IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

SOLDA', GIULIA MARIA EMILIA ANTONIETTA
 Distribuzione geografica
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Continente #
EU - Europa 3.875
NA - Nord America 3.340
AS - Asia 2.418
SA - Sud America 296
AF - Africa 59
OC - Oceania 30
Continente sconosciuto - Info sul continente non disponibili 16
Totale 10.034
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Nazione #
US - Stati Uniti d'America 3.226
GB - Regno Unito 1.502
CN - Cina 1.010
SG - Singapore 628
IT - Italia 602
DE - Germania 438
SE - Svezia 349
RU - Federazione Russa 251
BR - Brasile 204
HK - Hong Kong 201
NL - Olanda 143
FR - Francia 117
TR - Turchia 117
IN - India 110
KR - Corea 108
UA - Ucraina 108
CA - Canada 95
IE - Irlanda 91
FI - Finlandia 75
EU - Europa 52
VN - Vietnam 52
PL - Polonia 43
CO - Colombia 37
DK - Danimarca 36
IR - Iran 32
ID - Indonesia 29
JP - Giappone 29
AU - Australia 26
BE - Belgio 24
AR - Argentina 19
ES - Italia 19
GR - Grecia 17
LU - Lussemburgo 15
IQ - Iraq 14
BD - Bangladesh 13
MA - Marocco 12
MX - Messico 11
TH - Thailandia 11
TW - Taiwan 11
EC - Ecuador 10
CH - Svizzera 9
CI - Costa d'Avorio 9
NO - Norvegia 8
VE - Venezuela 8
ZA - Sudafrica 8
AT - Austria 7
DZ - Algeria 7
UZ - Uzbekistan 7
CL - Cile 6
EG - Egitto 6
KE - Kenya 6
SA - Arabia Saudita 6
IL - Israele 5
MY - Malesia 5
PK - Pakistan 5
PY - Paraguay 5
NP - Nepal 4
NZ - Nuova Zelanda 4
AE - Emirati Arabi Uniti 3
AZ - Azerbaigian 3
KZ - Kazakistan 3
PA - Panama 3
UY - Uruguay 3
AL - Albania 2
AO - Angola 2
BY - Bielorussia 2
CZ - Repubblica Ceca 2
ET - Etiopia 2
HN - Honduras 2
HU - Ungheria 2
IS - Islanda 2
MU - Mauritius 2
NG - Nigeria 2
PE - Perù 2
PH - Filippine 2
PT - Portogallo 2
RO - Romania 2
A1 - Anonimo 1
AM - Armenia 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
CG - Congo 1
CR - Costa Rica 1
EE - Estonia 1
GY - Guiana 1
KG - Kirghizistan 1
LB - Libano 1
LT - Lituania 1
LV - Lettonia 1
MD - Moldavia 1
MK - Macedonia 1
MM - Myanmar 1
MN - Mongolia 1
MO - Macao, regione amministrativa speciale della Cina 1
NI - Nicaragua 1
OM - Oman 1
PS - Palestinian Territory 1
QA - Qatar 1
SC - Seychelles 1
Totale 10.068
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Città #
Southend 1.388
Singapore 378
Ashburn 326
Chandler 320
Milan 258
Beijing 250
Hong Kong 189
Frankfurt am Main 148
Houston 144
Seattle 144
Dallas 137
Wilmington 137
Princeton 136
Ann Arbor 119
Mountain View 119
Fairfield 101
Council Bluffs 95
Dublin 91
Dearborn 85
Jacksonville 77
Redmond 74
Nanjing 66
Los Angeles 65
Santa Clara 55
Woodbridge 53
Shanghai 50
Serra 48
Des Moines 46
Bengaluru 44
Boardman 44
Guangzhou 44
Toronto 42
Somerville 40
Sakarya 38
Buffalo 37
Cambridge 37
Warsaw 37
Ottawa 33
Bogotá 32
Columbus 32
The Dalles 30
Andover 28
Moscow 28
Redwood City 26
Jinan 25
New York 25
Falls Church 24
Medford 24
Hefei 23
Tianjin 23
Shenyang 22
Sunnyvale 22
Cangzhou 21
São Paulo 21
Berlin 19
Changsha 19
Athens 18
Brussels 18
Ho Chi Minh City 18
Munich 18
Phoenix 18
Seoul 18
Roxbury 15
Wuhan 15
Jakarta 14
Nanchang 13
Tokyo 13
Hebei 12
Helsinki 12
London 12
Rio de Janeiro 12
Fuzhou 11
Hangzhou 11
Ningbo 11
San Francisco 11
Cagliari 10
Eitensheim 10
Kiez 10
Abidjan 9
Istanbul 9
Zhengzhou 9
Atlanta 8
Bühl 8
Chengdu 8
Haikou 8
Hanoi 8
Manchester 8
Mumbai 8
Odernheim 8
Rome 8
San Diego 8
Turin 8
Verona 8
Bangkok 7
Belo Horizonte 7
Casablanca 7
Hamburg 7
Kunming 7
Lanzhou 7
Norwalk 7
Totale 6.411
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Nome #
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing 305
Identification of genetic factors associated with neural tube defects 271
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 267
Role of miRNAs in neural tube development 259
Non-random retention of protein-coding overlapping genes in Metazoa 250
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p 245
Clinical Relevance of Clonal Hematopoiesis in the Oldest-Old Population: Analysis of the "Health and Anemia" Study 238
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest 237
A novel mutation within the MIR96 gene causes nonsyndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 235
Characterization of long noncoding RNAs associated with developmental genes in vertebrates 230
The double-faced association of the PRKCA gene with multiple sclerosis 229
Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcript 229
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 219
Identification of novel deafness-causing variants in the tmprss3 gene by whole-exome sequencing 217
Search for novel deafness genes by exome sequencing of autosomal recessive NSHL families 213
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 205
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 204
Differential expression of microRNAs in peripheral blood mononuclear cells of multiple sclerosis patients 199
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 199
Identification by exome sequencing and functional characterization of novel deafness-causing mutations in PRPS1 198
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 198
Exome sequencing identifies PRPS1 as a major locus for X-linked nonsyndromic hearing loss in the Italian population 197
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis 197
Identification by whole-exome sequencing of two novel LARS2 mutations in an Italian family with Perrault syndrome 193
Type II mutation (Glu117stop) causes factor XI deficiency by inducing allele specific mRNA degradation 187
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 183
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 179
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 177
Identification of novel NSHL-causing mutations by whole exome sequencing 177
Understanding genetic variation in the CFTR gene by next-generation sequencing 176
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 175
Alpha3 and alpha5 neuronal nicotinic receptor subunit genes : a case of tail-to-tail overlap in humans 172
Regulated independent expression of 3' untranslated regions in mammals 165
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 165
A type mutation II (Glu117stop), induction of allele-specific mRNA degradation and FXI deficiency 164
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs 162
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 162
Response: Further thoughts on the "phantom" delta6/7 FXI isoform 161
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis : identification of novel mutations 157
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 156
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis 154
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis 152
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 151
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 144
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 140
Evolution, identification and expression of noncoding RNAs in animals 133
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes 132
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 131
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 130
Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease 129
In-depth study of breast cancer tumor promoting cell transcriptome using RNA-seq and microarrays 126
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population 121
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation 117
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 114
Expression of distinct RNAs from 3' untranslated regions 113
Glucocerebrosidase mutations in primary parkinsonism 112
No association of GBA mutations and multiple system atrophy 109
Improving mRNA 5' coding sequence determination in the mouse genome 104
Totale 10.464
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Categoria #
all - tutte 26.610
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 26.610
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021534 0 0 0 0 0 59 68 50 69 90 159 39
2021/2022721 82 20 18 12 52 50 61 27 89 99 37 174
2022/2023929 119 112 104 91 109 185 18 67 80 5 28 11
2023/2024567 10 58 28 51 132 51 24 47 14 27 55 70
2024/20251.506 48 173 35 156 114 71 82 142 83 146 123 333
2025/20261.397 369 148 316 235 308 21 0 0 0 0 0 0
Totale 10.464