(Q37590819)

21 August 2017

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

1 reference

21 August 2017

0 references

4

1 reference

21 August 2017

Kasmintan A Schrader

8

0 references

Kenneth Offit

10

object named as

Kenneth Offit

1 reference

Heather Spencer Feigelson

21 August 2017

11

object named as

Heather Spencer Feigelson

1 reference

21 August 2017

9

Doug Campos-Outcalt

1 reference

21 August 2017

2

Evelyn P Whitlock

1 reference

21 August 2017

3

Jonathan S Berg

1 reference

21 August 2017

Katrina A B Goddard

1

1 reference

21 August 2017

Elizabeth M Webber

5

1 reference

21 August 2017

Jennifer A Webster

6

1 reference

21 August 2017

Jennifer S Lin

7

1 reference

21 August 2017

Celine Hollombe

12

1 reference

21 August 2017

language of work or name

English

0 references

publication date

4 April 2013

1 reference

21 August 2017

1 reference

21 August 2017

15

1 reference

21 August 2017

9

1 reference

21 August 2017

721-728

1 reference

https://scigraph.springernature.com/pub.10.1038/gim.2013.37

21 August 2017

0 references

cites work

Next-generation sequencing in the clinic: are we ready?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

An informatics approach to analyzing the incidentalome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Improving the efficiency and relevance of evidence-based recommendations in the era of whole-genome sequencing: an EGAPP methods update

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Evidence summaries: the evolution of a rapid review approach

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

AGREE II: advancing guideline development, reporting and evaluation in health care

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Clinical assessment incorporating a personal genome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

The 1000 Genomes Project: new opportunities for research and social challenges

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Committee report: Method for evaluating conditions nominated for population-based screening of newborns and children

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Outcomes of interest in evidence-based evaluations of genetic tests

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Towards universal newborn screening in developing countries: obstacles and the way forward.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

AMSTAR is a reliable and valid measurement tool to assess the methodological quality of systematic reviews

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

The diploid genome sequence of an Asian individual

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Accurate whole human genome sequencing using reversible terminator chemistry

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: methods of the EGAPP Working Group

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

The complete genome of an individual by massively parallel DNA sequencing

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

The diploid genome sequence of an individual human

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Current status of newborn screening: decision-making about the conditions to include in screening programs

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

The incidentalome: a threat to genomic medicine

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Population screening in the age of genomic medicine

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Reconsidering the criteria for evaluating proposed screening programs: reflections from 4 current and former members of the U.S. Preventive services task force

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Considerations in choosing screening conditions: one (US) approach.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

EASL clinical practice guidelines for HFE hemochromatosis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Update on the methods of the U.S. Preventive Services Task Force: estimating certainty and magnitude of net benefit

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

A Coefficient of Agreement for Nominal Scales

1 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FGIM.2013.37

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3927794

Epigenome effort makes its mark

5 November 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FGIM.2013.37

Iron overload, public health, and genetics: evaluating the evidence for hemochromatosis screening

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23558254

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Human genome: Genomes by the thousand

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23558254

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hemochromatosis genotypes and risk of 31 disease endpoints: meta-analyses including 66,000 cases and 226,000 controls

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23558254

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/GIM.2013.37

1 reference

21 August 2017

Microsoft Academic ID

0 references

1 reference

21 August 2017

PubMed publication ID

23558254

1 reference