Zobrazeno 1 - 10
of 120
pro vyhledávání: '"Robin Z Hayeems"'
Autor:
Trevor Jamieson, Kevin Thorpe, Francois Bernier, Melyssa Aronson, Marc Clausen, Rita Kodida, Emma Reble, June C Carroll, Jordan Lerner-Ellis, Yvonne Bombard, Matthew Osmond, Muhammad Mamdani, Ronald Cohn, Emily Seto, Hanna Faghfoury, Josh Silver, Maureen Smith, Lauren Chad, Jan M Friedman, Robin Z Hayeems, Michael Brudno, Gregory Costain, Quynh Pham, Anne-Marie Laberge, Christian Marshall, Cheryl Shuman, Rebekah Jobling, Irfan Dhalla, Serena Shastri-Estrada, Daniel Assamad, Stephanie Luca, Stacy Hewson, Eriskay Liston, Frank Rudzicz, Wendy Ungar, Guylaine D'Amours
Publikováno v:
BMJ Open, Vol 14, Iss 9 (2024)
Introduction Genetic testing is used across medical disciplines leading to unprecedented demand for genetic services. This has resulted in excessive waitlists and unsustainable pressure on the standard model of genetic healthcare. Alternative models
Externí odkaz:
https://doaj.org/article/8affa2793f8c4b6b9384324d8a29b5cd
Autor:
Gillian Parker, Sarah Hunter, Samer Ghazi, Robin Z Hayeems, Francois Rousseau, Fiona A Miller
Publikováno v:
PLoS ONE, Vol 18, Iss 3, p e0280582 (2023)
BackgroundDecision impact studies have become increasingly prevalent in cancer prognostic research in recent years. These studies aim to evaluate the impact of a genomic test on decision-making and appear to be a new form of evidence of clinical util
Externí odkaz:
https://doaj.org/article/cd4cf6ed78ea498d8abd4d7fc4f771f2
Autor:
Deborah A Marshall, Francois Bernier, Christine Michaels-Igbokwe, Kym M Boycott, Robin Z Hayeems, Taila Hartley
Publikováno v:
BMJ Open, Vol 12, Iss 10 (2022)
Introduction Despite the superior diagnostic performance of exome and genome sequencing compared with conventional genetic tests, evidence gaps related to clinical utility and cost effectiveness have limited their availability in routine clinical pra
Externí odkaz:
https://doaj.org/article/aec2df602453457092d42a23f8299358
Autor:
Monica Taljaard, Sarah Dyack, Jeremy M Grimshaw, Andreas Schulze, Ian D Graham, Jamie Brehaut, Kumanan Wilson, Pranesh Chakraborty, Nathalie Major, Eyal Cohen, Yannis Trakadis, Clara van Karnebeek, Maureen Smith, Kathy Speechley, Komudi Siriwardena, Robin Z Hayeems, Sharan Goobie, Beth K Potter, Jagdeep S Walia, Jennifer J MacKenzie, Chitra Prasad, Stuart G Nicholls, Ann Jolly, Brenda J Wilson, Lisa A Prosser, Andrea J Chow, Ryan Iverson, Monica Lamoureux, Kylie Tingley, Isabel Jordan, Nicole Pallone, Zobaida Al-Baldawi, Alicia Chan, Lisa Jane Gillis, Cheryl R Greenberg, Shailly Jain-Ghai, Sara Khangura, John J Mitchell, Amy Pender, Murray Potter, Rebecca Sparkes, Sylvia Stockler, Mari Teitelbaum
Publikováno v:
BMJ Open, Vol 12, Iss 2 (2022)
Externí odkaz:
https://doaj.org/article/369201d5c61346f4959e8868e0a7f579
Autor:
Ashish R. Deshwar, Kyoko E. Yuki, Huayun Hou, Yijing Liang, Tayyaba Khan, Alper Celik, Arun Ramani, Roberto Mendoza-Londono, Christian R. Marshall, Michael Brudno, Adam Shlien, M. Stephen Meyn, Robin Z. Hayeems, Brandon J. McKinlay, Panagiota Klentrou, Michael D. Wilson, Lianna Kyriakopoulou, Gregory Costain, James J. Dowling
Publikováno v:
The American Journal of Human Genetics. 110:895-900
Autor:
Gillian R. Currie, Brittany Gerber, Diane Lorenzetti, Karen MacDonald, Susanne M. Benseler, Francois P. Bernier, Kym M. Boycott, K. Vanessa Carias, Bettina Hamelin, Robin Z. Hayeems, Claire LeBlanc, Marinka Twilt, Gijs van Rooijen, Durhane Wong-Rieger, Rae S. M. Yeung, Deborah A. Marshall
Publikováno v:
PharmacoEconomics. 41:803-818
Autor:
Robin Z. Hayeems, Stephanie Luca, Anna C. E. Hurst, Meagan Cochran, Chelsea Owens, Alomgir Hossain, Lauren Chad, M. Stephen Meyn, Eleanor Pullenayegum, Wendy J. Ungar, David Bick
Publikováno v:
European Journal of Human Genetics. 30:1423-1431
Genome sequencing (GS) outperforms other rare disease diagnostics, but standardized approaches to assessing its clinical utility are limited. This study assessed the validity of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE), a novel
Autor:
Eriskay J. Liston, Kelsey J. Kalbfleisch, Kaitlin J. Stanley, Rajiv R. Chaturvedi, Iris Cohn, Kirsten M. Farncombe, Robin Z. Hayeems, Marci L.B. Schwartz, Cherith B. Somerville, Raymond H. Kim, Rebekah K. Jobling
Publikováno v:
Canadian Journal of Cardiology. 38:1454-1457
Autor:
Jathishinie Jegathisawaran, Kate Tsiplova, Robin Z. Hayeems, Christian R. Marshall, Dimitri J. Stavropoulos, Sergio L. Pereira, Bhooma Thiruvahindrapuram, Eriskay Liston, Miriam S. Reuter, Roozbeh Manshaei, Iris Cohn, Rebekah Jobling, Raymond H. Kim, Seema Mital, Wendy J. Ungar
Publikováno v:
Genetics in Medicine. 24:1027-1036
Genome sequencing (GS) can aid clinical management of multiple pediatric conditions. Insurers require accurate cost information to inform funding and implementation decisions. The objective was to compare the laboratory workflows and microcosts of tr
Autor:
Robin Z. Hayeems, Christine Michaels-Igbokwe, Viji Venkataramanan, Taila Hartley, Meryl Acker, Meredith Gillespie, Wendy J. Ungar, Roberto Mendoza-Londona, Francois P. Bernier, Kym M. Boycott, Deborah A. Marshall
Publikováno v:
Genetics in Medicine. 24:694-702
To facilitate robust economic analyses of clinical exome and genome sequencing, this study was taken up with the objective of establishing a framework for organizing diagnostic testing trajectories for patients with rare disease.We collected diagnost