CLIA-tested genetic variants on commercial SNP arrays: Potential for incidental findings in genome-wide association studies

An Open Access Database of Genome-wide Association Results

(2009) Andrew D Johnson et al.   BMC Medical Genetics

Single-Nucleotide Polymorphism Bioinformatics

(2009) Andrew D. Johnson   Circulation-Cardiovascular Genetics

The SPINK1 N34S variant is associated with acute pancreatitis

(2009) Derek A. OʼReilly et al.   EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY

Direct to consumer genetic testing: Avoiding a culture war

(2009) James P Evans et al.   GENETICS IN MEDICINE

A Critical Appraisal of the Scientific Basis of Commercial Genomic Profiles Used to Assess Health Risks and Personalize Health Interventions

(2008) A. Cecile J.W. Janssens et al.   AMERICAN JOURNAL OF HUMAN GENETICS

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

(2008) A. D. Johnson et al.   BIOINFORMATICS

A HapMap harvest of insights into the genetics of common disease

(2008) Teri A. Manolio et al.   JOURNAL OF CLINICAL INVESTIGATION

Understanding Incidental Findings in the Context of Genetics and Genomics

(2008) Mildred K. Cho   JOURNAL OF LAW MEDICINE & ETHICS

Genomic Research and Incidental Findings

(2008) Brian Van Ness   JOURNAL OF LAW MEDICINE & ETHICS

Managing Incidental Findings in Human Subjects Research: Analysis and Recommendations

(2008) Susan M. Wolf et al.   JOURNAL OF LAW MEDICINE & ETHICS

Keeping Pace with the Times — The Genetic Information Nondiscrimination Act of 2008

(2008) Kathy L. Hudson et al.   NEW ENGLAND JOURNAL OF MEDICINE