(Q35033000)

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

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Europe PubMed Central

PubMed publication ID

5 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

incidental finding

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corrigendum / erratum

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

1 reference

10.1038/GIM.2013.191

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1038/GIM.2013.191

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Wylie Burke

1 reference

Europe PubMed Central

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5 August 2017

17

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Gail P Jarvik

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Eliezer Van Allen

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Eliezer Van Allen

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Heidi L Rehm

7

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Robert C. Green

14

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Robert C Green

1 reference

Europe PubMed Central

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5 August 2017

Levi A Garraway

13

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Levi Garraway

1 reference

Europe PubMed Central

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5 August 2017

Christine M. Eng

3

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Christine Eng

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Europe PubMed Central

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5 August 2017

Laura M Amendola

2

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Laura M Amendola

1 reference

Europe PubMed Central

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5 August 2017

Jonathan S Berg

1

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Jonathan S Berg

1 reference

Europe PubMed Central

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5 August 2017

5

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Stacy W Gray

1 reference

Europe PubMed Central

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5 August 2017

Nancy B Spinner

12

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Nancy B Spinner

1 reference

Europe PubMed Central

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5 August 2017

Matthew C Dulik

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Matthew C Dulik

1 reference

Europe PubMed Central

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5 August 2017

15

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Sharon Plon

1 reference

Europe PubMed Central

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5 August 2017

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Nikhil Wagle

6

1 reference

Europe PubMed Central

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5 August 2017

Elizabeth T DeChene

8

1 reference

Europe PubMed Central

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5 August 2017

Fuki M Hisama

10

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

James P Evans

16

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Europe PubMed Central

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5 August 2017

Members of the CSER Actionability and Return of Results Working Group

18

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Europe PubMed Central

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5 August 2017

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publication date

24 October 2013

1 reference

Europe PubMed Central

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5 August 2017

Genetics in Medicine

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Europe PubMed Central

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5 August 2017

15

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Europe PubMed Central

PubMed publication ID

5 August 2017

11

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Europe PubMed Central

PubMed publication ID

5 August 2017

860-867

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935342

8 July 2018

Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935342

8 July 2018

Exploring concordance and discordance for return of incidental findings from clinical sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935342

8 July 2018

Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935342

8 July 2018

Charting a course for genomic medicine from base pairs to bedside

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935342

8 July 2018

Screening for hereditary hemochromatosis: a systematic review for the U.S. Preventive Services Task Force

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935342

8 July 2018

The incidentalome: a threat to genomic medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935342

8 July 2018

American College of Medical Genetics consensus statement on factor V Leiden mutation testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935342

8 July 2018

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%2FGIM.2013.133

21 January 2018

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10.1038/GIM.2013.133

1 reference

https://api.fatcat.wiki/v0/release/u6flutx6cbgmvpx3ovkoo4xkle

30 July 2022

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https://api.fatcat.wiki/v0/release/u6flutx6cbgmvpx3ovkoo4xkle

30 July 2022

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PMC publication ID

1 reference

https://api.fatcat.wiki/v0/release/u6flutx6cbgmvpx3ovkoo4xkle

30 July 2022

based on heuristic

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PubMed publication ID

1 reference

https://api.fatcat.wiki/v0/release/u6flutx6cbgmvpx3ovkoo4xkle

30 July 2022

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