Evidence map›Paper›PMID 32605438›Full record

ArticleThe American journal of psychiatry2020

Subcortical Signatures of Hemizygosity and Psychosis in 22q11.2 Deletion Syndrome: Finding Common Ground in Rare Genetic Variation.

Daniel P Eisenberg, Michael D Gregory, Karen F Berman

Open access · bronzeAbstract readEditorialComment
PubMed Full text at PMC Publisher
In one paragraph

Article in The American journal of psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 46% of its field
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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Daniel P EisenbergClinical and Translational Neuroscience Branch, NIMH, Intramural Research Program, Bethesda, Md.
Michael D GregoryClinical and Translational Neuroscience Branch, NIMH, Intramural Research Program, Bethesda, Md.
Karen F BermanClinical and Translational Neuroscience Branch, NIMH, Intramural Research Program, Bethesda, Md.
Office of Extramural Research · US

Funding

Imaging of Neuropsychiatric Disorders with Developmental and Genetic MechanismsZIAMH002652 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI BERMAN, KAREN FAITH · 2009 to 2025
$17.3M
PET STUDIES OF FRONTAL LOBE IN NEUROPSYCHIATRIC DISEASE, SCHIZOPHRENIAZ01MH002652 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI BERMAN, KAREN FAITH · 1993 to 2008
$2.0M
Intramural NIH HHS Z01 MH002652Intramural NIH HHS ZIA MH002652
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ArachnodactylyDiGeorge SyndromeMarfan SyndromePsychotic DisordersGenetic VariationHumans22q11.2 Deletion SyndromeCopy Number VariantNeuroanatomyNeurodevelopmentPsychosisSchizophrenia

Identifiers

PMID32605438
PMCPMC9583700
OpenAlexW3040584310

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.