(Q34243496)

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Comparative effectiveness of next generation genomic sequencing for disease diagnosis: design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromes

journal article published in 2014

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scholarly article

2 references

Europe PubMed Central

PubMed publication ID

31 July 2017

16 August 2019

Comparative effectiveness of next generation genomic sequencing for disease diagnosis: design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromes (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

National Institute for Occupational Safety and Health

1 reference

16 August 2019

1 reference

29 March 2020

colorectal cancer

1 reference

29 March 2020

16

object named as

Wylie Burke

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Martha Horike-Pyne

5

object named as

Martha Horike-Pyne

0 references

18

object named as

Gail P Jarvik

0 references

Peter Tarczy-Hornoch

10

object named as

Peter Tarczy-Hornoch

0 references

Susan B. Trinidad

object named as

Susan B Trinidad

13

0 references

Donald L. Patrick

17

object named as

Donald L Patrick

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

David L Veenstra

19

object named as

David L Veenstra

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Deborah A Nickerson

15

object named as

Deborah A Nickerson

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

Carlos J Gallego

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Caroline S Bennette

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Patrick Heagerty

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Bryan Comstock

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Fuki Hisama

6

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Laura M Amendola

7

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Robin L Bennett

8

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Michael O Dorschner

9

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

William M Grady

11

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

S Malia Fullerton

12

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Dean A Regier

14

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

language of work or name

0 references

publication date

3 July 2014

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Contemporary Clinical Trials

2 references

Europe PubMed Central

PubMed publication ID

31 July 2017

8 December 2019

39

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1-8

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

performing organization

University of Washington

object named as

University of Washington

1 reference

2 February 2024

on focus list of Wikimedia project

Wikimedia–NIOSH collaboration

0 references

1 reference

25 September 2023

Return of genomic results to research participants: the floor, the ceiling, and the choices in between

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Genetic counselors' views and experiences with the clinical integration of genome sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

The promise and challenges of next-generation genome sequencing for clinical care

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Recommendations for returning genomic incidental findings? We need to talk!

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

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=4175052

6 July 2018

Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Implementing genomic medicine in the clinic: the future is here

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Randomized trial of personal genomics for preventive cardiology: design and challenges

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Human genome sequencing in health and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Effect of direct-to-consumer genomewide profiling to assess disease risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

The Patient Health Questionnaire Somatic, Anxiety, and Depressive Symptom Scales: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Value for money? Array genomic hybridization for diagnostic testing for genetic causes of intellectual disability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Disclosure of APOE genotype for risk of Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Updated U.S. population standard for the Veterans RAND 12-item Health Survey (VR-12).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Estimating the Danish populations' preferences for pharmacogenetic testing using a discrete choice experiment. The case of treating depression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Economic methods for valuing the outcomes of genetic testing: beyond cost-effectiveness analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

The Rapid Assessment of Physical Activity (RAPA) among older adults.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Analyses of cost data in economic evaluations conducted alongside randomized controlled trials

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

A brief measure for assessing generalized anxiety disorder: the GAD-7.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Good research practices for cost-effectiveness analysis alongside clinical trials: the ISPOR RCT-CEA Task Force report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

An economic viewpoint on alternative strategies for identifying persons with hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

A genetic study of carcinoma of the large intestine.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Cost-effectiveness of microsatellite instability screening as a method for detecting hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

The PHQ-9: validity of a brief depression severity measure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Cost and outcomes of Medicare reimbursement for HMO preventive services.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

6 July 2018

Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

28 October 2018

The potential clinical and economic outcomes of pharmacogenomic approaches to EGFR-tyrosine kinase inhibitor therapy in non-small-cell lung cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

28 October 2018

The impact of predictive genetic testing for hereditary nonpolyposis colorectal cancer: three years after testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

28 October 2018

Validity of the Brief Patient Health Questionnaire Mood Scale (PHQ-9) in the general population

1 reference

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28 October 2018

Gene expression profiling and breast cancer care: what are the potential benefits and policy implications?

1 reference

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28 October 2018

A brief assessment of concerns associated with genetic testing for cancer: the Multidimensional Impact of Cancer Risk Assessment (MICRA) questionnaire.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

28 October 2018

Incidental findings in genetic research and clinical diagnostic tests: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

28 October 2018

Valuing pharmacogenetic testing services: A comparison of patients' and health care professionals' preferences

1 reference

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28 October 2018

Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4175052

28 October 2018

Predictive testing for hereditary nonpolyposis colorectal cancer: subjective perception regarding colorectal and endometrial cancer, distress, and health-related behavior at one year post-test

1 reference

https://pubmed.ncbi.nlm.nih.gov/24997220

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Probabilistic analysis of cost-effectiveness models: statistical representation of parameter uncertainty

1 reference

https://pubmed.ncbi.nlm.nih.gov/24997220

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/24997220

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FDA guidance on patient reported outcomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/24997220

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/24997220

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.CCT.2014.06.016

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

release_rx22cccmybcdzes3ibjhxsqbdu

1 reference

https://api.fatcat.wiki/v0/release/rx22cccmybcdzes3ibjhxsqbdu

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

16 August 2019

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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