Хайлтын үр дүнгүүд - Robin Z. Hayeems

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  1. 1
    How digital tools can advance quality and equity in genomic medicine

    How digital tools can advance quality and equity in genomic medicine -н Yvonne Bombard, Robin Z. Hayeems

    Хэвлэсэн 2020
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  2. 2
    What is a meaningful result? Disclosing the results of genomic research in autism to research participants

    What is a meaningful result? Disclosing the results of genomic research in autism to research participants -н Fiona A. Miller, Robin Z. Hayeems, Jessica Bytautas

    Хэвлэсэн 2010
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    Artigo
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  3. 3
    Parents’ Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling

    Parents’ Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling -н Robin Z. Hayeems, Riyana Babul‐Hirji, Ny Hoang, Rosanna Weksberg, Cheryl Shuman

    Хэвлэсэн 2015
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    Artigo
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  4. 4
    Utility of Genetic Testing from the Perspective of Parents/Caregivers: A Scoping Review

    Utility of Genetic Testing from the Perspective of Parents/Caregivers: A Scoping Review -н Robin Z. Hayeems, Stephanie Luca, Daniel Assamad, Ayushi Bhatt, Wendy J. Ungar

    Хэвлэсэн 2021
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  5. 5
    Health system strategies supporting transition to adult care

    Health system strategies supporting transition to adult care -н Charlotte Moore Hepburn, Eyal Cohen, Jasmin Bhawra, Natalie Weiser, Robin Z. Hayeems, Astrid Guttmann

    Хэвлэсэн 2015
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    Artigo
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  6. 6
    Patient-facing digital tools for delivering genetic services: a systematic review

    Patient-facing digital tools for delivering genetic services: a systematic review -н Whiwon Lee, Salma Shickh, Daniel Assamad, Stephanie Luca, Marc Clausen, Cherith Somerville, Abby Tafler, Angela Shaw, Robin Z. Hayeems, Yvonne Bombard

    Хэвлэсэн 2022
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  7. 7
    Public views on participating in newborn screening using genome sequencing

    Public views on participating in newborn screening using genome sequencing -н Yvonne Bombard, Fiona A. Miller, Robin Z. Hayeems, Carolyn J. Barg, Céline Cressman, June C. Carroll, Brenda J. Wilson, Julian Little, Denise Avard, Michael Painter‐Main, Judith Allanson, Yves Giguère, Pranesh Chakraborty

    Хэвлэсэн 2014
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    Artigo
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  8. 8
    Clinical utility of genomic sequencing: a measurement toolkit

    Clinical utility of genomic sequencing: a measurement toolkit -н Robin Z. Hayeems, David Dimmock, David Bick, John W. Belmont, Robert C. Green, Brendan C. Lanpher, Vaidehi Jobanputra, Roberto Mendoza‐Londono, Shashi Kulkarni, Megan E. Grove, Stacie L. Taylor, Euan A. Ashley

    Хэвлэсэн 2020
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  9. 9
    Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study

    Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study -н Iris Cohn, Tara Paton, Christian R. Marshall, Raveen Basran, Dimitri J. Stavropoulos, Peter N. Ray, Nasim Monfared, Robin Z. Hayeems, M. Stephen Meyn, Sarah Bowdin, Stephen W. Scherer, Ronald D. Cohn, Shinya Ito

    Хэвлэсэн 2017
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    Artigo
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  10. 10
    Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care

    Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care -н Fiona A. Miller, Robin Z. Hayeems, Jessica Bytautas, Philippe L. Bédard, Scott Ernst, Hal W. Hirte, Sébastien J. Hotte, Amit M. Oza, Albiruni Ryan Abdul Razak, Stephen Welch, Eric Winquist, Janet Dancey, Lillian L. Siu

    Хэвлэсэн 2013
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    Artigo
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  11. 11
    Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting

    Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting -н Iris Cohn, Roozbeh Manshaei, Eriskay Liston, John B. A. Okello, Reem Khan, Meredith Curtis, Abby J. Krupski, Rebekah Jobling, Kelsey Kalbfleisch, Tara Paton, Miriam S. Reuter, Robin Z. Hayeems, Ruud H J Verstegen, Aaron Goldman, Raymond H. Kim, Shinya Ito

    Хэвлэсэн 2021
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    Artigo
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  12. 12
    Trio RNA sequencing in a cohort of medically complex children

    Trio RNA sequencing in a cohort of medically complex children -н 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

    Хэвлэсэн 2023
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    Artigo
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  13. 13
    The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease

    The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease -н Miriam S. Reuter, Rajiv Chaturvedi, Eriskay Liston, Roozbeh Manshaei, Ritu B. Aul, Sarah Bowdin, Iris Cohn, Meredith Curtis, Priya Dhir, Robin Z. Hayeems, S. Mohsen Hosseini, Reem Khan, Linh Ly, Christian R. Marshall, Luc Mertens, John B. A. Okello, Sérgio L. Pereira, Akshaya Raajkumar, Mike Seed, Bhooma Thiruvahindrapuram, Stephen W. Scherer, Raymond H. Kim, Rebekah Jobling

    Хэвлэсэн 2020
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    Artigo
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  14. 14
    Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity

    Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity -н Gregory Costain, Susan Walker, Maria Marano, Danielle Veenma, Meaghan Snell, Meredith Curtis, Stephanie Luca, Jason Buera, Danielle Arje, Miriam S. Reuter, Bhooma Thiruvahindrapuram, Brett Trost, Wilson W. L. Sung, Ryan K. C. Yuen, David Chitayat, Roberto Mendoza‐Londono, Dimitri J. Stavropoulos, Stephen W. Scherer, Christian R. Marshall, Ronald D. Cohn, Eyal Cohen, Julia Orkin, M. Stephen Meyn, Robin Z. Hayeems

    Хэвлэсэн 2020
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    Artigo
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  15. 15
    Experiences of caregivers of children with inherited metabolic diseases: a qualitative study

    Experiences of caregivers of children with inherited metabolic diseases: a qualitative study -н Shabnaz Siddiq, Brenda J. Wilson, Ian D. Graham, Monica Lamoureux, Sara D. Khangura, Kylie Tingley, Laure Tessier, Pranesh Chakraborty, Doug Coyle, Sarah Dyack, Jane Gillis, Cheryl R. Greenberg, Robin Z. Hayeems, Shailly Jain‐Ghai, Jonathan B. Kronick, Anne‐Marie Laberge, Julian Little, John J. Mitchell, Chitra Prasad, Komudi Siriwardena, Rebecca Sparkes, Kathy N. Speechley, Sylvia Stöckler, Yannis Trakadis, S. Wafa, Jagdeep S. Walia, Kumanan Wilson, Nataliya Yuskiv, Beth K. Potter

    Хэвлэсэн 2016
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    Artigo
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  16. 16
    Finding the sweet spot: a qualitative study exploring patients’ acceptability of chatbots in genetic service delivery

    Finding the sweet spot: a qualitative study exploring patients’ acceptability of chatbots in genetic service delivery -н Stephanie Luca, Marc Clausen, Angela Shaw, Whiwon Lee, Suvetha Krishnapillai, Ella Adi-Wauran, Hanna Faghfoury, Gregory Costain, Rebekah Jobling, Melyssa Aronson, Eriskay Liston, Josh Silver, Cheryl Shuman, Lauren Chad, Robin Z. Hayeems, Yvonne Bombard, François Bernier, Michael Brudno, June C. Carroll, Ronald D. Cohn, Irfan A. Dhalla, Jan M. Friedman, Stacy Hewson, Trevor Jamieson, Rita Kodida, Anne‐Marie Laberge, Jordan Lerner‐Ellis, Muhammad Mamdani, Christian R. Marshall, Matthew Osmond, Quỳnh Phạm, Emma Reble, Frank Rudzicz, Emily Seto, Serena Shastri-Estrada, Maureen Smith, Kevin E. Thorpe, Wendy J. Ungar

    Хэвлэсэн 2023
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    Artigo
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  17. 17
    Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study

    Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort stu... -н Alissa M. D’Gama, Sarah Mulhern, Beth Rosen Sheidley, Fadil Boodhoo, Sarah Buts, Natalie Chandler, Joanna Cobb, Meredith Curtis, Edward J. Higginbotham, Jonathon Holland, Tayyaba Khan, Julia Koh, Nicole Si Yan Liang, Lyndsey McRae, Sarah E Nesbitt, Brandon T. Oby, Ben Paternoster, Alistair Patton, Graham Rose, Elizabeth Scotchman, Rozalia Valentine, Kimberly Wiltrout, Robin Z. Hayeems, Puneet Jain, Sebastian Lunke, Christian R. Marshall, Shira Rockowitz, Neil J. Sebire, Zornitza Stark, Susan M. White, Lyn S. Chitty, J. Helen Cross, Ingrid E. Scheffer, Vann Chau, Gregory Costain, Annapurna Poduri, Katherine B. Howell, Amy McTague

    Хэвлэсэн 2023
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    Artigo
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  18. 18
    Family‐centred care interventions for children with chronic conditions: A scoping review

    Family‐centred care interventions for children with chronic conditions: A scoping review -н Andrea Chow, Ammar Saad, Zobaida Al‐Baldawi, Ryan Iverson, Becky Skidmore, Isabel Jordán, Nicole Pallone, Maureen Smith, Pranesh Chakraborty, Jamie Brehaut, Eyal Cohen, Sarah Dyack, Jane Gillis, Sharan Goobie, Cheryl R. Greenberg, Robin Z. Hayeems, Brian Hutton, Michal Inbar‐Feigenberg, Shailly Jain‐Ghai, Sara D. Khangura, Jennifer MacKenzie, John J. Mitchell, Zeinab Moazin, Stuart G. Nicholls, Amy Pender, Chitra Prasad, Andreas Schulze, Komudi Siriwardena, Rebecca N. Sparkes, Kathy N. Speechley, Sylvia Stöckler, Monica Taljaard, Mari Teitelbaum, Yannis Trakadis, Clara van Karnebeek, Jagdeep S. Walia, Kumanan Wilson, Beth K. Potter

    Хэвлэсэн 2024
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  19. 19
    Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

    Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test -н Anath C. Lionel, Gregory Costain, Nasim Monfared, Susan Walker, Miriam S. Reuter, S. Mohsen Hosseini, Bhooma Thiruvahindrapuram, Daniele Merico, Rebekah Jobling, Thomas Nalpathamkalam, Giovanna Pellecchia, Wilson W. L. Sung, Zhuozhi Wang, Peter Bikangaga, Cyrus Boelman, Melissa T. Carter, Dawn Cordeiro, Cheryl Cytrynbaum, Sharon Dell, Priya Dhir, James J. Dowling, Elise Héon, Stacy Hewson, Linda T. Hiraki, Michal Inbar‐Feigenberg, Regan Klatt, Jonathan B. Kronick, Ronald M. Laxer, Christoph Licht, H. Robson MacDonald, Saadet Mercimek‐Andrews, Roberto Mendoza‐Londono, Tino D. Piscione, Rayfel Schneider, Andreas Schulze, Earl D. Silverman, Komudi Siriwardena, O. Carter Snead, Neal Sondheimer, Joanne Sutherland, Ajoy Vincent, Jonathan D. Wasserman, Rosanna Weksberg, Cheryl Shuman, Chris Carew, Michael J. Szego, Robin Z. Hayeems, Raveen Basran, Dimitri J. Stavropoulos, Peter N. Ray, Sarah Bowdin, M. Stephen Meyn, Ronald D. Cohn, Stephen W. Scherer, Christian R. Marshall

    Хэвлэсэн 2017
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    Artigo
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  20. 20
    Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine

    Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine -н Dimitri J. Stavropoulos, Daniele Merico, Rebekah Jobling, Sarah Bowdin, Nasim Monfared, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Giovanna Pellecchia, Ryan K. C. Yuen, Michael J. Szego, Robin Z. Hayeems, Randi Zlotnik Shaul, Michael Brudno, Marta Gîrdea, Brendan J. Frey, Babak Alipanahi, Sohnee Ahmed, Riyana Babul‐Hirji, Ramses Badilla Porras, Melissa T. Carter, Lauren Chad, Ayeshah Chaudhry, David Chitayat, Soghra Jougheh Doust, Cheryl Cytrynbaum, Lucie Dupuis, Resham Ejaz, Leona Fishman, Andrea Guerin, Bita Hashemi, Mayada Helal, Stacy Hewson, Michal Inbar‐Feigenberg, Pekka Kannus, Natalya Karp, Raymond H. Kim, Jonathan B. Kronick, Eriskay Liston, H. Robson MacDonald, Saadet Mercimek‐Mahmutoglu, Roberto Mendoza‐Londono, Enas Nasr, Graeme Nimmo, Nicole Parkinson, Nada Quercia, Julian Raiman, Maian Roifman, Andreas Schulze, Andrea Shugar, Cheryl Shuman, Pierre Sinajon, Komudi Siriwardena, Rosanna Weksberg, Grace Yoon, Chris Carew, Raith Erickson, Richard A. Leach, Robert J. Klein, Peter N. Ray, M. Stephen Meyn, Stephen W. Scherer, Ronald D. Cohn, Christian R. Marshall

    Хэвлэсэн 2016
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    Artigo
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