Search Results - Linlea Armstrong

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  1. 1

    The Identification of Lynch Syndrome in British Columbia by Carol M Cremin, Linlea Armstrong, Sharlene Gill, David Huntsman, Chris Bajdik

    Published in Canadian Journal of Gastroenterology (2009-01-01)
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  2. 2

    Expanding the genotype-phenotype spectrum in SCN8A-related disorders by Malavika Hebbar, Nawaf Al-Taweel, Inderpal Gill, Cyrus Boelman, Richard A. Dean, Samuel J. Goodchild, Janette Mezeyova, Noah Gregory Shuart, J. P. Johnson, James Lee, Aspasia Michoulas, Linda L. Huh, Linlea Armstrong, Mary B. Connolly, Michelle K. Demos

    Published in BMC Neurology (2024-01-01)
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  3. 3

    Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability by Farah R. Zahir, Jill C. Mwenifumbo, Hye-Jung E. Chun, Emilia L. Lim, Clara D. M. Van Karnebeek, Madeline Couse, Karen L. Mungall, Leora Lee, Nancy Makela, Linlea Armstrong, Cornelius F. Boerkoel, Sylvie L. Langlois, Barbara M. McGillivray, Steven J. M. Jones, Jan M. Friedman, Marco A. Marra

    Published in BMC Genomics (2017-05-01)
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  4. 4

    The practice of genomic medicine: A delineation of the process and its governing principles by Julia Handra, Julia Handra, Adrienne Elbert, Adrienne Elbert, Nour Gazzaz, Nour Gazzaz, Nour Gazzaz, Nour Gazzaz, Ashley Moller-Hansen, Ashley Moller-Hansen, Stephanie Hyunh, Stephanie Hyunh, Hyun Kyung Lee, Hyun Kyung Lee, Pierre Boerkoel, Emily Alderman, Emily Alderman, Erin Anderson, Erin Anderson, Lorne Clarke, Lorne Clarke, Sara Hamilton, Sara Hamilton, Ronnalea Hamman, Shevaun Hughes, Simon Ip, Sylvie Langlois, Sylvie Langlois, Mary Lee, Laura Li, Frannie Mackenzie, Millan S. Patel, Millan S. Patel, Leah M. Prentice, Karan Sangha, Karan Sangha, Laura Sato, Kimberly Seath, Kimberly Seath, Margaret Seppelt, Anne Swenerton, Anne Swenerton, Lynn Warnock, Jessica L. Zambonin, Jessica L. Zambonin, Cornelius F. Boerkoel, Cornelius F. Boerkoel, Hui-Lin Chin, Hui-Lin Chin, Hui-Lin Chin, Linlea Armstrong, Linlea Armstrong

    Published in Frontiers in Medicine (2023-01-01)
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  5. 5

    P531: Developing the patient-reported Genetic testing Utility InDEx (P-GUIDE): Assessing value of genetic testing from patients’ perspectives in multiple clinical contexts by Elise Poole, Stephanie Luca, Daniel Assamad, Bowen Xiao, Joyce Yan, Pooja Banglorewala, Cheryl Xia, Wendy Ungar, Lesleigh Abbott, Linlea Armstrong, Patricia Birch, Kym Boycott, June Carroll, Lauren Chad, David Chitayat, Avram Denburg, Rebecca Deyell, Alison Elliott, Catherine Goudie, Anne-Marie Laberge, Melissa Maio, Iskra Peltekova, Becky Quinlan, Sarah Sawyer, Rachel Silver, Maureen Smith, Ronni Teitelbaum, Anita Villani, Tasha Wainstein, Robin Hayeems

    Published in Genetics in Medicine Open (2024-01-01)
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  6. 6

    Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers by Rebecca J. Deyell, Yaoqing Shen, Emma Titmuss, Katherine Dixon, Laura M. Williamson, Erin Pleasance, Jessica M. T. Nelson, Sanna Abbasi, Martin Krzywinski, Linlea Armstrong, Melika Bonakdar, Carolyn Ch’ng, Eric Chuah, Chris Dunham, Alexandra Fok, Martin Jones, Anna F. Lee, Yussanne Ma, Richard A. Moore, Andrew J. Mungall, Karen L. Mungall, Paul C. Rogers, Kasmintan A. Schrader, Alice Virani, Kathleen Wee, Sean S. Young, Yongjun Zhao, Steven J. M. Jones, Janessa Laskin, Marco A. Marra, Shahrad R. Rassekh

    Published in Nature Communications (2024-05-01)
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  7. 7

    How does personal utility depend on clinical setting? Evidence from 3 cohorts by Elise Poole, Stephanie Luca, Daniel Assamad, Bowen Xiao, Joyce Yan, Yue Yin Xia, Lesleigh S. Abbott, Linlea Armstrong, Patricia Birch, Kym M. Boycott, June C. Carroll, Lauren Chad, David Chitayat, Avram Denburg, Rebecca J. Deyell, Alison M. Elliott, Catherine Goudie, Anne-Marie Laberge, Melissa Maio, Iskra T. Peltekova, Becky Quinlan, Sarah L. Sawyer, Rachel Silver, Maureen Smith, Ronni Teitelbaum, Anita Villani, Wendy J. Ungar, Robin Z. Hayeems, Andrea Staines, Bailey Gallinger, Claire Newman, Elisabeth Soubry, Grace Tam, Gregory Costain, Kimberly Seath, Kristal Louie, Nada Quercia, Nicole Gojska, Olivia M. Moran, Rosemarie E. Venier, Simina McDermott, Stephanie Hedges, Tami Uster, Tithi Paul

    Published in Genetics in Medicine Open (2025-01-01)
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