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Record W2738622934 · doi:10.17863/cam.1180

Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.

2016· article· en· W2738622934 on OpenAlexfundno aff
Elena Vigorito, Karoline Kuchenbaecker, Jonathan Beesley, Julian Adlard, Bjarni A. Agnarsson, Irene L. Andrulis, Banu Arun, Laure Barjhoux, Muriel Belotti, Javier Benı́tez, Andreas Berger, Anders Bojesen, Bernardo Bonanni, Carole Brewer, Trinidad Caldés, Maria A. Caligo, Ian Campbell, Salina Chan, Kathleen Claes, David E. Cohn, Jackie Cook, Mary B. Daly, Francesca Damiola, Rosemarie Davidson, Antoine De Pauw, Capucine Delnatte, Orland Dı́ez, Susan M. Domchek, Martine Dumont, Katarzyna Durda, Bernd Dworniczak, Douglas F. Easton, Diana Eccles, Ardnor Christina Edwinsdotter, Rosalind A. Eeles, Bent Ejlertsen, D. Gareth Evans, Lídia Feliubadaló, Florentia Fostira, William D. Foulkes, Eitan Friedman, Debra Frost, Pragna Gaddam, Patricia A. Ganz, Judy E. Garber, Vanesa García‐Barberán, Marion Gauthier‐Villars, Andrea Gehrig, Anne‐Marie Gerdes, Sophie Giraud, Andrew K. Godwin, David E. Goldgar, Christopher R. Hake, Thomas van Overeem Hansen, Sue Healey, Shirley Hodgson, Frans B.L. Hogervorst, Claude Houdayer, Peter J. Hulick, Evgeny N. Imyanitov, Claudine Isaacs, Louise Izatt, Á. Izquierdo, Lauren Jacobs, Anna Jakubowska, Ramūnas Janavičius, Katarzyna Jaworska–Bieniek, Uffe Birk Jensen, Esther M. John, Joseph Vijai, Beth Y. Karlan, Karin Kast, kConFab Investigators, Sofia Khan, Ava Kwong, Yael Laitman, Jenny Lester, Fabienne Lesueur, Annelie Liljegren, Jan Lubiński, Siranoush Manoukian, Sylvie Mazoyer, Alfons Meindl, Arjen R. Mensenkamp, Marco Montagna, Katherine L. Nathanson, Susan L. Neuhausen, Heli Nevanlinna, Dieter Niederacher, Edith Oláh, Olufunmilayo I. Olopade, Kai-Ren Ong, Ana Osório, Sue K. Park, Ylva Paulsson-Karlsson, Inge Søkilde Pedersen, Bernard Peissel, Paolo Peterlongo, Georg Pfeiler, Catherine M. Phelan, Marion Piedmonte, Bruce Poppe, Miguel Ángel Pujana, Paolo Radice, Gad Rennert, Gustavo C. Rodriguez, Matti A. Rookus, Eric A. Ross, Rita K. Schmutzler, Jacques Simard, Christian F. Singer, Thomas P. Slavin, Penny Soucy, Melissa C. Southey, Doris Steinemann, Dominique Stoppa‐Lyonnet, Grzegorz Sukiennicki, Christian Sutter, Csilla I. Szabo, Muy‐Kheng M. Tea, Manuel R. Teixeira, Soo‐Hwang Teo, Mary Beth Terry, Mads Thomassen, Maria Grazia Tibiletti, Laima Tihomirova, Silvia Tognazzo, Elizabeth J. van Rensburg, Liliana Varesco, Raymonda Varon-Mateeva, Athanassios Vratimos, Jeffrey N. Weitzel, Lesley McGuffog, Judy Kirk, Amanda E. Toland, Ute Hamann, Noralane M. Lindor, Susan J. Ramus, Mark H. Greene, Fergus J. Couch, Kenneth Offit, Paul D.P. Pharoah, Georgia Chenevix‐Trench, Antonis C. Antoniou

Bibliographic record

VenueApollo (University of Cambridge) · 2016
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicCRISPR and Genetic Engineering
Canadian institutionsnot available
FundersNational Health and Medical Research CouncilMedical Research Councillékařská fakulta Univerzity KarlovyNational Institutes of HealthMinistero dello Sviluppo EconomicoNational Cancer InstituteHospices Civils de LyonInstitut Gustave-RoussySahlgrenska UniversitetssjukhusetUniversità degli Studi di FirenzeJewish General HospitalLunds UniversitetUppsala UniversitetCancer AustraliaUniversity of California, San FranciscoLinköpings UniversitetCancer Research UKUniversity of ChicagoMcGill UniversityUniverzita Karlova v PrazeNational Breast Cancer FoundationUmeå UniversitetUniversity of PennsylvaniaMinistère du Développement Économique, de l’Innovation et de l’ExportationCentre Léon BérardBreast Cancer Research FoundationSusan G. Komen for the Cure
KeywordsScale (ratio)Ovarian cancerMutationCancerComputer scienceGeneticsBiologyGeneGeographyCartography

Abstract

fetched live from OpenAlex

Population-based genome wide association studies have identified a locus at 9p22.2 associated with ovarian cancer risk, which also modifies ovarian cancer risk in BRCA1 and BRCA2 mutation carriers. We conducted fine-scale mapping at 9p22.2 to identify potential causal variants in BRCA1 and BRCA2 mutation carriers. Genotype data were available for 15,252 (2,462 ovarian cancer cases) BRCA1 and 8,211 (631 ovarian cancer cases) BRCA2 mutation carriers. Following genotype imputation, ovarian cancer associations were assessed for 4,873 and 5,020 SNPs in BRCA1 and BRCA 2 mutation carriers respectively, within a retrospective cohort analytical framework. In BRCA1 mutation carriers one set of eight correlated candidate causal variants for ovarian cancer risk modification was identified (top SNP rs10124837, HR: 0.73, 95%CI: 0.68 to 0.79, p-value 2× 10-16). These variants were located up to 20 kb upstream of BNC2. In BRCA2 mutation carriers one region, up to 45 kb upstream of BNC2, and containing 100 correlated SNPs was identified as candidate causal (top SNP rs62543585, HR: 0.69, 95%CI: 0.59 to 0.80, p-value 1.0 × 10-6). The candidate causal in BRCA1 mutation carriers did not include the strongest associated variant at this locus in the general population. In sum, we identified a set of candidate causal variants in a region that encompasses the BNC2 transcription start site. The ovarian cancer association at 9p22.2 may be mediated by different variants in BRCA1 mutation carriers and in the general population. Thus, potentially different mechanisms may underlie ovarian cancer risk for mutation carriers and the general population.

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.

How this classification was reachedexpand

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: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.718
Threshold uncertainty score0.829

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 head0.007
GPT teacher head0.226
Teacher spread0.219 · 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

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2016
Admission routes1
Has abstractyes

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