Incidental findings in clinical genomics: a clarification.
about
Whole Genome Sequencing as a Genetic Test for Autism Spectrum Disorder: From Bench to Bedside and then Back AgainIncidental Findings with Genomic Testing: Implications for Genetic Counseling PracticeRecommendations for returning genomic incidental findings? We need to talk!Findings made in gene panel to whole genome sequencing: data, knowledge, ethics - and consequences?Cancer screening and genetics: a tale of two paradigmsAttitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing.Clinical genome sequencing and population preferences for information about 'incidental' findings-From medically actionable genes (MAGs) to patient actionable genes (PAGs)Return of genomic results to research participants: the floor, the ceiling, and the choices in between.The "right not to know" in the genomic era: time to break from tradition?Genetic counseling in direct-to-consumer exome sequencing: a case report.Returning incidental findings from genetic research to children: views of parents of children affected by rare diseasesThe best interests of the child and the return of results in genetic research: international comparative perspectives.Addressing the ethical challenges in genetic testing and sequencing of children.Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.The challenge of informed consent and return of results in translational genomics: empirical analysis and recommendations.The fiduciary relationship model for managing clinical genomic "incidental" findings.Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis.Management of Incidental Findings in the Era of Next-generation SequencingResearchers' views on informed consent for return of secondary results in genomic research.Identification of Medically Actionable Secondary Findings in the 1000 Genomes.Pragmatic and Ethical Challenges of Incorporating the Genome into the Electronic Medical Record.Association of Researcher Characteristics with Views on Return of Incidental Findings from Genomic Research.Professionally Responsible Disclosure of Genomic Sequencing Results in Pediatric Practice.How Much Control Do Children and Adolescents Have over Genomic Testing, Parental Access to Their Results, and Parental Communication of Those Results to Others?Mapping the Ethics of Translational Genomics: Situating Return of Results and Navigating the Research-Clinical Divide.Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.Towards a European consensus for reporting incidental findings during clinical NGS testing.Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age.Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling studyRaising Genomic Citizens: Adolescents and the Return of Secondary Genomic Findings.A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation.Legal approaches regarding health-care decisions involving minors: implications for next-generation sequencing.Managing incidental genomic findings in clinical trials: fulfillment of the principle of justice.Minimizing liability risks under the ACMG recommendations for reporting incidental findings in clinical exome and genome sequencing.Ethics and genomic medicine, how to navigate decisions in surgical oncology.Genomic Testing: a Genetic Counselor's Personal Reflection on Three Years of Consenting and Testing.Ethical perspectives on translational pharmacogenetic research involving children.Return of genetic testing results in the era of whole-genome sequencing.Interest and Attitudes of Patients With Advanced Cancer With Regard to Secondary Germline Findings From Tumor Genomic Profiling.Genetics of movement disorders in the next-generation sequencing era.
P2860
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P2860
Incidental findings in clinical genomics: a clarification.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh
2013年學術文章
@zh-hant
name
Incidental findings in clinical genomics: a clarification.
@en
Incidental findings in clinical genomics: a clarification.
@nl
type
label
Incidental findings in clinical genomics: a clarification.
@en
Incidental findings in clinical genomics: a clarification.
@nl
prefLabel
Incidental findings in clinical genomics: a clarification.
@en
Incidental findings in clinical genomics: a clarification.
@nl
P356
P1433
P1476
Incidental findings in clinical genomics: a clarification.
@en
P2093
American College of Medical Genetics and Genomics
P2860
P2888
P304
P356
10.1038/GIM.2013.82
P407
P577
2013-07-04T00:00:00Z