Search Results - Jasmine Healy
- Showing 1 - 11 results of 11
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SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencing by Jean-François Spinella, Pamela Mehanna, Ramón Vidal, Virginie Saillour, Pauline Cassart, Chantal Richer, Manon Ouimet, Jasmine Healy, Daniel Sinnett
Published 2016Artigo -
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Association of interleukin‐6 and interleukin‐10 genotypes with radiographic damage in rheumatoid arthritis is dependent on autoantibody status by Ιωάννα Μαρίνου, Jasmine Healy, Devesh Mewar, David Moore, Marion C. Dickson, Michael Binks, D. S. Montgomery, Kevin Walters, Anthony G. Wilson
Published 2007Artigo -
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Integration of High-Resolution Methylome and Transcriptome Analyses to Dissect Epigenomic Changes in Childhood Acute Lymphoblastic Leukemia by Stephan Busche, Bing Ge, Ramón Vidal, Jean-François Spinella, Virginie Saillour, Chantal Richer, Jasmine Healy, Shu‐Huang Chen, Arnaud Droit, Daniel Sinnett, Tomi Pastinen
Published 2013Artigo -
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Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutations by Jean-François Spinella, Pauline Cassart, Chantal Richer, Virginie Saillour, Manon Ouimet, Sylvie Langlois, Pascal St-Onge, Thomas Sontag, Jasmine Healy, Mark D. Minden, Daniel Sinnett
Published 2016Artigo -
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A first-in-human study of the anti-LAG-3 antibody favezelimab plus pembrolizumab in previously treated, advanced microsatellite stable colorectal cancer by Elena Garralda, Ammar Sukari, Nehal J. Lakhani, Akash Patnaik, Yiyun Lou, Seock‐Ah Im, Talia Golan, Ravit Geva, Martin Wermke, Maria J. de Miguel, J. Palcza, S. Jha, Marya Chaney, Anson K. Abraham, Jasmine Healy, Gerald S. Falchook
Published 2022Artigo -
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Rare allelic forms of <i>PRDM9</i> associated with childhood leukemogenesis by Julie Hussin, Daniel Sinnett, Ferrán Casals, Youssef Idaghdour, Vanessa Bruat, Virginie Saillour, Jasmine Healy, Jean‐Christophe Grenier, Thibault de Malliard, Stephan Busche, Jean-François Spinella, Mathieu Larivière, Greg Gibson, Anna Andersson, Linda Holmfeldt, Jing Ma, Lei Wei, Jinghui Zhang, Grégor Andelfinger, James R. Downing, Charles G. Mullighan, Philip Awadalla
Published 2012Artigo -
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Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans by Ferrán Casals, Alan Hodgkinson, Julie Hussin, Youssef Idaghdour, Vanessa Bruat, Thibault de Maillard, Jean‐Christophe Grenier, Elias Gbeha, Fadi F. Hamdan, Simon Girard, Jean-François Spinella, Mathieu Larivière, Virginie Saillour, Jasmine Healy, Isabel Fernández, Daniel Sinnett, Jacques L. Michaud, Guy A. Rouleau, Élie Haddad, Françoise Le Deist, Philip Awadalla
Published 2013Artigo -
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Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome by Adam J. de Smith, Kyle M. Walsh, Libby M. Morimoto, Stephen Francis, Helen M. Hansen, Soyoung Jeon, Semira Gonseth, Minhui Chen, Hanxiao Sun, Sandra Luna‐Fineman, Federico Antillón, Verónica Girón, Alice Y. Kang, I. Smirnov, Xiaorong Shao, Todd P. Whitehead, Lisa F. Barcellos, Kent W. Jolly, Jasmine Healy, Caroline Laverdière, Daniel Sinnett, Jeffrey W. Taub, Jillian M. Birch, Pamela Thompson, Maria S. Pombo‐de‐Oliveira, Logan G. Spector, Andrew T. DeWan, Beth A. Mueller, Charleston W. K. Chiang, Catherine Metayer, Xiaomei Ma, Joseph L. Wiemels
Published 2019Revisão -
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Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk by Amy L. Sherborne, Fay J. Hosking, Rashmi B. Prasad, Rajiv Kumar, Rolf Koehler, Jayaram Vijayakrishnan, Elli Papaemmanuil, Claus R. Bartram, Martin Stanulla, Martin Schrappe, Andreas Gast, Sara E. Dobbins, Yussanne Ma, Eamonn Sheridan, Malcolm Taylor, Sally E. Kinsey, T. Lightfoot, Eve Roman, Julie Irving, James M. Allan, Anthony V. Moorman, Christine J. Harrison, Ian Tomlinson, Sue Richards, Martin Zimmermann, Csaba Szalai, Ágnes F. Semsei, Dániel J. Erdélyi, Maja Krajinović, Daniel Sinnett, Jasmine Healy, Anna González‐Neira, Norihiko Kawamata, Seishi Ogawa, H. Phillip Koeffler, Kari Hemminki, Mel Greaves, Richard S. Houlston
Published 2010Artigo -
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Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome by Austin L. Brown, Adam J. de Smith, Vincent U. Gant, Wenjian Yang, Michael E. Scheurer, Kyle M. Walsh, Jonathan M. Chernus, Noah A. Kallsen, Stephen Peyton, Gareth E. Davies, Erik A. Ehli, Naomi J. Winick, Nyla A. Heerema, Andrew J. Carroll, Michael J. Borowitz, Brent L. Wood, William L. Carroll, Elizabeth A. Raetz, Eleanor Feingold, Meenakshi Devidas, Lisa F. Barcellos, Helen M. Hansen, Libby M. Morimoto, Alice Y. Kang, I. Smirnov, Jasmine Healy, Caroline Laverdière, Daniel Sinnett, Jeffrey W. Taub, Jillian M. Birch, Pamela Thompson, Logan G. Spector, Maria S. Pombo‐de‐Oliveira, Andrew T. DeWan, Charles G. Mullighan, Stephen P. Hunger, Ching‐Hon Pui, Mignon L. Loh, Michael E. Zwick, Catherine Metayer, Xiaomei Ma, Beth A. Mueller, Stephanie L. Sherman, Joseph L. Wiemels, Mary V. Relling, Jun J. Yang, Philip J. Lupo, Karen R. Rabin
Published 2019Revisão
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