Evidence map›Paper›PMID 37415806›Full record

ArticleHGG advances2023

Transcriptome-wide association study identifies novel candidate susceptibility genes for migraine.

Travis J Meyers, Jie Yin, Victor A Herrera, Alice R Pressman, Thomas J Hoffmann, Catherine Schaefer, Andrew L Avins, Hélène Choquet

Abstract read
In one paragraph

Article in HGG advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
–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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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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

8 authors.

Travis J MeyersDivision of Research, Kaiser Permanente Northern California, Oakland, CA 94612, USA.
Jie YinDivision of Research, Kaiser Permanente Northern California, Oakland, CA 94612, USA.
Victor A HerreraDivision of Research, Kaiser Permanente Northern California, Oakland, CA 94612, USA.
Alice R PressmanDepartment of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA 94158, USA.
Thomas J HoffmannDepartment of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA 94158, USA.
Catherine SchaeferDivision of Research, Kaiser Permanente Northern California, Oakland, CA 94612, USA.
Andrew L AvinsDivision of Research, Kaiser Permanente Northern California, Oakland, CA 94612, USA.
Hélène ChoquetDivision of Research, Kaiser Permanente Northern California, Oakland, CA 94612, USA.

Funding

A Resource for Genetic Epidemiology Research in Adult Health and AgingRC2AG036607 · NIA · KAISER FOUNDATION RESEARCH INSTITUTE · PI RISCH, NEIL J., SCHAEFER, CATHERINE ANN · 2009 to 2010
$24.8M
Genetic Etiology of Abdominal Hernia SusceptibilityR01DK116738 · NIDDK · KAISER FOUNDATION RESEARCH INSTITUTE · PI AHITUV, NADAV, CHOQUET, HELENE · 2018 to 2020
$1.8M
The Role of Genetic Risk Factors in Keratinocyte Carcinoma SusceptibilityR01CA241623 · NCI · KAISER FOUNDATION RESEARCH INSTITUTE · PI ASGARI, MARYAM MANDANA, CHOQUET, HELENE · 2020 to 2025
$1.7M
The Role of Refractive Error in the Etiology of GlaucomaR01EY027004 · NEI · KAISER FOUNDATION RESEARCH INSTITUTE · PI CHOQUET, HELENE · 2017 to 2020
$1.6M
The Role of Genetic and Non-Genetic Factors and Causal Mechanisms Underlying Cataract Susceptibility For Risk PredictionR01EY033010 · NEI · KAISER FOUNDATION RESEARCH INSTITUTE · PI CHOQUET, HELENE, LACHKE, SALIL · 2022 to 2025
$1.6M
Genetics and Comorbidity of MigraineR01NS080863 · NINDS · KAISER FOUNDATION RESEARCH INSTITUTE · PI PRESSMAN, ALICE ROGOT · 2012 to 2014
$979k
Identification of genetic loci and pathways underlying hidradenitis suppurativa riskR21AR076009 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI ASGARI, MARYAM MANDANA, CHOQUET, HELENE · 2020 to 2021
$359k
NCI NIH HHS R01 CA241623NEI NIH HHS R01 EY027004NEI NIH HHS R01 EY033010NIAMS NIH HHS R21 AR076009NIA NIH HHS RC2 AG036607NIDDK NIH HHS R01 DK116738NINDS NIH HHS R01 NS080863
6 · The paper itself

Abstract

Genome-wide association studies (GWASs) have identified more than 130 genetic susceptibility loci for migraine; however, how most of these loci impact migraine development is unknown. To identify novel genes associated with migraine and interpret the transcriptional products of those genes, we conducted a transcriptome-wide association study (TWAS). We performed tissue-specific and multi-tissue TWAS analyses to assess associations between imputed gene expression from 53 tissues and migraine susceptibility using FUSION software. Meta-analyzed GWAS summary statistics from 26,052 migraine cases and 487,214 controls, all of European ancestry and from two cohorts (the Kaiser Permanente GERA and the UK Biobank), were used. We evaluated the associations for genes after conditioning on variant-level effects from GWAS, and we tested for colocalization of GWAS migraine-associated loci and expression quantitative trait loci (eQTLs). Across tissue-specific and multi-tissue analyses, we identified 53 genes for which genetically predicted gene expression was associated with migraine after correcting for multiple testing. Of these 53 genes, 10 (

Indexed as

DNA GlycosylasesMigraine DisordersDNA Repair EnzymesGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMembrane ProteinsPhosphotransferases (Alcohol Group Acceptor)Quantitative Trait LociTranscriptomeDNA GlycosylasesDNA Repair EnzymesKTN1 protein, humanMembrane ProteinsNEIL1 protein, humanPhosphotransferases (Alcohol Group Acceptor)PNKP protein, humangeneticsmigraineTWAS

Identifiers

PMID37415806
PMCPMC10319829

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.