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dc.contributor.authorOstrom, QT
dc.contributor.authorKinnersley, B
dc.contributor.authorWrensch, MR
dc.contributor.authorEckel-Passow, JE
dc.contributor.authorArmstrong, G
dc.contributor.authorRice, T
dc.contributor.authorChen, Y
dc.contributor.authorWiencke, JK
dc.contributor.authorMcCoy, LS
dc.contributor.authorHansen, HM
dc.contributor.authorAmos, CI
dc.contributor.authorBernstein, JL
dc.contributor.authorClaus, EB
dc.contributor.authorIl'yasova, D
dc.contributor.authorJohansen, C
dc.contributor.authorLachance, DH
dc.contributor.authorLai, RK
dc.contributor.authorMerrell, RT
dc.contributor.authorOlson, SH
dc.contributor.authorSadetzki, S
dc.contributor.authorSchildkraut, JM
dc.contributor.authorShete, S
dc.contributor.authorRubin, JB
dc.contributor.authorLathia, JD
dc.contributor.authorBerens, ME
dc.contributor.authorAndersson, U
dc.contributor.authorRajaraman, P
dc.contributor.authorChanock, SJ
dc.contributor.authorLinet, MS
dc.contributor.authorWang, Z
dc.contributor.authorYeager, M
dc.contributor.authorGliomaScan consortium,
dc.contributor.authorHoulston, RS
dc.contributor.authorJenkins, RB
dc.contributor.authorMelin, B
dc.contributor.authorBondy, ML
dc.contributor.authorBarnholtz-Sloan, JS
dc.date.accessioned2020-10-21T13:36:36Z
dc.date.issued2018-05-09
dc.identifier.citationScientific reports, 2018, 8 (1), pp. 7352 - ?
dc.identifier.issn2045-2322
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4184
dc.identifier.eissn2045-2322
dc.identifier.doi10.1038/s41598-018-24580-z
dc.description.abstractIncidence of glioma is approximately 50% higher in males. Previous analyses have examined exposures related to sex hormones in women as potential protective factors for these tumors, with inconsistent results. Previous glioma genome-wide association studies (GWAS) have not stratified by sex. Potential sex-specific genetic effects were assessed in autosomal SNPs and sex chromosome variants for all glioma, GBM and non-GBM patients using data from four previous glioma GWAS. Datasets were analyzed using sex-stratified logistic regression models and combined using meta-analysis. There were 4,831 male cases, 5,216 male controls, 3,206 female cases and 5,470 female controls. A significant association was detected at rs11979158 (7p11.2) in males only. Association at rs55705857 (8q24.21) was stronger in females than in males. A large region on 3p21.31 was identified with significant association in females only. The identified differences in effect of risk variants do not fully explain the observed incidence difference in glioma by sex.
dc.formatElectronic
dc.format.extent7352 - ?
dc.languageeng
dc.language.isoeng
dc.publisherNATURE PORTFOLIO
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectGliomaScan consortium
dc.subjectChromosomes, Human, Pair 3
dc.subjectChromosomes, Human, Pair 7
dc.subjectChromosomes, Human, Pair 8
dc.subjectHumans
dc.subjectGlioma
dc.subjectBrain Neoplasms
dc.subjectGenetic Predisposition to Disease
dc.subjectLogistic Models
dc.subjectOdds Ratio
dc.subjectRisk Factors
dc.subjectCase-Control Studies
dc.subjectSex Factors
dc.subjectGenotype
dc.subjectPolymorphism, Single Nucleotide
dc.subjectAlleles
dc.subjectAdult
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectMale
dc.subjectGenome-Wide Association Study
dc.titleSex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21.
dc.typeJournal Article
dcterms.dateAccepted2018-04-06
rioxxterms.versionofrecord10.1038/s41598-018-24580-z
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2018-05-09
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfScientific reports
pubs.issue1
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/Genetics and 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/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Cancer Genomics
pubs.publication-statusPublished
pubs.volume8
pubs.embargo.termsNot known
icr.researchteamCancer Genomics
dc.contributor.icrauthorKinnersley, Benjamin
dc.contributor.icrauthorHoulston, Richard


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