Evidence map›Paper›PMID 36653477›Full record

ArticleCommunications biology2023

Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population.

Pyry Helkkula, Shabbeer Hassan, Elmo Saarentaus, Emilia Vartiainen, Sanni Ruotsalainen, Jaakko T Leinonen, FinnGen, Aarno Palotie, Juha Karjalainen, Mitja Kurki and 2 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

11 citing papers in PubMed, 21 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

12 authors at 3 institutions in 2 countries.

Pyry HelkkulaInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.ORCID 0000-0001-5094-3208
Shabbeer HassanInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
Elmo SaarentausInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.ORCID 0000-0002-8475-7187
Emilia VartiainenInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
Sanni RuotsalainenInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
Jaakko T LeinonenInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
FinnGen
Aarno PalotieInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.ORCID 0000-0002-2527-5874
Juha KarjalainenInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
Mitja KurkiInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
Samuli RipattiInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.ORCID 0000-0002-0504-1202
Taru TukiainenInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland. taru.tukiainen@helsinki.fi.ORCID 0000-0002-5404-8398
University of Helsinki · FIBroad Institute · USInstitute for Molecular Medicine Finland · FI

Funding

Medical Research Council MC_PC_17228
6 · The paper itself

Abstract

Varicose veins is the most common manifestation of chronic venous disease that displays female-biased incidence. To identify protein-inactivating variants that could guide identification of drug target genes for varicose veins and genetic evidence for the disease prevalence difference between the sexes, we conducted a genome-wide association study of varicose veins in Finns using the FinnGen dataset with 17,027 cases and 190,028 controls. We identified 50 associated genetic loci (P < 5.0 × 10

Indexed as

Genome-Wide Association StudyVaricose VeinsChronic DiseaseConnexinsFemaleFinlandHumansConnexins

Identifiers

PMID36653477
PMCPMC9849365
OpenAlexW4317242072

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.