Evidence map›Paper›PMID 31417727›Full record

ArticleRoyal Society open science2019

Disease classification via gene network integrating modules and pathways.

Zhilong Mi, Binghui Guo, Ziqiao Yin, Jiahui Li, Zhiming Zheng

Open access · goldAbstract read
In one paragraph

Article in Royal Society open science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Zhilong MiBeijing Advanced Innovation Center for Big Data and Brain Computing, Beihang University, Beijing 100191, People's Republic of China.ORCID 0000-0002-7811-7204
Binghui GuoBeijing Advanced Innovation Center for Big Data and Brain Computing, Beihang University, Beijing 100191, People's Republic of China.ORCID 0000-0002-0540-3779
Ziqiao YinBeijing Advanced Innovation Center for Big Data and Brain Computing, Beihang University, Beijing 100191, People's Republic of China.
Jiahui LiBeijing Advanced Innovation Center for Big Data and Brain Computing, Beihang University, Beijing 100191, People's Republic of China.
Zhiming ZhengBeijing Advanced Innovation Center for Big Data and Brain Computing, Beihang University, Beijing 100191, People's Republic of China.
Peng Cheng Laboratory · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disease classification based on gene information has been of significance as the foundation for achieving precision medicine. Previous works focus on classifying diseases according to the gene expression data of patient samples, and constructing disease network based on the overlap of disease genes, as many genes have been confirmed to be associated with diseases. In this work, the effects of diseases on human biological functions are assessed from the perspective of gene network modules and pathways, and the distances between diseases are defined to carry out the classification models. In total, 1728 diseases are divided into 12 and 14 categories by the intensity and scope of effects on pathways, respectively. Each category is a mix of several types of diseases identified based on congenital and acquired factors as well as diseased tissues and organs. The disease classification models on the basis of gene network are parallel with traditional pathology classification based on anatomic and clinical manifestations, and enable us to look at diseases in the viewpoint of commonalities in etiology and pathology. Our models provide a foundation for exploring combination therapy of diseases, which in turn may inform strategies for future gene-targeted therapy.

Indexed as

disease classificationgene networkmodulespathways

Identifiers

PMID31417727
PMCPMC6689581
OpenAlexW2963997030

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.