Evidence map›Paper›PMID 24012080›Full record

ReviewChild and adolescent psychiatric clinics of North America2013

Genetics of childhood-onset schizophrenia.

Robert F Asarnow, Jennifer K Forsyth

Open access · greenAbstract readReview
In one paragraph

Review in Child and adolescent psychiatric clinics of North America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Genetic aspects in schizophrenia. Receptoral theories. Metabolic theories.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie · 2020
    Article
  7. Article
  8. Childhood-Onset Schizophrenia: Insights from Induced Pluripotent Stem Cells.International journal of molecular sciences · 2018
    Review
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Robert F AsarnowDepartment of Psychiatry and Biobehavioral Sciences, University of California at Los Angeles, Los Angeles, CA 90024, USA; Department of Psychology, University of California at Los Angeles, Los Angeles, CA 90024, USA. Electronic address: rasarnow@mednet.ucla.edu.
Jennifer K Forsyth
University of California, Los Angeles · US

Funding

FAMILIAL PSYCHIATRIC DIS &ATTENTION IN SCHIZOPHRENIAR01MH045112 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ASARNOW, ROBERT F · 2000 to 2004
$2.7M
Cortical-Striatal Dysfunction and Vulnerability to SchizophreniaR24MH072697 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ASARNOW, ROBERT F · 2005 to 2007
$1.0M
NIMH NIH HHS MH 72697NIMH NIH HHS R01 MH045112NIMH NIH HHS R24 MH072697
6 · The paper itself

Abstract

Schizophrenia is a heritable disorder. The genetic architecture of schizophrenia is complex and heterogeneous. This article discusses genetic studies of childhood-onset schizophrenia (COS) and compares findings in familial aggregation, common allele, and rare allele studies of COS with those for adult-onset schizophrenia (AOS). COS seems to be a rare variant of AOS with greater familial aggregation of schizophrenia spectrum disorders and higher occurrence of rare allelic variants. The usefulness of genetic screening for diagnosis and individualized treatment is limited; however, identifying common pathways through which multiple genes adversely affect neural systems offers great promise toward developing novel pharmacologic interventions.

Indexed as

Genome-Wide Association StudyAge of OnsetAllelesAutistic DisorderChildEndophenotypesGene-Environment InteractionGenetic PleiotropyGenetic Predisposition to DiseaseGenetic TestingGenetic VariationGenomic Structural VariationHumansNational Institute of Mental Health (U.S.)Precision MedicineSchizophreniaAutismChildhood-onset schizophreniaCommon allelesCopy number variantsGeneticsGWASRare alleles

Identifiers

PMID24012080
PMCPMC4364758
OpenAlexW2095911762

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.