Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Marianne Eliou"'
Autor:
Lynette Lau, Edward Higginbotham, Wilson Sung, Venuja Sriretnakumar, Meredith Curtis, Caitlin Chisholm, Meredith Gillespie, Anna Pan, Sean Kim, Sean Simko, E. Magda Price, Marianne Eliou, Anna Szuto, Michelle Axford, Martin Somerville, Kym Boycott, Jean McGowan-Jordan, Melaine Beaulieu Bergeron, James Stavropoulos, Lijia Huang, Christian Marshall
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101548- (2024)
Externí odkaz:
https://doaj.org/article/8fc9fec7563e4535ace9bbc1d04d8659
The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations
Autor:
Anita Villani, Scott Davidson, Nisha Kanwar, Winnie W. Lo, Yisu Li, Sarah Cohen-Gogo, Fabio Fuligni, Lisa-Monique Edward, Nicholas Light, Mehdi Layeghifard, Ricardo Harripaul, Larissa Waldman, Bailey Gallinger, Federico Comitani, Ledia Brunga, Reid Hayes, Nathaniel D. Anderson, Arun K. Ramani, Kyoko E. Yuki, Sasha Blay, Brittney Johnstone, Cara Inglese, Rawan Hammad, Catherine Goudie, Andrew Shuen, Jonathan D. Wasserman, Rosemarie E. Venier, Marianne Eliou, Miranda Lorenti, Carol Ann Ryan, Michael Braga, Meagan Gloven-Brown, Jianan Han, Maria Montero, Famida Spatare, James A. Whitlock, Stephen W. Scherer, Kathy Chun, Martin J. Somerville, Cynthia Hawkins, Mohamed Abdelhaleem, Vijay Ramaswamy, Gino R. Somers, Lianna Kyriakopoulou, Johann Hitzler, Mary Shago, Daniel A. Morgenstern, Uri Tabori, Stephen Meyn, Meredith S. Irwin, David Malkin, Adam Shlien
Publikováno v:
Nature Cancer. 4:203-221
We conducted integrative somatic–germline analyses by deeply sequencing 864 cancer-associated genes, complete genomes and transcriptomes for 300 mostly previously treated children and adolescents/young adults with cancer of poor prognosis or with r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cc564393b318b298215f3cddc8037c8
https://doi.org/10.1038/s43018-022-00474-y
https://doi.org/10.1038/s43018-022-00474-y
Autor:
MStephen Meyn, Chris Carew, Christian R. Marshall, Jennifer Orr, Adam Shlien, Melissa T. Carter, Lynette Lau, Ronald D. Cohn, Marianne Eliou, Dimitri J. Stavropoulos, Sarah Bowdin, Peter N. Ray, Eriskay Liston, Raveen K. Basran
Publikováno v:
Journal of Medical Genetics. 52:A11.2-A11
Background The rapid pace of innovation within the era of genomic sequencing has provided unprecedented insights into the genetic basis of human disease. Clinical whole exome sequencing provides a means for clinicians and clinical labs to take advant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d30a1f281db91af3888536f6928c7d21
https://doi.org/10.1136/jmedgenet-2015-103578.29
https://doi.org/10.1136/jmedgenet-2015-103578.29