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dc.contributor.authorUji, Makoto
dc.contributor.authorWilson, Ross
dc.contributor.authorFrancis, Susan
dc.contributor.authorMullinger, Karen
dc.contributor.authorMayhew, Stephen
dc.date.accessioned2018-03-26T16:30:10Z
dc.date.available2018-03-26T16:30:10Z
dc.date.issued2017-06-26
dc.identifier252085293
dc.identifier345f213b-82d2-4849-acff-1f07c0368bf9
dc.identifier.citationUji , M , Wilson , R , Francis , S , Mullinger , K & Mayhew , S 2017 , ' Detecting gamma frequency neural activity using simultaneous multiband EEG-fMRI ' , Organization for Human Brain Mapping , Vancouver , Canada , 25/06/17 - 29/06/17 . < https://ww5.aievolution.com/hbm1701/index.cfm?do=abs.viewAbs&abs=2230 >en
dc.identifier.citationconferenceen
dc.identifier.otherORCID: /0000-0002-9445-6353/work/43150051
dc.identifier.urihttps://hdl.handle.net/10023/13020
dc.description.abstractSynchronization of gamma frequency (>35Hz) EEG activity is linked to cognitive and sensory behaviour as well as being widely cited as the closest neuronal correlate of the BOLD fMRI signal[1]. However, the majority of gamma-BOLD studies were conducted in the visual[2,3] or auditory[4,5] modalities, therefore a deeper understanding necessitates extension to the motor domain. Simultaneous EEG-fMRI is an ideal method to investigate gamma-BOLD correlates non-invasively in humans, however, residual gradient artefacts typically obscure gamma frequency EEG activity when acquired with fMRI. Accelerated fMRI methods such as multiband (MB)[6,7] allow whole-brain coverage in a sparse fMRI scheme which incorporates MR gradient “quiet periods” thus potentially useful to overcome EEG gradient artefacts during fMRI acquisition
dc.format.extent1134544
dc.language.isoeng
dc.subjectRC0321 Neuroscience. Biological psychiatry. Neuropsychiatryen
dc.subject.lccRC0321en
dc.titleDetecting gamma frequency neural activity using simultaneous multiband EEG-fMRIen
dc.typeConference posteren
dc.contributor.institutionUniversity of St Andrews. School of Psychology and Neuroscienceen
dc.description.statusPeer revieweden
dc.identifier.urlhttps://ww5.aievolution.com/hbm1701/index.cfm?do=abs.viewAbs&abs=2230en


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