Evidence map›Paper›PMID 19302770›Full record

ReviewCurrent psychiatry reports2009

The genetics of childhood-onset schizophrenia: when madness strikes the prepubescent.

Anjené M Addington, Judith L Rapoport

Open access · greenAbstract readReview
In one paragraph

Review in Current psychiatry reports, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 4 pooled it
4.2field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 4 syntheses or guidelines pooled it, 87 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Article
  7. Article
  8. Copy Number Variations in Neuropsychiatric Disorders.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. Obstacles to diagnostic investigation of a child with comorbid psychiatric conditions.Scandinavian journal of child and adolescent psychiatry and psychology · 2021
    Article
  13. Article
  14. Progress in iPSC-Based Modeling of Psychiatric Disorders.International journal of molecular sciences · 2019
    Review
  15. Social skills, executive functioning and social engagement.Schizophrenia research. Cognition · 2019
    Article
  16. Review
  17. Childhood-Onset Schizophrenia: Insights from Induced Pluripotent Stem Cells.International journal of molecular sciences · 2018
    Review
  18. Synaptic Actin Dysregulation, a Convergent Mechanism of Mental Disorders?The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Review
  19. A novel de novo mutation in ATP1A3 and childhood-onset schizophrenia.Cold Spring Harbor molecular case studies · 2016
    Article
  20. 15q13.3 duplication in two patients with childhood-onset schizophrenia.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2016
    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.

Anjené M AddingtonChild Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Room 3N202, Bethesda, MD 20892, USA. addingta@mail.nih.gov
Judith L Rapoport
National Institute of Mental Health · US

Funding

Childhood Onset SchizophreniaZIAMH002581 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI RAPOPORT, JUDITH L. · 2009 to 2017
$25.5M
CHILDHOOD ONSET SCHIZOPHRENIAZ01MH002581 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI RAPOPORT, JUDITH L. · 1991 to 2008
$2.5M
Intramural NIH HHS Z01 MH002581
6 · The paper itself

Abstract

Stratification by age at onset has been useful for genetic studies across all of medicine. For the past 20 years, the National Institute of Mental Health has been systematically recruiting patients with onset of schizophrenia before age 13 years. Examination of familial transmission of known candidate risk genes was carried out, and a 10% rate of cytogenetic abnormalities was found. Most recently, high-density, array-based scans for submicroscopic rare copy number variations (CNVs) have suggested that this kind of genetic variation occurs more frequently than expected by chance in childhood-onset schizophrenia (COS) and at a higher rate than observed in adult-onset disorder. Several CNVs and cytogenetic abnormalities associated with COS are also seen in autism and mental retardation. Populations with COS may have more salient genetic influence than adult-onset cases. The relationship of rare CNVs to prepsychotic development is being studied further.

Indexed as

ChildChromosome AberrationsGene ExpressionHumansSchizophrenia, Childhood

Identifiers

PMID19302770
PMCPMC2763299
OpenAlexW2064017214

What OpenQuestion holds

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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.