Evidence map›Paper›PMID 22005598›Full record

ReviewPharmacology, biochemistry, and behavior2012

Expression profiling in neuropsychiatric disorders: emphasis on glutamate receptors in bipolar disorder.

Stephen D Ginsberg, Scott E Hemby, John F Smiley

Abstract readReview
In one paragraph

Review in Pharmacology, biochemistry, and behavior, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Teneurin-4 promotes cellular protrusion formation and neurite outgrowth through focal adhesion kinase signaling.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2014
    Article
  12. Article
  13. Integrated neurobiology of bipolar disorder.Frontiers in psychiatry · 2014
    Review
  14. Article
  15. 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

3 authors at 3 institutions in 1 country.

Stephen D GinsbergCenter for Dementia Research, Nathan Kline Institute, Orangeburg, NY, USA. ginsberg@nki.rfmh.org
Scott E Hemby
John F Smiley
Nathan Kline Institute for Psychiatric Research · USNYU Langone Health · USWake Forest University · US

Funding

TAU, AB, SYNUCLEIN AND NITRATIVE/OXIDATIVE DAMAGE IN MCIP01AG014449 · NIA · UNIVERSITY OF PITTSBURGH · PI COUNTS, SCOTT E · 1997 to 2024
$39.7M
The Conte Center for Schizophrenia ResearchP50MH086385 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI JAVITT, DANIEL C. · 2009 to 2013
$10.7M
Cellular and Molecular Medial Temporal Lobe Pathology in Elderly PreMCI subjectsR01AG043375 · NIA · ST. JOSEPH'S HOSPITAL AND MEDICAL CENTER · PI GINSBERG, STEPHEN D, MUFSON, ELLIOTT JAY · 2013 to 2017
$3.6M
Cortical interneuron number and expression profile in schizophreniaR21MH085208 · NIMH · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI SMILEY, JOHN F · 2009 to 2010
$435k
NIA NIH HHS P01 AG014449NIA NIH HHS R01 AG043375NIMH NIH HHS MH085208NIMH NIH HHS MH086385NIMH NIH HHS P50 MH086385NIMH NIH HHS R21 MH085208
6 · The paper itself

Abstract

Functional genomics and proteomics approaches are being employed to evaluate gene and encoded protein expression changes with the tacit goal to find novel targets for drug discovery. Genome-wide association studies (GWAS) have attempted to identify valid candidate genes through single nucleotide polymorphism (SNP) analysis. Furthermore, microarray analysis of gene expression in brain regions and discrete cell populations has enabled the simultaneous quantitative assessment of relevant genes. The ability to associate gene expression changes with neuropsychiatric disorders, including bipolar disorder (BP), and their response to therapeutic drugs provides a novel means for pharmacotherapeutic interventions. This review summarizes gene and pathway targets that have been identified in GWAS studies and expression profiling of human postmortem brain in BP, with an emphasis on glutamate receptors (GluRs). Although functional genomic assessment of BP is in its infancy, results to date point towards a dysregulation of GluRs that bear some similarity to schizophrenia (SZ), although the pattern is complex, and likely to be more complementary than overlapping. The importance of single population expression profiling of specific neurons and intrinsic circuits is emphasized, as this approach provides informative gene expression profile data that may be underappreciated in regional studies with admixed neuronal and non-neuronal cell types.

Indexed as

Gene Expression ProfilingBipolar DisorderGenome-Wide Association StudyHumansReceptors, GlutamateReceptors, Glutamate

Identifiers

PMID22005598
PMCPMC3253885
OpenAlexW2159910813

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.