The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop (Q34113976)

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English	The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop	scientific article

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scholarly article

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Europe PubMed Central

31 July 2017

The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop (English)

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Europe PubMed Central

31 July 2017

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personal genomics

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based on heuristic

inferred from title

4

object named as

John P A Ioannidis

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Francis Collins

14

object named as

Francis S Collins

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Centers for Disease Control and Prevention

43

object named as

Centers for Disease Control and Prevention

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31 July 2017

Rebekah Rasooly

object named as

Rebekah S Rasooly

35

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Jay M. Bernhardt

object named as

Jay M Bernhardt

9

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Michael S. Lauer

object named as

Michael S Lauer

30

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George M. Church

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George M Church

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Robert C. Green

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object named as

Robert C Green

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31 July 2017

Stephen Chanock

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object named as

Stephen J Chanock

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32

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Kenneth Offit

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7

object named as

Marta Gwinn

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Muin J Khoury

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Sheri D Schully

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object named as

Sheri D Schully

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Cecile Janssens

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object named as

A Cecile J W Janssens

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42

object named as

Jianfeng Xu

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Kári Stefánsson

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object named as

Kari Stefansson

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Sharon L R Kardia

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object named as

Sharon L R Kardia

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Sharon F. Terry

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object named as

Sharon F Terry

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Jeffrey Gulcher

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object named as

Jeffrey R Gulcher

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Philip Greenland

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object named as

Philip Greenland

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Ralph J. Coates

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object named as

Ralph J Coates

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author name string

Colleen M McBride

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W Gregory Feero

5

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31 July 2017

Denise G Simons-Morton

8

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Michele Cargill

10

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Robert T Croyle

15

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Gregory J Downing

17

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Amy Duross

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Susan Friedman

19

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Mitchell H Gail

20

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Geoffrey S Ginsburg

21

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Mark H Greene

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Andro Hsu

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Kathy L Hudson

27

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Paul L Kimmel

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Amy M Miller

31

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David F Ransohoff

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J Scott Roberts

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Steven M Teutsch

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Angela Trepanier

39

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Kay L Wanke

40

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John S Witte

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language of work or name

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publication date

1 August 2009

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31 July 2017

number of pages

9

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Genetics in Medicine

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11

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559-567

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8

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31 July 2017

https://scigraph.springernature.com/pub.10.1097/gim.0b013e3181b13a6c

0 references

Impact of adding a single allele in the 9p21 locus to traditional risk factors on reclassification of coronary heart disease risk and implications for lipid-modifying therapy in the Atherosclerosis Risk in Communities study

1 reference

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Disclosure of APOE genotype for risk of Alzheimer's disease

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The genomic applications in practice and prevention network

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A health services research agenda for cellular, molecular and genomic technologies in cancer care

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Psychosocial aspects of DNA testing for hereditary hemochromatosis in at-risk individuals: a systematic review

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Estimation of the warfarin dose with clinical and pharmacogenetic data

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Meta-analysis in genome-wide association studies

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Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers

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Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3.

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Recommendations from the EGAPP Working Group: can UGT1A1 genotyping reduce morbidity and mortality in patients with metastatic colorectal cancer treated with irinotecan?

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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

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Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans.

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Pharmacogenomic dosing of warfarin: ready or not?

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Assessing the value of risk predictions by using risk stratification tables

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Genetic mapping in human disease

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Looking to the future of new media in health marketing: deriving propositions based on traditional theories.

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Pharmacogenomics: candidate gene identification, functional validation and mechanisms

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Genome-based prediction of common diseases: advances and prospects

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

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Predicting type 2 diabetes based on polymorphisms from genome-wide association studies: a population-based study

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Size matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiology

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Putting science over supposition in the arena of personalized genomics

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Psychosocial issues in genetic testing for familial adenomatous polyposis: a review of the literature.

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Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk

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Gauging the performance of SNPs, biomarkers, and clinical factors for predicting risk of breast cancer

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Assessing the combined impact of 18 common genetic variants of modest effect sizes on type 2 diabetes risk

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A HapMap harvest of insights into the genetics of common disease

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Genome-wide association studies for complex traits: consensus, uncertainty and challenges

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Rare independent mutations in renal salt handling genes contribute to blood pressure variation

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A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions

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Health behavior changes after genetic risk assessment for Alzheimer disease: The REVEAL Study

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Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men.

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General cardiovascular risk profile for use in primary care: the Framingham Heart Study

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Letting the genome out of the bottle--will we get our wish?

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Assessment of cumulative evidence on genetic associations: interim guidelines

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The impact of genotype frequencies on the clinical validity of genomic profiling for predicting common chronic diseases

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Self-regulation and the behavioural response to DNA risk information: a theoretical analysis and framework for future research

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Blazing a trail: a public health research agenda in genomics and chronic disease

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On criteria for evaluating models of absolute risk

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1 reference

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5 July 2018

Who seeks genetic susceptibility testing for Alzheimer's disease? Findings from a multisite, randomized clinical trial

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Population screening in the age of genomic medicine

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5 July 2018

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21 January 2018

Misdirected precaution

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21 January 2018

A navigator for human genome epidemiology.

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21 January 2018

Time to check CHEK2 in families with breast cancer?

1 reference

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21 January 2018

What is the clinical utility of genetic testing?

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B13A6C

21 January 2018

Developing a center for comparative effectiveness information.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B13A6C

21 January 2018

Genetic susceptibility testing versus family history-based risk assessment: Impact on perceived risk of Alzheimer disease.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B13A6C

21 January 2018

Evaluating the utility of personal genomic information.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B13A6C

21 January 2018

Pharmacogenomics--ready for prime time?

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181B13A6C

21 January 2018

Pharmacogenetics--tailoring treatment for the outliers

1 reference

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21 January 2018

Cost-effectiveness of using pharmacogenetic information in warfarin dosing for patients with nonvalvular atrial fibrillation

1 reference

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21 January 2018

Effects of attributing serious mental illnesses to genetic causes on orientations to treatment.

1 reference

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21 January 2018

The feasibility of online genetic testing for lung cancer susceptibility: uptake of a web-based protocol and decision outcomes

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21 January 2018

Predictors of attrition and weight loss in an adolescent weight control program.

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21 January 2018

The evidence dilemma in genomic medicine.

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21 January 2018

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28 October 2018

Turning the Pump Handle: Evolving Methods for Integrating the Evidence on Gene-Disease Association

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21 January 2018

Beyond odds ratios — communicating disease risk based on genetic profiles

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21 January 2018

Update on the methods of the U.S. Preventive Services Task Force: insufficient evidence

1 reference

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12 December 2020

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Difficulty in losing weight by behavioral intervention for women with Trp64Arg polymorphism of the beta3-adrenergic receptor gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19617843

12 December 2020

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Psychological impact of genetic testing for familial hypercholesterolemia within a previously aware population: A randomized controlled trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/19617843

12 December 2020

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The case for a global human genome epidemiology initiative

1 reference

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12 December 2020

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When is measuring sensitivity and specificity sufficient to evaluate a diagnostic test, and when do we need randomized trials?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19617843

12 December 2020

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Risky communication: pitfalls in counseling about risk, and how to avoid them

1 reference

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12 December 2020

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Point: genetic risk feedback for common disease time to test the waters

1 reference

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12 December 2020

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Counterpoint: genetic risk feedback for common disease time to test the waters

1 reference

https://pubmed.ncbi.nlm.nih.gov/19617843

12 December 2020

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The genome gets personal--almost

1 reference

https://pubmed.ncbi.nlm.nih.gov/19617843

12 December 2020

based on heuristic

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Genomic profiles for disease risk: predictive or premature?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19617843

12 December 2020

based on heuristic

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Cohort studies and the genetics of complex disease

1 reference

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12 December 2020

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Personalized genetic prediction: too limited, too expensive, or too soon?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19617843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1097/GIM.0B013E3181B13A6C

1 reference

Europe PubMed Central

31 July 2017

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0 references

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

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