Genetics patients’ perspectives on clinical genomic testing

The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases

(2012) William A. Gahl et al.   GENETICS IN MEDICINE

Stakeholder assessment of the evidence for cancer genomic tests: insights from three case studies

(2012) Patricia A. Deverka et al.   GENETICS IN MEDICINE

Exploring concordance and discordance for return of incidental findings from clinical sequencing

(2012) Robert C. Green et al.   GENETICS IN MEDICINE

Perception of Direct-To-Consumer Genetic Testing and Direct-To-Consumer Advertising of Genetic Tests among Members of a Large Managed Care Organization

(2012) Alanna Kulchak Rahm et al.   Journal of Genetic Counseling

Downsizing genomic medicine: Approaching the ethical complexity of whole-genome sequencing by starting small

(2011) Richard R Sharp   GENETICS IN MEDICINE

Effect of Direct-to-Consumer Genomewide Profiling to Assess Disease Risk

(2011) Cinnamon S. Bloss et al.   NEW ENGLAND JOURNAL OF MEDICINE

Motivations and Perceptions of Early Adopters of Personalized Genomics: Perspectives from Research Participants

(2011) S.E. Gollust et al.   Public Health Genomics

Making a definitive diagnosis: Successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

(2010) Elizabeth A Worthey et al.   GENETICS IN MEDICINE

A timely arrival for genomic medicine

(2010) Alan N Mayer et al.   GENETICS IN MEDICINE

The personal genome—the future of personalised medicine?

(2010) Nilesh J Samani et al.   LANCET

Effect of genome-wide association studies, direct-to-consumer genetic testing, and high-speed sequencing technologies on predictive genetic counselling for cancer risk

(2010) Michael R Speicher et al.   LANCET ONCOLOGY

Taking DNA from the dead

(2010) Amy L. McGuire et al.   NATURE REVIEWS GENETICS

Individual Genomes on the Horizon

(2010) Richard P. Lifton   NEW ENGLAND JOURNAL OF MEDICINE

Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy

(2010) James R. Lupski et al.   NEW ENGLAND JOURNAL OF MEDICINE

Personal genomics and individual identities: motivations and moral imperatives of early users

(2010) Michelle L. McGowan et al.   NEW GENETICS AND SOCIETY

Personal genome research : what should the participant be told?

(2010) Amy L. McGuire et al.   TRENDS IN GENETICS

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

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

Are Social Networkers and Genome Testers One in the Same? The Limitations of Public Opinion Research for Guiding Clinical Practice

(2009) Michelle L. McGowan et al.   AMERICAN JOURNAL OF BIOETHICS

How Attitudes Research Contributes to Overoptimistic Expectations of Personal Genome Testing

(2009) Eline Bunnik et al.   AMERICAN JOURNAL OF BIOETHICS

Social Networkers' Attitudes Toward Direct-to-Consumer Personal Genome Testing

(2009) Amy L. McGuire et al.   AMERICAN JOURNAL OF BIOETHICS

“Personalizing” academic medicine: opportunities and challenges in implementing genomic profiling

(2009) David J. Tweardy et al.   Translational Research

Comparing test-specific distress of susceptibility versus deterministic genetic testing for Alzheimer's disease

(2008) Michael R. Cassidy et al.   Alzheimers & Dementia

An Unwelcome Side Effect of Direct-to-Consumer Personal Genome Testing

(2008) Amy L. McGuire et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Misdirected precaution

(2008) Barbara Prainsack et al.   NATURE