IRIS
Vallortigara, Giorgio
 Distribuzione geografica
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Continente #
NA - Nord America 17.385
EU - Europa 3.762
AS - Asia 2.086
SA - Sud America 84
AF - Africa 57
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 6
Totale 23.387
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Nazione #
US - Stati Uniti d'America 17.303
SG - Singapore 1.258
IT - Italia 994
SE - Svezia 738
UA - Ucraina 557
CN - Cina 478
GB - Regno Unito 408
FI - Finlandia 376
DE - Germania 199
BG - Bulgaria 153
RU - Federazione Russa 128
VN - Vietnam 119
CA - Canada 69
BR - Brasile 68
ID - Indonesia 66
JO - Giordania 65
MU - Mauritius 49
FR - Francia 46
BE - Belgio 32
NL - Olanda 24
AT - Austria 18
TR - Turchia 18
CZ - Repubblica Ceca 16
JP - Giappone 15
RO - Romania 14
HK - Hong Kong 13
IN - India 13
SK - Slovacchia (Repubblica Slovacca) 10
LT - Lituania 9
ES - Italia 8
MX - Messico 7
A2 - ???statistics.table.value.countryCode.A2??? 6
CH - Svizzera 6
IR - Iran 6
AU - Australia 5
NO - Norvegia 5
TW - Taiwan 5
CL - Cile 4
IL - Israele 4
AE - Emirati Arabi Uniti 3
BD - Bangladesh 3
CO - Colombia 3
GR - Grecia 3
IE - Irlanda 3
KZ - Kazakistan 3
MA - Marocco 3
PE - Perù 3
PH - Filippine 3
PL - Polonia 3
PT - Portogallo 3
BA - Bosnia-Erzegovina 2
HN - Honduras 2
HR - Croazia 2
NZ - Nuova Zelanda 2
PA - Panama 2
PK - Pakistan 2
TH - Thailandia 2
UY - Uruguay 2
AL - Albania 1
AM - Armenia 1
AR - Argentina 1
AZ - Azerbaigian 1
BO - Bolivia 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
CY - Cipro 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EC - Ecuador 1
HU - Ungheria 1
IQ - Iraq 1
KH - Cambogia 1
KR - Corea 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
MD - Moldavia 1
MY - Malesia 1
NP - Nepal 1
SC - Seychelles 1
SI - Slovenia 1
TN - Tunisia 1
VE - Venezuela 1
ZA - Sudafrica 1
Totale 23.387
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Città #
Fairfield 2.522
Chandler 1.815
Jacksonville 1.275
Woodbridge 1.265
Ashburn 1.178
Seattle 1.042
Wilmington 972
Houston 940
Singapore 832
Cambridge 814
Ann Arbor 630
Santa Clara 545
Columbus 533
Trento 502
San Mateo 450
Princeton 435
Beijing 209
Helsinki 171
San Diego 162
Sofia 153
Dearborn 147
Boardman 125
Lawrence 125
New York 121
Moscow 97
London 89
Council Bluffs 70
San Paolo di Civitate 67
Dong Ket 66
Jakarta 65
Falls Church 52
Norwalk 45
Philadelphia 39
Fremont 35
Düsseldorf 34
Toronto 34
Washington 33
Brussels 30
Shanghai 29
Altamura 26
Dallas 26
Padova 26
Rome 26
Guangzhou 25
Milan 25
Des Moines 24
Los Angeles 24
Ottawa 24
Hefei 23
Phoenix 22
Pordenone 22
Andover 20
Falkenstein 20
Verona 20
Mountain View 17
Kilburn 16
Nanjing 16
Como 15
Trieste 15
Nuremberg 14
Kunming 13
Munich 13
Frankfurt am Main 12
Izmir 12
Nanchang 11
Amsterdam 10
Bratislava 10
Chiswick 10
Paris 9
Redmond 9
Treviso 9
Brno 8
Chicago 8
Desenzano Del Garda 8
Hong Kong 8
Hounslow 8
Olomouc 8
Prescot 8
São Paulo 8
Clearwater 7
Lappeenranta 7
Redwood City 7
Shenyang 7
Travagliato 7
Vienna 7
Acton 6
Auburn Hills 6
Augusta 6
Moncalieri 6
Rio de Janeiro 6
Dormagen 5
Islington 5
Laurel 5
Montreal 5
North Bergen 5
San Francisco 5
San Michele All'adige 5
San Zeno Naviglio 5
Vicenza 5
Austin 4
Totale 18.497
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Nome #
Working memory and reference memory tests of spatial navigation in mice (Mus musculus) 428
Neonicotinoid-induced impairment of odour coding in the honeybee 246
Cortical route for facelike pattern processing in human newborns 186
A mental number line in human newborns 178
Embryonic Exposure to Valproic Acid Impairs Social Predispositions of Newly-Hatched Chicks 172
Seeing left- or right-asymmetric tail wagging produces different emotional responses in dogs 170
Number-space mapping in the newborn chick resembles humans' mental number line 166
Differential Odour Coding of Isotopomers in the Honeybee Brain 163
The Bee as a Model to Investigate Brain and Behavioural Asymmetries 160
Searching for anatomical correlates of olfactory lateralization in the honeybee antennal lobes: a morphological and behavioural study 159
Asymmetric neural coding revealed by in vivo calcium imaging in the honey bee brain 158
A transient time window for early predispositions in newborn chicks 158
Selective response of the nucleus taeniae of the amygdala to a naturalistic social stimulus in visually naive domestic chicks 146
Embryonic exposure to valproic acid affects social predispositions for dynamic cues of animate motion in newly-hatched chicks 144
Ratio abstraction over discrete magnitudes by newly hatched domestic chicks (Gallus gallus) 141
Spontaneous and light-induced lateralization of immediate early genes expression in domestic chicks 137
Reorienting strategies in a rectangular array of landmarks by domestic chicks (Gallus gallus). 135
Quantity discrimination by zebrafish (Danio rerio) 134
Forelimb preferences in human beings and other species: Multiple models for testing hypotheses on lateralization 134
A left-sided visuospatial bias in birds 132
Morphofunctional experience-dependent plasticity in the honeybee brain 127
In-vivo two-photon imaging of the honey bee antennal lobe 126
Representation of environmental shape in the hippocampus of domestic chicks (Gallus gallus) 126
Navigation by environmental geometry: the use of zebrafish as a model. 126
Origins of knowledge: insights from precocial species 125
Individual-Level and Population-Level Lateralization: Two Sides of the Same Coin 124
Hippocampus and medial striatum dissociation during goal navigation by geometry or features in the domestic chick: An immediate early gene study 121
From natural geometry to spatial cognition. 120
Newborn chicks show inherited variability in early social predispositions for hen-like stimuli 119
Learning of geometry and features in bumblebees (Bombus terrestris). 118
Filial responses as predisposed and learned preferences: Early attachment in chicks and babies 118
View-based strategy for reorientation by geometry. 117
Intuitive physical reasoning about occluded objects by inexperienced chicks 117
Discrimination of small quantities by fish (redtail splitfin, Xenotoca eiseni. 117
Boundary primacy in spatial mapping: evidence from zebrafish (Danio rerio) 116
Core knowledge of object, number, and geometry: A comparative and neural approach. 114
Dynamic features of animate motion activate septal and preoptic areas in visually naïve chicks ( Gallus gallus ) 114
A multimodal approach for tracing lateralisation along the olfactory pathway in the honeybee through electrophysiological recordings, morpho-functional imaging, and behavioural studies 111
Spontaneous learning of visual structures in domestic chicks 111
Spatial impairment and memory in genetic disorders: Insights from mouse models 110
First exposure to an alive conspecific activates septal and amygdaloid nuclei in visually-naïve domestic chicks (Gallus gallus) 110
Domestic chicks perceive stereokinetic illusions. 109
Olfactory lateralization in homing pigeons: a GPS study on birds released with unilateral olfactory inputs. 108
Lateralization in the invertebrate brain: left-right asymmetry of olfaction in bumble bee, Bombus terrestris. 108
Naïve chicks prefer hollow objects 108
Encoding of geometric and landmark information in the left and right hemispheres of the avian brain. 108
Spatial Reorientation by Geometry in Bumblebees 108
Advantages of having a lateralized brain. 107
Visually inexperienced chicks exhibit a spontaneous preference for biological motion patterns 107
Naïve 3-Day-Old Domestic Chicks (Gallus gallus) Are Attracted to Discrete Acoustic Patterns Characterizing Natural Vocalizations 107
Navigating through an asymmetrical brain: lateralisation and homing in Pigeon. 106
Summation of large numerousness by newborn chicks. 104
Roots of a social brain: Developmental models of emerging animacy-detection mechanisms 104
Bumblebees spontaneously map location of conspecific using geometry and features 104
Social predisposition dependent neuronal activity in the intermediate medial mesopallium of domestic chicks (Gallus gallus domesticus) 104
The evolution of brain lateralization: A game theoretical analysis of population structure. 103
Chicks like consonant music. 102
Early- and late-light embryonic stimulation modulates similarly chicks' ability to filter out distractors 102
Roots of brain specializations: Preferential left-eye use during mirror- image inspection in six species of teleost fish. 102
A misunderstanding of principal and medial axes? Reply to Sturz & Bodily 102
Inexperienced preys know when to flee or to freeze in front of a threat 102
Spontaneous generalization of abstract multimodal patterns in young domestic chicks 101
Stable panoramic views facilitate snap-shot like memories for spatial reorientation in homing pigeons. 100
Advantages of a lateralised brain for reasoning about the social world in chicks. 100
Chicks, like children, spontaneously reorient by three-dimensional environmental geometry, not by image matching 100
In-vivo two-photon imaging of the honeybee antennal lobe 100
Animals’ representation of enclosed spaces: Evidence for use of a similar frame of reference following different disorientation procedures in the domestic chick (Gallus gallus). 99
Early-light embryonic stimulation suggests a second route, via gene activation, to cerebral lateralization in vertebrates 99
Animal's use of landmarks and metric information to reorient: Effects of size of experimental space 98
Chicks prefer to peck at insect-like elongated stimuli moving in a direction orthogonal to their longer axis. 98
Spatial reorientation by geometry with freestanding objects and extended surfaces: A unifying view 98
Working memory in the chick: Parallel and lateralized mechanisms for encoding of object- and position-specific information. 98
Delayed search for a concealed imprinted object in the domestic chick. 97
Bilateral participation of the hippocampus in familiar landmark navigation by homing pigeons. 97
Detour behaviour in three species of birds, quails (Coturnix sp.), herring gulls (Larus cachinnans) and canaries (Serinus canaria). 97
Asymmetric tail-wagging responses by dogs to different emotive stimuli. 97
One, two, three, four, or is there something more? Numerical discrimination in day-old domestic chicks. 97
The cradle of causal reasoning: newborns' preference for physical causality. 97
Asymmetrical number-space mapping in the avian brain. 97
Unlearned visual preferences for the head region in domestic chicks 97
Modularity and spatial reorientation in a simple mind: encoding of geometric and nongeometric properties of a spatial environment by fish 96
Functional asymmetry of left and right avian piriform cortex in homing pigeons' navigation. 96
Is it only humans that count from left to right? 96
Re-orienting in space: Do animals use global or local geometry strategies? 96
Young chickens learn to localize the centre of a spatial environment. 96
Spontaneous discrimination of possible and impossible objects by newly hatched chicks. 96
Conjoining information from different modules: a comparative perspective 95
Arithmetic in newborn chicks. 95
Dogs turn left to emotional stimuli 95
Volumetric assessment of cerebral asymmetries in dogs. 95
Chicken –  Cognition in the Poultry Yard. 95
How fish do geometry in large and in small spaces 94
Separate geometric and non-geometric modules for spatial reorientation: evidence from a lopsided animal brain 94
The use of proportion by young domestic chicks (Gallus gallus) 94
Paw preference in dogs: relations between lateralised behaviour and immunity. 94
Complementary right and left hemifield use for predatory and agonistic behaviour in toads. 93
Heritability of lateralization in fish: Concordance of right-left asymmetry between parents and offspring. 93
Consistency among different tasks of left-right asymmetries in lines of fish originally selected for opposite direction of lateralization in a detour task 93
The evolution of social orienting: Evidence from chicks (Gallus gallus) and human newborns. 93
Introduction: the origins of numerical abilities 93
Totale 11.798
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Categoria #
all - tutte 121.999
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 4.835
Totale 126.834
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.492 0 0 0 0 0 0 0 0 664 325 198 305
2020/20213.794 162 446 145 397 345 375 325 207 308 294 406 384
2021/20223.513 156 508 65 153 154 173 211 600 177 322 412 582
2022/20233.915 747 446 57 536 391 575 37 261 489 36 219 121
2023/20241.407 111 113 105 43 133 244 113 126 37 117 70 195
2024/20253.138 41 71 256 1.082 402 722 77 358 129 0 0 0
Totale 24.279