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Jennifer B McCormick

Showing results (31-40 of 74) with videos related to

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Plos One|April 8, 2014
Challenges in translational research: the views of addiction scientistsJenny E Ostergren, Rachel R Hammer, Molly J Dingel, et al.
Journal of Autism and Developmental Disorders|March 24, 2019
Parent Perspectives Towards Genetic and Epigenetic Testing for Autism Spectrum DisorderKayla E Wagner, Jennifer B McCormick, Sarah Barns, et al.
BMC Medical Ethics|July 25, 2013
Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trialsAdam Nishimura, Jantey Carey, Patricia J Erwin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2013
Preserving personal autonomy in a genomic testing eraNoralane M Lindor, Kiley J Johnson, Jennifer B McCormick, et al.
Public Health Genomics|March 21, 2015
Public perceptions of disease severity but not actionability correlate with interest in receiving genomic results: nonalignment with current trends in practiceKristi D Graves, Pamela S Sinicrope, Jennifer B McCormick, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 18, 2019
Pancreatic cancer and melanoma related perceptions and behaviors following disclosure of CDKN2A variant status as a research resultEmma R Leof, Xuan Zhu, Kari G Rabe, et al.
Public Health Genomics|April 19, 2019
Psychological Impact of Learning CDKN2A Variant Status as a Genetic Research ResultXuan Zhu, Emma R Leof, Kari G Rabe, et al.
Public Health Genomics|May 13, 2020
At a Moment's Notice: Community Advisory Board Perspectives on Biobank Communication to Supplement Broad ConsentKaren M Meagher, Susan H Curtis, Kylie O Gamm, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|February 21, 2013
Incorporating expert terminology and disease risk factors into consumer health vocabulariesMichael Seedorff, Kevin J Peterson, Laurie A Nelsen, et al.
Journal of Personalized Medicine|September 29, 2020
"They're Not Going to Do Nothing for Me": Research Participants' Attitudes towards Elective Genetic CounselingErica J Sutton, Annika T Beck, Kylie O Gamm, et al.
Pageof 8

Showing results (31-40 of 74) with videos related to

Sort By:
Pageof 8
Plos One|April 8, 2014
Challenges in translational research: the views of addiction scientistsJenny E Ostergren, Rachel R Hammer, Molly J Dingel, et al.
Journal of Autism and Developmental Disorders|March 24, 2019
Parent Perspectives Towards Genetic and Epigenetic Testing for Autism Spectrum DisorderKayla E Wagner, Jennifer B McCormick, Sarah Barns, et al.
BMC Medical Ethics|July 25, 2013
Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trialsAdam Nishimura, Jantey Carey, Patricia J Erwin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2013
Preserving personal autonomy in a genomic testing eraNoralane M Lindor, Kiley J Johnson, Jennifer B McCormick, et al.
Public Health Genomics|March 21, 2015
Public perceptions of disease severity but not actionability correlate with interest in receiving genomic results: nonalignment with current trends in practiceKristi D Graves, Pamela S Sinicrope, Jennifer B McCormick, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 18, 2019
Pancreatic cancer and melanoma related perceptions and behaviors following disclosure of CDKN2A variant status as a research resultEmma R Leof, Xuan Zhu, Kari G Rabe, et al.
Public Health Genomics|April 19, 2019
Psychological Impact of Learning CDKN2A Variant Status as a Genetic Research ResultXuan Zhu, Emma R Leof, Kari G Rabe, et al.
Public Health Genomics|May 13, 2020
At a Moment's Notice: Community Advisory Board Perspectives on Biobank Communication to Supplement Broad ConsentKaren M Meagher, Susan H Curtis, Kylie O Gamm, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|February 21, 2013
Incorporating expert terminology and disease risk factors into consumer health vocabulariesMichael Seedorff, Kevin J Peterson, Laurie A Nelsen, et al.
Journal of Personalized Medicine|September 29, 2020
"They're Not Going to Do Nothing for Me": Research Participants' Attitudes towards Elective Genetic CounselingErica J Sutton, Annika T Beck, Kylie O Gamm, et al.
Pageof 8