Evidence map›Paper›PMID 19259126›Full record

ArticleEuropean journal of human genetics : EJHG2009

Genetic horoscopes: is it all in the genes? Points for regulatory control of direct-to-consumer genetic testing.

Christine Patch, Jorge Sequeiros, Martina C Cornel

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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  15. Direct to consumer genetic tests.European journal of human genetics : EJHG · 2009
    Article
  16. Challenges of incorporating pharmacogenomics into clinical practice.Gastrointestinal cancer research : GCR · 2009
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Christine PatchPublic and Professional Policy Committee of the European Society of Human Genetics, Vienna, Austria. christine.patch@gstt.nhs.uk
Jorge Sequeiros
Martina C Cornel

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of tests for genetic susceptibility to common complex diseases has raised concerns. These concerns relate to evaluation of the scientific and clinical validity and utility of the tests, quality assurance of laboratories and testing services, advice and protection for the consumer and the appropriate regulatory and policy response. How these concerns are interpreted and addressed is an ongoing debate. If the possibility of using the discoveries from genomic science to improve health is to be realised without losing public confidence, then improvements in the evaluation and mechanisms for control of supply of tests may be as important as the science itself.

Indexed as

Government RegulationMarketing of Health ServicesAttitude to HealthConsumer AdvocacyGenesGenetic CounselingGenetic PrivacyGenetic TestingHumansQuality ControlReproducibility of Results

Identifiers

PMID19259126
PMCPMC2986502

What OpenQuestion holds

Textmetadata
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.