Evidence map›Paper›PMID 21386875›Full record

ArticleEuropean journal of human genetics : EJHG2011

The expanded human disease network combining protein-protein interaction information.

Xuehong Zhang, Ruijie Zhang, Yongshuai Jiang, Peng Sun, Guoping Tang, Xing Wang, Hongchao Lv, Xia Li

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. MultiSourcDSim: an integrated approach for exploring disease similarity.BMC medical informatics and decision making · 2019
    Article
  7. Computational Methods for Identifying Similar Diseases.Molecular therapy. Nucleic acids · 2019
    Review
  8. Article
  9. Review
  10. Applications of molecular networks in biomedicine.Biology methods & protocols · 2019
    Review
  11. Article
  12. Article
  13. Article
  14. Network mirroring for drug repositioning.BMC medical informatics and decision making · 2017
    Article
  15. Article
  16. Article
  17. Observational
  18. Mechanism-based disease similarity.Journal of rare diseases research & treatment · 2016
    Article
  19. Article
  20. 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

8 authors.

Xuehong ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Ruijie Zhang
Yongshuai Jiang
Peng Sun
Guoping Tang
Xing Wang
Hongchao Lv
Xia Li

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human disease network (HDN) has become a powerful tool for revealing disease-disease associations. Some studies have shown that genes that share similar or same disease phenotypes tend to encode proteins that interact with each other. Therefore, protein-protein interactions (PPIs) may help us to further understand the relationships between diseases with overlapping clinical phenotypes. In this study, we constructed the expanded HDN (eHDN) by combining disease gene information with PPI information, and analyzed its topological features and functional properties. We found that the network is hierarchical and, most diseases are connected to only a few diseases, whereas a small part of diseases are linked to many different diseases. Diseases in a specific disease class tend to cluster together, and genes associated with the same disease are functionally related. Comparing the eHDN with the original HDN (oHDN, constructed using disease gene information) revealed high consistency over all topological and functional properties. This, to some extent, indicates that our eHDN is reliable. In the eHDN, we found some new associations among diseases resulting from the shared genes interacting with disease genes. The new eHDN will provide a valuable reference for clinicians and medical researchers.

Indexed as

Databases, GeneticProtein Interaction MappingCluster AnalysisComputational BiologyGenetic Predisposition to DiseaseHumansProteinsProteins

Identifiers

PMID21386875
PMCPMC3137500

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.