Evidence map›Paper›PMID 20351723›Full record

ArticleMolecular psychiatry2010

Response to Mitchell and Porteus.

P F Sullivan, P V Gejman

Abstract readCommentLetter
In one paragraph

Article in Molecular psychiatry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Genome-wide association studies: a primer.Psychological medicine · 2010
    Article
  3. The role of genetics in the etiology of schizophrenia.The Psychiatric clinics of North America · 2010
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

P F Sullivan
P V Gejman

Funding

Decoding schizophrenia-From GWAS to functional regulatory variantsR01MH105472 · NIMH · DUKE UNIVERSITY · PI CRAWFORD, GREGORY E, SULLIVAN, PATRICK F · 2014 to 2017
$2.9M
NIMH NIH HHS R01 MH105472
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genome-Wide Association StudyDNA Copy Number VariationsHumansMental Disorders

Identifiers

PMID20351723
PMCPMC4188919

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.