Evidence map›Paper›PMID 21309772›Full record

ReviewJournal of child psychology and psychiatry, and allied disciplines2011

Annual Research Review: Transgenic mouse models of childhood-onset psychiatric disorders.

Holly R Robertson, Guoping Feng

Open access · greenAbstract readReview
In one paragraph

Review in Journal of child psychology and psychiatry, and allied disciplines, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. TheJournal of clinical medicine · 2019
    Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Autistic-like syndrome in mu opioid receptor null mice is relieved by facilitated mGluR4 activity.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2014
    Article
  8. Expression of Nampt in hippocampal and cortical excitatory neurons is critical for cognitive function.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  9. Genetic effects on cerebellar structure across mouse models of autism using a magnetic resonance imaging atlas.Autism research : official journal of the International Society for Autism Research · 2014
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
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.

Holly R RobertsonDuke University, Neurobiology Department, Durham, NC, USA.
Guoping Feng
Massachusetts Institute of Technology · US

Funding

Roles of SAPAP Proteins in Synaptic Function and Compulsive-like BehaviorR01MH081201 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI FENG, GUOPING · 2007 to 2011
$1.8M
NIMH NIH HHS R01 MH081201
6 · The paper itself

Abstract

Childhood-onset psychiatric disorders, such as attention deficit hyperactivity disorder (ADHD), autism spectrum disorder (ASD), mood disorders, obsessive compulsive spectrum disorders (OCSD), and schizophrenia (SZ), affect many school-age children, leading to a lower quality of life, including difficulties in school and personal relationships that persist into adulthood. Currently, the causes of these psychiatric disorders are poorly understood, resulting in difficulty diagnosing affected children, and insufficient treatment options. Family and twin studies implicate a genetic contribution for ADHD, ASD, mood disorders, OCSD, and SZ. Identification of candidate genes and chromosomal regions associated with a particular disorder provide targets for directed research, and understanding how these genes influence the disease state will provide valuable insights for improving the diagnosis and treatment of children with psychiatric disorders. Transgenic mouse models are one important approach in the study of human diseases, allowing for the use of a variety of experimental approaches to dissect the contribution of a specific chromosomal or genetic abnormality in human disorders. While it is impossible to model an entire psychiatric disorder in a single mouse model, these models can be extremely valuable in dissecting out the specific role of a gene, pathway, neuron subtype, or brain region in a particular abnormal behavior. In this review we discuss existing transgenic mouse models for childhood-onset psychiatric disorders. We compare the strength and weakness of various transgenic mouse models proposed for each of the common childhood-onset psychiatric disorders, and discuss future directions for the study of these disorders using cutting-edge genetic tools.

Indexed as

Disease Models, AnimalModels, GeneticAnimalsBrainChildDiseases in TwinsDNA Mutational AnalysisGene ExpressionGenetic Association StudiesGenetic LinkageGenotypeHumansMental DisordersMiceMice, TransgenicNerve Net

Identifiers

PMID21309772
PMCPMC3075087
OpenAlexW2110812713

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.