Evidence map›Paper›PMID 40869943›Full record

ArticleGenes2025

Genetic Insights into Hemiplegic Migraine: Whole Exome Sequencing Highlights Vascular Pathway Involvement via Association Analysis.

Zizi Molaee, Robert A Smith, Neven Maksemous, Lyn R Griffiths

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Zizi MolaeeGenomics Research Centre, School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, 60 Musk Ave, Kelvin Grove, QLD 4059, Australia.ORCID 0009-0000-2917-6251
Robert A SmithGenomics Research Centre, School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, 60 Musk Ave, Kelvin Grove, QLD 4059, Australia.
Neven MaksemousGenomics Research Centre, School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, 60 Musk Ave, Kelvin Grove, QLD 4059, Australia.ORCID 0000-0002-4891-4333
Lyn R GriffithsGenomics Research Centre, School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, 60 Musk Ave, Kelvin Grove, QLD 4059, Australia.ORCID 0000-0002-6774-5475

Funding

NHMRC APP1122387
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Cerebral Small Vessel DiseasesMigraine with AuraAdultCalcium ChannelsCalcium Channels, N-TypeCase-Control StudiesExome SequencingFemaleGenetic Predisposition to DiseaseHumansLow Density Lipoprotein Receptor-Related Protein-1MaleMiddle AgedNAV1.1 Voltage-Gated Sodium ChannelSodium-Potassium-Exchanging ATPaseATP1A2 protein, humanCACNA1A protein, humanCalcium ChannelsCalcium Channels, N-TypeLow Density Lipoprotein Receptor-Related Protein-1LRP1 protein, humanNAV1.1 Voltage-Gated Sodium ChannelSCN1A protein, humanSodium-Potassium-Exchanging ATPaseCOL4A1COL4A2genetic variantshemiplegic migraineLRP1migraine geneticssmall vessel diseaseTGFBR2vascular dysfunctionwhole exome sequencing

Identifiers

PMID40869943
PMCPMC12386144

What Socratic 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 Socratic graph.