MétaCan
Menu
Back to cohort
Record W2082458892 · doi:10.1002/gepi.21771

Identification of New Genetic Susceptibility Loci for Breast Cancer Through Consideration of Gene‐Environment Interactions

2013· article· en· W2082458892 on OpenAlex

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

affAt least one author lists a Canadian institution in the pinned OpenAlex snapshot.
fundA Canadian funder is recorded on the work.

Bibliographic record

VenueGenetic Epidemiology · 2013
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicMolecular Biology Techniques and Applications
Canadian institutionsUniversité du QuébecUniversité LavalUniversity Health NetworkMount Sinai HospitalLunenfeld-Tanenbaum Research InstituteOccupational Cancer Research CentreCentre hospitalier universitaire de Québec
FundersUniversitätsklinikum Hamburg-EppendorfInstituto de Salud Carlos IIIMedical Research CouncilRheinische Friedrich-Wilhelms-Universität BonnNational Health and Medical Research CouncilInstitut National Du CancerCancer Council VictoriaDeutsche KrebshilfeMedical Research and Materiel CommandAgence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du TravailVetenskapsrådetNational Cancer InstituteKuopion Yliopistollinen SairaalaCancer Research UKHerlev HospitalNederlandse Organisatie voor Wetenschappelijk OnderzoekCHIST-ERAAgence Nationale de la RechercheRobert Bosch StiftungAgency for Science, Technology and ResearchCanadian Institutes of Health ResearchCancerfondenOvarian Cancer Research FundCancer AustraliaNational Breast Cancer FoundationBundesministerium für Bildung und ForschungNational Institute for Health and Care ResearchNational Institutes of HealthDeutsche Gesetzliche UnfallversicherungDavid F. and Margaret T. Grohne Family FoundationLigue Contre le CancerDeutsches KrebsforschungszentrumCancer Care OntarioGénome QuébecMcGill UniversityFondation de FranceSundhed og Sygdom, Det Frie ForskningsrådItä-Suomen YliopistoU.S. Department of Health and Human ServicesBreast Cancer Research Foundation
KeywordsIdentification (biology)GeneticsBreast cancerBiologyGeneComputational biologyCancerEvolutionary biologyEcology

Abstract

fetched live from OpenAlex

Genes that alter disease risk only in combination with certain environmental exposures may not be detected in genetic association analysis. By using methods accounting for gene-environment (G × E) interaction, we aimed to identify novel genetic loci associated with breast cancer risk. Up to 34,475 cases and 34,786 controls of European ancestry from up to 23 studies in the Breast Cancer Association Consortium were included. Overall, 71,527 single nucleotide polymorphisms (SNPs), enriched for association with breast cancer, were tested for interaction with 10 environmental risk factors using three recently proposed hybrid methods and a joint test of association and interaction. Analyses were adjusted for age, study, population stratification, and confounding factors as applicable. Three SNPs in two independent loci showed statistically significant association: SNPs rs10483028 and rs2242714 in perfect linkage disequilibrium on chromosome 21 and rs12197388 in ARID1B on chromosome 6. While rs12197388 was identified using the joint test with parity and with age at menarche (P-values = 3 × 10(-07)), the variants on chromosome 21 q22.12, which showed interaction with adult body mass index (BMI) in 8,891 postmenopausal women, were identified by all methods applied. SNP rs10483028 was associated with breast cancer in women with a BMI below 25 kg/m(2) (OR = 1.26, 95% CI 1.15-1.38) but not in women with a BMI of 30 kg/m(2) or higher (OR = 0.89, 95% CI 0.72-1.11, P for interaction = 3.2 × 10(-05)). Our findings confirm comparable power of the recent methods for detecting G × E interaction and the utility of using G × E interaction analyses to identify new susceptibility loci.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: none
Teacher disagreement score0.462
Threshold uncertainty score0.628

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.032
GPT teacher head0.336
Teacher spread0.304 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it