| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2015PNAS..112E.361G |
| P356 | DOI | 10.1073/PNAS.1414974112 |
| P932 | PMC publication ID | 4313798 |
| P698 | PubMed publication ID | 25583504 |
| P5875 | ResearchGate publication ID | 270790159 |
| P50 | author | Geraint Rees | Q5548822 |
| Marlene Behrmann | Q6771717 | ||
| Lauren J Lorenzi | Q125331076 | ||
| Sharon Gilaie-Dotan | Q125331771 | ||
| Ayse Pinar Saygin | Q125331873 | ||
| P2860 | cites work | The Psychophysics Toolbox | Q27861071 |
| Brain areas involved in perception of biological motion | Q28142468 | ||
| Can face recognition really be dissociated from object recognition? | Q28143664 | ||
| A cortical area selective for visual processing of the human body | Q28189305 | ||
| Functional neuroanatomy of biological motion perception in humans | Q29030692 | ||
| Visual perception of biological motion and a model for its analysis | Q29038554 | ||
| What does visual agnosia tell us about perceptual organization and its relationship to object perception? | Q29039169 | ||
| The VideoToolbox software for visual psychophysics: transforming numbers into movies | Q29547363 | ||
| Temporal cortex neurons encode articulated actions as slow sequences of integrated poses | Q30453910 | ||
| Perception of biological motion without local image motion | Q30476190 | ||
| Seeing with profoundly deactivated mid-level visual areas: non-hierarchical functioning in the human visual cortex | Q30488105 | ||
| Human functional magnetic resonance imaging reveals separation and integration of shape and motion cues in biological motion processing. | Q33459689 | ||
| The role of human ventral visual cortex in motion perception | Q33598187 | ||
| fMR-Adaptation Reveals Invariant Coding of Biological Motion on the Human STS | Q33817875 | ||
| Brain Areas Active during Visual Perception of Biological Motion | Q34152299 | ||
| Normal form from biological motion despite impaired ventral stream function | Q34159162 | ||
| The functional neuroanatomy of object agnosia: a case study | Q34199466 | ||
| Separate face and body selectivity on the fusiform gyrus. | Q34469967 | ||
| A model of biological motion perception from configural form cues. | Q34502488 | ||
| Superior temporal and premotor brain areas necessary for biological motion perception | Q34657011 | ||
| Neural mechanisms for the recognition of biological movements | Q35075740 | ||
| Not one extrastriate body area: using anatomical landmarks, hMT+, and visual field maps to parcellate limb-selective activations in human lateral occipitotemporal cortex | Q35110449 | ||
| Brain regions involved in human movement perception: A quantitative voxel-based meta-analysis | Q57516235 | ||
| Specific involvement of human parietal systems and the amygdala in the perception of biological motion | Q71106336 | ||
| Perception of biological motion | Q74621081 | ||
| Highlighting human form and motion information enhances the conspicuity of pedestrians at night | Q82290153 | ||
| Structural processing in biological motion perception | Q82294603 | ||
| Seeing pedestrians at night: visual clutter does not mask biological motion | Q83731289 | ||
| Sparing of sensitivity to biological motion but not of global motion after early visual deprivation | Q84400003 | ||
| Form overshadows 'opponent motion' information in processing of biological motion from point light walker stimuli | Q84893225 | ||
| Neuroanatomical correlates of biological motion detection | Q36726889 | ||
| The neural basis of visual body perception. | Q36887537 | ||
| Effects of spatial transformation on regional brain volume estimates | Q36969417 | ||
| Linking form and motion in the primate brain. | Q37158841 | ||
| Perceptual deficits in patients with impaired recognition of biological motion after temporal lobe lesions | Q37695829 | ||
| Pure alexia and covert reading: Evidence from Stroop tasks | Q38423514 | ||
| Bilateral hemispheric processing of words and faces: evidence from word impairments in prosopagnosia and face impairments in pure alexia | Q38459381 | ||
| Probing the face-space of individuals with prosopagnosia | Q39923920 | ||
| Intact "biological motion" and "structure from motion" perception in a patient with impaired motion mechanisms: a case study | Q41216008 | ||
| Quantifying and modeling the strength of motion illusions perceived in static patterns. | Q42168378 | ||
| Perception of biological motion in visual agnosia | Q42321438 | ||
| Using biological motion to enhance the conspicuity of roadway workers | Q42693286 | ||
| Repetitive TMS over posterior STS disrupts perception of biological motion | Q43537670 | ||
| Snap! Recognising implicit actions in static point-light displays | Q43819162 | ||
| Perception and production of biological movement in patients with early periventricular brain lesions | Q44302034 | ||
| Configural processing of biological motion in human superior temporal sulcus. | Q44913936 | ||
| Effects of TMS over premotor and superior temporal cortices on biological motion perception. | Q45351015 | ||
| Point-light biological motion perception activates human premotor cortex. | Q46041410 | ||
| Individual differences in the perception of biological motion: links to social cognition and motor imagery | Q46048655 | ||
| Long-term deprivation affects visual perception and cortex | Q46100354 | ||
| Distinct mechanisms for coding of visual actions in macaque temporal cortex. | Q46143209 | ||
| Perception of global gestalt by temporal integration in simultanagnosia | Q46176807 | ||
| Motion processing at low light levels: Differential effects on the perception of specific motion types | Q46591996 | ||
| Visual perception and neural correlates of novel 'biological motion'. | Q46847075 | ||
| Patterns of fMRI activity dissociate overlapping functional brain areas that respond to biological motion | Q47217637 | ||
| The human premotor cortex is 'mirror' only for biological actions. | Q47248540 | ||
| The retinotopic organization of the human middle temporal area MT/V5 and its cortical neighbors | Q48112068 | ||
| Cells in monkey STS responsive to articulated body motions and consequent static posture: a case of implied motion? | Q48180574 | ||
| Brain activity evoked by the perception of human walking: controlling for meaningful coherent motion. | Q48238753 | ||
| The overlap of the EBA and the MT/V5 cluster. | Q48316972 | ||
| Visual complexity in letter-by-letter reading: "pure" alexia is not pure | Q48334950 | ||
| Limitations in drivers' ability to recognize pedestrians at night | Q48459668 | ||
| Visual motion perception after brain damage: II. Deficits in form-from-motion perception | Q48597219 | ||
| Parallel visual motion processing streams for manipulable objects and human movements | Q48640278 | ||
| Visuoperceptual deficits in letter-by-letter reading? | Q48642714 | ||
| Acquiring long-term representations of visual classes following extensive extrastriate damage | Q48792405 | ||
| A functional MRI study of face recognition in patients with prosopagnosia | Q48838900 | ||
| Specificity of regions processing biological motion | Q48876304 | ||
| From word superiority to word inferiority: visual processing of letters and words in pure alexia. | Q50664938 | ||
| Seeing biological motion. | Q50858806 | ||
| Impairments in part-whole representations of objects in two cases of integrative visual agnosia. | Q51896307 | ||
| Visual perception of biological motion by form: a template-matching analysis. | Q51935877 | ||
| Recruitment of periventricular parietal regions in processing cluttered point-light biological motion. | Q52088017 | ||
| Subconfigurations of the human form in the perception of biological motion displays. | Q52174217 | ||
| QUEST: a Bayesian adaptive psychometric method. | Q52708519 | ||
| Individual Comparisons by Ranking Methods | Q56028075 | ||
| Phonological Activation in Pure Alexia | Q57408865 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | E361-70 | |
| P577 | publication date | 2015-01-12 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Ventral aspect of the visual form pathway is not critical for the perception of biological motion | |
| P478 | volume | 112 |
| Q30827033 | A comparison of form processing involved in the perception of biological and nonbiological movements. |
| Q36015055 | A new technique for generating disordered point-light animations for the study of biological motion perception |
| Q55438198 | Attraction of posture and motion-trajectory elements of conspecific biological motion in medaka fish. |
| Q40082094 | Cognitive estimation: Performance of patients with focal frontal and posterior lesions. |
| Q48650393 | Cognitive neuropsychology and its vicissitudes: The fate of Caramazza's axioms |
| Q64941161 | Differential sustained and transient temporal processing across visual streams. |
| Q36730540 | Face-selective regions differ in their ability to classify facial expressions |
| Q47555839 | Heritable aspects of biological motion perception and its covariation with autistic traits |
| Q95318974 | Investigating face and house discrimination at foveal to parafoveal locations reveals category-specific characteristics |
| Q44125909 | Natural Translating Locomotion Modulates Cortical Activity at Action Observation |
| Q35211732 | Perception of biological motion from size-invariant body representations |
| Q90258889 | Structural and effective brain connectivity underlying biological motion detection |
| Q34498631 | Three-Dimensional Representations of Objects in Dorsal Cortex are Dissociable from Those in Ventral Cortex |
| Q26738547 | Visual motion serves but is not under the purview of the dorsal pathway |
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