Perceptual, motor, cognitive, and social abilities are critical for people’s interactions with the physical and social world in their everyday lives.
By using a technique called electroencephalography (EEG), which measures electrical activity in the brain with high temporal resolution, we can find out more about the neural processes that support these abilities, advancing not only basic research but, ultimately, research in mental health and other applied fields.
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Investigating the neural bases of perceptual, motor, cognitive, and social abilities
EEG Laboratory Lead, Dr Giorgio Ganis, Associate Professor, has been using electroencephalography (EEG), brain stimulation (TMS), functional magnetic resonance imaging (fMRI), as well as behavioural method, to study the neuroscience of perceptual, motor, cognitive, and social abilities.
BRIC Director, Professor Stephen Hall has been using electro-and magneto-physiological measures (EEG and MEG) as well as fMRI and TMS to characterise the neural network mechanisms, such as oscillatory processes, underlying cognitive and behavioural function in health and disease. Recent research has primarily focussed on the neuroscience of sensorimotor function.
Dr Jeremy Goslin,
has been adopting a multidisciplinary research approach to investigate both the behaviour and the cognitive neuroscience of topics in language, economics, and trust. His current research has centred around using behavioural and EEG methods to investigate areas such as the neuroscience of reinforcement learning, tool use in virtual reality, and language and language development.
Research expertiseLab lead: Dr Giorgio Ganis, Associate Professor in Cognitive Neuroscience
Other research in this lab will be carried out by:
Professor Stephen Hall, Dr Elsa Fouragnan, Dr Jeremy Goslin
Ward E, Ganis G & Bach P 2019. Spontaneous vicarious perception of the content of others’ visual perspective. Current Biology 29(5) 874-880.
Hsu CW, Begliomini C, Dall'Acqua T, Ganis G 2019. The effect of mental countermeasures on neuroimaging-based concealed information tests. Human Brain Mapping 40(10):2899-2916.
Zabelina DL, Ganis G 2018. Creativity and cognitive control: Behavioral and ERP evidence that divergent thinking, but not real-life creative achievement, relates to better cognitive control. Neuropsychologia 118, 20-28.
Ganis G, Bridges D, Hsu CW, Schendan HE 2016. Is anterior N2 enhancement a reliable electrophysiological index of concealed information? Neuroimage 143, 152-165.Battaglini L, Casco C, Isaacs BR, Bridges D & Ganis G 2016. Electrophysiological correlates of motion extrapolation: An investigation on the CNV. Neuropsychologia. 95, 86-93.
Battaglini, L., Casco, C., Isaacs, B. R., Bridges, D., & Ganis, G. (2017). Electrophysiological correlates of motion extrapolation: An investigation on the CNV. Neuropsychologia, 95, 86-93.
Ganis, G., Bridges, D., Hsu, C. W., & Schendan, H. E. (2016). Is anterior N2 enhancement a reliable electrophysiological index of concealed information? Neuroimage, 143, 152-165.
Ganis, G., & Kutas, M. (2003). An electrophysiological study of scene effects on object identification. Brain Res Cogn Brain Res, 16(2), 123-144.
Ganis, G., Kutas, M., & Sereno, M. I. (1996). The search for "common sense": an electrophysiological study of the comprehension of words and pictures in reading. J Cogn Neurosci, 8(2), 89-106.
Ganis, G., & Schendan, H. E. (2008). Visual mental imagery and perception produce opposite adaptation effects on early brain potentials. Neuroimage, 42(4), 1714-1727.
Ganis, G., & Schendan, H. E. (2012). Concealed semantic and episodic autobiographical memory electrified. Front Hum Neurosci, 6, 354.
Ganis, G., Smith, D., & Schendan, H. E. (2012). The N170, not the P1, indexes the earliest time for categorical perception of faces, regardless of interstimulus variance. Neuroimage, 62(3), 1563-1574.
Schendan, H. E., & Ganis, G. (2012). Electrophysiological potentials reveal cortical mechanisms for mental imagery, mental simulation, and grounded (embodied) cognition. Front Psychol, 3, 329.
Schendan, H. E., & Ganis, G. (2013). Face-specificity is robust across diverse stimuli and individual people, even when interstimulus variance is zero. Psychophysiology, 50(3), 287-291.
Schendan, H. E., Ganis, G., & Kutas, M. (1998). Neurophysiological evidence for visual perceptual categorization of words and faces within 150 ms. Psychophysiology, 35(3), 240-251.
Zabelina, D. L., & Ganis, G. (2018). Creativity and cognitive control: Behavioral and ERP evidence that divergent thinking, but not real-life creative achievement, relates to better cognitive control. Neuropsychologia, 118(Pt A), 20-28.
Sambrook, T.D, Roser, M., Goslin, J. (2012). Prospect theory does not describe the feedback-related negativity value function. Psychophysiology, 49(12), 1533-44.
Marrett, N. E., de-Wit, L. H., Roser, M. E., Kentridge, R. W., Milner, A. D., & Lambert, A. J. (2011). Testing the dorsal stream attention hypothesis: Electrophysiological correlates and the effects of ventral stream damage. Visual Cognition, 19(9), 1089-1121. (THIS COMBINES fMRI, PATIENTS AND EEG).Roser, M.E., Fugelsang, J., Handy, T.C., Dunbar, K.N., & Gazzaniga, M.S. (2009). Representations of physical plausibility revealed by event-related potentials. NeuroReport, 20,1081-1086.
Gaetz W, Rhodes E, Bloy L, Blaskey L, Jackel CR, Brodkin ES, Waldman A, Embick D, Hall S, Roberts TP. (2019). Evaluating motor cortical oscillations and age-related change in autism spectrum disorder. Neuroimage. 11:116349. doi: 10.1016/j.neuroimage.2019.116349.
Prokic E., Woodhall, GL, Williams AC, Stanford IM, Hall SD. (2019). Bradykinesia is driven by cumulative beta power during continuous movement and alleviated by GABAergic modulation in Parkinson’s disease. Frontiers in Neurology 10: 1298. https://doi.org/10.3389/fneur.2019.01298.
Hall SD, Prokic EJ, McAllister CJ, Ronnqvist KC, Williams AC, Witton C, Woodhall GL, Stanford IM.(2014). GABA-mediated changes in inter-hemispheric beta frequency activity in early-stage Parkinson’s disease. Neuroscience 281 :68-76.
Rossiter HE, Worthen SF, Hall SD & Furlong PL. (2013). Gamma Oscillatory Amplitude EncodesStimulus Intensity in Primary Somatosensory Cortex. Frontiers in Human Neuroscience. 15;7:362
Ronnqvist KC, McAllister CJ, Woodhall GL, Stanford & Hall SD. (2013). A multimodal perspectiveon the composition of cortical oscillations. Frontiers in Human Neuroscience. 7, 132.
Mcallister CJ, Ronnqvist KC, Woodhall GL, Stanford IM, Furlong PL & Hall SD. (2013). OscillatoryBeta Activity Mediates Neuroplastic Effects of Motor Cortex Stimulation in Humans. Journal of Neuroscience 33(18):7919-7927
Hall SD, Stanford IM, Yamawaki N, McAllister CJ, Rönnqvist KC, Woodhall GL & Furlong PL.(2011) The role of GABAergic modulation in motor function related neuronal network activity. NeuroImage. 56(3):1506-10.
Worthen SF, Furlong PL, Hall SD, Aziz Q & Hobson AR. (2011) Primary and secondary somatosensory cortex responses to anticipation and pain: a magnetoencephalography study. European Journal of Neuroscience. 33(5): 946-59
Hall SD, Yamawaki N, Fisher AE, Clauss RP, Woodhall GL & Stanford IM. (2010). Desynchronisation of pathological low-frequency brain activity by the hypnotic drug zolpidem. Clinical Neurophysiology. 121(4): 549-55.
Hall SD, Barnes GR, Furlong PL, Seri S & Hillebrand A. (2010) Neuronal network pharmacodynamics of GABAergic modulation in the human cortex determined using pharmaco-MEG. Human Brain Mapping. 31(4): 581-94.
Sambrook, T.D., Wills, A.J., Hardwick, B., & Goslin, J. (2018). Model-free and model-based reward prediction errors in EEG. NeuroImage, 178, 162-171.
Wills, A.J., Lavric, A., Hemmings, Y., & Surrey, E. (2014). Attention, predictive learning, and the inverse base-rate effect: Evidence from event-related potentials. NeuroImage, 87, 61-71.
Wills, A.J., Lavric, A., Croft, G., & Hodgson, T.L. (2007). Predictive learning, prediction errors and attention: Evidence from event-related potentials and eye tracking. Journal of Cognitive Neuroscience, 19, 843-854.
Enhancing research through BRIC
The Fundamental and Applied Electroencephalography lab in the BRIC facility will include stationary and mobile EEG systems.
This cutting-edge facility will provide an integrated research environment where EEG can be combined with other neuroimaging and neurostimulation techniques to further investigate the mechanisms behind visual and social cognition, and help facilitate further funding and collaboration opportunities.