(Q92503067)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

review article

1 reference

title

Improving recommendations for genomic medicine: building an evolutionary process from clinical practice advisory documents to guidelines (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

1

1 reference

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30 April 2020

Ellen Wright Clayton

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

Susan A. Berry

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

Barbara J Evans

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

Diane M Korngiebel

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

9

Anne-Marie Laberge

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

11

Amy L McGuire

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

3

Susan M Wolf

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

10

Bonnie S LeRoy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

author name string

James P Evans

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

Ralph Hall

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

publication date

4 June 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

volume

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

page(s)

2431-2438

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium

30 April 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

1 reference

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7 January 2021

NSGC practice guideline: risk assessment and genetic counseling for hereditary breast and ovarian cancer

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7 January 2021

Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives

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https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Screening for Breast Cancer: U.S. Preventive Services Task Force Recommendation Statement

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https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Clinical integration of next generation sequencing: coverage and reimbursement challenges.

1 reference

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7 January 2021

Payer Coverage for Hereditary Cancer Panels: Barriers, Opportunities, and Implications for the Precision Medicine Initiative

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https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

A proposed approach to accelerate evidence generation for genomic-based technologies in the context of a learning health system

1 reference

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7 January 2021

Rationality versus reality: the challenges of evidence-based decision making for health policy makers

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7 January 2021

Evidence-based medicine in the United States--de rigueur or dream deferred?

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7 January 2021

The usefulness of whole-exome sequencing in routine clinical practice.

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https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Clinical exome sequencing for genetic identification of rare Mendelian disorders

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7 January 2021

Clinical application of whole-exome sequencing across clinical indications

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7 January 2021

Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience.

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Molecular findings among patients referred for clinical whole-exome sequencing

1 reference

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7 January 2021

Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.

1 reference

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7 January 2021

Practical considerations in the clinical application of whole-exome sequencing

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https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Clinical exome sequencing: the new standard in genetic diagnosis

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

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https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Technical report: Ethical and policy issues in genetic testing and screening of children

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https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists

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7 January 2021

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Clinical exome sequencing in neurogenetic and neuropsychiatric disorders

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: variant reclassification and surgical decisions.

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Point-counterpoint. Ethics and genomic incidental findings

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Specialty Society Clinical Practice Guidelines: Time for Evolution or Revolution?

1 reference

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7 January 2021

Clinical Practice Guidelines: Expanded Use and Misuse.

1 reference

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7 January 2021

Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

1 reference

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7 January 2021

Clinical Practice Guidelines: What's Next?

1 reference

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7 January 2021

Making policy when the evidence is in dispute.

1 reference

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7 January 2021

Molecular testing for Lynch syndrome in people with colorectal cancer: systematic reviews and economic evaluation.

1 reference

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7 January 2021

Reducing Test Utilization in Hospital Settings: A Narrative Review

1 reference

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7 January 2021

Reducing Unnecessary Imaging and Pathology Tests: A Systematic Review

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Incidental variants are critical for genomics

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

Standardized Clinical Assessment And Management Plans (SCAMPs) provide a better alternative to clinical practice guidelines

1 reference

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7 January 2021

EXAMINING EVIDENCE IN U.S. PAYER COVERAGE POLICIES FOR MULTI-GENE PANELS AND SEQUENCING TESTS.

1 reference

https://api.crossref.org/works/10.1038%2FS41436-019-0549-3

7 January 2021

10.1038/S41436-019-0549-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31160753%20AND%20SRC:MED&resulttype=core&format=json

30 April 2020

1 reference