Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16274
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dc.contributor.authorRoberts, James A-
dc.contributor.authorPerry, Alistair-
dc.contributor.authorLord, Anton R-
dc.contributor.authorRoberts, Gloria-
dc.contributor.authorMitchell, Philip B-
dc.contributor.authorSmith, Robert E-
dc.contributor.authorCalamante, Fernando-
dc.contributor.authorBreakspear, Michael-
dc.date2015-09-11-
dc.date.accessioned2016-09-15T06:39:50Z-
dc.date.available2016-09-15T06:39:50Z-
dc.date.issued2016-01-01-
dc.identifier.citationNeuroImage 2016; 124(A): 379-393en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16274-
dc.description.abstractThe human connectome is a topologically complex, spatially embedded network. While its topological properties have been richly characterized, the constraints imposed by its spatial embedding are poorly understood. By applying a novel resampling method to tractography data, we show that the brain's spatial embedding makes a major, but not definitive, contribution to the topology of the human connectome. We first identify where the brain's structural hubs would likely be located if geometry was the sole determinant of brain topology. Empirical networks show a widespread shift away from this geometric center toward more peripheral interconnected skeletons in each hemisphere, with discrete clusters around the anterior insula, and the anterior and posterior midline regions of the cortex. A relatively small number of strong inter-hemispheric connections assimilate these intra-hemispheric structures into a rich club, whose connections are locally more clustered but globally longer than predicted by geometry. We also quantify the extent to which the segregation, integration, and modularity of the human brain are passively inherited from its geometry. These analyses reveal novel insights into the influence of spatial geometry on the human connectome, highlighting specific topological features that likely confer functional advantages but carry an additional metabolic cost.en_US
dc.subjectBrainen_US
dc.subjectConnectomeen_US
dc.titleThe contribution of geometry to the human connectomeen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleNeuroImageen_US
dc.identifier.affiliationAustin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationSystems Neuroscience Group, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australiaen_US
dc.identifier.affiliationCentre for Healthy Brain Ageing (CHeBA), School of Psychiatry, University of New South Wales, Sydney, NSW, Australiaen_US
dc.identifier.affiliationSchool of Psychiatry, University of New South Wales, Sydney, NSW, Australiaen_US
dc.identifier.affiliationLeibniz Institute for Neurobiology, Magdeburg, Germanyen_US
dc.identifier.affiliationBlack Dog Institute, Prince of Wales Hospital, Hospital Road, Randwick, NSW, Australiaen_US
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, Austin Health and Northern Health, University of Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationFlorey Department of Neuroscience and Mental Health, University of Melbourne, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationMetro North Mental Health Service, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/26364864en_US
dc.identifier.doi10.1016/j.neuroimage.2015.09.009en_US
dc.type.contentTexten_US
dc.type.austinJournal Articleen_US
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
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