Evidence map›Paper›PMID 24056909›Full record

ArticleMolecular psychiatry2013

Questions about DISC1 as a genetic risk factor for schizophrenia.

P F Sullivan

Abstract readEditorial
In one paragraph

Article in Molecular psychiatry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 3 pooled it
–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

57 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
  6. Article
  7. Zebrafish as a model to investigate the CRH axis and interactions with DISC1.Current opinion in endocrine and metabolic research · 2022
    Review
  8. Advantages and Limitations of Animal Schizophrenia Models.International journal of molecular sciences · 2022
    Review
  9. Review
  10. Article
  11. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

P F SullivanDepartments of Genetics and Psychiatry, Center for Psychiatric Genomics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Funding

1/4 Psychiatric GWAS Consortium: Genomic Follow-up Next-Gen Sequencing & GenotypiU01MH094421 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2012 to 2015
$1.9M
NIMH NIH HHS U01 MH094421
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

CausalityChromosome BreakpointsChromosomes, Human, Pair 1Chromosomes, Human, Pair 11Conduct DisorderGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLod ScoreMental DisordersMood DisordersNerve Tissue ProteinsPedigreePhenotypeRisk FactorsRNA, Long NoncodingDISC1 protein, humanNerve Tissue ProteinsRNA, Long Noncoding

Identifiers

PMID24056909
PMCPMC3967792

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.