Evidence map›Paper›PMID 34294844›Full record

ArticleCommunications biology2021

New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis.

Hélène Choquet, Jie Yin, Alice S Jacobson, Brandon H Horton, Thomas J Hoffmann, Eric Jorgenson, Andrew L Avins, Alice R Pressman

Abstract read
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 5 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

52 citing papers in PubMed, 5 syntheses or guidelines pooled it.

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  12. Early-childhood temperament deviations mark psychiatric risk into early adulthood.medRxiv : the preprint server for health sciences · 2026
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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.

Hélène ChoquetDivision of Research, Kaiser Permanente Northern California (KPNC), Oakland, CA, USA. Helene.Choquet@kp.org.ORCID http://orcid.org/0000-0001-9839-8667
Jie YinDivision of Research, Kaiser Permanente Northern California (KPNC), Oakland, CA, USA.
Alice S JacobsonSutter Health, Walnut Creek, CA, USA.
Brandon H HortonDivision of Research, Kaiser Permanente Northern California (KPNC), Oakland, CA, USA.
Thomas J HoffmannInstitute for Human Genetics, University of California, San Francisco (UCSF), San Francisco, CA, USA.ORCID http://orcid.org/0000-0001-6893-4449
Eric JorgensonDivision of Research, Kaiser Permanente Northern California (KPNC), Oakland, CA, USA.ORCID http://orcid.org/0000-0002-5829-8191
Andrew L AvinsDivision of Research, Kaiser Permanente Northern California (KPNC), Oakland, CA, USA.ORCID http://orcid.org/0000-0003-1723-7904
Alice R PressmanSutter Health, Walnut Creek, CA, USA. PressmAR@sutterhealth.org.ORCID http://orcid.org/0000-0003-2775-3275

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
Genetics and Comorbidity of MigraineR01NS080863 · NINDS · KAISER FOUNDATION RESEARCH INSTITUTE · PI PRESSMAN, ALICE ROGOT · 2012 to 2014
$979k
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NCI NIH HHS R01 CA241623NEI NIH HHS R01 EY027004NIA NIH HHS RC2 AG036607NIDDK NIH HHS R01 DK116738NINDS NIH HHS R01 NS080863
6 · The paper itself

Abstract

Migraine is a common disabling primary headache disorder that is ranked as the most common neurological cause of disability worldwide. Women present with migraine much more frequently than men, but the reasons for this difference are unknown. Migraine heritability is estimated to up to 57%, yet much of the genetic risk remains unaccounted for, especially in non-European ancestry populations. To elucidate the etiology of this common disorder, we conduct a multiethnic genome-wide association meta-analysis of migraine, combining results from the GERA and UK Biobank cohorts, followed by a European-ancestry meta-analysis using public summary statistics. We report 79 loci associated with migraine, of which 45 were novel. Sex-stratified analyses identify three additional novel loci (CPS1, PBRM1, and SLC25A21) specific to women. This large multiethnic migraine study provides important information that may substantially improve our understanding of the etiology of migraine susceptibility.

Indexed as

Meta-Analysis as TopicAdultAgedAsianBlack or African AmericanChromosome MappingCohort StudiesFemaleGenetic Association StudiesGenetic LociGenetic Predisposition to DiseaseGenome-Wide Association StudyHispanic or LatinoHumansMaleMiddle Aged

Identifiers

PMID34294844
PMCPMC8298472

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.