SANSALONE, Gabriele
 Distribuzione geografica
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Continente #
AS - Asia 3.620
NA - Nord America 2.956
EU - Europa 1.044
SA - Sud America 500
Continente sconosciuto - Info sul continente non disponibili 69
OC - Oceania 62
AF - Africa 51
Totale 8.302
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Nazione #
US - Stati Uniti d'America 2.851
CN - Cina 1.350
SG - Singapore 939
HK - Hong Kong 452
BR - Brasile 397
IT - Italia 316
KR - Corea 251
VN - Vietnam 227
GB - Regno Unito 185
BD - Bangladesh 157
RU - Federazione Russa 111
SE - Svezia 86
FR - Francia 78
DE - Germania 49
IN - India 47
CA - Canada 46
ID - Indonesia 39
NZ - Nuova Zelanda 37
AR - Argentina 35
LT - Lituania 35
FI - Finlandia 31
NL - Olanda 29
AU - Australia 25
JP - Giappone 25
ES - Italia 24
MX - Messico 22
BE - Belgio 21
IQ - Iraq 18
AT - Austria 17
EC - Ecuador 17
TR - Turchia 17
CO - Colombia 14
PK - Pakistan 14
ZA - Sudafrica 14
CL - Cile 12
MY - Malesia 12
MA - Marocco 11
IE - Irlanda 10
UA - Ucraina 10
UZ - Uzbekistan 9
VE - Venezuela 9
AE - Emirati Arabi Uniti 8
JM - Giamaica 8
PL - Polonia 8
PY - Paraguay 8
TN - Tunisia 7
JO - Giordania 6
NP - Nepal 6
PH - Filippine 6
RS - Serbia 6
CZ - Repubblica Ceca 5
EG - Egitto 5
KG - Kirghizistan 5
PE - Perù 5
CR - Costa Rica 4
HR - Croazia 4
KZ - Kazakistan 4
NI - Nicaragua 4
SA - Arabia Saudita 4
SI - Slovenia 4
SV - El Salvador 4
AL - Albania 3
AZ - Azerbaigian 3
BH - Bahrain 3
DO - Repubblica Dominicana 3
IL - Israele 3
TH - Thailandia 3
TT - Trinidad e Tobago 3
TW - Taiwan 3
AO - Angola 2
BO - Bolivia 2
GR - Grecia 2
GT - Guatemala 2
HN - Honduras 2
IR - Iran 2
LK - Sri Lanka 2
MD - Moldavia 2
PT - Portogallo 2
QA - Qatar 2
RO - Romania 2
BB - Barbados 1
BG - Bulgaria 1
BS - Bahamas 1
BZ - Belize 1
CG - Congo 1
CH - Svizzera 1
CM - Camerun 1
ET - Etiopia 1
GA - Gabon 1
GM - Gambi 1
IS - Islanda 1
KE - Kenya 1
KH - Cambogia 1
LB - Libano 1
MQ - Martinica 1
NE - Niger 1
NG - Nigeria 1
OM - Oman 1
PA - Panama 1
PR - Porto Rico 1
Totale 8.226
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Città #
Hefei 913
Santa Clara 825
Singapore 504
Hong Kong 440
San Jose 350
Ashburn 327
Seoul 250
London 135
The Dalles 116
Los Angeles 101
Council Bluffs 86
Beijing 68
Ho Chi Minh City 68
Hanoi 62
Kent 55
Modena 51
Lauterbourg 49
Chicago 45
Buffalo 43
São Paulo 43
New York 41
Milan 40
Moscow 38
Dallas 37
Reggio Emilia 34
Columbus 32
Shanghai 31
Jakarta 29
Boardman 28
Atlanta 24
Rome 23
Helsinki 21
Amsterdam 20
Tokyo 19
Redondo Beach 17
Rio de Janeiro 16
Belo Horizonte 15
Melbourne 15
Salt Lake City 15
Brooklyn 14
Mexico City 13
Da Nang 12
Florence 12
Haiphong 12
Orem 12
San Francisco 12
Naples 11
Phoenix 11
Brussels 10
Dublin 10
Lappeenranta 10
Auckland 9
Bologna 9
Elk Grove Village 9
Guayaquil 9
Liège 9
Nuremberg 9
Stockholm 9
Brasília 8
Chennai 8
Hackney 8
Kuala Lumpur 8
Miano 8
Montreal 8
Munich 8
Newark 8
Philadelphia 8
Tashkent 8
Vienna 8
Dunedin 7
Kilburn 7
Ninh Bình 7
Santiago 7
Toronto 7
Amman 6
Barcelona 6
Birmingham 6
Campinas 6
Frankfurt am Main 6
Guangzhou 6
Hangzhou 6
Miami 6
North Bergen 6
Seattle 6
Stuttgart 6
Warsaw 6
Albuquerque 5
Bauru 5
Belgrade 5
Detroit 5
Fairfax 5
Gainesville 5
Houston 5
Istanbul 5
Jacksonville 5
Johannesburg 5
Kingston 5
Madison 5
Novo Hamburgo 5
Ribeirão Preto 5
Totale 5.493
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Nome #
Geometric morphometrics and finite element analyses reveal the Haast's eagle (Harpagornis moorei) to be a mixed predator-scavenger 338
How domestication, feralization and experience-dependent plasticity affect brain size variation in Sus scrofa 222
Evolutionary trends and stasis in carnassial teeth of European Pleistocene wolf Canis lupus (Mammalia, Canidae) 205
Evolution of the vomer and its implications for cranial kinesis in Paraves 195
RRmorph—a new R package to map phenotypic evolutionary rates and patterns on 3D meshes 193
Condylura (Mammalia, Talpidae) reloaded: New insights about the fossil representatives of the genus 181
Systematics and macroevolution of extant and fossil scalopine moles (Mammalia, Talpidae) 169
Abdominal contents reveal Cretaceous crocodyliforms ate dinosaurs 161
Marsupial Functional Morphology, Biomechanics, and Feeding Ecology 160
New systematic insights about Plio-Pleistocene moles from Poland 152
Cortical areas associated to higher cognition drove primate brain evolution 150
One among many: The enigmatic case of the Miocene mammal, Kolponomos newportensis 146
DIFFERENTIAL RATES OF EVOLUTION WITHIN HIGHLY FOSSORIAL MOLES (TALPINAE) CONSTRAIN TRAJECTORIES AND EVOLUTIONARY ALLOMETRIES OF HUMERAL MORPHOLOGY 143
UNVEILING THE DIGGING ADAPTATIONS IN PROSCALOPIDAE HUMERUS BY MEANS OF COMPARATIVE 3D FINITE ELEMENT ANALYSIS 142
Examining the effect of feralization on craniomandibular morphology in pigs, Sus scrofa (Artiodactyla: Suidae) 140
When moles became diggers: Tegulariscaptor gen. nov., from the early Oligocene of south Germany, and the evolution of talpid fossoriality 135
Reassessing the earliest Oligocene vertebrate assemblage of Monteviale (Vicenza, Italy) 130
Decoupling Functional and Morphological Convergence, the Study Case of Fossorial Mammalia 129
REASSESSING THE (?)EARLY OLIGOCENE VERTEBRATE ASSEMBLAGE OF MONTEVIALE (VICENZA, ITALY) 128
Evolution of the sabertooth mandible: A deadly ecomorphological specialization 127
Macroevolutionary trends of brain mass in Primates 124
Did the Late Pleistocene climatic changes influence evolutionary trends in body size of the red deer? The study case of the Italian Peninsula 124
Digging adaptation in insectivorous subterranean eutherians. The enigma of Mesoscalops montanensis unveiled by geometric morphometrics and finite element analysis 124
Head to head: the case for fighting behaviour in Megaloceros giganteus using finite-element analysis 123
Think Big, Evolutionary Allometry as a Major Factor in Rates, Trajectories and Scaling of Morphological Evolution of the Primate Brain Shape 123
How Changes in Functional Demands Associated with Captivity Affect the Skull Shape of a Wild Boar (Sus scrofa) 123
FEEDING BIOMECHANICS INFLUENCES CRANIOFACIAL MORPHOLOGY AMONG EAST AUSTRALIAN PADEMELONS (MACROPODIDAE: THYLOGALE) 123
UNRAVELING THE MYSTERY OF DIGGING ADAPTATION OF MESOSCALOPS MONTANENSIS BY MEANS OF GEOMETRIC MORPHOMETRICS AND FINITE ELEMENT ANALYSIS 122
Raptor talon shape and biomechanical performance are controlled by relative prey size but not by allometry 122
Basicranium and face: Assessing the impact of morphological integration on primate evolution 121
Talpa fossilis or Talpa europaea? Using geometric morphometrics and allometric trajectories of humeral moles remains from Hungary to answer a taxonomic debate 118
Small vertebrates from the Late Pleistocene of Avetrana (Apulia, southern Italy) karst filling 118
Relationship between foramen magnum position and locomotion in extant and extinct hominoids 117
THE ORAL APPARATUS OF MARSUPIALS IS MORE INTEGRATED BUT NOT LESS MORPHOLOGICALLY DIVERSE THAN THAT OF PLACENTAL CARNIVORES 116
Influence of evolutionary allometry on rates of morphological evolution and disparity in strictly subterranean moles (Talpinae, Talpidae, Eulipotyphla, Mammalia) 115
Condylura reloaded: a review of fossil star nosed moles 115
A new integrated tool to calculate and map bilateral asymmetry on three-dimensional digital models 115
A method for mapping morphological convergence on three-dimensional digital models: the case of the mammalian sabre-tooth 114
The prodigious alliance: molecular systematics and morphometrics dig out the puzzling origin and diversification of European moles (Soricomorpha: Talpidae) 112
A NEW CROCODYLIFORM FROM THE WINTON FORMATION (CA 95 MA) OF QUEENSLAND (AUSTRALIA) 112
The influence of domestication, insularity and sociality on the tempo and mode of brain size evolution in mammals 112
THINK BIG: EVOLUTIONARY ALLOMETRY AS A MAJOR FACTOR IN RATES OF MORPHOLOGICAL EVOLUTION OF THE PRIMATE BRAIN SHAPE 111
EVOLUTIONARY TRENDS AND STASIS IN MOLAR MORPHOLOGY OF RHAGAPODEMUS-RHAGAMYS LINEAGE IN THE PLEISTOCENE OF SARDINIA 111
Homo sapiens and Neanderthals share high cerebral cortex integration into adulthood 111
Trapped in the morphospace: The relationship between morphological integration and functional performance 111
Tuning Geometric Morphometrics: an R tool to reduce information loss caused by surface smoothing 111
From Smart Apes to Human Brain Boxes. A Uniquely Derived Brain Shape in Late Hominins Clade 110
Human face-off: a new method for mapping evolutionary rates on three-dimensional digital models 107
Morphological integration and functional modularity in the crocodilian skull 106
Skull shape of a widely distributed, endangered marsupial reveals little evidence of local adaptation between fragmented populations 105
Finite element analyses on the skull and talon of Haast's eagle (Harpagornis moorei) 101
New Zealand's extinct giant raptor (Hieraaetus moorei) killed like an eagle, ate like a condor 100
Testing convergent and parallel adaptations in talpids humeral mechanical performance by means of geometric morphometrics and finite element analysis 99
Morfometria geometrica dell' omero di specie attuali e fossili del genere Talpa 99
Unexpectedly uneven distribution of functional trade-offs explains cranial morphological diversity in carnivores 99
Morphological integration affects the evolution of midline cranial base, lateral basicranium, and face across primates 98
Domestication, insularity and sociality. Determinants of brain size evolutionary rate and trends in mammals 96
Variation in the strength of allometry drives rates of evolution in primate brain shape 96
THE ORAL APPARATUS OF MARSUPIALS IS MORE INTEGRATED BUT NOT LESS MORPHOLOGICALLY DIVERSE THAN THAT OF PLACENTAL CARNIVORES 95
Impact of transition to a subterranean lifestyle on morphological disparity and integration in talpid moles (Mammalia, Talpidae) 93
Reassessing the Eocene-Oligocene Transition vertebrate assemblage of Monteviale (Vicenza, Italy) 91
Feeding Biomechanics Influences Craniofacial Morphology at the Subspecies Scale among Australian Pademelons (Macropodidae: Thylogale) 89
Palaeoecological significance of the “wolf event” as revealed by skull ecometrics of the canid guilds 89
Evolution of hypsodonty reveals a long-standing ecological separation in the Japanese shrew-moles 89
Reassessing the faunal assemblages of the late pleistocene stratified karst filling from avetrana (Apulia, Southern Italy): The BED 8, palaeoenvironment and biochronology 84
Cytosolic PCNA is localised in Pomacea canaliculata circulating hemocytes, independently from active cell proliferation 37
Parallel Recovery Dynamics of Circulating and Tissue-Resident Hemocytes Following Hemolymph Withdrawal in Pomacea canaliculata 25
Totale 8.302
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Categoria #
all - tutte 35.371
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 35.371
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/2024334 0 0 56 18 61 13 20 17 21 35 55 38
2024/20252.912 93 16 14 174 568 436 160 193 296 209 398 355
2025/20264.535 475 489 564 462 299 196 544 158 285 473 349 241
2026/2027521 325 196 0 0 0 0 0 0 0 0 0 0
Totale 8.302