The Preparation and Execution of Self-Initiated and Externally-Triggered Movement: A Study of Event-Related fMRI

By Ross Cunnington, C. Windischberger, L. Deecke, E. Moser. NeuroImage, 2002

574 citations recorded by the source corpus.

Subfields: Cognitive Neuroscience, Neurology

View Paper: https://www.semanticscholar.org/paper/007a229329ba32bd9b356772565f302cf8451e84

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Citations in the corpus

When thoughts become action: An fMRI paradigm to study volitional brain activity in non-communicative brain injured patients (2007, background): “A number of studies have reported pre-SMA activation in motor imagery (Deiber et al., 1998; Jenkins et al., 2000; Cunnington et al., 2002; Malouin et al., 2003) as well as in other mental imagery modalities (Paulesu et al.”
Neuroanatomical and Neurochemical Substrates of Timing (2011, background): “On the other hand, when subjects were required to produce their own internal representation of a variable time interval (Cunnington et al, 2002; Garraux et al, 2005) the BG alone were activated.”
Functional role of the supplementary and pre-supplementary motor areas (2008, result): “In one event-related functional MRI (fMRI) study, SMA activity before internally generated and externally triggered actions was similar, but there was earlier activation of the pre-SMA for internally generated movements than for externally generated movement”
Co-activation patterns distinguish cortical modules, their connectivity and functional differentiation (2011, background): “Based on these observations and functional activation studies, the SMA has been implicated in executive aspects of motor control, e.g. movement initiation (Chouinard and Paus, 2006; Cunnington et al., 2002; Eickhoff et al., 2008a; Picard and Strick, 1996).”
Human volition: towards a neuroscience of will (2008, background): “Studies that focused on voluntary action alone confirmed that the timing of an action can be predicted from preparatory activity in the preSM”
Functional neuroimaging correlates of finger-tapping task variations: An ALE meta-analysis (2008, background): “…(Mushiake et al., 1990, 1991; Tanji, 1994; Tanji and Shima, 1994, 1996; Brinkman, 1984; Chen et al., 1995, Taniwaki et al., 2003; Romo and Schultz, 1987; Middleton and Strick, 2000), however this distinction has not been consistently reported in humans (Menon et al., 1998; Cunnington et al., 2002).”
Rhythm and Beat Perception in Motor Areas of the Brain (2007, background): “Given that the basal ganglia and SMA are not only involved in attention to time (Coull et al., 2004), but are critical to temporal sequencing (Shima & Tanji, 2000; Brotchie, Iansek, & Horne, 1991) and predictable, internally generated movements ( Cunnington, Windischberger, Deecke, & Moser, 2002; F”
Audiovisual integration of emotional signals in voice and face: An event-related fMRI study (2007, background): “One possible explanation for the emergence of these areas in the context of the connectivity analysis is that they are part of a network of brain regions subserving response selection and response prepara- tion (Cunnington et al., 2002; Elsinger et al., 2006, Rushworth et al., 2004).”
The Use of Vibration as an Exercise Intervention (2003, background): “8% after a total of 10 min of whole-body vibration (5), and an increase of 13% in the average power recorded during arm flexion in welltrained subjects (4) after 5 min of locally applied vibration.”
Internal vs external generation of movements: differential neural pathways involved in bimanual coordination performed in the presence or absence of augmented visual feedback (2003, background): “Imaging studies often failed to show a differential activation of the basal ganglia when directly comparing internally and externally generated tasks (Jenkins et al., 2000; Jahanshahi et al., 1995; Cunnington et al., 2002).”
What is the Bereitschaftspotential? (2006, methodology): “As pointed out originally by Kornhuber and Deecke (1964, 1965) and in their subsequent reports (Deecke et al., 1969, 1976), and later by Kutas and Donchin (1980), BP suddenly increases its gradient about 400 ms before the movement onset. Based on the clearly different scalp distribution of the late ”