Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117351
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dc.contributorDepartment of Applied Mathematics-
dc.contributorMainland Development Office-
dc.creatorNg, HM-
dc.creatorWong, KY-
dc.date.accessioned2026-02-13T02:41:05Z-
dc.date.available2026-02-13T02:41:05Z-
dc.identifier.issn0962-2802-
dc.identifier.urihttp://hdl.handle.net/10397/117351-
dc.language.isoenen_US
dc.publisherSAGE Publicationsen_US
dc.rightsThis is the accepted version of the publication Ng HM, Wong KY. Penalized estimation for varying coefficient additive hazards models. Statistical Methods in Medical Research. 2025;34(7):1373-1384. Copyright © 2025 The Author(s). DOI: 10.1177/09622802251338978.en_US
dc.subjectCensored dataen_US
dc.subjectKernel smoothingen_US
dc.subjectSemiparametric modelen_US
dc.subjectSurvival analysisen_US
dc.subjectVariable selectionen_US
dc.titlePenalized estimation for varying coefficient additive hazards modelsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1373-
dc.identifier.epage1384-
dc.identifier.volume34-
dc.identifier.issue7-
dc.identifier.doi10.1177/09622802251338978-
dcterms.abstractVarying coefficient models are commonly used to capture intricate interaction effects among covariates in regression models, allowing for the modification of one covariate’s effect by another. Although these models offer increased flexibility, they also introduce greater estimation and computational complexity as a trade-off. This complexity is particularly evident in genomic studies, where the covariates are often high-dimensional, rendering conventional estimation methods inapplicable. In this paper, we study a penalized estimation method for the varying coefficient additive hazards model. We adopt the group lasso penalty along with the kernel smoothing technique to estimate the varying coefficients. In contrast to existing kernel methods, which only use a “local” neighborhood of subjects to estimate the varying coefficient function at any given point, the proposed method takes a “global” approach that incorporates all subjects and is more efficient. Through extensive simulation studies, we demonstrate that the proposed method produces interpretable results with satisfactory predictive performance. We provide an application to a major cancer genomic study.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationStatistical methods in medical research, July 2025, v. 34, no. 7, p. 1373-1384-
dcterms.isPartOfStatistical methods in medical research-
dcterms.issued2025-07-
dc.identifier.scopus2-s2.0-105005546400-
dc.identifier.pmid40368379-
dc.identifier.eissn1477-0334-
dc.description.validate202602 bcjz-
dc.description.oaAccepted Manuscripten_US
dc.identifier.SubFormIDG000939/2025-11en_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis research was partially supported by the Guangdong Basic and Applied Basic Research Foundation (Project No. 2021A1515110048) and the Hong Kong Research Grants Council Grant 15303422.en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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