Evidence map›Paper›PMID 20954426›Full record

ReviewDialogues in clinical neuroscience2010

Genetics in schizophrenia: where are we and what next?

Arun K Tiwari, Clement C Zai, Daniel J Müller, James L Kennedy

Open access · diamondAbstract readReview
In one paragraph

Review in Dialogues in clinical neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.1field-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

15 citing papers in PubMed, 60 citations in OpenAlex.

  1. Influence of ANKK1 and DRD2 polymorphisms in response to haloperidol.European archives of psychiatry and clinical neuroscience · 2013
    Trial
  2. Review
  3. Article
  4. Article
  5. Neuroimaging in schizophrenia: A review article.Frontiers in neuroscience · 2022
    Review
  6. Review
  7. Role of calcium channels in bipolar disorder.Current psychopharmacology · 2017
    Article
  8. Article
  9. Review
  10. Article
  11. Abnormal activity of the MAPK- and cAMP-associated signaling pathways in frontal cortical areas in postmortem brain in schizophrenia.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2012
    Article
  12. Article
  13. AKT/GSK3 signaling pathway and schizophrenia.Frontiers in molecular neuroscience · 2012
    Article
  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

4 authors at 1 institution in 1 country.

Arun K TiwariNeurogenetics section, Neuroscience department, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Clement C Zai
Daniel J Müller
James L Kennedy
Centre for Addiction and Mental Health · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the genetic basis of schizophrenia continues to be major challenge. The research done during the last two decades has provided several candidate genes which unfortunately have not been consistently replicated across or within a population. The recent genome-wide association studies (GWAS) and copy number variation (CNV) studies have provided important evidence suggesting a role of both common and rare large CNVs in schizophrenia genesis. The burden of rare copy number variations appears to be increased in schizophrenia patients. A consistent observation among the GWAS studies is the association with schizophrenia of genetic markers in the major histocompatibility complex (6p22.1)-containing genes including NOTCH4 and histone protein loci. Molecular genetic studies are also demonstrating that there is more overlap between the susceptibility genes for schizophrenia and bipolar disorder than previously suspected. In this review we summarize the major findings of the past decade and suggest areas of future research.

Indexed as

GeneticsDNA Copy Number VariationsGenome-Wide Association StudyHumansProto-Oncogene ProteinsReceptor, Notch4Receptors, NotchSchizophreniaNOTCH4 protein, humanProto-Oncogene ProteinsReceptor, Notch4Receptors, Notch

Identifiers

PMID20954426
PMCPMC3181975
OpenAlexW101570666

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.