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dc.contributor.authorClaus, EB
dc.contributor.authorCornish, AJ
dc.contributor.authorBroderick, P
dc.contributor.authorSchildkraut, JM
dc.contributor.authorDobbins, SE
dc.contributor.authorHolroyd, A
dc.contributor.authorCalvocoressi, L
dc.contributor.authorLu, L
dc.contributor.authorHansen, HM
dc.contributor.authorSmirnov, I
dc.contributor.authorWalsh, KM
dc.contributor.authorSchramm, J
dc.contributor.authorHoffmann, P
dc.contributor.authorNöthen, MM
dc.contributor.authorJöckel, K-H
dc.contributor.authorSwerdlow, A
dc.contributor.authorLarsen, SB
dc.contributor.authorJohansen, C
dc.contributor.authorSimon, M
dc.contributor.authorBondy, M
dc.contributor.authorWrensch, M
dc.contributor.authorHoulston, RS
dc.contributor.authorWiemels, JL
dc.date.accessioned2018-05-17T15:05:30Z
dc.date.issued2018-10-09
dc.identifier.citationNeuro-oncology, 2018, 20 (11), pp. 1485 - 1493
dc.identifier.issn1522-8517
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/1675
dc.identifier.eissn1523-5866
dc.identifier.doi10.1093/neuonc/noy077
dc.description.abstractBACKGROUND: Meningiomas are adult brain tumors originating in the meningeal coverings of the brain and spinal cord, with significant heritable basis. Genome-wide association studies (GWAS) have previously identified only a single risk locus for meningioma, at 10p12.31. METHODS: To identify a susceptibility locus for meningioma, we conducted a meta-analysis of 2 GWAS, imputed using a merged reference panel from the 1000 Genomes Project and UK10K data, with validation in 2 independent sample series totaling 2138 cases and 12081 controls. RESULTS: We identified a new susceptibility locus for meningioma at 11p15.5 (rs2686876, odds ratio = 1.44, P = 9.86 × 10-9). A number of genes localize to the region of linkage disequilibrium encompassing rs2686876, including RIC8A, which plays a central role in the development of neural crest-derived structures, such as the meninges. CONCLUSIONS: This finding advances our understanding of the genetic basis of meningioma development and provides additional support for a polygenic model of meningioma.
dc.formatPrint
dc.format.extent1485 - 1493
dc.languageeng
dc.language.isoeng
dc.publisherOXFORD UNIV PRESS INC
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectChromosomes, Human, Pair 11
dc.subjectHumans
dc.subjectMeningioma
dc.subjectMeningeal Neoplasms
dc.subjectGenetic Predisposition to Disease
dc.subjectPrognosis
dc.subjectRisk Factors
dc.subjectCase-Control Studies
dc.subjectFollow-Up Studies
dc.subjectGenotype
dc.subjectLinkage Disequilibrium
dc.subjectPolymorphism, Single Nucleotide
dc.subjectAdult
dc.subjectAged
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectMale
dc.subjectGenome-Wide Association Study
dc.subjectYoung Adult
dc.subjectGenetic Loci
dc.subjectBiomarkers, Tumor
dc.titleGenome-wide association analysis identifies a meningioma risk locus at 11p15.5.
dc.typeJournal Article
dcterms.dateAccepted2018-05-08
rioxxterms.versionofrecord10.1093/neuonc/noy077
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc/4.0
rioxxterms.licenseref.startdate2018-10
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfNeuro-oncology
pubs.issue11
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Aetiological Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Aetiological Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Cancer Genomics
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Aetiological Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Aetiological Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Cancer Genomics
pubs.publication-statusPublished
pubs.volume20
pubs.embargo.termsNot known
icr.researchteamAetiological Epidemiology
icr.researchteamCancer Genomics
dc.contributor.icrauthorCornish, Alexander
dc.contributor.icrauthorBroderick, Peter
dc.contributor.icrauthorSwerdlow, Anthony
dc.contributor.icrauthorHoulston, Richard


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