Evidence map›Paper›PMID 40297163›Full record

ArticleFrontiers in cardiovascular medicine2025

Identification of signature genes and subtypes for heart failure diagnosis based on machine learning.

Yanlong Zhang, Yanming Fan, Fei Cheng, Dan Chen, Hualong Zhang

Abstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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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.

Yanlong ZhangDepartment of Cardiology, Xingtai People's Hospital, Xingtai, Hebei, China.
Yanming FanDepartment of Cardiology, Xingtai People's Hospital, Xingtai, Hebei, China.
Fei ChengDepartment of Cardiology, Xingtai People's Hospital, Xingtai, Hebei, China.
Dan ChenDepartment of Pediatrics Hematology and Oncology, Xingtai People's Hospital, Xingtai, Hebei, China.
Hualong ZhangDepartment of Cardiology, Xingtai People's Hospital, Xingtai, Hebei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Heart failure (HF) is a multifaceted clinical condition, and our comprehension of its genetic pathogenesis continues to be significantly limited. Consequently, identifying specific genes for HF at the transcriptomic level may enhance early detection and allow for more targeted therapies for these individuals. Methods: HF datasets were acquired from the Gene Expression Omnibus (GEO) database (GSE57338), and through the application of bioinformatics and machine-learning algorithms. We identified four candidate genes ( Results: A total of 295 differential genes were identified in the HF dataset, and intersected with the blue module gene with the highest correlation to HF identified by weighted correlation network analysis ( Conclusions: Our research identified four unique genes (

Indexed as

heart failureimmune characteristicsmachine learningpan-cancersubtypes

Identifiers

PMID40297163
PMCPMC12034685

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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.