Incidental copy-number variants identified by routine genome testing in a clinical population
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Incidental copy-number variants identified by routine genome testing in a clinical population
Authors
Keywords
-
Journal
GENETICS IN MEDICINE
Volume 15, Issue 1, Pages 45-54
Publisher
Springer Nature
Online
2012-08-09
DOI
10.1038/gim.2012.95
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Taxonomizing, sizing and overcoming the incidentalome
- (2012) Isaac S. Kohane et al. GENETICS IN MEDICINE
- A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes
- (2012) D. G. MacArthur et al. SCIENCE
- Social and ethical implications of BRCA testing
- (2011) A. Surbone ANNALS OF ONCOLOGY
- Human Genome Sequencing in Health and Disease
- (2011) Claudia Gonzaga-Jauregui et al. Annual Review of 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
- Disclosing pathogenic genetic variants to research participants: Quantifying an emerging ethical responsibility
- (2011) C. A. Cassa et al. GENOME RESEARCH
- Next-Generation DNA Sequencing, Regulation, and the Limits of Paternalism
- (2011) James P. Evans et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues?
- (2011) G. Pichert et al. JOURNAL OF MEDICAL GENETICS
- Mapping copy number variation by population-scale genome sequencing
- (2011) Ryan E. Mills et al. NATURE
- Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes
- (2011) Santhosh Girirajan et al. PLoS Genetics
- Ethical and Practical Guidelines for Reporting Genetic Research Results to Study Participants
- (2010) Richard R. Fabsitz et al. Circulation-Cardiovascular Genetics
- Deletion and duplication of 15q24: Molecular mechanisms and potential modification by additional copy number variants
- (2010) Ayman W El-Hattab et al. GENETICS IN MEDICINE
- CLIA-tested genetic variants on commercial SNP arrays: Potential for incidental findings in genome-wide association studies
- (2010) Andrew D Johnson et al. GENETICS IN MEDICINE
- Detection of clinically relevant exonic copy-number changes by array CGH
- (2010) Philip M. Boone et al. HUMAN MUTATION
- Clinical assessment incorporating a personal genome
- (2010) Euan A Ashley et al. LANCET
- A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
- (2010) Santhosh Girirajan et al. NATURE GENETICS
- Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH
- (2009) Sara Anne Adams et al. GENETICS IN MEDICINE
- Direct to consumer genetic testing: Avoiding a culture war
- (2009) James P Evans et al. GENETICS IN MEDICINE
- The Current Landscape for Direct-to-Consumer Genetic Testing: Legal, Ethical, and Policy Issues
- (2008) Stuart Hogarth et al. Annual Review of Genomics and Human Genetics
- Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses
- (2008) Zhishuo Ou et al. GENETICS IN MEDICINE
- Understanding Incidental Findings in the Context of Genetics and Genomics
- (2008) Mildred K. Cho 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
- Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH
- (2008) Weimin Bi et al. PRENATAL DIAGNOSIS
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started