Evidence map›Paper›PMID 17043677›Full record

ArticleMolecular psychiatry2007

Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia.

L M Camargo, V Collura, J-C Rain, K Mizuguchi, H Hermjakob, S Kerrien, T P Bonnert, P J Whiting, N J Brandon

Abstract read
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In one paragraph

Article in Molecular psychiatry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 232 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
232citing papers in PubMed, 3 pooled it
10.7field-weighted citation impact, top 1% 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

232 citing papers in PubMed, 3 syntheses or guidelines pooled it, 406 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. A missense mutation in theJournal of medicine and life · 2024
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  10. TransgenicCurrent issues in molecular biology · 2024
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  15. Review
  16. Genetic Influences on Cognitive Dysfunction in Schizophrenia.Current topics in behavioral neurosciences · 2023
    Article
  17. Article
  18. Article
  19. Polysialylation in a DISC1 Mutant Mouse.International journal of molecular sciences · 2022
    Article
  20. Article

172 more citing papers are in PubMed but not listed here.

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

9 authors at 6 institutions in 3 countries.

L M CamargoMerck Research Labs, Merck & Co., Boston, MA 02115, USA. miguel_camargo@merck.com
V Collura
J-C Rain
K Mizuguchi
H Hermjakob
S Kerrien
T P Bonnert
P J Whiting
N J Brandon
MSD (UK) Limited (United Kingdom) · GBHybrigenics (France) · FREuropean Bioinformatics Institute · GBMerck & Co., Inc., Rahway, NJ, USA (United States) · USUniversity of Cambridge · GBWellcome Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disrupted in Schizophrenia 1 (DISC1) is a schizophrenia risk gene associated with cognitive deficits in both schizophrenics and the normal ageing population. In this study, we have generated a network of protein-protein interactions (PPIs) around DISC1. This has been achieved by utilising iterative yeast-two hybrid (Y2H) screens, combined with detailed pathway and functional analysis. This so-called 'DISC1 interactome' contains many novel PPIs and provides a molecular framework to explore the function of DISC1. The network implicates DISC1 in processes of cytoskeletal stability and organisation, intracellular transport and cell-cycle/division. In particular, DISC1 looks to have a PPI profile consistent with that of an essential synaptic protein, which fits well with the underlying molecular pathology observed at the synaptic level and the cognitive deficits seen behaviourally in schizophrenics. Utilising a similar approach with dysbindin (DTNBP1), a second schizophrenia risk gene, we show that dysbindin and DISC1 share common PPIs suggesting they may affect common biological processes and that the function of schizophrenia risk genes may converge.

Indexed as

Biological TransportCarrier ProteinsCell DivisionCognitionCytoskeletonDysbindinDystrophin-Associated ProteinsHumansNerve Tissue ProteinsRisk FactorsSchizophreniaSynapsesTwo-Hybrid System TechniquesCarrier ProteinsDISC1 protein, humanDTNBP1 protein, humanDysbindinDystrophin-Associated ProteinsNerve Tissue Proteins

Identifiers

PMID17043677
OpenAlexW2049733177

What OpenQuestion holds

Textmetadata
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.