Evidence map›Paper›PMID 20733502›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2010

Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium.

Ellen Wright Clayton, Maureen Smith, Stephanie M Fullerton, Wylie Burke, Catherine A McCarty, Barbara A Koenig, Amy L McGuire, Laura M Beskow, Lynn Dressler, Amy A Lemke and 3 more

Abstract read
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Preferences for Accessing Electronic Health Records for Research Purposes: Views of Parents Who Have a Child With a Known or Suspected Genetic Condition.Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research · 2020
    Article
  5. Article
  6. Enabling phenotypic big data with PheNorm.Journal of the American Medical Informatics Association : JAMIA · 2018
    Article
  7. How Sensitive Is Genetic Data?Biopreservation and biobanking · 2017
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The translational potential of research on the ethical, legal, and social implications of genomics.Genetics in medicine : official journal of the American College of Medical Genetics · 2015
    Review
  18. Secondary use of clinical data: the Vanderbilt approach.Journal of biomedical informatics · 2014
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Ellen Wright ClaytonCenter for Biomedical Ethics and Society, Vanderbilt University, Nashville, TN, USA. ellen.clayton@vanderbilt.edu
Maureen Smith
Stephanie M Fullerton
Wylie Burke
Catherine A McCarty
Barbara A Koenig
Amy L McGuire
Laura M Beskow
Lynn Dressler
Amy A Lemke
Erin M Ramos
Laura Lyman Rodriguez
Consent and Community Consultation Working Group of the eMERGE Consortium

Funding

Vanderbilt Genome-Electronic Records ProjectU01HG004603 · NHGRI · VANDERBILT UNIVERSITY · PI RODEN, DAN M · 2007 to 2011
$7.3M
Development and Use of Network Infrastructure for High-Throughput GWA StudiesU01HG004610 · NHGRI · KAISER FOUNDATION HEALTH PLAN OF WASHINGTON · PI LARSON, ERIC B · 2007 to 2010
$4.2M
Genetic Discovery and Application in a Clinical Setting Continuing a PartnershipU01HG006375 · NHGRI · KAISER FOUNDATION HEALTH PLAN OF WASHINGTON · PI JARVIK, GAIL PAIRITZ, LARSON, ERIC B · 2011 to 2014
$4.1M
EMR Phenotypes and Community Engaged Genomic AssociationsU01HG004599 · NHGRI · MAYO CLINIC ROCHESTER · PI CHUTE, CHRISTOPHER G · 2007 to 2010
$3.7M
Genome-wide Studies from the NUgene BiorespositoryU01HG004609 · NHGRI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CHISHOLM, REX L · 2007 to 2010
$3.7M
Genome-Wide Study of Cataract and Low HDL in the Personalized Medicine Research PU01HG004608 · NHGRI · MARSHFIELD CLINIC RESEARCH FOUNDATION · PI MCCARTY, CATHERINE ANNE · 2007 to 2010
$3.3M
NHGRI NIH HHS U01 HG004599NHGRI NIH HHS U01 HG004603NHGRI NIH HHS U01 HG004608NHGRI NIH HHS U01-HG-004608NHGRI NIH HHS U01 HG004609NHGRI NIH HHS U01HG004609NHGRI NIH HHS U01 HG004610NHGRI NIH HHS U01-HG-004610NHGRI NIH HHS U01 HG006375NHGRI NIH HHS U01-HG-04599NHGRI NIH HHS U01-HG-04603
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Electronic Health RecordsGenetic ResearchGenome-Wide Association StudyCommunity-Based Participatory ResearchConfidentialityEthics Committees, ResearchEthics, MedicalGenomicsHumansInformation DisseminationInformed ConsentInterinstitutional RelationsNational Human Genome Research Institute (U.S.)National Institutes of Health (U.S.)Physician-Patient RelationsResearch Design

Identifiers

PMID20733502
PMCPMC3090678

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.