A novel clinician interface to improve clinician access to up-to-date genetic results. - Wikidata - awgldk - TriplyDB

A novel clinician interface to improve clinician access to up-to-date genetic results.

A novel clinician interface to improve clinician access to up-to-date genetic results.

http://www.wikidata.org/entity/Q37642944

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Genetic Misdiagnoses and the Potential for Health Disparities Are physicians prepared for whole genome sequencing? a qualitative analysis Evaluation: A Qualitative Pilot Study of Novel Information Technology Infrastructure to Communicate Genetic Variant Updates.A proposed clinical decision support architecture capable of supporting whole genome sequence information.Data resources for the identification and interpretation of actionable mutations by clinicians.Providing Access to Genomic Variant Knowledge in a Healthcare Setting: A Vision for the ClinGen Electronic Health Records Workgroup.Computational Pathology: A Path Ahead.Developing knowledge resources to support precision medicine: principles from the Clinical Pharmacogenetics Implementation Consortium (CPIC).User-centered design of multi-gene sequencing panel reports for clinicians.The BabySeq project: implementing genomic sequencing in newborns

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A novel clinician interface to improve clinician access to up-to-date genetic results.

http://www.wikidata.org/entity/Q37642944

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 07 September 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

A novel clinician interface to improve clinician access to up-to-date genetic results.

@en

A novel clinician interface to improve clinician access to up-to-date genetic results.

@nl

type

label

A novel clinician interface to improve clinician access to up-to-date genetic results.

@en

A novel clinician interface to improve clinician access to up-to-date genetic results.

@nl

prefLabel

A novel clinician interface to improve clinician access to up-to-date genetic results.

@en

A novel clinician interface to improve clinician access to up-to-date genetic results.

@nl

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AMIAJNL-2013-001965

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Journal of the American Medical Informatics Association

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A novel clinician interface to improve clinician access to up-to-date genetic results.

@en

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Allison R Wilcox

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David W Bates

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Eugene H Clark

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Lawrence J Babb

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Lisa P Newmark

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Lynn A Volk

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Matthew Varugheese

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Pamela M Neri

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Samuel J Aronson

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P2860

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.

Usability of a novel clinician interface for genetic results

Lack of MEF2A mutations in coronary artery disease.

Free the data: one laboratory's approach to knowledge-based genomic variant classification and preparation for EMR integration of genomic data.

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results.

The GeneInsight Suite: a platform to support laboratory and provider use of DNA-based genetic testing.

Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.

Deleterious- and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases, and population-scale resequencing.

Carrier testing for severe childhood recessive diseases by next-generation sequencing

Inherited susceptibility to common cancers.

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e117-21

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10.1136/AMIAJNL-2013-001965

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e1

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21

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