Association of the CPT1A p.P479L Metabolic Gene Variant With Childhood Respiratory and Other Infectious Illness in Nunavut

por Collins, Sorcha A., Edmunds, Sharon, Akearok, Gwen Healey, Thompson, J. Robert, Erickson, Anders C., Hildes-Ripstein, Elske, Miners, Amber, Somerville, Martin, Goldfarb, David M., Rockman-Greenberg, Cheryl, Arbour, Laura
Publicado 2021

Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario

por Hayeems, Robin Z., Marshall, Christian R., Gillespie, Meredith K., Szuto, Anna, Chisholm, Caitlin, Stavropoulos, Dimitri J., Venkataramanan, Viji, Tsiplova, Kate, Sawyer, Sarah, Price, E. Magda, Lau, Lynette, Khan, Reem, Lee, Whiwon, Huang, Lijia, Jarinova, Olga, Ungar, Wendy J., Mendoza-Londono, Roberto, Somerville, Martin J., Boycott, Kym M.
Publicado 2022

The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations

por Villani, Anita, Davidson, Scott, Kanwar, Nisha, Lo, Winnie W., Li, Yisu, Cohen-Gogo, Sarah, Fuligni, Fabio, Edward, Lisa-Monique, Light, Nicholas, Layeghifard, Mehdi, Harripaul, Ricardo, Waldman, Larissa, Gallinger, Bailey, Comitani, Federico, Brunga, Ledia, Hayes, Reid, Anderson, Nathaniel D., Ramani, Arun K., Yuki, Kyoko E., Blay, Sasha, Johnstone, Brittney, Inglese, Cara, Hammad, Rawan, Goudie, Catherine, Shuen, Andrew, Wasserman, Jonathan D., Venier, Rosemarie E., Eliou, Marianne, Lorenti, Miranda, Ryan, Carol Ann, Braga, Michael, Gloven-Brown, Meagan, Han, Jianan, Montero, Maria, Spatare, Famida, Whitlock, James A., Scherer, Stephen W., Chun, Kathy, Somerville, Martin J., Hawkins, Cynthia, Abdelhaleem, Mohamed, Ramaswamy, Vijay, Somers, Gino R., Kyriakopoulou, Lianna, Hitzler, Johann, Shago, Mary, Morgenstern, Daniel A., Tabori, Uri, Meyn, Stephen, Irwin, Meredith S., Malkin, David, Shlien, Adam
Publicado 2022