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

From Wikidata

Jump to navigation Jump to search

scientific article

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

Statements

scholarly article

1 reference

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)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

0 references

personal genomics

1 reference

based on heuristic

inferred from title

4

object named as

John P A Ioannidis

0 references

Francis Collins

14

object named as

Francis S Collins

0 references

Centers for Disease Control and Prevention

43

object named as

Centers for Disease Control and Prevention

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Rebekah Rasooly

object named as

Rebekah S Rasooly

35

0 references

Jay M. Bernhardt

object named as

Jay M Bernhardt

9

0 references

Michael S. Lauer

object named as

Michael S Lauer

30

0 references

George M. Church

object named as

George M Church

12

0 references

Robert C. Green

22

object named as

Robert C Green

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Stephen Chanock

11

object named as

Stephen J Chanock

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

32

object named as

Kenneth Offit

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

7

object named as

Marta Gwinn

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1

object named as

Muin J Khoury

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Sheri D Schully

3

object named as

Sheri D Schully

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Cecile Janssens

6

object named as

A Cecile J W Janssens

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

42

object named as

Jianfeng Xu

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Kári Stefánsson

36

object named as

Kari Stefansson

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Sharon L R Kardia

28

object named as

Sharon L R Kardia

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Sharon F. Terry

37

object named as

Sharon F Terry

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Jeffrey Gulcher

25

object named as

Jeffrey R Gulcher

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

16

0 references

Philip Greenland

24

object named as

Philip Greenland

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Ralph J. Coates

13

object named as

Ralph J Coates

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

29

object named as

Paul L Kimmel

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

Colleen M McBride

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

W Gregory Feero

5

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Denise G Simons-Morton

8

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Michele Cargill

10

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Robert T Croyle

15

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Gregory J Downing

17

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Amy Duross

18

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Susan Friedman

19

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Mitchell H Gail

20

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Geoffrey S Ginsburg

21

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Mark H Greene

23

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Andro Hsu

26

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Kathy L Hudson

27

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Amy M Miller

31

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

David F Ransohoff

33

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

J Scott Roberts

34

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Steven M Teutsch

38

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Angela Trepanier

39

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Kay L Wanke

40

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

John S Witte

41

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

language of work or name

0 references

publication date

1 August 2009

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

number of pages

9

1 reference

based on heuristic

inferred from page(s)

Genetics in Medicine

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

559-567

1 reference

Europe PubMed Central

PubMed publication ID

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Disclosure of APOE genotype for risk of Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

The genomic applications in practice and prevention network

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Estimation of the warfarin dose with clinical and pharmacogenetic data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Meta-analysis in genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Pharmacogenomic dosing of warfarin: ready or not?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Assessing the value of risk predictions by using risk stratification tables

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Genetic mapping in human disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Pharmacogenomics: candidate gene identification, functional validation and mechanisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Genome-based prediction of common diseases: advances and prospects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Putting science over supposition in the arena of personalized genomics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

A HapMap harvest of insights into the genetics of common disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Integrating the predictiveness of a marker with its performance as a classifier

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Assessment of cumulative evidence on genetic associations: interim guidelines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Pharmacogenetics and pharmacogenomics: development, science, and translation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

On criteria for evaluating models of absolute risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

A meta-analysis of the effect of mediated health communication campaigns on behavior change in the United States

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Simple tools for understanding risks: from innumeracy to insight

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

Population screening in the age of genomic medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

5 July 2018

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

1 reference

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

21 January 2018

Misdirected precaution

1 reference

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

21 January 2018

A navigator for human genome epidemiology.

1 reference

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

21 January 2018

Time to check CHEK2 in families with breast cancer?

1 reference

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

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?

1 reference

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

21 January 2018

Pharmacogenetics--tailoring treatment for the outliers

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

The evidence dilemma in genomic medicine

1 reference

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

21 January 2018

Incorporating biomarkers of exposure and genetic susceptibility into smoking cessation treatment: effects on smoking-related cognitions, emotions, and behavior change

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2936269

28 October 2018

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

1 reference

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

21 January 2018

Beyond odds ratios — communicating disease risk based on genetic profiles

1 reference

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

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

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34113976&oldid=2255062830"