(Q36825747)

16 August 2017

Toward clinical genomics in everyday medicine: perspectives and recommendations (English)

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16 August 2017

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John Quackenbush

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Susan K Delaney

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Susan K Delaney

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Robert C. Green

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Robert C Green

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16 August 2017

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Sharon F Terry

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W Andrew Faucett

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16 August 2017

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David H Ledbetter

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16 August 2017

Michael L Hultner

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16 August 2017

Howard J Jacob

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16 August 2017

Jeanette J McCarthy

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16 August 2017

Michael Ball

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16 August 2017

Kenneth B Beckman

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16 August 2017

John W Belmont

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16 August 2017

Cinnamon S Bloss

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16 August 2017

Michael F Christman

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16 August 2017

Andy Cosgrove

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16 August 2017

Stephen A Damiani

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16 August 2017

Timothy Danis

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16 August 2017

Massimo Delledonne

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16 August 2017

Michael J Dougherty

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16 August 2017

Joel T Dudley

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16 August 2017

Jennifer R Friedman

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16 August 2017

David H Haase

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Tom S Hays

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16 August 2017

Stu Heilsberg

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16 August 2017

Jeff Huber

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Leah Kaminsky

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Nikki Ledbetter

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Warren H Lee

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16 August 2017

Elissa Levin

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16 August 2017

Ondrej Libiger

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Michael Linderman

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Richard L Love

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16 August 2017

David C Magnus

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16 August 2017

AnneMarie Martland

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Susan L McClure

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Scott E Megill

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Helen Messier

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Robert L Nussbaum

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Latha Palaniappan

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16 August 2017

Bradley A Patay

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Bradley W Popovich

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16 August 2017

Mark J Savant

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16 August 2017

Michael M Su

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16 August 2017

Steven Tucker

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16 August 2017

William T Wong

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16 August 2017

25 January 2016

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Expert Review of Molecular Diagnostics: new diagnostic technologies are set to revolutionise healthcare

16 August 2017

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16 August 2017

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16 August 2017

521-532

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Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International

16 August 2017

start time

24 February 2016

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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April 2022 Public Data File from Crossref

cites work

Next-generation sequencing to guide cancer therapy

1 reference

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Core Concept: Homomorphic encryption

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

ClinGen--the Clinical Genome Resource

29 September 2017

1 reference

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The FDA and genomic tests--getting regulation right

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

How to know when physicians are ready for genomic medicine

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Common genetic risk for melanoma encourages preventive behavior change.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Whole-exome sequencing as a diagnostic tool in a family with episodic ataxia type 1.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

A new initiative on precision medicine

29 September 2017

1 reference

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Personalized medicine and cancer

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Insurance coverage policies for personalized medicine

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Exome sequencing in undiagnosed inherited and sporadic ataxias

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Redefining genomic privacy: trust and empowerment

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

An approach to pediatric exome and genome sequencing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Next generation sequencing and tumor mutation profiling: are we ready for routine use in the oncology clinic?

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

"Is it going to hurt?": the impact of the diagnostic odyssey on children and their families

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Diagnostic clinical genome and exome sequencing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Routes for breaching and protecting genetic privacy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Enabling a genetically informed approach to cancer medicine: a retrospective evaluation of the impact of comprehensive tumor profiling using a targeted next-generation sequencing panel

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Clinical utility of whole-exome sequencing in rare diseases: Galactosialidosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Professional medical education and genomics

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Informed decision-making among students analyzing their personal genomes on a whole genome sequencing course: a longitudinal cohort study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

First FDA authorization for next-generation sequencer

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Evidence that personal genome testing enhances student learning in a course on genomics and personalized medicine.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Pharmacogenetics and pharmacogenomics: a bridge to individualized cancer therapy.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Identifying personal genomes by surname inference

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Implementing genomic medicine in the clinic: the future is here

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Use of targeted exome sequencing as a diagnostic tool for Familial Hypercholesterolaemia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Exome sequencing can improve diagnosis and alter patient management

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Use of CYP2D6 genotyping in practice: tamoxifen dose adjustment

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Genomic information as a behavioral health intervention: can it work?

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

When public health and genetic privacy collide: positive and normative theories explaining how ACA's expansion of corporate wellness programs conflicts with GINA's privacy rules

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Medical and graduate students' attitudes toward personal genomics

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Personalized medicine in oncology: tailoring the right drug to the right patient

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Does genomic risk information motivate people to change their behavior?

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

GINA, genetic discrimination, and genomic medicine.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Regulation of next generation sequencing.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

College of American Pathologists' laboratory standards for next-generation sequencing clinical tests

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

The diagnostic utility of exome sequencing in Joubert syndrome and related disorders

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Cost-effectiveness of KRAS testing in metastatic colorectal cancer patients in the United States and Germany

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Lessons learned from the introduction of personalized genotyping into a medical school curriculum.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

The evidence dilemma in genomic medicine.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4841021

Clinical Genome Sequencing

5 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1586%2F14737159.2016.1146593

Addressing gaps in physician education using personal genomic testing

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1586%2F14737159.2016.1146593

Coverage options for promising technologies: Medicare's 'coverage with evidence development'

21 January 2018

1 reference

12 December 2020

Diagnostic clinical genome and exome sequencing

1 reference

12 December 2020

Genetic testing and FDA regulation: overregulation threatens the emergence of genomic medicine

1 reference

12 December 2020

Clinical utility of genetic and genomic services: a position statement of the American College of Medical Genetics and Genomics

1 reference

12 December 2020

Coverage With Evidence Development Activities Around The World: An Environment Scan

1 reference

12 December 2020

BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes

1 reference

12 December 2020

10.1586/14737159.2016.1146593

Identifiers

DOI

1 reference

16 August 2017

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16 August 2017

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