IRIS
Sperandio, Irene
 Distribuzione geografica
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Continente #
NA - Nord America 4.063
AS - Asia 1.850
EU - Europa 1.712
SA - Sud America 570
Continente sconosciuto - Info sul continente non disponibili 271
AF - Africa 35
OC - Oceania 26
Totale 8.527
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Nazione #
US - Stati Uniti d'America 3.941
IT - Italia 952
SG - Singapore 738
BR - Brasile 452
VN - Vietnam 434
CN - Cina 271
RU - Federazione Russa 129
GB - Regno Unito 96
DE - Germania 92
KR - Corea 90
CA - Canada 79
FI - Finlandia 78
FR - Francia 76
HK - Hong Kong 69
LV - Lettonia 69
AR - Argentina 45
ID - Indonesia 44
IN - India 43
BG - Bulgaria 40
SE - Svezia 40
CO - Colombia 32
BD - Bangladesh 29
AT - Austria 27
AU - Australia 23
IQ - Iraq 21
MX - Messico 20
NL - Olanda 20
JP - Giappone 19
PL - Polonia 16
ES - Italia 14
CH - Svizzera 13
EC - Ecuador 13
UA - Ucraina 13
ZA - Sudafrica 13
CL - Cile 11
TR - Turchia 11
PK - Pakistan 10
PY - Paraguay 9
SA - Arabia Saudita 9
IR - Iran 8
JM - Giamaica 8
AE - Emirati Arabi Uniti 6
BE - Belgio 6
IE - Irlanda 6
IL - Israele 6
RO - Romania 6
KE - Kenya 5
VE - Venezuela 5
CR - Costa Rica 4
JO - Giordania 4
MA - Marocco 4
MY - Malesia 4
PH - Filippine 4
TW - Taiwan 4
DZ - Algeria 3
EE - Estonia 3
GT - Guatemala 3
KH - Cambogia 3
MK - Macedonia 3
NP - Nepal 3
RS - Serbia 3
TH - Thailandia 3
UZ - Uzbekistan 3
BH - Bahrain 2
ET - Etiopia 2
HU - Ungheria 2
LK - Sri Lanka 2
LT - Lituania 2
NI - Nicaragua 2
PE - Perù 2
PT - Portogallo 2
SV - El Salvador 2
SY - Repubblica araba siriana 2
TN - Tunisia 2
XK - ???statistics.table.value.countryCode.XK??? 2
YE - Yemen 2
AM - Armenia 1
AZ - Azerbaigian 1
BW - Botswana 1
CI - Costa d'Avorio 1
CZ - Repubblica Ceca 1
EG - Egitto 1
EU - Europa 1
GA - Gabon 1
GE - Georgia 1
HN - Honduras 1
HR - Croazia 1
HT - Haiti 1
KW - Kuwait 1
KZ - Kazakistan 1
LB - Libano 1
MD - Moldavia 1
NR - Nauru 1
NZ - Nuova Zelanda 1
PR - Porto Rico 1
SI - Slovenia 1
SR - Suriname 1
TT - Trinidad e Tobago 1
TZ - Tanzania 1
UG - Uganda 1
Totale 8.258
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Città #
Ashburn 505
Rome 461
Singapore 436
Dallas 311
San Jose 293
Chandler 202
Fairfield 185
Santa Clara 182
Verona 158
Ho Chi Minh City 147
Columbus 141
Hanoi 100
Princeton 100
Council Bluffs 97
Seoul 90
Woodbridge 81
Houston 74
Riga 69
Los Angeles 67
Seattle 63
Wilmington 63
Cambridge 62
Lauterbourg 59
San Mateo 58
Trento 55
Milan 51
Moscow 50
Chicago 49
Helsinki 49
Hong Kong 47
Ann Arbor 45
Phoenix 45
Beijing 41
New York 40
Sofia 40
São Paulo 33
London 32
Da Nang 31
San Diego 29
Jakarta 27
The Dalles 26
Turku 25
Toronto 21
Brescia 20
Munich 20
Atlanta 18
Melbourne 18
Vienna 18
Buffalo 17
Boardman 16
Haiphong 16
Nuremberg 16
Orem 16
Rio de Janeiro 14
Salt Lake City 14
St Louis 14
Brooklyn 12
Denver 12
Chennai 11
Frankfurt am Main 11
Guangzhou 11
Shanghai 11
Bogotá 10
Stockholm 10
Tokyo 10
Baghdad 9
Belo Horizonte 9
Brasília 9
Falls Church 9
Lancaster 9
Povo 9
Riverside 9
Tampa 9
Warsaw 9
Washington 9
Biên Hòa 8
Curitiba 8
Hefei 8
Johannesburg 8
Naples 8
Norwalk 8
Springfield 8
Thái Bình 8
Venice 8
Amsterdam 7
Boston 7
Montreal 7
Can Tho 6
Canterbury 6
Chaozhou 6
Charlotte 6
Dhaka 6
Dublin 6
Guarulhos 6
Madrid 6
Ninh Bình 6
Padua 6
Recife 6
Rovereto 6
Santiago 6
Totale 5.316
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Nome #
The contribution of proprioception to size constancy in perception and action: an fMRI study 270
Editorial: perceiving and acting in the real world: from neural activity to behavior 197
A review on various explanations of Ponzo-like illusions 182
A review of abnormalities in the perception of visual illusions in schizophrenia 177
Behavioural relevance of foveal cortex processing for haptic size estimation 174
The 44th European Conference on Visual Perception (ECVP) 2022, Nijmegen, The Netherlands 168
Fading boundaries between the physical and the social world: Insights and novel techniques from the intersection of these two fields 162
Behavioural significance of foveal cortical processing for haptic size estimation 160
Evidence for a functional and anatomical dissociation in the use of size constancy for perceptual report and goal-directed grasping. 154
Behavioural significance of foveal cortex processing for haptic size estimation 151
Does Emmert’s law operate in primary visual cortex? 151
Afterimage size is modulated by size-contrast illusions 150
Electrophysiological correlates of size constancy 149
Preservation of size constancy for action, but not perception, in a patient with bilateral occipital lesions. 147
Behavioural relevance of foveal cortex processing for haptic size estimation 146
Differences in the Effects of Crowding on Size Perception and Grip Scaling in Densely Cluttered 3-D Scenes 143
Temporal features of size constancy for perception and action in a real-world setting: A combined EEG-kinematics study 140
A reaction time approach to size constancy and visual illusions 140
Does reaction time depend upon perceived or retinal stimulus size? 139
Simple actions modulate context-dependent visual size perception at late processing stages 136
Grip Constancy but Not Perceptual Size Constancy Survives Lesions of Early Visual Cortex 136
Haptic size decoding in the early visual cortex 133
Network dynamics underlying alterations in apparent object size 131
Cortical areas involved in haptic and imagined size decoding 131
Developmental Trajectories of Size Constancy as Implicitly Examined by Simple Reaction Times 126
The contribution of semantic distance knowledge to size constancy in perception and grasping when visual cues are limited. 123
The influence of crowding on grip scaling during grasping. 123
Human brain areas involved in imagined and haptically explored objects 122
The mechanisms of size constancy 119
A Comparison Between the Use of Afterimages and Physical Stimuli in the Examination of Size Constancy 118
Cortical areas involved in imagery and haptic exploration of object size 117
The influence of familiar size on simple reaction times. 110
Linear perspective cues have a greater effect on the perceptual rescaling of distant stimuli than textures in the virtual environment 109
Dissociation between size constancy for perception and action in a patient with bilateral occipital lesions. 106
The contribution of linear perspective cues and texture gradients in the perceptual rescaling of stimuli inside a Ponzo illusion corridor 105
Pupillary responses to perceived brightness require visual awareness 105
Extracurricular sports activities modify the proprioceptive map in children aged 5–8 years 105
Changing the Real Viewing Distance Reveals the Temporal Evolution of Size Constancy in Visual Cortex 103
Looking at the Ebbinghaus illusion: Differences in neurocomputational requirements, not gaze-mediated attention, explain a classic perception-action dissociation 102
Editorial: Introduction to the special issue on Visual Cognition and Visuomotor Control: A tribute to Mel Goodale. 101
Is simple reaction time affected by visual illusions? 100
The contribution of stereopsis in Emmert’s law 96
Perceptual Discrimination of Basic Object Features Is Not Facilitated When Priming Stimuli Are Prevented From Reaching Awareness by Means of Visual Masking 96
Do those with schizophrenia more accurately perceive reality? And why is this ‘abnormal’? 95
Conscious awareness is required for the perceptual discrimination of threatening animal stimuli: A visual masking and continuous flash suppression study 94
Susceptibility to Optical Illusions Varies as a Function of the Autism-Spectrum Quotient but not in Ways Predicted by Local–Global Biases 93
Proprioception calibrates object size constancy for grasping but not perception in limited viewing conditions. 93
Perceptual size discrimination requires awareness and late visual areas: A continuous flash suppression and interocular transfer study 92
Evidence of midline retinal nasotemporal overlap in healthy humans: A model for foveal sparing in hemianopia? 90
The conceptual understanding of depth rather than the low-level processing of spatial frequencies drives the corridor illusion. 89
The role of vergence and proprioception in the Taylor illusion. 87
Evaluating bodily self-consciousness and the brain using multisensory perturbation and fMRI 86
Pupil Size as a Gateway Into Conscious Interpretation of Brightness 86
Visual illusions in young people reporting psychotic-like experiences 83
Size constancy is preserved but afterimages are prolonged in typical individuals with higher degrees of self-reported autistic traits 82
Perceived size change induced by non-visual signals in darkness: the relative contribution of vergence and proprioception. 81
Real objects maintain superior size-distance scaling to afterimages under sudden and adapted darkness conditions 79
Interocular transfer effects of linear perspective cues and texture gradients in the perceptual rescaling of size 79
Visual reaction time and size constancy 75
Retinotopic activity in V1 reflects the perceived not the retinal size of an afterimage 73
Size constancy is not accomplished in the early stages of visual processing 71
The Shepard illusion is reduced in children with an autism spectrum disorder because of perceptual rather than attentional mechanisms. Frontiers in Psychology. 71
Contribution of auditory distance cues to size constancy in perception and grasping in restricted viewing 69
Size after effects are eliminated when adaptor stimuli are prevented from reaching awareness by continuous flash suppression 68
The Size-Distance Scaling of Real Objects and Afterimages is Equivalent in Typical but Not Reduced Visual Environments 66
Global processing during the Muller-Lyer illusion is distinctively affected by the degree of autistic traits in the typical population 66
Acute technostress, but not schizotypy, selectively changes the strength of the Müller-Lyer and Poggendorff illusions. 63
Simple reaction times as an implicit measure of the development of size constancy. 63
Familiar size effects on reaction time: When congruent is better 63
Implicit redundant target effect across the vertical meridian, but not horizontal, in a stroke patient with an inferior left quadrantanopia 63
Proprioceptive Distance Cues Restore Perfect Size Constancy in Grasping, but Not Perception, When Vision Is Limited 61
The temporal features of size constancy in two- and three-dimensional stimuli reveals a real-world advantage 60
Unconscious processing of threatening stimuli: behavioural and physiological evidence 58
Retinotopic organization of the visual cortex before and after decompression of the optic chiasm in a patient with pituitary macroadenoma 55
Seeing Size Through the Hand: fMRI Evidence for Visuo-Proprioceptive Size Constancy 49
How do individuals who report psychotic-like experiences process visual illusions? 43
Effects of Visual Awareness on Behavioral and Autonomic Responses to Threatening Animals: A bCFS Study 41
The role of awareness and specific phobias in visual perception and autonomic responses to threatening animals 37
Decoding haptic and imagined stimulus size in the human cortex 35
Mind the snake in the shadows: Preattentive processing and autonomic responses to subliminal evolutionary threats 32
Temporal dynamics of size constancy reveals an advantage for real-world stimuli 26
What contributes to our perception of the Shepard Tabletop Illusion? 21
null 16
The contribution of proprioception to size constancy in perception and action: an fMRI study 11
Monocular size and distance scaling is modulated by the presence of a fixation point 8
Perspective matters: using past experiences to understand others’ insensitivity to physical pain 1
Totale 8.527
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Categoria #
all - tutte 41.551
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 41.551
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022346 0 0 0 17 13 24 28 87 10 31 44 92
2022/2023493 116 49 10 33 39 61 12 37 76 24 32 4
2023/2024267 18 19 17 12 31 23 27 5 1 40 20 54
2024/20251.165 26 18 50 240 84 159 43 41 131 163 97 113
2025/20264.262 150 158 572 785 261 187 815 382 259 249 190 254
2026/20271.318 390 237 459 232 0 0 0 0 0 0 0 0
Totale 8.527