Multisensory convergence in calcarine visual areas in macaque monkey.

By K. Rockland, H. Ojima. 2003

577 citations recorded by the source corpus.

Subfields: Cognitive Neuroscience, Experimental and Cognitive Psychology

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In Cognitive Neuroscience

In Experimental and Cognitive Psychology

Citations in the corpus

Assessing the Role of the ‘Unity Assumption’ on Multisensory Integration: A Review (2017, background): “…compared to central visual field (e.g., Charbonneau et al., 2013; Gleiss and Kayser, 2013; Chen et al., submitted), which is thought to be partly attributable to the more extensive neural connectivity across sensory-dominant areas in the periphery (Falchier et al., 2002; Rockland and Ojima, 2003).”
Synesthesia: a new approach to understanding the development of perception. (2013, background): “Also in monkeys, there is evidence that neurons in the primary visual cortex with receptive fields in the periphery receive input from the primary auditory cortex (Falchier, Clavagnier , Barone, & Kennedy, 2002; see also Cappe & Barone, 2005; Rockland & Ojima, 2003).”
Sound-induced flash illusion as an optimal percept (2005, background): “the pattern of interconnectivity between the sensory areas [13,14]), as well as biases imposed by the task, the observer’s state, etc.”
Diffusion tensor imaging shows white matter tracts between human auditory and visual cortex (2011, unknown): “They found direct axonal connections between auditory cortex and the primary and secondary visual cortex (Falchier et al. 2002; Rockland and Ojima 2003).”
Multisensory Interplay Reveals Crossmodal Influences on ‘Sensory-Specific’ Brain Regions, Neural Responses, and Judgments (2008, unknown): “Another study reported bidirectional fibers between auditory belt areas and primary visual cortex in macaques (Rockland and Ojima, 2003).”
The origins of metamodality in visual object area LO: Bodily topographical biases and increased functional connectivity to S1 (2016, unknown): “Similarly, previous studies have suggested that the extent of multisensory processing and connectivity of low-level visual areas is modulated by their topographic organization (Borra and Rockland, 2011; Falchier et al., 2002; Gleiss and Kayser, 2013; Rockland and Ojima, 2003).”
The multisensory function of the human primary visual cortex. (2016, background): “Finally, some have claimed that these projections are heterogeneously distributed across the retinotopic representations within the primary visual cortex, with more peripheral visual field representations receiving denser projections (Falchier et al., 2002; Rockland and Ojima, 2003).”
The ventriloquist in periphery: impact of eccentricity-related reliability on audio-visual localization. (2013, background): “…region of the auditory cortex and visual areas representing peripheral visual space in monkeys (Falchier, Clavagnier, Barone, & Kennedy, 2002; Rockland & Ojima, 2003) and humans (Beer, Plank, & Greenlee, 2011) provided a neurophysiological support to hypothesize enhanced audio-visual…”
Looming Signals Reveal Synergistic Principles of Multisensory Integration (2012, background): “…monosynaptic projections identified between unisensory (including primary) cortices raise the possibility of interactions during early stimulus processing stages (Falchier et al., 2002, 2010; Rockland and Ojima, 2003; Cappe and Barone, 2005; Cappe et al., 2009a; see also Beer et al., 2011).”
Distinct Functional Contributions of Primary Sensory and Association Areas to Audiovisual Integration in Object Categorization (2010, background): “Indeed, their extensive bidirectional anatomical connectivity to visual and auditory areas renders them ideal for integrating inputs from multiple senses (Neal et al., 1990; Seltzer and Pandya, 1994; Falchier et al., 2002; Rockland and Ojima, 2003).”
Multisensory integration: flexible use of general operations (2014, unknown): “…cortices have been put forward, including direct ‘‘crossing’’ projections from sensory cortices of different modalities (e.g., Falchier et al., 2002; Rockland and Ojima, 2003), direct ascending inputs from so-called ‘‘nonspecific’’ thalamic regions (Hackett et al., 2007; Schroeder et al.,…”