(Q35012563)

5 August 2017

'Someday it will be the norm': physician perspectives on the utility of genome sequencing for patient care in the MedSeq Project (English)

1 reference

5 August 2017

1 reference

Kurt D Christensen

2

0 references

Amy L McGuire

12

object named as

Amy L McGuire

1 reference

5 August 2017

11

Robert C Green

1 reference

5 August 2017

Jason L Vassy

1

1 reference

5 August 2017

Melody J Slashinski

3

1 reference

5 August 2017

Denise M Lautenbach

4

1 reference

5 August 2017

Sridharan Raghavan

5

1 reference

5 August 2017

Jill Oliver Robinson

6

1 reference

5 August 2017

Jennifer Blumenthal-Barby

7

1 reference

5 August 2017

Lindsay Zausmer Feuerman

8

1 reference

5 August 2017

Lisa Soleymani Lehmann

9

1 reference

5 August 2017

Michael F Murray

10

1 reference

5 August 2017

language of work or name

English

0 references

publication date

1 January 2015

1 reference

5 August 2017

Personalized Medicine

1 reference

5 August 2017

12

1 reference

5 August 2017

1

1 reference

5 August 2017

23-32

1 reference

Diagnostic clinical genome and exome sequencing

5 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Clinical interpretation and implications of whole-genome sequencing

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Economic analyses of genetic tests in personalized medicine: clinical utility first, then cost utility.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Clinical whole-exome sequencing for the diagnosis of mendelian disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

The EGAPP initiative: lessons learned

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physicians

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Academic family physicians' perception of genetic testing and integration into practice: a CERA study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

How can polygenic inheritance be used in population screening for common diseases?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Inviting patients to read their doctors' notes: a quasi-experimental study and a look ahead

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Personalized genetic risk counseling to motivate diabetes prevention: a randomized trial

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Incidental copy-number variants identified by routine genome testing in a clinical population

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Attitudes and practices among internists concerning genetic testing

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Personal omics profiling reveals dynamic molecular and medical phenotypes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Adoption of pharmacogenomic testing by US physicians: results of a nationwide survey

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Primary care physicians' awareness, experience and opinions of direct-to-consumer genetic testing

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Whole-genome sequencing for optimized patient management

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Genomic risk profiling: attitudes and use in personal and clinical care of primary care physicians who offer risk profiling.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Charting a course for genomic medicine from base pairs to bedside

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Effects of communicating DNA-based disease risk estimates on risk-reducing behaviours

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

The behavioral response to personalized genetic information: will genetic risk profiles motivate individuals and families to choose more healthful behaviors?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

The clinical application of genetic testing in type 2 diabetes: a patient and physician survey

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Population screening for genetic disorders in the 21st century: evidence, economics, and ethics

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Does comparative-effectiveness research threaten personalized medicine?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Genetic susceptibility to cancer. Family physicians' experience.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306284

Patient and family engagement: a framework for understanding the elements and developing interventions and policies.

8 July 2018

1 reference

Why we should care about what you get for "only $99" from a personal genomic service.

21 January 2018

1 reference

Regulation: The FDA is overcautious on consumer genomics

21 January 2018

1 reference

Primary care physicians' concerns about offering a genetic test to tailor smoking cessation treatment.

21 January 2018

1 reference

Barriers for integrating personalized medicine into clinical practice: a qualitative analysis.

21 January 2018

1 reference

Predictive genetics in primary care: expectations for the motivational impact of genetic testing affects the importance family physicians place on screening for familial cancer risk

21 January 2018

1 reference

Psychological and behavioural impact of genetic testing smokers for lung cancer risk: a phase II exploratory trial.

21 January 2018

1 reference

Deflating the Genomic Bubble

21 January 2018

1 reference

How Many Interviews Are Enough?

21 January 2018

1 reference

Applied Thematic Analysis

21 January 2018

1 reference

Physicians' perceived usefulness of and satisfaction with test reports for cystic fibrosis (DeltaF508) and factor V Leiden

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25642274

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Special report: exome sequencing for clinical diagnosis of patients with suspected genetic disorders

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25642274

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Direct-to-consumer genomics reinvents itself

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25642274

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.2217/PME.14.68

1 reference

5 August 2017

1 reference

5 August 2017

1 reference