(Q30585056)

15 October 2017

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine (English)

1 reference

15 October 2017

whole genome sequencing

1 reference

Kurt D Christensen

5

0 references

Carolyn Ho

Carolyn Y Ho

12

0 references

Heidi L. Rehm

Heidi L Rehm

18

0 references

Amy L McGuire

17

Amy L McGuire

1 reference

15 October 2017

19

Robert C Green

1 reference

15 October 2017

7

Isaac S Kohane

1 reference

15 October 2017

Sek Won Kong

4

0 references

Peter A. Ubel

13

Peter A Ubel

1 reference

15 October 2017

15

Christine E Seidman

1 reference

15 October 2017

6

Joel Krier

1 reference

15 October 2017

Jason L Vassy

1

1 reference

15 October 2017

Denise M Lautenbach

2

1 reference

15 October 2017

Heather M McLaughlin

3

1 reference

15 October 2017

Lindsay Z Feuerman

8

1 reference

15 October 2017

Jennifer Blumenthal-Barby

9

1 reference

15 October 2017

J Scott Roberts

10

1 reference

15 October 2017

Lisa Soleymani Lehmann

11

1 reference

15 October 2017

Calum A MacRae

14

1 reference

15 October 2017

Michael F Murray

16

1 reference

15 October 2017

MedSeq Project

20

1 reference

15 October 2017

20 March 2014

1 reference

15 October 2017

1 reference

15 October 2017

15

1 reference

15 October 2017

85

1 reference

https://scigraph.springernature.com/pub.10.1186/1745-6215-15-85

15 October 2017

0 references

cites work

Clinical whole-exome sequencing for the diagnosis of mendelian disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

A systematic approach to assessing the clinical significance of genetic variants.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Whole-genome sequencing for rapid susceptibility testing of M. tuberculosis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Delayed puberty and estrogen resistance in a woman with estrogen receptor α variant

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

A culture-independent sequence-based metagenomics approach to the investigation of an outbreak of Shiga-toxigenic Escherichia coli O104:H4.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Long QT syndrome-associated mutations in intrauterine fetal death

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Analysis of circulating tumor DNA to monitor metastatic breast cancer

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Genotyping of fanconi anemia patients by whole exome sequencing: advantages and challenges

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Personal genomic measurements: the opportunity for information integration

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Clinical diagnosis by whole-genome sequencing of a prenatal sample

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Effects of informed consent for individual genome sequencing on relevant knowledge

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Rapid whole-genome sequencing for investigation of a neonatal MRSA outbreak

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Patients' understanding of and responses to multiplex genetic susceptibility test results

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Barriers to integrating personalized medicine into clinical practice: a best-worst scaling choice experiment

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Whole-genome sequencing for optimized patient management

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Charting a course for genomic medicine from base pairs to bedside

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

CONSORT 2010 statement: updated guidelines for reporting parallel group randomized trials

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Social networkers' attitudes toward direct-to-consumer personal genome testing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Accurate whole human genome sequencing using reversible terminator chemistry

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Report of the Banbury Summit Meeting on the evolving role of the medical geneticist, February 12-14, 2006.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Delivery of genomic medicine for common chronic adult diseases: a systematic review

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Extending the CONSORT statement to randomized trials of nonpharmacologic treatment: explanation and elaboration

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

The incidentalome: a threat to genomic medicine

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Fearing the unknown: a short version of the Intolerance of Uncertainty Scale

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Predicting mortality and healthcare utilization with a single question

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Genetic testing for Alzheimer's disease and its impact on insurance purchasing behavior

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Population screening in the age of genomic medicine

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Quality of informed consent: a new measure of understanding among research subjects

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Validation of a decisional conflict scale

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

The hospital anxiety and depression scale

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

Personalized medicine vs guideline-based medicine

20 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1745-6215-15-85

An unwelcome side effect of direct-to-consumer personal genome testing: raiding the medical commons

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1745-6215-15-85

Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1745-6215-15-85

Measuring trust in medical researchers

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1745-6215-15-85

The Health Information National Trends Survey (HINTS): development, design, and dissemination.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1745-6215-15-85

Validation of a decision regret scale.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1745-6215-15-85

Exome sequencing deciphers rare diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1745-6215-15-85

The evidence dilemma in genomic medicine.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113228

The Human Gene Mutation Database (HGMD) and its exploitation in the study of mutational mechanisms

26 November 2018

1 reference

12 December 2020

The state of the medical geneticist workforce: findings of the 2003 survey of American Board of Medical Genetics certified geneticists

1 reference

12 December 2020

The Roter interaction analysis system (RIAS): utility and flexibility for analysis of medical interactions

1 reference

12 December 2020

Decision making in the transtheoretical model of behavior change

1 reference

12 December 2020

The Control Preferences Scale.

1 reference

12 December 2020

Identifiers

DOI

10.1186/1745-6215-15-85

1 reference

Dimensions Publication ID

15 October 2017

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1745-6215-15-85

1 reference

15 October 2017

PubMed publication ID

24645908

1 reference