IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

CASTRONOVO, CHIARA
 Distribuzione geografica
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Continente #
NA - Nord America 2.240
EU - Europa 1.968
AS - Asia 1.589
SA - Sud America 171
OC - Oceania 97
AF - Africa 60
Continente sconosciuto - Info sul continente non disponibili 2
Totale 6.127
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Nazione #
US - Stati Uniti d'America 2.051
CN - Cina 505
GB - Regno Unito 478
IT - Italia 392
SG - Singapore 283
DE - Germania 250
CA - Canada 147
HK - Hong Kong 142
IN - India 138
VN - Vietnam 128
FR - Francia 127
BR - Brasile 120
ES - Italia 109
SE - Svezia 95
RU - Federazione Russa 86
PL - Polonia 83
AU - Australia 78
BD - Bangladesh 76
NL - Olanda 65
TR - Turchia 64
JP - Giappone 57
KR - Corea 40
MX - Messico 37
FI - Finlandia 36
IE - Irlanda 36
IL - Israele 34
CI - Costa d'Avorio 30
BE - Belgio 29
DK - Danimarca 29
SI - Slovenia 21
ID - Indonesia 20
NZ - Nuova Zelanda 19
SA - Arabia Saudita 19
ZA - Sudafrica 17
UA - Ucraina 16
CZ - Repubblica Ceca 15
HU - Ungheria 15
TH - Thailandia 15
CO - Colombia 13
CH - Svizzera 12
EC - Ecuador 12
TW - Taiwan 12
IQ - Iraq 11
AT - Austria 10
EE - Estonia 10
GR - Grecia 10
AR - Argentina 9
PT - Portogallo 8
CL - Cile 6
NO - Norvegia 6
RS - Serbia 6
LT - Lituania 5
LV - Lettonia 5
MY - Malesia 5
SK - Slovacchia (Repubblica Slovacca) 5
UZ - Uzbekistan 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
EU - Europa 4
JO - Giordania 4
LK - Sri Lanka 4
PK - Pakistan 4
IR - Iran 3
PH - Filippine 3
TN - Tunisia 3
AL - Albania 2
BG - Bulgaria 2
BO - Bolivia 2
CY - Cipro 2
KZ - Kazakistan 2
NG - Nigeria 2
PY - Paraguay 2
QA - Qatar 2
SN - Senegal 2
AD - Andorra 1
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BS - Bahamas 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GE - Georgia 1
GT - Guatemala 1
HN - Honduras 1
HR - Croazia 1
KE - Kenya 1
MA - Marocco 1
MT - Malta 1
NP - Nepal 1
OM - Oman 1
PE - Perù 1
PR - Porto Rico 1
PS - Palestinian Territory 1
RO - Romania 1
SC - Seychelles 1
TL - Timor Orientale 1
TM - Turkmenistan 1
UY - Uruguay 1
ZM - Zambia 1
ZW - Zimbabwe 1
Totale 6.129
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Città #
Southend 309
Singapore 183
Ashburn 173
Chandler 119
Hong Kong 105
Redwood City 94
Fairfield 80
Frankfurt am Main 80
Wilmington 80
Beijing 74
Milan 72
Ann Arbor 66
Seattle 60
San Jose 56
Houston 53
Ho Chi Minh City 49
Cambridge 42
Dallas 42
Los Angeles 42
Woodbridge 42
Guangzhou 38
Rome 38
Hanoi 37
Montreal 36
Council Bluffs 35
Shanghai 35
Dearborn 33
Toronto 33
Warsaw 32
Dublin 31
Paris 31
Abidjan 30
Princeton 30
Chicago 28
New York 27
Delhi 26
Brisbane 24
Phoenix 22
Santa Clara 22
Minneapolis 21
Naples 21
Bengaluru 20
Helsinki 20
Melbourne 20
Tokyo 20
Ankara 18
Barcelona 18
Boardman 18
Falls Church 18
Nanjing 18
São Paulo 18
Brussels 17
Hangzhou 17
Ljubljana 17
Madrid 17
Jakarta 16
Jinan 16
Lexington 16
San Diego 16
Lauterbourg 15
Munich 15
Atlanta 14
Moscow 14
Bangkok 13
Da Nang 13
Hyderabad 13
Manchester 13
Sydney 13
Turin 13
Buffalo 12
Des Moines 12
Hefei 12
Jacksonville 12
Seoul 12
Shenzhen 12
Boston 11
Columbus 11
Fremont 11
Glasgow 11
London 11
Washington 11
Changsha 10
Istanbul 10
Montréal 10
Ottawa 10
Strasbourg 10
Tartu 10
Cardiff 9
Jeddah 9
Kayseri 9
Philadelphia 9
Surrey 9
Wuhan 9
Birmingham 8
Bogotá 8
Budapest 8
Guadalajara 8
Haifa 8
Indianapolis 8
Providence 8
Totale 3.215
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Nome #
9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression 2.311
RARE DE NOVO AND TRANSMITTED COPY NUMBER VARIATIONS IN AUTISM SPECTRUM DISORDERS: IMPLICATIONS FOR FUNCTIONAL NETWORKS OF GENES INVOLVED IN NEUROGENESIS, NEURONAL METABOLISM, SYNAPTIC FUNCTION, NEUROIMMUNITY, INTRACELLULAR SIGNALING AND CHROMATIN REMODELING 831
Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features 308
13q mosaic deletion including RB1 associated to mild phenotype and no cancer outcome-case report and review of the literature 288
Familial intragenic duplication of ANKRD11 underlying three patients of KBG syndrome 286
Identification of rare CNVs involving genes acting in oocyte maturation and differentiation in a cohort of patients affected by Primary Ovarian Insufficiency 271
Identification of balanced 4p16 paracentric inversions in three patients with Wolf-Hirschhorn phenotype not deleted for the WHS critical region 251
Submicroscopic genomic alterations detected by array CGH analysis in a cohort of patients with Silver Russell syndrome found negative to classical genetic and epigenetic tests 249
Complex de novo chromosomal rearrangement at 15q11-q13 involving an intrachromosomal triplication in a patient with a severe neuropsychological phenotype: Clinical report and review of the literature. 247
Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes 241
New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene 234
Sindrome di Cornelia de Lange in un paziente portatore della Traslocazione t(5;15)(p13;q25.1): possibile effetto di posizione su NIPBL 216
A novel nonsense ATP7A pathogenic variant in a family exhibiting a variable occipital horn syndrome phenotype 205
Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome 196
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes 164
Totale 6.298
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Categoria #
all - tutte 13.200
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 13.200
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202138 0 0 0 0 0 0 0 0 0 0 0 38
2021/2022549 46 38 43 40 45 44 18 43 55 60 27 90
2022/2023736 51 68 46 62 50 71 35 115 85 39 68 46
2023/2024833 43 71 70 72 128 81 57 72 32 64 47 96
2024/20251.004 64 107 59 97 68 54 72 82 94 122 63 122
2025/20261.400 155 81 119 133 124 92 223 53 126 86 169 39
Totale 6.298