The evolving picture of the glioblastoma genome

Por Parsons, Donald W.
Publicado em 2010

Somatic cancer variant curation and harmonization through consensus minimum variant level data

Por Ritter, Deborah I., Roychowdhury, Sameek, Roy, Angshumoy, Rao, Shruti, Landrum, Melissa J., Sonkin, Dmitriy, Shekar, Mamatha, Davis, Caleb F., Hart, Reece K., Micheel, Christine, Weaver, Meredith, Van Allen, Eliezer M., Parsons, Donald W., McLeod, Howard L., Watson, Michael S., Plon, Sharon E., Kulkarni, Shashikant, Madhavan, Subha
Publicado no Genome Med (2016)

Germline Mutations in Shelterin Complex Genes Are Associated With Familial Glioma

Por Bainbridge, Matthew N., Armstrong, Georgina N., Gramatges, M. Monica, Bertuch, Alison A., Jhangiani, Shalini N., Doddapaneni, Harsha, Lewis, Lora, Tombrello, Joseph, Tsavachidis, Spyros, Liu, Yanhong, Jalali, Ali, Plon, Sharon E., Lau, Ching C., Parsons, Donald W., Claus, Elizabeth B., Barnholtz-Sloan, Jill, Il’yasova, Dora, Schildkraut, Joellen, Ali-Osman, Francis, Sadetzki, Siegal, Johansen, Christoffer, Houlston, Richard S., Jenkins, Robert B., Lachance, Daniel, Olson, Sara H., Bernstein, Jonine L., Merrell, Ryan T., Wrensch, Margaret R., Walsh, Kyle M., Davis, Faith G., Lai, Rose, Shete, Sanjay, Aldape, Kenneth, Amos, Christopher I., Thompson, Patricia A., Muzny, Donna M., Gibbs, Richard A., Melin, Beatrice S., Bondy, Melissa L.
Publicado no J Natl Cancer Inst (2014)

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

Por Green, Robert C., Goddard, Katrina A.B., Jarvik, Gail P., Amendola, Laura M., Appelbaum, Paul S., Berg, Jonathan S., Bernhardt, Barbara A., Biesecker, Leslie G., Biswas, Sawona, Blout, Carrie L., Bowling, Kevin M., Brothers, Kyle B., Burke, Wylie, Caga-anan, Charlisse F., Chinnaiyan, Arul M., Chung, Wendy K., Clayton, Ellen W., Cooper, Gregory M., East, Kelly, Evans, James P., Fullerton, Stephanie M., Garraway, Levi A., Garrett, Jeremy R., Gray, Stacy W., Henderson, Gail E., Hindorff, Lucia A., Holm, Ingrid A., Lewis, Michelle Huckaby, Hutter, Carolyn M., Janne, Pasi A., Joffe, Steven, Kaufman, David, Knoppers, Bartha M., Koenig, Barbara A., Krantz, Ian D., Manolio, Teri A., McCullough, Laurence, McEwen, Jean, McGuire, Amy, Muzny, Donna, Myers, Richard M., Nickerson, Deborah A., Ou, Jeffrey, Parsons, Donald W., Petersen, Gloria M., Plon, Sharon E., Rehm, Heidi L., Roberts, J. Scott, Robinson, Dan, Salama, Joseph S., Scollon, Sarah, Sharp, Richard R., Shirts, Brian, Spinner, Nancy B., Tabor, Holly K., Tarczy-Hornoch, Peter, Veenstra, David L., Wagle, Nikhil, Weck, Karen, Wilfond, Benjamin S., Wilhelmsen, Kirk, Wolf, Susan M., Wynn, Julia, Yu, Joon-Ho
Publicado no Am J Hum Genet (2016)

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

Por Green, Robert C., Goddard, Katrina A.B., Jarvik, Gail P., Amendola, Laura M., Appelbaum, Paul S., Berg, Jonathan S., Bernhardt, Barbara A., Biesecker, Leslie G., Biswas, Sawona, Blout, Carrie L., Bowling, Kevin M., Brothers, Kyle B., Burke, Wylie, Caga-anan, Charlisse F., Chinnaiyan, Arul M., Chung, Wendy K., Clayton, Ellen W., Cooper, Gregory M., East, Kelly, Evans, James P., Fullerton, Stephanie M., Garraway, Levi A., Garrett, Jeremy R., Gray, Stacy W., Henderson, Gail E., Hindorff, Lucia A., Holm, Ingrid A., Lewis, Michelle Huckaby, Hutter, Carolyn M., Janne, Pasi A., Joffe, Steven, Kaufman, David, Knoppers, Bartha M., Koenig, Barbara A., Krantz, Ian D., Manolio, Teri A., McCullough, Laurence, McEwen, Jean, McGuire, Amy, Muzny, Donna, Myers, Richard M., Nickerson, Deborah A., Ou, Jeffrey, Parsons, Donald W., Petersen, Gloria M., Plon, Sharon E., Rehm, Heidi L., Roberts, J. Scott, Robinson, Dan, Salama, Joseph S., Scollon, Sarah, Sharp, Richard R., Shirts, Brian, Spinner, Nancy B., Tabor, Holly K., Tarczy-Hornoch, Peter, Veenstra, David L., Wagle, Nikhil, Weck, Karen, Wilfond, Benjamin S., Wilhelmsen, Kirk, Wolf, Susan M., Wynn, Julia, Yu, Joon-Ho
Publicado no Am J Hum Genet (2016)