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Barbara A Bernhardt

Showing results (41-50 of 75) with videos related to

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Journal of Genetic Counseling|December 20, 2011
"It's not like judgment day": public understanding of and reactions to personalized genomic risk informationErynn S Gordon, Georgia Griffin, Lisa Wawak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 16, 2009
Distress and burnout among genetic service providersBarbara A Bernhardt, Cynda H Rushton, Joseph Carrese, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2004
Perceptions of genetic discrimination among at-risk relatives of colorectal cancer patientsKira A Apse, Barbara B Biesecker, Francis M Giardiello, et al.
Journal of Genetic Counseling|September 17, 2013
A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practiceMarian Reiff, Rebecca Mueller, Surabhi Mulchandani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2012
Women's experiences receiving abnormal prenatal chromosomal microarray testing resultsBarbara A Bernhardt, Danielle Soucier, Karen Hanson, et al.
Personalized Medicine|June 25, 2013
Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physiciansBarbara A Bernhardt, Cara Zayac, Erynn S Gordon, et al.
Personalized Medicine|October 3, 2017
How do providers discuss the results of pediatric exome sequencing with families?Sarah A Walser, Allison Werner-Lin, Rebecca Mueller, et al.
Community Genetics|August 23, 2005
The quality of media reports on discoveries related to human genetic diseasesNeil A Holtzman, Barbara A Bernhardt, Eliza Mountcastle-Shah, et al.
Journal of Genetic Counseling|July 13, 2013
Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consentBrooke L Levenseller, Danielle J Soucier, Victoria A Miller, et al.
American Journal of Medical Genetics. Part A|February 16, 2018
Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable resultsAllison Werner-Lin, Lori Zaspel, Mae Carlson, et al.
Pageof 8

Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Journal of Genetic Counseling|December 20, 2011
"It's not like judgment day": public understanding of and reactions to personalized genomic risk informationErynn S Gordon, Georgia Griffin, Lisa Wawak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 16, 2009
Distress and burnout among genetic service providersBarbara A Bernhardt, Cynda H Rushton, Joseph Carrese, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2004
Perceptions of genetic discrimination among at-risk relatives of colorectal cancer patientsKira A Apse, Barbara B Biesecker, Francis M Giardiello, et al.
Journal of Genetic Counseling|September 17, 2013
A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practiceMarian Reiff, Rebecca Mueller, Surabhi Mulchandani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2012
Women's experiences receiving abnormal prenatal chromosomal microarray testing resultsBarbara A Bernhardt, Danielle Soucier, Karen Hanson, et al.
Personalized Medicine|June 25, 2013
Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physiciansBarbara A Bernhardt, Cara Zayac, Erynn S Gordon, et al.
Personalized Medicine|October 3, 2017
How do providers discuss the results of pediatric exome sequencing with families?Sarah A Walser, Allison Werner-Lin, Rebecca Mueller, et al.
Community Genetics|August 23, 2005
The quality of media reports on discoveries related to human genetic diseasesNeil A Holtzman, Barbara A Bernhardt, Eliza Mountcastle-Shah, et al.
Journal of Genetic Counseling|July 13, 2013
Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consentBrooke L Levenseller, Danielle J Soucier, Victoria A Miller, et al.
American Journal of Medical Genetics. Part A|February 16, 2018
Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable resultsAllison Werner-Lin, Lori Zaspel, Mae Carlson, et al.
Pageof 8