Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Bartha, Knoppers"'
Autor:
Lauren C. Tindale, Almira Zhantuyakova, Stephanie Lam, Michelle Woo, Janice S. Kwon, Gillian E. Hanley, Bartha Knoppers, Kasmintan A. Schrader, Stuart J. Peacock, Aline Talhouk, Trevor Dummer, Kelly Metcalfe, Nora Pashayan, William D. Foulkes, Ranjit Manchanda, David Huntsman, Gavin Stuart, Jacques Simard, Lesa Dawson
Publikováno v:
Current Oncology, Vol 29, Iss 7, Pp 4632-4646 (2022)
Individuals with proven hereditary cancer syndrome (HCS) such as BRCA1 and BRCA2 have elevated rates of ovarian, breast, and other cancers. If these high-risk people can be identified before a cancer is diagnosed, risk-reducing interventions are high
Externí odkaz:
https://doaj.org/article/bff72e27330148d4a6cecedac5991628
Autor:
Saima Ahmed, Emmanuelle Lévesque, Rosalind Garland, Bartha Knoppers, Michel Dorval, Jacques Simard, Carmen G. Loiselle
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 20, Iss 1, Pp 1-9 (2022)
Abstract Background Breast cancer risk stratification categorizes a woman’s potential risk of developing the disease as near-population, intermediate, or high. In accordance, screening and follow up for breast cancer can readily be tailored followi
Externí odkaz:
https://doaj.org/article/43dbffb27d754a1ca907491789d58c0f
Autor:
Rong Zhang, Xi Yang, Jun Zhang, Hong Li, Jian Shen, Jian Xu, Yan Jin, Louise Mâsse, Zhong-Cheng Luo, Lise Dubois, Huijuan Zhang, Bartha Knoppers, He-Feng Huang, Jiahao Wu, Liping Wang, Benoît Mâsse, Fengxiu Ouyang, Yamei Yu, Wenguang Sun, William Fraser, Isabel Fortier, Sonia Semenic, Yanting Wu, Isabelle Marc, Luigi Bouchard, Jianxia Fan, Peter C K Leung, Xiang Peng Liao, C M Herba, Linda Booij, Antoine Lewin, Weibin Wu, Chen Lei, Anita Kozyrskyj, N Chaillet, Janelle Zhan, Catherine Allard, Ma'n Zawati, Jean-Patrice Baillargeon, Maria P Velez, Hanqiu Zhang, Wen Yu, Caroline Vaillancourt, Han Liu, Amelie Tetu, Wenli Fang, Xinzhi Zhao, Xin-Mei Liu, Zhirou Chen, Yan-Hui Hao, Nadia Abdelouahab
Publikováno v:
BMJ Open, Vol 11, Iss 4 (2021)
Introduction Childhood overweight and obesity (OWO) is a primary global health challenge. Childhood OWO prevention is now a public health priority in China. The Sino-Canadian Healthy Life Trajectories Initiative (SCHeLTI), one of four trials being un
Externí odkaz:
https://doaj.org/article/13f2399c7f704861a6276cb7f166fbe4
Publikováno v:
BMJ Open, Vol 9, Iss 8 (2019)
ObjectiveAnonymised patient-level data from clinical research are increasingly recognised as a fundamental and valuable resource. It has value beyond the original research project and can help drive scientific research and innovations and improve pat
Externí odkaz:
https://doaj.org/article/ee5f3f55881b44e387f58a051bc5e945
Autor:
Melissa S Cline, Rachel G Liao, Michael T Parsons, Benedict Paten, Faisal Alquaddoomi, Antonis Antoniou, Samantha Baxter, Larry Brody, Robert Cook-Deegan, Amy Coffin, Fergus J Couch, Brian Craft, Robert Currie, Chloe C Dlott, Lena Dolman, Johan T den Dunnen, Stephanie O M Dyke, Susan M Domchek, Douglas Easton, Zachary Fischmann, William D Foulkes, Judy Garber, David Goldgar, Mary J Goldman, Peter Goodhand, Steven Harrison, David Haussler, Kazuto Kato, Bartha Knoppers, Charles Markello, Robert Nussbaum, Kenneth Offit, Sharon E Plon, Jem Rashbass, Heidi L Rehm, Mark Robson, Wendy S Rubinstein, Dominique Stoppa-Lyonnet, Sean Tavtigian, Adrian Thorogood, Can Zhang, Marc Zimmermann, BRCA Challenge Authors, John Burn, Stephen Chanock, Gunnar Rätsch, Amanda B Spurdle
Publikováno v:
PLoS Genetics, Vol 14, Iss 12, p e1007752 (2018)
The BRCA Challenge is a long-term data-sharing project initiated within the Global Alliance for Genomics and Health (GA4GH) to aggregate BRCA1 and BRCA2 data to support highly collaborative research activities. Its goal is to generate an informed and
Externí odkaz:
https://doaj.org/article/3d040669de2049168c109d5c746eac9a
Autor:
Sonia S. Anand, Jack V. Tu, Philip Awadalla, Sandra Black, Catherine Boileau, David Busseuil, Dipika Desai, Jean-Pierre Després, Russell J. de Souza, Trevor Dummer, Sébastien Jacquemont, Bartha Knoppers, Eric Larose, Scott A. Lear, Francois Marcotte, Alan R. Moody, Louise Parker, Paul Poirier, Paula J. Robson, Eric E. Smith, John J. Spinelli, Jean-Claude Tardif, Koon K. Teo, Natasa Tusevljak, Matthias G. Friedrich, on behalf of the CAHHM Study Investigators
Publikováno v:
BMC Public Health, Vol 16, Iss 1, Pp 1-15 (2016)
Abstract Background The Canadian Alliance for Healthy Hearts and Minds (CAHHM) is a pan-Canadian, prospective, multi-ethnic cohort study being conducted in Canada. The overarching objective of the CAHHM is to understand the association of socio-envir
Externí odkaz:
https://doaj.org/article/81d4f3f1ea134ca0bbf2e4efacba63ea
Autor:
Erika Kleiderman, Vasiliki Rahimzadeh, Bartha Knoppers, Marie-Christine Roy, Anne-Marie Laberge, Vardit Ravitsky
Publikováno v:
The American Journal of Bioethics. 22:23-25
Autor:
Matthew Osmond, Taila Hartley, David A. Dyment, Kristin D. Kernohan, Michael Brudno, Orion J. Buske, A. Micheil Innes, Kym M. Boycott, Kym Boycott, Francois Bernier, Clara van Karnebeek, David Dyment, Kristin Kernohan, Micheil Innes, Ryan Lamont, Jillian Parboosingh, Deborah Marshall, Christian Marshall, Roberto Mendoza, James Dowling, Robin Hayeems, Bartha Knoppers, Anna Lehman, Sara Mostafavi
Publikováno v:
Genetics in Medicine, 24(1), 100-108. Lippincott Williams and Wilkins
Genetics in medicine, 24(1), 100-108. Lippincott Williams and Wilkins
Care4Rare Canada Consortium 2022, ' Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery : The 2-year experience of Care4Rare Canada ', Genetics in Medicine, vol. 24, no. 1, pp. 100-108 . https://doi.org/10.1016/j.gim.2021.08.014
Genetics in medicine, 24(1), 100-108. Lippincott Williams and Wilkins
Care4Rare Canada Consortium 2022, ' Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery : The 2-year experience of Care4Rare Canada ', Genetics in Medicine, vol. 24, no. 1, pp. 100-108 . https://doi.org/10.1016/j.gim.2021.08.014
Purpose: Matchmaking has emerged as a useful strategy for building evidence toward causality of novel disease genes in patients with undiagnosed rare diseases. The Matchmaker Exchange (MME) is a collaborative initiative that facilitates international
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7efeb0aa7a0464da98a39699fed7beed
https://research.vumc.nl/en/publications/3f110bf7-df13-477a-b69e-084e3705637e
https://research.vumc.nl/en/publications/3f110bf7-df13-477a-b69e-084e3705637e
Autor:
Saima Ahmed, Emmanuelle Lévesque, Rosalind Garland, Bartha Knoppers, Michel Dorval, Jacques Simard, Carmen G. Loiselle
Publikováno v:
Hereditary cancer in clinical practice. 20(1)
Background Breast cancer risk stratification categorizes a woman’s potential risk of developing the disease as near-population, intermediate, or high. In accordance, screening and follow up for breast cancer can readily be tailored following risk a
Autor:
Dianne, Nicol, Yann, Joly, Jane, Kaye, Bartha, Knoppers, Eric M, Meslin, Jane, Nielsen, Margaret, Otlowski, Kate, Warner
Publikováno v:
Journal of law and medicine. 28(1)
Distinguished Professor Don Chalmers retired from the Law Faculty at the University of Tasmania on Friday 10 July 2020. This article is dedicated to Don, providing a brief account and acknowledgment of his fine contributions to legal research and edu