Evidence map›Paper›PMID 23190151›Full record

ReviewAnnual review of medicine2013

Treating the developing brain: implications from human imaging and mouse genetics.

B J Casey, Siobhan S Pattwell, Charles E Glatt, Francis S Lee

Abstract readReview
In one paragraph

Review in Annual review of medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Trial
  2. Review
  3. Individual-specific functional connectivity of the amygdala: A substrate for precision psychiatry.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  4. Article
  5. Adolescent ΔBiological psychiatry · 2019
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. The Genetics of Stress-Related Disorders: PTSD, Depression, and Anxiety Disorders.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Review
  11. Review
  12. Article
  13. Review
  14. Sensitive periods in affective development: nonlinear maturation of fear learning.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2015
    Review
  15. 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
  16. Article
  17. 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

4 authors.

B J CaseySackler Institute for Developmental Psychology, Department of Psychiatry, Weill Cornell MedicalCollege, New York, New York 10065, USA. bjc2002@med.cornell.edu
Siobhan S Pattwell
Charles E Glatt
Francis S Lee

Funding

Role of conflict in memoryP50MH062196 · NIMH · PRINCETON UNIVERSITY · PI COHEN, JONATHAN D · 2000 to 2009
$18.9M
Statistical Genetics Core: Impact of BDNF Genotype and Stress on LearningP50MH079513 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI CASEY, BETTY J · 2008 to 2012
$9.4M
The Impact of the BDNF Val66Met Prodomain on Cognitive Function in a Mouse Model of Alzheimer's DiseaseR01NS052819 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI HEMPSTEAD, BARBARA L, LEE, FRANCIS SANG YONG · 2005 to 2019
$5.3M
Molecular Mechanisms of SSRI Action in Childhood and AdolescenceRC1MH088814 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI LEE, FRANCIS SANG YONG · 2009 to 2010
$1.0M
NIMH NIH HHS P50 MH079513NIMH NIH HHS P50 MH62196NIMH NIH HHS RC1 MH088814NINDS NIH HHS R01 NS052819
6 · The paper itself

Abstract

A fundamental issue in psychiatric medicine is the lack of empirical evidence indicating when, during development, a treatment will be most effective for a patient. We review behavioral and brain changes that occur across development, focusing on the period of adolescence, when there is a peak in diagnosis of many psychiatric disorders. We use anxiety disorders as an example because of their high prevalence in youth (affecting as many as 1 in 10). Basic forms of fear learning, which are at the core of anxiety disorders and are the targets of behavioral therapeutics, are examined as a function of age. We also discuss how fear learning has been genetically modulated in mice and humans. Based on these findings, we provide future directions for determining the efficacy of innovative therapies and preventive strategies for anxiety disorders as a function of age and potential genetic effects inferred from mice and humans.

Indexed as

Mental DisordersAnimalsBehavior TherapyBrainDiagnostic ImagingDisease Models, AnimalHumansMicePsychiatric Status Rating Scales

Identifiers

PMID23190151
PMCPMC4372469

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.