry, Steven, Feolo, Mike, Misquitta, Leonie, Lee, Eduardo, Greenhut, Susan F, Schaefer, Carl F, Buetow, Kenneth, Bonner, Tom I, Haussler, David, Kent, Jim, Kiekhaus, Mark, Furey, Terry, Brent, Michael, Prange, Christa, Schreiber, Kirsten, Shapiro, Nicole, Bhat, Narayan K, Hsie, Florence, Driscoll, Tom, Soares, M Bento, Casavant, Tom L, Scheetz, Todd E, Brown-stein, Michael J, Usdin, Ted B, Toshiyuki, Shiraki, Carninci, Piero, Piao, Yulan, Dudekula, Dawood B, Ko, Minoru S H, Suzuki, Yutaka, Sugano, Sumio, Gruber, C E, Smith, M R, Simmons, Blake, Moore, Troy, Waterman, Richard, Johnson, Stephen L, Ruan, Yijun, Wei, Chia Lin, Mathavan, S, Gunaratne, Preethi H, Wu, Jiaqian, Garcia, Angela M, Hulyk, Stephen W, Sneed, Anna, Kowis, Carla, Hodgson, Anne, Muzny, Donna M, Gibbs, Richard A, Fahey, Jessica, Helton, Erin, Ketteman, Mark, Madan, Anuradha, Rodrigues, Stephanie, Sanchez, Amy, Whiting, Michelle, Madari, Anup, Young, Alice C, Wetherby, Keith D, Granite, Steven J, Kwong, Peggy N, Brinkley, Charles P, Bouffard, Gerard G, Blakesly, Robert W, Green, Eric D, Dickson, Mark C, Rodriguez, Alex C, Myers, Richard M, Griffith, Malachi, Griffith, Obi L, Krzywinski, Martin I, Liao, Nancy, Morin, Ryan, Morrin, Ryan, Palmquist, Diana, Smailus, Duane E, Stott, Jeff M, Schnerch, Angelique, Schein, Jacqueline E, Holt, Robert A, Baross, Agnes, Makowski, Kathryn A, Bosak, Stephanie, Malek, Joel

    Published in Genome research
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    The completion of the Mammalian Gene Collection (MGC) by Temple, Gary, Rasooly, Rebekah, Feingold, Elise A, Good, Peter J, Robinson, Cristen, Derge, Jeffrey G, Lewis, Jeanne, Shoaf, Debonny, Collins, Francis S, Jang, Wonhee, Wagner, Lukas, Shenmen, Carolyn M, Buetow, Kenneth H, Bonner, Tom I, Ward, Ming, Brown, Garth, Farrell, Catherine, Hart, Jennifer, Maidak, Bonnie L, Murphy, Terence, Rajput, Bhanu, Webb, David, Weber, Janet, Wu, Wendy, Pruitt, Kim D, Maglott, Donna, Siepel, Adam, Brejova, Brona, Diekhans, Mark, Harte, Rachel, Baertsch, Robert, Kent, Jim, Haussler, David, Brent, Michael, Langton, Laura, Comstock, Charles L G, Stevens, Michael, Wei, Chaochun, van Baren, Marijke J, Murray, Ryan R, Ghamsari, Lila, Mello, Elizabeth, Lin, Chenwei, Pennacchio, Christa, Schreiber, Kirsten, Shapiro, Nicole, Moore, Troy, Muratet, Mike, Kloske, David, Sieja, Stephanie, Hudson, James, Sethupathy, Praveen, Brownstein, Michael, Bhat, Narayan, Smith, Mark R, McPherson, John, Garcia, Angela M, Gunaratne, Preethi H, Wu, Jiaqian, Muzny, Donna, Gibbs, Richard A, Young, Alice C, Bouffard, Gerard G, Blakesley, Robert W, Mullikin, Jim, Green, Eric D, Dickson, Mark C, Rodriguez, Alex C, Grimwood, Jane, Schmutz, Jeremy, Myers, Richard M, Hirst, Martin, Tse, Kane, Deng, Merinda, Mah, Diana, Taylor, Greg, Deng, Athena, Fichter, Keith, Go, Anne, Lee, Stephanie, Griffith, Malachi, Morin, Ryan, Moore, Richard A, Mayo, Michael, Munro, Sarah, Wagner, Susan, Holt, Robert A, Marra, Marco A, Lu, Sun, Yang, Shuwei, Graf, Marcus, Letovksy, Stanley, Pulido, Jacqueline C, Robison, Keith, Esposito, Dominic, Hartley, James, Wall, Vanessa E, Hopkins, Ralph F, Ohara, Osamu, Wiemann, Stefan

    Published in Genome research
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    Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants by Bommireddipalli, Shobhana, Ades, Lesley, Archibald, Alison D., Berman, Yemima, Bojadzieva, Jasmina, Brown, Natasha J., Bryen, Samantha J., Engel, Amanda, Ewans, Lisa J., Fennell, Andrew, Freckmann, Mary-Louise, Gear, Russell, Goel, Himanshu, Goh, Shuxiang, Harraway, James, Higgins, Megan, Ho, Gladys, Hunter, Matthew F., Joshi, Himanshu, Krzesinski, Emma, Leventer, Richard J., Macaskill, Steven, McCarthy, Hugh J., McLean, Alison, Patel, Chirag, Regan, Matthew, Schindler, Tim, Tantsis, Esther, Tchan, Michel C., van Spaendonck-Zwarts, Karin, White, Susan M., Williams, Mark G., Wright, Dale C., Yap, Patrick, Yeung, Alison, Jones, Kristi J., Cooper, Sandra T., Arts, Peer, Barnett, Christopher, Beshay, Victoria, Blombery, Piers, Boggs, Kirsten, Branford, Susan, Bryen, Samantha J., Canson, Daffodil, Chew, Edward, Chong, Belinda, Chung, Seo-Kyung, Clark, Mike, Compton, Alison, Corbett, Mark, Davis, Mark R., Dudding, Tracy, Ewans, Lisa J., Eyras, Eduardo, Fellowes, Andrew, Field, Michael, Freckmann, Mary-Louise, Gaff, Clara, Galea, Melanie, Hanna, Bernadette, Harraway, James, Hayashi, Rippei, Henderson, Alex, Jackson, Matilda, Jones, Kristi J., Wong, Justin Jong-Leong, Joshi, Himanshu, Krzesinski, Emma, Kumble, Smitha, Laing, Nigel, Lau, Chiyan, Lee, Eric, Lundie, Ben, Mallawaarachchi, Amali, McLean, Alison, Meldrum, Cliff, Mina, Kym, Mowat, David, Oshlack, Alicia, Parsons, Michael, Patel, Chirag, Pinner, Jason R., Quinn, Michael, Ravenscroft, Gina, Regan, Matthew, Ronan, Anne, Sadedin, Simon, Schreiber, Andreas, Scott, Rodney, Simons, Cas, Smyth, Renee, Thompson, Bryony A., Thorburn, David, Trent, Ronald, Tudini, Emma, Wallis, Mathew, Wilson, Meredith J., Winship, Ingrid, Yeung, Alison

    Published in Genetics in medicine
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