Evidence map›Paper›PMID 37895035›Full record

ArticleInternational journal of molecular sciences2023

Evaluation of Density-Based Spatial Clustering for Identifying Genomic Loci Associated with Ischemic Stroke in Genome-Wide Data.

Gennady V Khvorykh, Nikita A Sapozhnikov, Svetlana A Limborska, Andrey V Khrunin

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. The Use of AI for Phenotype-Genotype Mapping.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  4. 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

4 authors at 1 institution in 1 country.

Gennady V KhvorykhNational Research Centre "Kurchatov Institute", Kurchatov Sq. 2, Moscow 123182, Russia.ORCID 0000-0001-8927-5921
Nikita A SapozhnikovNational Research Centre "Kurchatov Institute", Kurchatov Sq. 2, Moscow 123182, Russia.
Svetlana A LimborskaNational Research Centre "Kurchatov Institute", Kurchatov Sq. 2, Moscow 123182, Russia.
Andrey V KhruninNational Research Centre "Kurchatov Institute", Kurchatov Sq. 2, Moscow 123182, Russia.ORCID 0000-0002-7848-4688
Kurchatov Institute · RU

Funding

Russian Foundation for Basic Research 19-29-01151Russian Science Foundation 23-14-00131
6 · The paper itself

Abstract

The genetic architecture of ischemic stroke (IS), which is one of the leading causes of death worldwide, is complex and underexplored. The traditional approach for associative gene mapping is genome-wide association studies (GWASs), testing individual single-nucleotide polymorphisms (SNPs) across the genomes of case and control groups. The purpose of this research is to develop an alternative approach in which groups of SNPs are examined rather than individual ones. We proposed, validated and applied to real data a new workflow consisting of three key stages: grouping SNPs in clusters, inferring the haplotypes in the clusters and testing haplotypes for the association with phenotype. To group SNPs, we applied the clustering algorithms DBSCAN and HDBSCAN to linkage disequilibrium (LD) matrices, representing pairwise r

Indexed as

Genome-Wide Association StudyIschemic StrokeCluster AnalysisGenomicsGenotypeHaplotypesHumansLinkage DisequilibriumPolymorphism, Single Nucleotideclustering algorithmsGWASischemic strokemulti-locus approach

Identifiers

PMID37895035
PMCPMC10607504
OpenAlexW4387780371

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.