Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Kathy Hudson

Showing results (21-30 of 29) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 29 results.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 15, 2008
Ethical implications of including children in a large biobank for genetic-epidemiologic research: a qualitative study of public opinionDavid Kaufman, Gail Geller, Lisa Leroy, et al.
The American Journal of Bioethics : AJOB|December 9, 2008
Public expectations for return of results from large-cohort genetic researchJuli Murphy, Joan Scott, David Kaufman, et al.
American Journal of Public Health|October 17, 2009
Public perspectives on informed consent for biobankingJuli Murphy, Joan Scott, David Kaufman, et al.
Academic Radiology|October 15, 2013
Comparative analysis of data collection methods for individualized modeling of radiologists' visual similarity judgments in mammogramsGeorgia Tourassi, Hong-Jun Yoon, Songhua Xu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2008
Confidentiality, privacy, and security of genetic and genomic test information in electronic health records: points to considerAmy L McGuire, Rebecca Fisher, Paul Cusenza, et al.
Fertility and Sterility|June 14, 2005
Opinions about new reproductive genetic technologies: hopes and fears for our genetic futureAndrea L Kalfoglou, Teresa Doksum, Barbara Bernhardt, et al.
Nucleic Acids Research|November 30, 2012
The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparencyWendy S Rubinstein, Donna R Maglott, Jennifer M Lee, et al.
American Journal of Epidemiology|March 14, 2012
New models for large prospective studies: is there a better way?Teri A Manolio, Brenda K Weis, Catherine C Cowie, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|June 13, 2008
Managing incidental findings in human subjects research: analysis and recommendationsSusan M Wolf, Frances P Lawrenz, Charles A Nelson, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 15, 2008
Ethical implications of including children in a large biobank for genetic-epidemiologic research: a qualitative study of public opinionDavid Kaufman, Gail Geller, Lisa Leroy, et al.
The American Journal of Bioethics : AJOB|December 9, 2008
Public expectations for return of results from large-cohort genetic researchJuli Murphy, Joan Scott, David Kaufman, et al.
American Journal of Public Health|October 17, 2009
Public perspectives on informed consent for biobankingJuli Murphy, Joan Scott, David Kaufman, et al.
Academic Radiology|October 15, 2013
Comparative analysis of data collection methods for individualized modeling of radiologists' visual similarity judgments in mammogramsGeorgia Tourassi, Hong-Jun Yoon, Songhua Xu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2008
Confidentiality, privacy, and security of genetic and genomic test information in electronic health records: points to considerAmy L McGuire, Rebecca Fisher, Paul Cusenza, et al.
Fertility and Sterility|June 14, 2005
Opinions about new reproductive genetic technologies: hopes and fears for our genetic futureAndrea L Kalfoglou, Teresa Doksum, Barbara Bernhardt, et al.
Nucleic Acids Research|November 30, 2012
The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparencyWendy S Rubinstein, Donna R Maglott, Jennifer M Lee, et al.
American Journal of Epidemiology|March 14, 2012
New models for large prospective studies: is there a better way?Teri A Manolio, Brenda K Weis, Catherine C Cowie, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|June 13, 2008
Managing incidental findings in human subjects research: analysis and recommendationsSusan M Wolf, Frances P Lawrenz, Charles A Nelson, et al.
Pageof 3