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Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.

http://www.wikidata.org/entity/Q30391601

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Governing the research-care divide in clinical biobanking: Dutch perspectives Genomic medicine in gastroenterology: A new approach or a new specialty?Clinical application of next-generation sequencing for Mendelian diseases Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics The challenges, advantages and future of phenome-wide association studies Are physicians prepared for whole genome sequencing? a qualitative analysis Review of current methods, applications, and data management for the bioinformatics analysis of whole exome sequencing.Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.To disclose, or not to disclose? Context matters.Translating personalized medicine using new genetic technologies in clinical practice: the ethical issues Availability of treatment drives decisions of genetic health professionals about disclosure of incidental findings.The best interests of the child and the return of results in genetic research: international comparative perspectives.Public views on participating in newborn screening using genome sequencing Finding Fault? Exploring Legal Duties to Return Incidental Findings in Genomic Research.Addressing the ethical challenges in genetic testing and sequencing of children.Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patients.The challenge of consent in clinical genome-wide testing.Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification.The unintended implications of blurring the line between research and clinical care in a genomic age.Delivery of a clinical genomics service Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism.Use of an electronic medical record to create the marshfield clinic twin/multiple birth cohort An implementation framework for the feedback of individual research results and incidental findings in research Exome Sequencing in Fetuses with Structural Malformations The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation.Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.It is time to take timing seriously in clinical genetics.A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication Compare and contrast: a cross-national study across UK, USA and Greek experts regarding return of incidental findings from clinical sequencing Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic Research.Towards a European consensus for reporting incidental findings during clinical NGS testing.Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes Regulating biobanking with children's tissue: a legal analysis and the experts' view Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.Attitudes towards personal genomics among older Swiss adults: An exploratory study Evolving Roles for Physicians and Genetic Counselors in Managing Complex Genetic Disorders.Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling study Whole exome sequencing diagnosis of inborn errors of metabolism and other disorders in United Arab Emirates

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Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.

http://www.wikidata.org/entity/Q30391601

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2013 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2013年の論文

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European Journal of Human Genetics

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Carla G van El

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ESHG Public and Professional Policy Committee

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Florence Fellmann

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Guido M W R de Wert

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Heidi C Howard

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Lisbeth Tranebjaerg

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Ros J Hastings

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Shirley V Hodgson

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Wybo Dondorp

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GENE SEQUENCING: The Race for the $1000 Genome

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

The complete genome of an individual by massively parallel DNA sequencing

Exome sequencing identifies the cause of a mendelian disorder

Clinical assessment incorporating a personal genome

A map of human genome variation from population-scale sequencing

Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy.

Diagnostic interpretation of array data using public databases and internet sources.

Disclosure of individual genetic data to research participants: the debate reconsidered.

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10.1038/EJHG.2013.46

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21

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Bartha Knoppers

Hanne Meijers-Heijboer

Anne Cambon-Thomsen

Heidi Carmen Howard

Martina C Cornel

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2013-06-01T00:00:00Z

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