A direct quantitative relationship between the functional properties of human and macaque V5

By Geraint E. Rees, Karl J. Friston, Christof Koch. Nature Neuroscience, 2000

721 citations recorded by the source corpus.

Subfields: Biophysics, Cognitive Neuroscience

View Paper: https://www.semanticscholar.org/paper/1428381485d887bef07a67ddc138f4a2df6b5e94

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Citations in the corpus

The neural basis of the blood-oxygen-level-dependent functional magnetic resonance imaging signal. (2002, methodology): “The instantaneous or mean rate of such spikes is the neuronal variable most frequently examined with respect to a sensory stimulus or behavioural state, and the one recently used to examine quantitatively the relationship of the BOLD signal to neural activity by comparing human fMRI data with electr”
Beyond the Visible—Imaging the Human Brain with Light (2003, background): “…interest in the correlation of the two and the surprise at the problems encountered when doing so (Heeger et al., 2000; Lauritzen 2001; Logothetis et al., 2001; Rees et al., 2000) may highlight the importance of considering the diversity of responses, many of which may be investigated optically.”
Dissociable Neural Pathways Are Involved in the Recognition of Emotion in Static and Dynamic Facial Expressions (2003, positive): “Compared to static displays, the perception of anger in dynamic expressions was associated with prominent activations in brain regions specialized for the visual processing of coherent stimulus motion (V5; Zeki et al., 1991; Watson et al., 1993; Tootell and Taylor, 1995; Rees et al., 2000) and facia”
Competing Theories of Binocular Rivalry: A Possible Resolution (2001, background): “Second, there is a strong agreement between single-unit estimates of neur onal firing rate and fMRI estimates of neural activity in studies measuring V1 responses to different stimulus contrasts (Heeger, Huk, Geisler and Albrecht, 2000) and MT responses to different motion velocities ( Rees, Fristo”
Abstract reward and punishment representations in the human orbitofrontal cortex (2001, background): “A full understanding of this effect may only be possible when the relationship between the underlying neural firing rate and the characteristics of the BOLD response are more completely understoo”
Neural correlates of beauty. (2004, background): “For example , a graded response in area V5 has been observed when the visibility of a pattern of moving dots is increased by increasing the coherence of the motion of the dots (Rees et al. 2000).”
Transient and linearly graded deactivation of the human default-mode network by a visual detection task (2008, positive): “Firstly, the positive BOLD effects in the primary and lateral visual cortices are only revealed by comparison to the null trials and are entirely consistent both with previous neuroimaging studies (e.g. Rees et al., 2000) and what we expect from animal neurophysiology (Newsome and Pare, 1988).”
Weakened Center-Surround Interactions in Visual Motion Processing in Schizophrenia (2006, background): “Of course, this statement assumes that the properties of human and macaque MT are comparable (Rees et al., 2000) and that the receptive field sizes are similar for two species (Kastner et al., 2001).”
Task-Related Changes in Cortical Synchronization Are Spatially Coincident with the Hemodynamic Response (2002, result): “The results support recent findings that the haemodynamic response is tightly linked to underlying neuronal function (Rees et al., 2000; Logothetis et al., 2001) and the assertion that event-related desynchronization is a correlate of increased neural activation in a cortical area (Pfurtscheller…”
Comparative mapping of higher visual areas in monkeys and humans. (2004, background): “The LOS region is motion sensitive [19,58, 59 ], but the motion-sensitive and shapesensitive parts are not co-extensive [20].”
Reorganization of global form and motion processing during human visual development. (2010, background): “Differential Vulnerability Areas V4 (sensitive to global form [10]) and V5 (sensitive to global motion [9, 11, 23]) are key structures in routing information to the ventral and dorsal cortical streams, respectively [41–43].”
Coupling between neuronal firing rate, gamma LFP, and BOLD fMRI is related to interneuronal correlations. (2007, result): “in humans and spike recordings obtained under comparable experimental conditions in macaque monkeys [15, 16].”
What does fMRI tell us about neuronal activity? (2002, background): “Two studies have compared human fMRI and monkey single-unit data to infer that fMRI signals are directly proportional to average neuronal firing rate”