Hasil Pencarian - Marc Clausen

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  1. 1
    P564: Doing no harm: Exploring the psychosocial impacts of receiving secondary findings from whole exome sequencing

    P564: Doing no harm: Exploring the psychosocial impacts of receiving secondary findings from whole exome sequencing oleh Vanessa Rokoszak, Daena Hirjikaka, Marc Clausen, Salma Shickh, Keven Cheung, Yvonne Bombard

    Diterbitkan 2024-01-01
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  2. 2
    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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  3. 3
    Greenotyper: Image-Based Plant Phenotyping Using Distributed Computing and Deep Learning

    Greenotyper: Image-Based Plant Phenotyping Using Distributed Computing and Deep Learning oleh Marni Tausen, Marni Tausen, Marc Clausen, Sara Moeskjær, ASM Shihavuddin, ASM Shihavuddin, Anders Bjorholm Dahl, Luc Janss, Stig Uggerhøj Andersen

    Diterbitkan 2020-08-01
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  4. 4
    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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  5. 5
    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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  6. 6
    P543: Comparing the analytical performance of exome sequencing and traditional panel testing in a cancer population

    P543: Comparing the analytical performance of exome sequencing and traditional panel testing in a cancer population oleh Emma Reble, Jordan Sam, Rita Kodida, Marc Clausen, Salma Shickh, Chloe Mighton, Jose-Mario Capo-Chichi, Elena Greenfeld, Abdul Noor, Raymond Kim, Jordan Lerner-Ellis, Yvonne Bombard

    Diterbitkan 2023-01-01
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  7. 7
    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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  8. 8
    P382: Professionals’ perspectives on the use of digital tools to support patient recontact in clinical genetics

    P382: Professionals’ perspectives on the use of digital tools to support patient recontact in clinical genetics oleh Guylaine D'Amours, Emma Reble, Vernie Aguda, Marc Clausen, Salma Shickh, Chloe Mighton, June Carroll, Jordan Lerner-Ellis, Tanya Nelson, Julie Richer, Kasmintan Schrader, Emily Seto, Serena Shastri-Estrada, Kevin Thorpe, Yvonne Bombard

    Diterbitkan 2023-01-01
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  9. 9
    P409: Clinical utility of genomic sequencing for hereditary cancer syndromes: An observational chart review

    P409: Clinical utility of genomic sequencing for hereditary cancer syndromes: An observational chart review oleh Salma Shickh, Chloe Mighton, Marc Clausen, Rita Kodida, Jordan Sam, Daena Hirjikaka, Emma Reble, Tracy Graham, Seema Panchal, Andrea Eisen, Christine Elser, Kasmintan Schrader, Nancy N. Baxter, Andreas Laupacis, Jordan Lerner-Ellis, Raymond Kim, Yvonne Bombard

    Diterbitkan 2023-01-01
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  10. 10
    P538: Curious but cautious: Patients’ preferences for all types of clinically actionable genomic incidental results

    P538: Curious but cautious: Patients’ preferences for all types of clinically actionable genomic incidental results oleh Salma Shickh, Rita Kodida, Chloe Mighton, Marc Clausen, Emma Reble, Jordan Sam, Sonya Grewal, Seema Panchal, Melyssa Aronson, Susan Armel, Tracy Graham, Christine Elser, Andrea Eisen, June Carroll, Emily Glogowski, Kasmintan Schrader, Kevin Thorpe, Jordan Lerner-Ellis, Raymond Kim, Yvonne Bombard

    Diterbitkan 2024-01-01
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  11. 11
    P862: How to conduct equitable genetics research to include underserved populations: A systematic review of best practices

    P862: How to conduct equitable genetics research to include underserved populations: A systematic review of best practices oleh Vernie Aguda, Sonya Grewal, Arielle Nsenga, Daena Hirjikaka, Saumeh Saeedi, Emma Reble, Marc Clausen, Charles Law, Francine Holness, Kristal John, Tracy Reece, Aaron Pollett, Aisha Lofters, Ambreen Sayani, Andrea Eisen, David Lightfoot, Harriet Feilotter, Jordan Lerner-Ellis, Melyssa Aronson, Nav Persaud, Yvonne Bombard

    Diterbitkan 2024-01-01
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  12. 12
    P406: Partnering with patients to explore the psychosocial and socioeconomic impacts of hereditary cancer syndromes

    P406: Partnering with patients to explore the psychosocial and socioeconomic impacts of hereditary cancer syndromes oleh Jordan Sam, Holly Etchegary, Marc Clausen, Derrick Bishop, Julee Pauling, Claudia Pavao, Catriona Remocker, Teresa Tiano, Angelina Tilley, Chloe Mighton, Sepideh Rajeziesfahani, Ridhi Gopalakrishnan, Melyssa Aronson, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Sevtap Savas, Sophie Sun, Kevin Thorpe, Kasmintan Schrader, Yvonne Bombard

    Diterbitkan 2023-01-01
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  13. 13
    Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol

    Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol oleh Stephanie Best, Melissa Martyn, Ling Lee, Zornitza Stark, Ilias Goranitis, Marc Clausen, Yvonne Bombard, Martin Delatycki, Lilian Downie, Sebastian Lunke, Elly Lynch, Belinda Chong, Lisette Curnow, Fiona Lynch, Sophie E Bouffler, Ivan Macciocca, Giulia McCorkell, Justine E Marum, Danya F Vears, Clara L Gaff

    Diterbitkan 2023-06-01
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  14. 14
    P375: Fragmented systems of care: An overview of Canadian health system care models for hereditary cancer syndromes

    P375: Fragmented systems of care: An overview of Canadian health system care models for hereditary cancer syndromes oleh Jordan Sam, Carly Butkowsky, Marc Clausen, Chloe Mighton, Sepideh Rajeziesfahani, Ridhi Gopalakrishnan, Melyssa Aronson, Derrick Bishop, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Julee Pauling, Claudia Pavao, Catriona Remocker, Sevtap Savas, Sophie Sun, Teresa Tiano, Angelina Tilley, Kevin Thorpe, Kasmintan Schrader, Holly Etchegary, Yvonne Bombard

    Diterbitkan 2023-01-01
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  15. 15
    P892: “Should I let them know I have this?”: Concerns and experiences of genetic discrimination amongst individuals with hereditary cancer syndromes

    P892: “Should I let them know I have this?”: Concerns and experiences of genetic discrimination amongst individuals with hereditary cancer syndromes oleh Ridhi Gopalakrishnan, Emma Reble, Jordan Sam, Carly Butkowsky, Marc Clausen, Sepideh Rajeziesfahani, Brooklyn Sparkes, Vernie Aguda, Melyssa Aronson, Derrick Bishop, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Chloe Mighton, Julee Pauling, Claudia Pavao, Petros Pechlivanoglou, Catriona Remocker, Sevtap Savas, Sophie Sun, Teresa Tiano, Angelina Tilley, Kevin Thorpe, Kasmintan Schrader, Holly Etchegary, Yvonne Bombard

    Diterbitkan 2024-01-01
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  16. 16
    P881: Revealing the hidden costs: Exploring the financial toxicity of hereditary cancer syndromes

    P881: Revealing the hidden costs: Exploring the financial toxicity of hereditary cancer syndromes oleh Sepideh Rajeziesfahani, Jordan Sam, Carly Butkowsky, Emma Reble, Marc Clausen, Brooklyn Sparkes, Ridhi Gopalakrishnan, Vernie Aguda, Melyssa Aronson, Derrick Bishop, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Chloe Mighton, Julee Pauling, Claudia Pavao, Petros Pechlivanoglou, Catriona Remocker, Sevtap Savas, Sophie Sun, Teresa Tiano, Angelina Tilley, Kevin Thorpe, Kasmintan Schrader, Yvonne Bombard, Holly Etchegary

    Diterbitkan 2024-01-01
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  17. 17
    P523: Returning all clinically relevant findings from genomic sequencing: Preliminary results from the incidental genomics RCT

    P523: Returning all clinically relevant findings from genomic sequencing: Preliminary results from the incidental genomics RCT oleh Yvonne Bombard, Chloe Mighton, Salma Shickh, Marc Clausen, Rita Kodida, Emma Reble, Jordan Sam, Sonya Grewal, Seema Panchal, Melyssa Aronson, Susan Armel, Tracy Graham, Nicole Forster, Jose-Mario Capo-Chichi, Elena Greenfeld, Abdul Noor, Iris Cohn, Chantal Morel, Christine Elser, Andrea Eisen, June Carroll, Emily Glogowski, Kasmintan Schrader, Jordan Lerner-Ellis, Raymond Kim, Kevin Thorpe

    Diterbitkan 2024-01-01
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  18. 18
    P867: “I worry I don’t have control”: The psychosocial impacts of living with a hereditary cancer syndrome

    P867: “I worry I don’t have control”: The psychosocial impacts of living with a hereditary cancer syndrome oleh Jordan Sam, Brooklyn Sparkes, Marc Clausen, Carly Butkowsky, Emma Reble, Sepideh Rajeziesfahani, Ridhi Gopalakrishnan, Vernie Aguda, Melyssa Aronson, Derrick Bishop, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Chloe Mighton, Julee Pauling, Claudia Pavao, Petros Pechlivanoglou, Catriona Remocker, Sevtap Savas, Sophie Sun, Teresa Tiano, Angelina Tilley, Kevin Thorpe, Kasmintan Schrader, Yvonne Bombard, Holly Etchegary

    Diterbitkan 2024-01-01
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  19. 19
    P555: Clinical utility returning of all types of medically relevant genomic sequencing findings: An observational study

    P555: Clinical utility returning of all types of medically relevant genomic sequencing findings: An observational study oleh Chloe Mighton, Rita Kodida, Salma Shickh, Marc Clausen, Emma Reble, Jordan Sam, Sonya Grewal, Seema Panchal, Melyssa Aronson, Susan Armel, Tracy Graham, Nicole Forster, Jose-Mario Capo-Chichi, Elena Greenfeld, Abdul Noor, Iris Cohn, Chantal Morel, Christine Elser, Andrea Eisen, June Carroll, Emily Glogowski, Kasmintan Schrader, Kelvin Chan, Kevin Thorpe, Jordan Lerner-Ellis, Raymond Kim, Yvonne Bombard

    Diterbitkan 2024-01-01
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  20. 20
    P553: How do patients with hereditary cancer syndromes navigate the healthcare system? A qualitative comparative study across Canada

    P553: How do patients with hereditary cancer syndromes navigate the healthcare system? A qualitative comparative study across Canada oleh Carly Butkowsky, Jordan Sam, Emma Reble, Marc Clausen, Sepideh Rajeziesfahani, Brooklyn Sparkes, Ridhi Gopalakrishnan, Vernie Aguda, Melyssa Aronson, June Carroll, Derrick Bishop, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Chloe Mighton, Julee Pauling, Claudia Pavao, Petros Pechlivanoglou, Catriona Remocker, Sevtap Savas, Sophie Sun, Teresa Tiano, Angelina Tilley, Kevin Thorpe, Kasmintan Schrader, Holly Etchegary, Yvonne Bombard

    Diterbitkan 2024-01-01
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