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Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk.

Naomi WilcoxMartine DumontAnna González-NeiraSara CarvalhoCharles Joly BeauparlantMarco CrottiCraig LuccariniPenny SoucyStéphane DuboisRocio Nuñez-TorresGuillermo PitaEugene J GardnerJoe DennisM Rosario AlonsoNuria ÁlvarezCaroline BaynesAnnie Claude Collin-DeschesnesSylvie DesjardinsHeiko BecherSabine BehrensManjeet K BollaJose E CastelaoJenny Chang-ClaudeSten CornelissenThilo DörkChristoph EngelManuela Gago-DominguezPascal GuénelAndreas HadjisavvasEric HahnenMikael HartmanBelén Herráeznull nullAudrey JungRenske KeemanMarion KiechleJingmei LiMaria A LoizidouMichael LushKyriaki MichailidouMihalis I PanayiotidisXueling S SimSoo-Hwang TeoJonathan P TyrerLizet E van der KolkCecilia WahlströmQin WangJohn R B PerryJavier BenitezMarjanka K SchmidtRita K SchmutzlerPaul David Peter PharoahArnaud DroitAlison M DunningAnders KvistPeter DevileeDouglas F EastonJacques Simard
Published in: Nature genetics (2023)
Keyphrases
  • breast cancer risk
  • genome wide
  • copy number
  • dna methylation
  • single cell
  • gene expression
  • bioinformatics analysis
  • genome wide analysis