The Fiduciary Relationship Model for Managing Clinical Genomic “Incidental” Findings

Currents in Contemporary Bioethics

(2015) Mark A. Rothstein   JOURNAL OF LAW MEDICINE & ETHICS

Individualized Medicine from Prewomb to Tomb

(2014) Eric J. Topol   CELL

Huntington Disease: Who Seeks Presymptomatic Genetic Testing, Why and What are the Outcomes?

(2014) Tracey M. Scuffham et al.   Journal of Genetic Counseling

Diagnostic Clinical Genome and Exome Sequencing

(2014) Leslie G. Biesecker et al.   NEW ENGLAND JOURNAL OF MEDICINE

Genomic Incidental Findings: Reducing the Burden to Be Fair

(2013) Velizara Anastasova et al.   AMERICAN JOURNAL OF BIOETHICS

Effect of Knowledge of APOE Genotype on Subjective and Objective Memory Performance in Healthy Older Adults

(2013) Tara T. Lineweaver et al.   AMERICAN JOURNAL OF PSYCHIATRY

Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer in Women: U.S. Preventive Services Task Force Recommendation Statement

(2013) Virginia A. Moyer   ANNALS OF INTERNAL MEDICINE

Genomics and epigenomics: new promises of personalized medicine for cancer patients

(2013) M.-R. Schweiger et al.   Briefings in Functional Genomics

We screen newborns, don’t we?: realizing the promise of public health genomics

(2013) James P. Evans et al.   GENETICS IN MEDICINE

Recommendations for returning genomic incidental findings? We need to talk!

(2013) Wylie Burke et al.   GENETICS IN MEDICINE

Managing incidental genomic findings: legal obligations of clinicians

(2013) Ellen Wright Clayton et al.   GENETICS IN MEDICINE

Incidental findings in clinical genomics: a clarification

(2013)   GENETICS IN MEDICINE

Minimizing liability risks under the ACMG recommendations for reporting incidental findings in clinical exome and genome sequencing

(2013) Barbara J. Evans   GENETICS IN MEDICINE

Points to consider for informed consent for genome/exome sequencing

(2013)   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

Ethical, legal and social implications of incorporating genomic information into electronic health records

(2013) Ribhi Hazin et al.   GENETICS IN MEDICINE

Genetics of healthy aging and longevity

(2013) Angela R. Brooks-Wilson   HUMAN GENETICS

Mandatory Extended Searches in All Genome Sequencing

(2013) Lainie Friedman Ross et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Return of Secondary Genomic Findings vs Patient Autonomy

(2013) Robert Klitzman et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Reporting Genomic Sequencing Results to Ordering Clinicians

(2013) Robert C. Green et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Patient Autonomy and Incidental Findings in Clinical Genomics

(2013) S. M. Wolf et al.   SCIENCE

Ethics and Genomic Incidental Findings

(2013) A. L. McGuire et al.   SCIENCE

Not-so-incidental findings: the ACMG recommendations on the reporting of incidental findings in clinical whole genome and whole exome sequencing

(2013) Megan Allyse et al.   TRENDS IN BIOTECHNOLOGY

Epigenetics: A New Link Toward Understanding Human Disease and Drug Response

(2012) A M Cressman et al.   CLINICAL PHARMACOLOGY & THERAPEUTICS

Chapter 11: Challenges in and Principles for Conducting Systematic Reviews of Genetic Tests used as Predictive Indicators

(2012) Daniel E. Jonas et al.   JOURNAL OF GENERAL INTERNAL MEDICINE

The expanding scope of DNA sequencing

(2012) Jay Shendure et al.   NATURE BIOTECHNOLOGY

Pharmacogenomics in clinical practice and drug development

(2012) Andrew R Harper et al.   NATURE BIOTECHNOLOGY

Reconsidering the Criteria for Evaluating Proposed Screening Programs: Reflections From 4 Current and Former Members of the U.S. Preventive Services Task Force

(2011) Russell Harris et al.   EPIDEMIOLOGIC REVIEWS

Studying the epigenome using next generation sequencing

(2011) C. S. Ku et al.   JOURNAL OF MEDICAL GENETICS

Charting a course for genomic medicine from base pairs to bedside

(2011) Eric D. Green et al.   NATURE

Exclusion of Genetic Information From the Medical Record

(2010) Robert Klitzman   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

(2010) Tom Walsh et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Disclosure ofAPOEGenotype for Risk of Alzheimer's Disease

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

Putting the Genetic Information Nondiscrimination Act in context

(2008) Mark A Rothstein   GENETICS IN MEDICINE