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Incidental Findings with Genomic Testing: Implications for Genetic Counseling PracticeReturn of individual research results and incidental findings: facing the challenges of translational sciencePublic preferences for the return of research results in genetic research: a conjoint analysisSequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence DataClinGen--the Clinical Genome ResourceACMG recommendations for reporting of incidental findings in clinical exome and genome sequencingShort read (next-generation) sequencing: a tutorial with cardiomyopathy diagnostics as an exemplar.Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results.Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencing.PhenoVar: a phenotype-driven approach in clinical genomics for the diagnosis of polymalformative syndromes.Traditional roles in a non-traditional setting: genetic counseling in precision oncologyClinical interpretation and implications of whole-genome sequencing.Bioinformatic approaches to augment study of epithelial-to-mesenchymal transition in lung cancerClinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype-phenotype correlations and unexpected diagnostic revisionsManagement of Incidental Findings in the Era of Next-generation SequencingIdentification of Medically Actionable Secondary Findings in the 1000 Genomes.Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.High Diagnostic Yield of Whole Exome Sequencing in Participants With Retinal Dystrophies in a Clinical Ophthalmology Setting.Secondary findings and carrier test frequencies in a large multiethnic sample.Mitigating false-positive associations in rare disease gene discoveryDefining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome.A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencingDealing with the unexpected: consumer responses to direct-access BRCA mutation testingIncidental variants are critical for genomicsClinical genomic database.Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles.Management of incidental findings in clinical genomic sequencingResearchers' views on return of incidental genomic research results: qualitative and quantitative findings.Genomic sequencing in clinical practice: applications, challenges, and opportunities.How could disclosing incidental information from whole-genome sequencing affect patient behavior?Communicating genetic risk information for common disorders in the era of genomic medicine.Next-generation sequencing in the clinic: are we ready?Cancer pharmacogenomics: early promise, but concerted effort needed.Ethical, legal, and social implications of incorporating genomic information into electronic health records.Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies.The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.Enhancing the incidental pipeline in genomic sequencing.GCH1 heterozygous mutation identified by whole-exome sequencing as a treatable condition in a patient presenting with progressive spastic paraplegia.Incidental findings from clinical genome-wide sequencing: a review.
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description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
An informatics approach to analyzing the incidentalome.
@ast
An informatics approach to analyzing the incidentalome.
@en
type
label
An informatics approach to analyzing the incidentalome.
@ast
An informatics approach to analyzing the incidentalome.
@en
prefLabel
An informatics approach to analyzing the incidentalome.
@ast
An informatics approach to analyzing the incidentalome.
@en
P2093
P2860
P356
P1433
P1476
An informatics approach to analyzing the incidentalome.
@en
P2093
Charles P Schmitt
Chris Bizon
James P Evans
Jonathan S Berg
Kirk C Wilhelmsen
Michael Adams
P2860
P2888
P356
10.1038/GIM.2012.112
P407
P577
2012-09-20T00:00:00Z
P5875
P6179
1026109703