(Q34113976)

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

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Europe PubMed Central

PubMed publication ID

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

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31 July 2017

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personal genomics

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4

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John P A Ioannidis

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Francis Collins

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Francis S Collins

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Centers for Disease Control and Prevention

43

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Centers for Disease Control and Prevention

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31 July 2017

Rebekah Rasooly

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Rebekah S Rasooly

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Jay M. Bernhardt

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Jay M Bernhardt

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Michael S. Lauer

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Michael S Lauer

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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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Robert C Green

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31 July 2017

Stephen Chanock

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Stephen J Chanock

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Kenneth Offit

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Marta Gwinn

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Muin J Khoury

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Sheri D Schully

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Sheri D Schully

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Cecile Janssens

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A Cecile J W Janssens

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Jianfeng Xu

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Kári Stefánsson

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Kari Stefansson

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Sharon L R Kardia

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Sharon L R Kardia

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Sharon F. Terry

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Sharon F Terry

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Jeffrey Gulcher

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Jeffrey R Gulcher

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Philip Greenland

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Philip Greenland

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Ralph J. Coates

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Ralph J Coates

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31 July 2017

author name string

Colleen M McBride

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31 July 2017

W Gregory Feero

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31 July 2017

Denise G Simons-Morton

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31 July 2017

Michele Cargill

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Robert T Croyle

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Gregory J Downing

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31 July 2017

Amy Duross

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Susan Friedman

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Mitchell H Gail

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Geoffrey S Ginsburg

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31 July 2017

Mark H Greene

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31 July 2017

Andro Hsu

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Kathy L Hudson

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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

41

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31 July 2017

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0 references

publication date

1 August 2009

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31 July 2017

number of pages

9

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inferred from page(s)

Genetics in Medicine

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31 July 2017

11

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31 July 2017

8

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31 July 2017

559-567

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31 July 2017

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

1 reference

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5 July 2018

The genomic applications in practice and prevention network

1 reference

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5 July 2018

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

1 reference

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

1 reference

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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

1 reference

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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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

1 reference

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5 July 2018

Recommendations from the EGAPP Working Group: can tumor gene expression profiling improve outcomes in patients with breast cancer?

1 reference

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

1 reference

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5 July 2018

Pharmacogenomic dosing of warfarin: ready or not?

1 reference

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5 July 2018

Assessing the value of risk predictions by using risk stratification tables

1 reference

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5 July 2018

Genetic mapping in human disease

1 reference

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

1 reference

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5 July 2018

Pharmacogenomics: candidate gene identification, functional validation and mechanisms

1 reference

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5 July 2018

Genome-based prediction of common diseases: advances and prospects

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

Putting science over supposition in the arena of personalized genomics

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

A HapMap harvest of insights into the genetics of common disease

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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

1 reference

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

1 reference

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Recommendations from the EGAPP Working Group: testing for cytochrome P450 polymorphisms in adults with nonpsychotic depression treated with selective serotonin reuptake inhibitors

1 reference

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The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention?

1 reference

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Assessment of cumulative evidence on genetic associations: interim guidelines

1 reference

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

1 reference

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Evaluating the added predictive ability of a new marker: from area under the ROC curve to reclassification and beyond

1 reference

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Using wireless handheld computers and tailored text messaging to reduce negative consequences of drinking alcohol.

1 reference

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5 July 2018

Use and misuse of the receiver operating characteristic curve in risk prediction

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Pharmacogenetics and pharmacogenomics: development, science, and translation

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Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

1 reference

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

1 reference

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

1 reference

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On criteria for evaluating models of absolute risk

1 reference

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

1 reference

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

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Simple tools for understanding risks: from innumeracy to insight

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Population screening in the age of genomic medicine

1 reference

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

1 reference

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21 January 2018

Misdirected precaution

1 reference

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21 January 2018

A navigator for human genome epidemiology.

1 reference

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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

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21 January 2018

Developing a center for comparative effectiveness information

1 reference

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21 January 2018

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

1 reference

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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?

1 reference

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

The evidence dilemma in genomic medicine.

1 reference

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21 January 2018

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1 reference

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28 October 2018

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

1 reference

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21 January 2018

Beyond odds ratios — communicating disease risk based on genetic profiles

1 reference

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21 January 2018

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

based on heuristic

inferred from PubMed ID database lookup

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

based on heuristic

inferred from PubMed ID database lookup

The case for a global human genome epidemiology initiative

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genome gets personal--almost

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic profiles for disease risk: predictive or premature?

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cohort studies and the genetics of complex disease

1 reference

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

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

PubMed publication ID

31 July 2017

Dimensions Publication ID

0 references

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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