The Development of a Preference-Setting Model for the Return of Individual Genomic Research Results

Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children’s Hospital Gene Partnership Informed Cohort Oversight Board

(2014) Ingrid A. Holm et al.   GENETICS IN MEDICINE

Parents' Preferences for Return of Results in Pediatric Genomic Research

(2014) S.I. Ziniel et al.   Public Health Genomics

Self-guided management of exome and whole-genome sequencing results: changing the results return model

(2013) Joon-Ho Yu et al.   GENETICS IN MEDICINE

Return of incidental findings in genomic medicine: measuring what patients value—development of an instrument to measure preferences for information from next-generation testing (IMPRINT)

(2013) Caroline Savage Bennette et al.   GENETICS IN MEDICINE

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

(2013) Robert C. Green et al.   GENETICS IN MEDICINE

“I want to know what's in Pandora's box”: Comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing

(2012) Anne Townsend et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Population studies: return of research results and incidental findings Policy Statement

(2012) Bartha Maria Knoppers et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The beliefs, motivations and expectations of parents who have enrolled their children in a genetic biorepository

(2012) Erin D. Harris et al.   GENETICS IN MEDICINE

Broadening research consent in the era of genome-informed medicine

(2012) Courtney Kronenthal et al.   GENETICS IN MEDICINE

Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study

(2012) Juli Murphy Bollinger et al.   GENETICS IN MEDICINE

The past, present and future of the debate over return of research results and incidental findings

(2012) Susan M. Wolf   GENETICS IN MEDICINE

Managing incidental findings and research results in genomic research involving biobanks and archived data sets

(2012) Susan M. Wolf et al.   GENETICS IN MEDICINE

Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time

(2011) Jonathan S Berg et al.   GENETICS IN MEDICINE

Ethical and Practical Guidelines for Reporting Genetic Research Results to Study Participants

(2010) Richard R. Fabsitz et al.   Circulation-Cardiovascular Genetics

Multidimensional Results Reporting to Participants in Genomic Studies: Getting It Right

(2010) I. S. Kohane et al.   Science Translational Medicine

Health Behavior Changes After Genetic Risk Assessment for Alzheimer Disease: The REVEAL Study

(2009) Serena Chao et al.   ALZHEIMER DISEASE & ASSOCIATED DISORDERS

The Scientific Foundation for Personal Genomics: Recommendations from a National Institutes of Health–Centers for Disease Control and Prevention Multidisciplinary Workshop

(2009) Muin J Khoury et al.   GENETICS IN MEDICINE

Personal utility and genomic information: Look before you leap

(2009) Scott D Grosse et al.   GENETICS IN MEDICINE

Evaluating the utility of personal genomic information

(2009) Morris W Foster et al.   GENETICS IN MEDICINE

Disclosure ofAPOEGenotype for Risk of Alzheimer's Disease

(2009) Robert C. Green et al.   NEW ENGLAND JOURNAL OF MEDICINE