IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

SOLDA', GIULIA MARIA EMILIA ANTONIETTA
 Distribuzione geografica
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Continente #
EU - Europa 4.083
NA - Nord America 3.916
AS - Asia 3.204
SA - Sud America 331
AF - Africa 70
OC - Oceania 33
Continente sconosciuto - Info sul continente non disponibili 16
Totale 11.653
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Nazione #
US - Stati Uniti d'America 3.769
GB - Regno Unito 1.517
CN - Cina 1.096
SG - Singapore 907
IT - Italia 653
DE - Germania 449
SE - Svezia 350
RU - Federazione Russa 304
HK - Hong Kong 265
VN - Vietnam 247
BR - Brasile 224
FR - Francia 168
NL - Olanda 144
IN - India 122
TR - Turchia 118
CA - Canada 114
BD - Bangladesh 113
KR - Corea 113
UA - Ucraina 110
IE - Irlanda 91
FI - Finlandia 80
EU - Europa 52
PL - Polonia 46
JP - Giappone 44
CO - Colombia 40
DK - Danimarca 36
IR - Iran 32
AU - Australia 29
ID - Indonesia 29
BE - Belgio 24
ES - Italia 23
AR - Argentina 22
GR - Grecia 18
IQ - Iraq 18
LU - Lussemburgo 17
MX - Messico 16
MA - Marocco 15
EC - Ecuador 13
TH - Thailandia 13
TW - Taiwan 13
ZA - Sudafrica 11
CH - Svizzera 10
PH - Filippine 10
VE - Venezuela 10
AT - Austria 9
CI - Costa d'Avorio 9
CL - Cile 8
DZ - Algeria 8
EG - Egitto 8
MY - Malesia 8
NO - Norvegia 8
PK - Pakistan 8
SA - Arabia Saudita 7
UZ - Uzbekistan 7
KE - Kenya 6
NP - Nepal 6
IL - Israele 5
PY - Paraguay 5
AZ - Azerbaigian 4
NZ - Nuova Zelanda 4
UY - Uruguay 4
AE - Emirati Arabi Uniti 3
ET - Etiopia 3
KZ - Kazakistan 3
PA - Panama 3
PE - Perù 3
PT - Portogallo 3
TT - Trinidad e Tobago 3
AL - Albania 2
AO - Angola 2
BG - Bulgaria 2
BH - Bahrain 2
BY - Bielorussia 2
CZ - Repubblica Ceca 2
DO - Repubblica Dominicana 2
GT - Guatemala 2
HN - Honduras 2
HU - Ungheria 2
IS - Islanda 2
LT - Lituania 2
MD - Moldavia 2
MU - Mauritius 2
NG - Nigeria 2
NI - Nicaragua 2
RO - Romania 2
TN - Tunisia 2
A1 - Anonimo 1
AM - Armenia 1
BO - Bolivia 1
BS - Bahamas 1
CG - Congo 1
CR - Costa Rica 1
CY - Cipro 1
EE - Estonia 1
GY - Guiana 1
JM - Giamaica 1
JO - Giordania 1
KG - Kirghizistan 1
LB - Libano 1
LV - Lettonia 1
Totale 11.680
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Città #
Southend 1.388
Singapore 561
Ashburn 392
Chandler 320
Milan 263
Beijing 257
Hong Kong 242
San Jose 182
Frankfurt am Main 158
Houston 146
Seattle 144
Dallas 138
Wilmington 137
Princeton 136
Ann Arbor 119
Mountain View 119
Council Bluffs 103
Fairfield 101
Los Angeles 100
Dublin 91
Dearborn 85
Ho Chi Minh City 84
Boardman 81
Jacksonville 77
Redmond 74
Santa Clara 72
Nanjing 67
Hanoi 63
Shanghai 57
Woodbridge 53
New York 51
Lauterbourg 49
Guangzhou 48
Serra 48
Toronto 47
Des Moines 46
Bengaluru 44
Buffalo 42
Somerville 40
Warsaw 40
Moscow 38
Sakarya 38
Cambridge 37
Columbus 35
Bogotá 33
Ottawa 33
The Dalles 30
Andover 28
Tokyo 27
Jinan 26
Redwood City 26
Hefei 25
Falls Church 24
Medford 24
Tianjin 24
Seoul 23
São Paulo 23
Phoenix 22
Shenyang 22
Sunnyvale 22
Cangzhou 21
Athens 19
Berlin 19
Changsha 19
Brussels 18
Munich 18
Wuhan 18
Helsinki 17
Roxbury 15
Jakarta 14
Rome 14
Haiphong 13
London 13
Nanchang 13
Hangzhou 12
Hebei 12
Rio de Janeiro 12
Atlanta 11
Fuzhou 11
Ningbo 11
San Francisco 11
Verona 11
Cagliari 10
Eitensheim 10
Kiez 10
Abidjan 9
Belo Horizonte 9
Da Nang 9
Istanbul 9
Manchester 9
Mumbai 9
San Diego 9
Zhengzhou 9
Bangkok 8
Bühl 8
Casablanca 8
Chengdu 8
Haikou 8
Odernheim 8
Quito 8
Totale 7.305
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Nome #
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing 351
Non-random retention of protein-coding overlapping genes in Metazoa 337
Role of miRNAs in neural tube development 316
Identification of genetic factors associated with neural tube defects 310
Clinical Relevance of Clonal Hematopoiesis in the Oldest-Old Population: Analysis of the "Health and Anemia" Study 288
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 285
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p 283
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest 282
Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcript 268
A novel mutation within the MIR96 gene causes nonsyndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 263
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 260
The double-faced association of the PRKCA gene with multiple sclerosis 253
Characterization of long noncoding RNAs associated with developmental genes in vertebrates 250
Identification of novel deafness-causing variants in the tmprss3 gene by whole-exome sequencing 250
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis 241
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 236
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 232
Search for novel deafness genes by exome sequencing of autosomal recessive NSHL families 232
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 228
Differential expression of microRNAs in peripheral blood mononuclear cells of multiple sclerosis patients 224
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 223
Exome sequencing identifies PRPS1 as a major locus for X-linked nonsyndromic hearing loss in the Italian population 223
Identification by exome sequencing and functional characterization of novel deafness-causing mutations in PRPS1 212
Identification by whole-exome sequencing of two novel LARS2 mutations in an Italian family with Perrault syndrome 210
Type II mutation (Glu117stop) causes factor XI deficiency by inducing allele specific mRNA degradation 208
Identification of novel NSHL-causing mutations by whole exome sequencing 208
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 207
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 206
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis : identification of novel mutations 200
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis 199
Understanding genetic variation in the CFTR gene by next-generation sequencing 197
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 195
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 195
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 193
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 190
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis 189
Regulated independent expression of 3' untranslated regions in mammals 187
Alpha3 and alpha5 neuronal nicotinic receptor subunit genes : a case of tail-to-tail overlap in humans 186
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 185
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 185
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs 184
Response: Further thoughts on the "phantom" delta6/7 FXI isoform 184
A type mutation II (Glu117stop), induction of allele-specific mRNA degradation and FXI deficiency 182
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 172
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 169
In-depth study of breast cancer tumor promoting cell transcriptome using RNA-seq and microarrays 166
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 165
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 163
Evolution, identification and expression of noncoding RNAs in animals 156
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes 152
Glucocerebrosidase mutations in primary parkinsonism 148
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population 144
Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease 140
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 134
No association of GBA mutations and multiple system atrophy 130
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation 128
Improving mRNA 5' coding sequence determination in the mouse genome 127
Expression of distinct RNAs from 3' untranslated regions 123
Totale 12.154
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Categoria #
all - tutte 29.774
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 29.774
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202139 0 0 0 0 0 0 0 0 0 0 0 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
2025/20263.087 369 148 316 235 308 200 458 126 277 281 297 72
Totale 12.154