Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/115682
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dc.contributorDepartment of Rehabilitation Sciencesen_US
dc.contributorUniversity Research Facility in Behavioral and Systems Neuroscienceen_US
dc.contributorMental Health Research Centreen_US
dc.contributorResearch Institute for Smart Ageingen_US
dc.creatorChau, BKHen_US
dc.creatorLaw, CKen_US
dc.creatorTo, JYLen_US
dc.creatorShum, DHKen_US
dc.creatorMars, RBen_US
dc.date.accessioned2025-10-20T01:25:09Z-
dc.date.available2025-10-20T01:25:09Z-
dc.identifier.issn0006-8950en_US
dc.identifier.urihttp://hdl.handle.net/10397/115682-
dc.language.isoenen_US
dc.rights© The Author(s) 2025. Published by Oxford University Press on behalf of the Guarantors of Brain.en_US
dc.rightsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication Chau, B. K. H., Law, C.-K., To, J. Y. L., Shum, D. H. K., & Mars, R. B. (2025). Complex functions of human lateral frontopolar cortex. Brain, awaf289 is available at https://doi.org/10.1093/brain/awaf289.en_US
dc.subjectAnterior prefrontal cortexen_US
dc.subjectArea 10en_US
dc.subjectDecision makingen_US
dc.subjectFrontopolar cortexen_US
dc.subjectNeuropsychologyen_US
dc.titleComplex functions of human lateral frontopolar cortexen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1093/brain/awaf289en_US
dcterms.abstractRecent anatomical studies have shown that, compared to other primates, the human frontal pole (FP) contains a unique lateral subdivision (FPl). This area provides an important target for understanding the uniqueness of human intelligence. Paradoxically, patients with FP lesions often perform normally on standard neuropsychological tests, while experiencing problems in real-life or simulated situations. This paper aims to review the complex functions of the FPl that may account for the dysfunctions observed in these patients. First, we consider studies of FP lesion patients that reveal deficits in analogical reasoning and prospective memory. Second, we review, mainly based on neuroimaging and neurostimulation studies, the FPl’s involvement in exploratory decision making, information integration and the representation of abstract rules. We argue that these functions primarily stem from the FPl’s capacity to manage multiple sources of information and to reduce that information into simpler features for guiding behaviour. Finally, we propose a model of the FPl that emphasizes its role in decomposing high-dimensional information to enhance decision making processes in conjunction with connected regions, including the posterior cingulate cortex, anterior cingulate cortex, and dorsolateral prefrontal cortex.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBrain, Published: 07 August 2025, Advance articles, awaf289, https://doi.org/10.1093/brain/awaf289en_US
dcterms.isPartOfBrainen_US
dcterms.issued2025-
dc.publisher.placeOxford University Pressen_US
dc.identifier.eissn1460-2156en_US
dc.identifier.artnawaf289en_US
dc.description.validate202510 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera4123, OA_TA-
dc.identifier.SubFormID52111-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextB.K.H.C. is supported by the Research Grants Council, University Grants Committee (C5001-23Y) and The Hong Kong Polytechnic University (Project of Strategic Importance:1-ZE0E). D.H.K.S. is supported by the Yeung Tsang Wing Yee and Tsang Wing Hing Endowed Professorship in Neuropsychology. R.B.M. is supported by the UK Medical Research Council [MR/Y010698/1]. The Wellcome Centre for Integrative Neuroimaging is supported by core funding from the Wellcome Trust [203139/Z/16/Z]. For the purpose of Open Access, the authors have applied a CC BY public copyright licence to any Author Accepted Manuscript version arising from this submission.en_US
dc.description.pubStatusEarly releaseen_US
dc.description.TAOUP (2025)en_US
dc.description.oaCategoryTAen_US
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