Human parietal cortex in action.

By Jody C. Culham, Kenneth F. Valyear. Current Opinion in Neurobiology, 2006

673 citations recorded by the source corpus.

Subfields: Cognitive Neuroscience, Social Psychology

View Paper: https://www.semanticscholar.org/paper/ee09f70f60e36dc68cb2b1c06dd9d8298f8f1638

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Cognitive Neuroscience

In Social Psychology

Citations in the corpus

The origins of metamodality in visual object area LO: Bodily topographical biases and increased functional connectivity to S1 (2016, neutral): “One cortical region which was associated to knowledge and the use of tool is a subarea of left anterior parietal cortex (Culham and Valyear, 2006).”
A new neural framework for visuospatial processing (2011, background): “…all of these regions in both monkeys 34,36,37,84,85 and humans 86,87 have been directly implicated in reaching and grasping objects, and some anterior regions of the parietal lobe contain three-dimensional representations of objects suited for guiding grip (see REFS 88,89 for reviews; BOX 1 ).”
Cultural recycling of cortical maps. (2007, positive): “The systematicity of this surrounding macromap was confirmed by subsequent research using more selective experiments specifically designed to isolate grasping, saccade, and attention-related functions (for review, see Culham et al., 2006).”
Human cortical representations for reaching: Mirror neurons for execution, observation, and imagery (2007, background): “A similar functional specialization of parieto-frontal circuits has recently been found in humans too (see Culham and Kanwisher, 2001; Culham et al., 2006; Culham and Valyear, 2006).”
Recurrent Processing during Object Recognition (2013, background): “This simple mechanism is likely responsible for a broad range of effects, such as action-related response properties in the ventral stream (due to connectivity with dorsal areas involved in object manipulation and tool use; Culham and Valyear, 2006; Mahon et al., 2007; Almeida et al., 2010; Mahon an”
ALE meta-analysis of action observation and imitation in the human brain (2010, neutral): “It has, however, also been argued that potential mirror neurons in the human brain may have an independent relevance for imitation tasks, even though they don't hold the same function in non-human primates (e.g., Brass and Heyes, 2005; Culham and Valyear, 2006; Heyes, 2001).”
The thing that should not be: predictive coding and the uncanny valley in perceiving human and humanoid robot actions (2011, background): “There was a significant Agent by Repetition interaction in the anterior portion of the intraparietal sulcus bilaterally, corresponding to area aIPS, the putative human homologue of macaque area AIP (Grefkes and Fink, 2005; Culham and Valyear, 2006; Grafton and Hamilton, 2007).”
Macroscopic EEG reveals discriminative low-frequency oscillations in plan-to-grasp visuomotor tasks (2025, unknown): “During the planning phase, discriminative theta patterns are predominantly localized to parieto-occipital regions (PO7, P4, Oz) and frontal electrodes (FP1), consistent with the dorsal visual stream’s role in transforming visual object information into motor intent [42, 43].”