Evidence map›Paper›PMID 39640032›Full record

ArticleHealth science reports2024

Genetic Variants and Haplotype Structures in the

Morteza Gholami, Mohsen Asouri, Ali Asghar Ahmadi

Abstract read
In one paragraph

Article in Health science reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Morteza GholamiDepartment of Paramedicine Amol School of Paramedicine, Mazandaran University of Medical Sciences Sari Iran.ORCID 0000-0003-0952-0654
Mohsen AsouriDepartment of Paramedicine Amol School of Paramedicine, Mazandaran University of Medical Sciences Sari Iran.ORCID https://orcid.org/0000-0001-7661-1172
Ali Asghar AhmadiNorth Research Center Pasteur Institute of Iran Amol Iran.ORCID https://orcid.org/0000-0003-2286-534X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: The cancer susceptibility ( Methods: Genome-wide association studies (GWAS) significant variants ( Results: There were six haplotypic blocks in four genes. The GC, TA, and AGAC haplotypes are located in the Conclusion: These haplotypic structures and lncRNA:miRNA:SNP interactions on

Indexed as

cancerCASC geneslncRNAmiRNAmRNAvariant

Identifiers

PMID39640032
PMCPMC11618408

What OpenQuestion holds

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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.