no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
A Family-Centered Model for Sharing Genetic Risk
|
Daly, Mary B. |
|
2015 |
43 |
3 |
p. 545-551 |
article |
2 |
Calendar of Events
|
|
|
2015 |
43 |
3 |
p. 666 |
article |
3 |
Canadian Research Ethics Board Leadership Attitudes to the Return of Genetic Research Results to Individuals and Their Families
|
Fernandez, Conrad V. |
|
2015 |
43 |
3 |
p. 514-522 |
article |
4 |
Certificates of Confidentiality: Protecting Human Subject Research Data in Law and Practice
|
Wolf, Leslie E. |
|
2015 |
43 |
3 |
p. 594-609 |
article |
5 |
Considerations for Returning Research Results to Culturally Diverse Participants and Families of Decedents
|
Garrison, Nanibaa' A. |
|
2015 |
43 |
3 |
p. 569-575 |
article |
6 |
Considering Actionability at the Participant's Research Setting Level for Anticipatable Incidental Findings from Clinical Research
|
Ortiz-Osorno, Alberto (Betto) |
|
2015 |
43 |
3 |
p. 619-632 |
article |
7 |
Disclosing Secondary Findings from Pediatric Sequencing to Families: Considering the “Benefit to Families”
|
Wilfond, Benjamin S. |
|
2015 |
43 |
3 |
p. 552-558 |
article |
8 |
Ethical Integrity in Health Care Organizations: Currents in Contemporary Bioethics
|
Mantel, Jessica |
|
2015 |
43 |
3 |
p. 661-665 |
article |
9 |
Funding the Costs of Disease Outbreaks Caused by Non-Vaccination
|
Moser, Charlotte A. |
|
2015 |
43 |
3 |
p. 633-647 |
article |
10 |
How Agencies Market Egg Donation on the Internet: A Qualitative Study
|
Keehn, Jason |
|
2015 |
43 |
3 |
p. 610-618 |
article |
11 |
How Much Control Do Children and Adolescents Have over Genomic Testing, Parental Access to Their Results, and Parental Communication of Those Results to Others?
|
Clayton, Ellen Wright |
|
2015 |
43 |
3 |
p. 538-544 |
article |
12 |
International Policies on Sharing Genomic Research Results with Relatives: Approaches to Balancing Privacy with Access
|
Branum, Rebecca |
|
2015 |
43 |
3 |
p. 576-593 |
article |
13 |
Mapping the Ethics of Translational Genomics: Situating Return of Results and Navigating the Research-Clinical Divide
|
Wolf, Susan M. |
|
2015 |
43 |
3 |
p. 486-501 |
article |
14 |
Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their Death
|
Amendola, Laura M. |
|
2015 |
43 |
3 |
p. 476-485 |
article |
15 |
Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject
|
Scollon, Sarah |
|
2015 |
43 |
3 |
p. 529-537 |
article |
16 |
Physician Dismissal of Families Who Refuse Vaccination: An Ethical Assessment
|
Diekema, Douglas S. |
|
2015 |
43 |
3 |
p. 654-660 |
article |
17 |
Preferences regarding Return of Genomic Results to Relatives of Research Participants, Including after Participant Death: Empirical Results from a Cancer Biobank
|
Breitkopf, Carmen Radecki |
|
2015 |
43 |
3 |
p. 464-475 |
article |
18 |
Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations
|
Wolf, Susan M. |
|
2015 |
43 |
3 |
p. 440-463 |
article |
19 |
Returning a Research Participant's Genomic Results to Relatives: Perspectives from Managers of Two Distinct Research Biobanks
|
Petersen, Gloria M. |
|
2015 |
43 |
3 |
p. 523-528 |
article |
20 |
Return of Genetic Research Results to Participants and Families: IRB Perspectives and Roles
|
Beskow, Laura M. |
|
2015 |
43 |
3 |
p. 502-513 |
article |
21 |
Return of Research Results: What about the Family?
|
Wolf, Susan M. |
|
2015 |
43 |
3 |
p. 437-439 |
article |
22 |
Return of Results from Research Using Newborn Screening Dried Blood Samples
|
Lewis, Michelle Huckaby |
|
2015 |
43 |
3 |
p. 559-568 |
article |
23 |
The Pediatrician's Dilemma: Refusing the Refusers of Infant Vaccines
|
Block, Stan L. |
|
2015 |
43 |
3 |
p. 648-653 |
article |