Hasil Pencarian - Robin Hayeems

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  1. 1
    Barriers to care for women with low-grade endometrial cancer and morbid obesity: a qualitative study

    Barriers to care for women with low-grade endometrial cancer and morbid obesity: a qualitative study oleh Angela Han, Robin Hayeems, Deborah Robertson, Sari L Kives, Abheha Satkunaratnam, Sarah E Ferguson

    Diterbitkan 2019-06-01
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  2. 2
    P383: The clinician-reported genetic testing utility InDEx in the NICU (C-GUIDETM-NICU): Quantifying genome-wide sequencing utility in neonatal critical care

    P383: The clinician-reported genetic testing utility InDEx in the NICU (C-GUIDETM-NICU): Quantifying genome-wide sequencing utility in neonatal critical care oleh Lena Dolman, Elise Poole, Joyce Yan, Stephanie Luca, Wendy Ungar, Lauren Chad, Martin Offringa, Robin Hayeems

    Diterbitkan 2023-01-01
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  3. 3
    O54: Reimagining genetics service delivery: Genetics providers’ perspectives on the integration of digital tools into clinical practice

    O54: Reimagining genetics service delivery: Genetics providers’ perspectives on the integration of digital tools into clinical practice oleh Whiwon Lee, Daena Hirjikaka, Sonya Grewal, Marc Clausen, Stephanie Luca, Angela Shaw, Yvonne Bombard, Robin Hayeems

    Diterbitkan 2023-01-01
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  4. 4
    P479: The Clinician-reported Genetic testing Utility InDEx: A revised tool to quantify genome-wide sequencing utility in neonatal intensive care (C-GUIDE NICU)

    P479: The Clinician-reported Genetic testing Utility InDEx: A revised tool to quantify genome-wide sequencing utility in neonatal intensive care (C-GUIDE NICU) oleh Lena Dolman, Elise Poole, Joyce Yan, Stephanie Luca, Bowen Xiao, Wendy Ungar, Lauren Chad, Martin Offringa, Robin Hayeems

    Diterbitkan 2024-01-01
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  5. 5
    P482: The clinical utility of genome-wide sequencing for rare disease: A multidimensional map

    P482: The clinical utility of genome-wide sequencing for rare disease: A multidimensional map oleh Robin Hayeems, Viji Venkataramanan, Katharine Fooks, Karen MacDonald, Trevor Seeger, Taila Hartley, Francois Bernier, Kym Boycott, Deborah Marshall

    Diterbitkan 2024-01-01
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  6. 6
    P477: Barriers and facilitators to implementing genomic medicine: A scoping review of the global landscape*

    P477: Barriers and facilitators to implementing genomic medicine: A scoping review of the global landscape* oleh Whiwon Lee, Joyce Yan, Katharine Fooks, Abby Tafler, Pooja Banglorewala, Melanie Barwick, Mark Dobrow, Jan Friedman, Christian Marshall, Robin Hayeems

    Diterbitkan 2024-01-01
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  7. 7
    P543: Design and early findings from a mixed-methods study exploring the genomics era role of the medical geneticist in Canada

    P543: Design and early findings from a mixed-methods study exploring the genomics era role of the medical geneticist in Canada oleh Michael Mackley, Kym Boycott, Shaimaa Helal, Lauren Chad, Gregory Costain, Ronald Cohn, Hanna Faghfoury, Aspasia Karalis, Roberto Mendoza-Londono, Robin Hayeems

    Diterbitkan 2024-01-01
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  8. 8
    P373: Patients’ and parents’ perspectives on the use of digital tools to deliver genetic services

    P373: Patients’ and parents’ perspectives on the use of digital tools to deliver genetic services oleh Daniel Assamad, Saumeh Saeedi, Sonya Grewal, Vedika Jha, Stephanie Luca, Marc Clausen, Angela Shaw, Whiwon Lee, Yvonne Bombard, Robin Hayeems, Genetics Navigator Study Team

    Diterbitkan 2023-01-01
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  9. 9
    P547: The clinician-reported Genetic testing Utility InDEX (C-GUIDE): Establishing content validity for a new measure for sequencing-based newborn screening

    P547: The clinician-reported Genetic testing Utility InDEX (C-GUIDE): Establishing content validity for a new measure for sequencing-based newborn screening oleh Stephanie Luca, Katharine Fooks, Elise Poole, Amanda Pichini, Joanna Ziff, Katrina Stone, Bowen Xiao, Salma Shickh, David Bick, Pranesh Chakraborty, Wendy Ungar, Robin Hayeems

    Diterbitkan 2024-01-01
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  10. 10
    P616: Genome-wide Sequencing Ontario (GSO): Insight into Ontario’s rare disease landscape

    P616: Genome-wide Sequencing Ontario (GSO): Insight into Ontario’s rare disease landscape oleh Meredith Gillespie, Robin Hayeems, Christian Marshall, Anna Szuto, Caitlin Chisholm, Wendy Ungar, James Stavropoulos, Lijia Huang, Viji Venkataramanan, Lynette Lau, Wilson Sung, Melanie Beaulieu Bergeron, Ted Higginbotham, Meredith Curtis, Venuja Sriretnakumar, Hassan Zaidi, Emma Hitchcock, Audrey Schaffer, Sarah Sawyer, Wendy Ungar, Gregory Costain, Roberto Mendoza-Londono, Robin Hayeems, Martin Somerville, Kym Boycott, Taila Hartley

    Diterbitkan 2024-01-01
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  11. 11
    P391: What are patients’ perspectives on the privacy and security of digital genomic tools? A qualitative study

    P391: What are patients’ perspectives on the privacy and security of digital genomic tools? A qualitative study oleh Vedika Jha, Saumeh Saeedi, Daniel Assamad, Sonya Grewal, Daena Hirjikaka, Whiwon Lee, Stephanie Luca, Angela Shaw, Robin Hayeems, Marc Clausen, Yvonne Bombard, Genetics Navigator Study Team

    Diterbitkan 2023-01-01
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  12. 12
    P823: Insights and strategies for inclusive adolescent and young adult participation in genetics research

    P823: Insights and strategies for inclusive adolescent and young adult participation in genetics research oleh Tasha Wainstein, Courtney Cook, Daniel Assamad, Julia Heaton, Manraj Randhawa, David Yeung, Lauren Jennings, Robin Hayeems, Harpreet Chhina, Anthony Cooper, GenCOUNSEL. Study, Jehannine Austin, Alison Elliott

    Diterbitkan 2024-01-01
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  13. 13
    Access to novel drugs and therapeutics for children and youth: Eliciting citizens' values to inform public funding decisions

    Access to novel drugs and therapeutics for children and youth: Eliciting citizens' values to inform public funding decisions oleh Cindy L. Gauvreau, Lisa Wight, Mathushan Subasri, Antonia Palmer, Robin Hayeems, Alysha Croker, Julia Abelson, Brent Fraser, Yvonne Bombard, Charlotte Moore Hepburn, Michael G. Wilson, Avram Denburg

    Diterbitkan 2023-04-01
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  14. 14
    P516: The Genetics Navigator: The development and usability testing of a new patient-facing digital health application to support clinical genetic testing

    P516: The Genetics Navigator: The development and usability testing of a new patient-facing digital health application to support clinical genetic testing oleh Marc Clausen, Stephanie Luca, Emma Reble, Rita Kodida, Saumeh Saeedi, Daena Hirjikaka, Lauren Chad, Gregory Costain, Hanna Faghfoury, Josh Silver, Serena Shastri-Estrada, Maureen Smith, Robin Hayeems, Yvonne Bombard

    Diterbitkan 2024-01-01
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  15. 15
    P873: “If you look for a problem, you’ll find one”: A qualitative study to understand why parents/adult patients decline secondary findings

    P873: “If you look for a problem, you’ll find one”: A qualitative study to understand why parents/adult patients decline secondary findings oleh Abigail Hansen, Stephanie Luca, Olivia Moran, Riyana Babul-Hirji, Joyce Yan, Katharine Fooks, Viji Venkataramanan, Wendy Ungar, Robin Hayeems, Secondary Findings Study Team, Elise Poole, Daniel Assamad, Pooja Banglorewala, Lydia Vermeer, Christian Marshall, Meredith Gillespie, Anna Szuto, Caitlin Chisholm, James Stavropoulos, Lijia Huang, Olga Jarinova, Lynette Lau, Whiwon Lee, Lauren Badalato, Tugce Balci, Lauren Chad, Cara Inglese, Virginie Ladouceur, Michael Mackley, Chantal Morel, Julie Richer, Mark Tarnopolsky, Anita Villani, Laura Zahavich, Sarah Sawyer, Roberto Mendoza-Londono, Martin Somerville, Kym Boycott, Wendy Ungar, Robin Hayeems

    Diterbitkan 2024-01-01
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  16. 16
    O05: A micro-costing and cost-effectiveness analysis of genome sequencing vs exome sequencing in pediatric rare diseases

    O05: A micro-costing and cost-effectiveness analysis of genome sequencing vs exome sequencing in pediatric rare diseases oleh Wendy Ungar, Vercancy Wu, Christian Marshall, Jackie Hwang, Robin Hayeems, Kate Tsiplova, Meredith Gillespie, Anna Szuto, Caitlin Chisholm, Dimitri Stavropoulos, Viji Venkataramanan, Bowen Xiao, Sheena Li, Gregory Costain, Melanie Beaulieu Bergeron, Sarah Sawyer, Lynette Lau, Lijia Huang, Roberto Mendoza-Londono, Brian Smith, Edward Higginbotham, Martin Somerville, Kym Boycott

    Diterbitkan 2024-01-01
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  17. 17
    P305: Evaluation of the feasibility, diagnostic yield, and utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): An international pilot study

    P305: Evaluation of the feasibility, diagnostic yield, and utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): An international pilot study oleh Nicole Si Yan Liang, Gregory Costain, Alissa D'Gama, Amy McTague, Katherine Howell, Vann Chau, Sarah Mulhern, Annapurna Poduri, Ingrid Scheffer, Beth Sheidley, Meredith Curtis, Edward Higginbotham, Tayyaba Khan, Lyndsey McRae, Kimberly Wiltrout, Robin Hayeems, Puneet Jain, Sebastian Lunke, Christian Marshall, Lyn Chitty, Shira Rockowitz, Zornitza Stark, Susan White

    Diterbitkan 2024-01-01
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  18. 18
    P540: Genome-wide Sequencing Ontario (GSO): Canada’s first provincial clinical genome-wide sequencing service

    P540: Genome-wide Sequencing Ontario (GSO): Canada’s first provincial clinical genome-wide sequencing service oleh Meredith Gillespie, Robin Hayeems, Christian Marshall, Anna Szuto, Caitlin Chisholm, James Stavropoulos, Lijia Huang, Lynette Lau, Wilson Sung, Melanie Beaulieu Bergeron, Ted Higginbotham, Meredith Curtis, Venuja Sriretnakumar, Hassan Zaidi, Emma Hitchcock, Audrey Schaffer, Taila Hartley, Sarah Sawyer, Wendy Ungar, Gregory Costain, Roberto Mendoza-Londono, Anna Pan, Jennifer Keating, Diana Matviychuk, Tamara Braid, Niri Carroll, Martin Somerville, Kym Boycott

    Diterbitkan 2024-01-01
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  19. 19
    P531: Developing the patient-reported Genetic testing Utility InDEx (P-GUIDE): Assessing value of genetic testing from patients’ perspectives in multiple clinical contexts

    P531: Developing the patient-reported Genetic testing Utility InDEx (P-GUIDE): Assessing value of genetic testing from patients’ perspectives in multiple clinical contexts oleh 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

    Diterbitkan 2024-01-01
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  20. 20
    P866: Exploring the impact of secondary findings in a cohort of patients and families receiving genome-wide sequencing

    P866: Exploring the impact of secondary findings in a cohort of patients and families receiving genome-wide sequencing oleh Katharine Fooks, Lydia Vermeer, Elise Poole, Stephanie Luca, Riyana Babul-Hirji, Lauren Chad, David Chitayat, Michael Mackley, Marci Schwartz, Wendy Ungar, Robin Hayeems, Secondary Findings Study Team, Joyce Yan, Abigail Hansen, Viji Venkataramanan, Daniel Assamad, Christian Marshall, Meredith Gillespie, Anna Szuto, Caitlin Chisholm, James Stavropoulos, Lijia Huang, Olga Jarinova, Lynette Lau, Whiwon Lee, Lauren Badalato, Tugce Balci, Cara Inglese, Virginie Beausejour Ladouceur, Chantal Morel, Julie Richer, Mark Tarnopolsky, Anita Villani, Laura Zahavich, Olivia Moran, Sarah Sawyer, Roberto Mendoza-Londono, Martin Somerville, Kym Boycott

    Diterbitkan 2024-01-01
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