Evidence map›Paper›PMID 29031917›Full record

ArticleBiological psychiatry2017

How Good Were Candidate Gene Guesses in Schizophrenia Genetics?

Patrick F Sullivan

Abstract readComment
In one paragraph

Article in Biological psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Genetic Architecture of Depression: Where Do We Stand Now?Advances in experimental medicine and biology · 2021
    Article
  5. Article
  6. How genome-wide association studies (GWAS) made traditional candidate gene studies obsolete.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    Review
  7. Review
  8. Review
  9. Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2019
    Article
  10. Article
  11. Review
  12. Combination ofFrontiers in psychiatry · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

Patrick F SullivanDepartments of Genetics and Psychiatry, University of North Carolina at Chapel Hill, North Carolina; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden. Electronic address: pfsulliv@med.unc.edu.

Funding

A Large-Scale Schizophrenia Association Study in SwedenR01MH077139 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2007 to 2018
$9.9M
1/7 Psychiatric Genomics Consortium: Finding actionable variationU01MH109528 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2016 to 2020
$2.5M
NIMH NIH HHS R01 MH077139NIMH NIH HHS U01 MH109528
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

SchizophreniaGenetic Predisposition to DiseaseHumans

Identifiers

PMID29031917
PMCPMC6950644

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.