Refining the structure and content of clinical genomic reports - Wikidata - awgldk - TriplyDB

Refining the structure and content of clinical genomic reports

Refining the structure and content of clinical genomic reports

http://www.wikidata.org/entity/Q33830276

about

The challenge of comprehensive and consistent sequence variant interpretation between clinical laboratories.Developing patient-friendly genetic and genomic test reports: formats to promote patient engagement and understanding.Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network.An informatics research agenda to support precision medicine: seven key areas Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing A primer on precision medicine informatics.The ins and outs of molecular pathology reporting.Barriers to clinical adoption of next-generation sequencing: a policy Delphi panel's solutions.Interactive or static reports to guide clinical interpretation of cancer genomics.Physician Experiences and Understanding of Genomic Sequencing in Oncology.Educating patients and providers through comprehensive pharmacogenetic test reports.Enhancing genomic laboratory reports: A qualitative analysis of provider review.

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P2860

Refining the structure and content of clinical genomic reports

http://www.wikidata.org/entity/Q33830276

description

2014 nî lūn-bûn

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2014 թուականի Մարտին հրատարակուած գիտական յօդուած

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2014 թվականի մարտին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Refining the structure and content of clinical genomic reports

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Refining the structure and content of clinical genomic reports

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Refining the structure and content of clinical genomic reports

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Refining the structure and content of clinical genomic reports

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Refining the structure and content of clinical genomic reports

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Refining the structure and content of clinical genomic reports

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P1433

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

P1476

Refining the structure and content of clinical genomic reports

@en

P2093

Adam S Gordon

http://www.w3.org/2001/XMLSchema#string

Brian H Shirts

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Joseph Salama

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Laura M Amendola

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Lesli Kiedrowski

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Michael O Dorschner

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P2860

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

Good laboratory practices for molecular genetic testing for heritable diseases and conditions.

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.

Clinician perspectives about molecular genetic testing for heritable conditions and development of a clinician-friendly laboratory report.

Actionable, pathogenic incidental findings in 1,000 participants' exomes.

A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record.

A report template for molecular genetic tests designed to improve communication between the clinician and laboratory.

Clinical laboratory reports in molecular pathology.

Effective communication of molecular genetic test results to primary care providers.

Medicare and Medicaid programs: hospital outpatient prospective payment and ambulatory surgical center payment systems and quality reporting programs; Hospital Value-Based Purchasing Program; organ procurement organizations; quality improvement orga

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85-92

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scholarly article

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10.1002/AJMG.C.31395

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1

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P478

166C

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Peter Tarczy-Hornoch

Stephanie M Fullerton

P577

2014-03-10T00:00:00Z

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260684579

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24616401

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4077592

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