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  1. The representing brain: Neural correlates of motor intention and imagery.Marc Jeannerod - 1994 - Behavioral and Brain Sciences 17 (2):187-202.
    This paper concerns how motor actions are neurally represented and coded. Action planning and motor preparation can be studied using a specific type of representational activity, motor imagery. A close functional equivalence between motor imagery and motor preparation is suggested by the positive effects of imagining movements on motor learning, the similarity between the neural structures involved, and the similar physiological correlates observed in both imaging and preparing. The content of motor representations can be inferred from motor images at a (...)
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  • The neuropsychology of schizophrenia.J. A. Gray, J. Feldon, J. N. P. Rawlins, D. R. Hemsley & A. D. Smith - 1991 - Behavioral and Brain Sciences 14 (1):1-20.
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  • The representation of egocentric space in the posterior parietal cortex.J. F. Stein - 1992 - Behavioral and Brain Sciences 15 (4):691-700.
    The posterior parietal cortex (PPC) is the most likely site where egocentric spatial relationships are represented in the brain. PPC cells receive visual, auditory, somaesthetic, and vestibular sensory inputs; oculomotor, head, limb, and body motor signals; and strong motivational projections from the limbic system. Their discharge increases not only when an animal moves towards a sensory target, but also when it directs its attention to it. PPC lesions have the opposite effect: sensory inattention and neglect. The PPC does not seem (...)
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  • Does the nervous system depend on kinesthetic information to control natural limb movements?S. C. Gandevia & David Burke - 1992 - Behavioral and Brain Sciences 15 (4):614-632.
    This target article draws together two groups of experimental studies on the control of human movement through peripheral feedback and centrally generated signals of motor commands. First, during natural movement, feedback from muscle, joint, and cutaneous afferents changes; in human subjects these changes have reflex and kinesthetic consequences. Recent psychophysical and microneurographic evidence suggests that joint and even cutaneous afferents may have a proprioceptive role. Second, the role of centrally generated motor commands in the control of normal movements and movements (...)
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  • The role of attention in auditory information processing as revealed by event-related potentials and other brain measures of cognitive function.Risto Näätänen - 1990 - Behavioral and Brain Sciences 13 (2):201-233.
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  • Context-switching and responsiveness to real relevance.Erik Rietveld - 2012 - In Julian Kiverstein & Michael Wheeler (eds.), Heidegger and Cognitive Science. New York: Palgrave-Macmillan.
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  • The frame/content theory of evolution of speech production.Peter F. MacNeilage - 1998 - Behavioral and Brain Sciences 21 (4):499-511.
    The species-specific organizational property of speech is a continual mouth open-close alternation, the two phases of which are subject to continual articulatory modulation. The cycle constitutes the syllable, and the open and closed phases are segments framescontent displays that are prominent in many nonhuman primates. The new role of Broca's area and its surround in human vocal communication may have derived from its evolutionary history as the main cortical center for the control of ingestive processes. The frame and content components (...)
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  • Does the nervous system use equilibrium-point control to guide single and multiple joint movements?E. Bizzi, N. Hogan, F. A. Mussa-Ivaldi & S. Giszter - 1992 - Behavioral and Brain Sciences 15 (4):603-613.
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  • Express saccades and visual attention.B. Fischer & H. Weber - 1993 - Behavioral and Brain Sciences 16 (3):553-567.
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  • How does the nervous system control the equilibrium trajectory?S. V. Adamovich - 1992 - Behavioral and Brain Sciences 15 (4):704-705.
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  • Is stiffness the mainspring of posture and movement?Z. Hasan - 1992 - Behavioral and Brain Sciences 15 (4):756-758.
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  • Equilibrium-point hypothesis, minimum effort control strategy and the triphasic muscle activation pattern.Ning Lan & Patrick E. Crago - 1992 - Behavioral and Brain Sciences 15 (4):769-771.
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  • Jeannerod's representing brain: Image or illusion?Jean Pailhous & Mireille Bonnard - 1994 - Behavioral and Brain Sciences 17 (2):215-216.
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  • Schiz bits: Misses, mysteries and hits.J. A. Gray, D. R. Hemsley, J. Feldon, N. S. Gray & J. N. P. Rawlins - 1991 - Behavioral and Brain Sciences 14 (1):56-84.
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  • What is schizophrenia?Janice R. Stevens & James M. Gold - 1991 - Behavioral and Brain Sciences 14 (1):50-51.
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  • A realistic model will be much more complex and will consider longitudinal neuropsychodevelopment.Terry Patterson - 1991 - Behavioral and Brain Sciences 14 (1):40-41.
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  • Medial frontal cortex: from self-generated action to reflection on one's own performance.Hakwan C. Lau Richard E. Passingham, Sara L. Bengtsson - 2010 - Trends in Cognitive Sciences 14 (1):16.
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  • The Meaning of Embodiment.Julian Kiverstein - 2012 - Topics in Cognitive Science 4 (4):740-758.
    There is substantial disagreement among philosophers of embodied cognitive science about the meaning of embodiment. In what follows, I describe three different views that can be found in the current literature. I show how this debate centers around the question of whether the science of embodied cognition can retain the computer theory of mind. One view, which I will label body functionalism, takes the body to play the functional role of linking external resources for problem solving with internal biological machinery. (...)
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  • Brain correlates of subjective freedom of choice.Elisa Filevich, Patricia Vanneste, Marcel Brass, Wim Fias, Patrick Haggard & Simone Kühn - 2013 - Consciousness and Cognition 22 (4):1271-1284.
    The subjective feeling of free choice is an important feature of human experience. Experimental tasks have typically studied free choice by contrasting free and instructed selection of response alternatives. These tasks have been criticised, and it remains unclear how they relate to the subjective feeling of freely choosing. We replicated previous findings of the fMRI correlates of free choice, defined objectively. We introduced a novel task in which participants could experience and report a graded sense of free choice. BOLD responses (...)
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  • Absent minds and absent agents: Attention-lapse induced alienation of agency.James Allan Cheyne, Jonathan S. A. Carriere & Daniel Smilek - 2009 - Consciousness and Cognition 18 (2):481-493.
    We report a novel task designed to elicit transient attention-lapse induced alienation of agency experiences in normal participants. When attention-related action slips occur during the task, participants reported substantially decreased self control as well as a high degree of perceived agency attributed to the errant hand. In addition, participants reported being surprised by, and annoyed with, the actions of the errant hand. We argue that ALIA experiences occur because of constraints imposed by the close and precise temporal relations between intention (...)
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  • Causally efficacious intentions and the sense of agency: In defense of real mental causation.Markus E. Schlosser - 2012 - Journal of Theoretical and Philosophical Psychology 32 (3):135-160.
    Empirical evidence, it has often been argued, undermines our commonsense assumptions concerning the efficacy of conscious intentions. One of the most influential advocates of this challenge has been Daniel Wegner, who has presented an impressive amount of evidence in support of a model of "apparent mental causation". According to Wegner, this model provides the best explanation of numerous curious and pathological cases of behavior. Further, it seems that Benjamin Libet's classic experiment on the initiation of action and the empirical evidence (...)
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  • Vectorial versus configural encoding ofbody space.Jacques Paillard - 2005 - In Helena de Preester & Veroniek Knockaert (eds.), Body image and body schema. John Benjamins. pp. 62--89.
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  • Neural systems and hormones mediating attraction to infant and child faces.Lizhu Luo - 2015 - Frontiers in Psychology 6.
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  • On the neural mechanisms of sequence learning.Tim Curran - 1995 - PSYCHE: An Interdisciplinary Journal of Research On Consciousness 2.
    Nissen and Bullemer's serial reaction time task has proven to be a useful model task for exploring implicit sequence learning. Neuropsychological research indicates that SRT learning may depend on the integrity of the basal ganglia, but not on medial temporal and diencephalic structures that are crucial for explicit learning. Recent neuroimaging research demonstrates that motor cortical areas , prefrontal, and parietal cortex also may be involved. This paper reviews this neuropsychological and neuroimaging research, but finds it lacking specific links between (...)
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  • Action-Effect Bindings and Ideomotor Learning in Intention- and Stimulus-Based Actions.Arvid Herwig & Florian Waszak - 2012 - Frontiers in Psychology 3.
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  • Responsible choices, desert-based legal institutions, and the challenges of contemporary neuroscience.Michael S. Moore - 2012 - Social Philosophy and Policy 29 (1):233-279.
    Research Articles Michael S. Moore, Social Philosophy and Policy, FirstView Article.
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  • Evolving concepts of sleep cycle generation: From brain centers to neuronal populations.J. A. Hobson, R. Lydic & H. A. Baghdoyan - 1986 - Behavioral and Brain Sciences 9 (3):371-400.
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  • Effects of Transcranial Direct Current Stimulation of Primary Motor Cortex on Reaction Time and Tapping Performance: A Comparison Between Athletes and Non-athletes.Oliver Seidel & Patrick Ragert - 2019 - Frontiers in Human Neuroscience 13.
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  • Neural Adaptations Associated with Interlimb Transfer in a Ballistic Wrist Flexion Task.Kathy L. Ruddy, Anne K. Rudolf, Barbara Kalkman, Maedbh King, Andreas Daffertshofer, Timothy J. Carroll & Richard G. Carson - 2016 - Frontiers in Human Neuroscience 10.
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  • Different Neural Information Flows Affected by Activity Patterns for Action and Verb Generation.Zijian Wang, Zuo Zhang & Yaoru Sun - 2022 - Frontiers in Psychology 13.
    Shared brain regions have been found for processing action and language, including the left inferior frontal gyrus, the premotor cortex, and the inferior parietal lobule. However, in the context of action and language generation that shares the same action semantics, it is unclear whether the activity patterns within the overlapping brain regions would be the same. The changes in effective connectivity affected by these activity patterns are also unclear. In this fMRI study, participants were asked to perform hand action and (...)
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  • Implications of neural networks for how we think about brain function.David A. Robinson - 1992 - Behavioral and Brain Sciences 15 (4):644-655.
    Engineers use neural networks to control systems too complex for conventional engineering solutions. To examine the behavior of individual hidden units would defeat the purpose of this approach because it would be largely uninterpretable. Yet neurophysiologists spend their careers doing just that! Hidden units contain bits and scraps of signals that yield only arcane hints about network function and no information about how its individual units process signals. Most literature on single-unit recordings attests to this grim fact. On the other (...)
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  • Locating volition.Jing Zhu - 2004 - Consciousness and Cognition 13 (2):302-322.
    In this paper, it is examined how neuroscience can help to understand the nature of volition by addressing the question whether volitions can be localized in the brain. Volitions, as acts of the will, are special mental events or activities by which an agent consciously and actively exercises her agency to voluntarily direct her thoughts and actions. If we can pinpoint when and where volitional events or activities occur in the brain and find out their neural underpinnings, this can substantively (...)
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  • Automatic and attention-dependent processing of auditory stimulus information.Risto Näätänen - 1990 - Behavioral and Brain Sciences 13 (2):261-288.
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  • Nonconscious motor images.Giacomo Rizzolatti - 1994 - Behavioral and Brain Sciences 17 (2):220-220.
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  • A mobility gradient in the organization of vertebrate movement: The perception of movement through symbolic language.Ilan Golani - 1992 - Behavioral and Brain Sciences 15 (2):249-266.
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  • Neuropsychological vulnerability or episode factors in schizophrenia?Keith H. Nuechterlein & Michael Foster Green - 1991 - Behavioral and Brain Sciences 14 (1):37-38.
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  • On the relation between motor imagery and visual imagery.Roberta L. Klatzky - 1994 - Behavioral and Brain Sciences 17 (2):212-213.
    Jeannerod's target article describes support, through empirical and neurological findings, for the intriguing idea of motor imagery, a form of representation hypothesized to have levels of functional equivalence with motor preparation, while being consciously accessible. Jeannerod suggests that the subjectively accessible content of motor imagery allows it to be distinguished from motor preparation, which is unconscious. Motor imagery is distinguished from visual imagery in terms of content. Motor images are kinesthetic in nature; they are parametrized by variables such as force (...)
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  • Heterogeneity, orienting and habituation in schizophrenia.Michael E. Dawson & Erin A. Hazlett - 1991 - Behavioral and Brain Sciences 14 (1):24-25.
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  • How does the physiology change with symptom exacerbation and remission in schizophrenia?George G. Dougherty, Stuart R. Steinhauer, Joseph Zubin & Daniel P. van Kammen - 1991 - Behavioral and Brain Sciences 14 (1):25-26.
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  • In what context is latent inhibition relevant to the symptoms of schizophrenia?Chris Frith - 1991 - Behavioral and Brain Sciences 14 (1):28-29.
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  • Call it what it is: Motor memory.Joaquin M. Fuster - 1994 - Behavioral and Brain Sciences 17 (2):208-208.
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  • Novelty value in associative learning.Jonathan C. Gewirtz - 1991 - Behavioral and Brain Sciences 14 (1):29-29.
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  • Schizophrenia and attention: In and out of context.R. E. Lubow - 1991 - Behavioral and Brain Sciences 14 (1):35-36.
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  • Express attentional shifts.Ken Nakayama & Manfred Mackeben - 1993 - Behavioral and Brain Sciences 16 (3):584-585.
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  • Bases for irrelevant information processing in schizophrenia: Room for manoeuvre.R. D. Oades - 1991 - Behavioral and Brain Sciences 14 (1):38-39.
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  • A hippocampal theory of schizophrenia.Nestor A. Schmajuk & James J. DiCarlo - 1991 - Behavioral and Brain Sciences 14 (1):47-49.
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  • Action and attention.A. H. C. Van der Heijden & Bruce Bridgeman - 1994 - Behavioral and Brain Sciences 17 (2):225-226.
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  • Precis of.D. M. Wegner - 2004 - Behavioral and Brain Sciences 27.
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  • The accumbens–substantia nigra pathway, mismatch and amphetamine.Ina Weiner - 1991 - Behavioral and Brain Sciences 14 (1):54-55.
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  • Moving beyond imagination.Robert Dufour, Martin H. Fischer & David A. Rosenbaum - 1994 - Behavioral and Brain Sciences 17 (2):206-207.
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