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Marsha Michie

Showing results (21-30 of 55) with videos related to

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Journal of Empirical Research on Human Research Ethics : JERHRE|June 18, 2011
"If I could in a small way help": motivations for and beliefs about sample donation for genetic researchMarsha Michie, Gail Henderson, Joanne Garrett, et al.
The American Journal of Bioethics : AJOB|September 29, 2018
Weaponizing Hope: Sources of Hope, Unrealistic Optimism, and DenialMarsha Michie, Megan Allyse, Katie A Stoll, et al.
American Journal on Intellectual and Developmental Disabilities|December 27, 2019
Evaluating the Risks and Benefits of Genetic and Pharmacologic Interventions for Down Syndrome: Views of ParentsKirsten A Riggan, Christina Nyquist, Marsha Michie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Conflicts of interest in genetic counseling: persistent underlying questionsKatie A Stoll, Amanda Mackison, Megan A Allyse, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2017
Conflicts of interest in genetic counseling: acknowledging and acceptingKatie A Stoll, Amanda Mackison, Megan A Allyse, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 1, 2012
Am I a control?: Genotype-driven research recruitment and self-understandings of study participantsMarsha Michie, R Jean Cadigan, Gail Henderson, et al.
Journal of Intellectual Disabilities : JOID|May 25, 2023
Views of parents of children with Down syndrome on Alzheimer's disease vaccinationSarah Batbold, Gabrielle Cummings, Kirsten A Riggan, et al.
Annual Review of Genomics and Human Genetics|September 1, 2015
Noninvasive Prenatal Genetic Testing: Current and Emerging Ethical, Legal, and Social IssuesMollie A Minear, Stephanie Alessi, Megan Allyse, et al.
Cleveland Clinic Journal of Medicine|March 1, 2023
The cost of 'free': Advising patients about sponsored genetic testingStephanie Allison Larson, Joseph Liu, David Flannery, et al.
AJOB Empirical Bioethics|May 2, 2015
"Don't Want No Risk and Don't Want No Problems": Public Understandings of the Risks and Benefits of Non-Invasive Prenatal Testing in the United StatesMegan Allyse, Lauren Carter Sayres, Taylor Goodspeed, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
Journal of Empirical Research on Human Research Ethics : JERHRE|June 18, 2011
"If I could in a small way help": motivations for and beliefs about sample donation for genetic researchMarsha Michie, Gail Henderson, Joanne Garrett, et al.
The American Journal of Bioethics : AJOB|September 29, 2018
Weaponizing Hope: Sources of Hope, Unrealistic Optimism, and DenialMarsha Michie, Megan Allyse, Katie A Stoll, et al.
American Journal on Intellectual and Developmental Disabilities|December 27, 2019
Evaluating the Risks and Benefits of Genetic and Pharmacologic Interventions for Down Syndrome: Views of ParentsKirsten A Riggan, Christina Nyquist, Marsha Michie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Conflicts of interest in genetic counseling: persistent underlying questionsKatie A Stoll, Amanda Mackison, Megan A Allyse, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2017
Conflicts of interest in genetic counseling: acknowledging and acceptingKatie A Stoll, Amanda Mackison, Megan A Allyse, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 1, 2012
Am I a control?: Genotype-driven research recruitment and self-understandings of study participantsMarsha Michie, R Jean Cadigan, Gail Henderson, et al.
Journal of Intellectual Disabilities : JOID|May 25, 2023
Views of parents of children with Down syndrome on Alzheimer's disease vaccinationSarah Batbold, Gabrielle Cummings, Kirsten A Riggan, et al.
Annual Review of Genomics and Human Genetics|September 1, 2015
Noninvasive Prenatal Genetic Testing: Current and Emerging Ethical, Legal, and Social IssuesMollie A Minear, Stephanie Alessi, Megan Allyse, et al.
Cleveland Clinic Journal of Medicine|March 1, 2023
The cost of 'free': Advising patients about sponsored genetic testingStephanie Allison Larson, Joseph Liu, David Flannery, et al.
AJOB Empirical Bioethics|May 2, 2015
"Don't Want No Risk and Don't Want No Problems": Public Understandings of the Risks and Benefits of Non-Invasive Prenatal Testing in the United StatesMegan Allyse, Lauren Carter Sayres, Taylor Goodspeed, et al.
Pageof 6