IRIS
SOLDA', GIULIA MARIA EMILIA ANTONIETTA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 3.714
AS - Asia 2.345
EU - Europa 785
SA - Sud America 487
AF - Africa 123
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 3
AN - Antartide 1
Totale 7.465
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 3.648
SG - Singapore 1.468
BR - Brasile 402
CN - Cina 382
VN - Vietnam 202
FI - Finlandia 166
IE - Irlanda 114
IT - Italia 101
DE - Germania 93
NG - Nigeria 83
HK - Hong Kong 73
FR - Francia 65
GB - Regno Unito 47
NL - Olanda 47
IN - India 44
CA - Canada 40
AR - Argentina 38
SE - Svezia 35
BE - Belgio 18
TR - Turchia 18
IQ - Iraq 17
PK - Pakistan 17
BD - Bangladesh 15
RU - Federazione Russa 15
IL - Israele 14
PL - Polonia 14
ZA - Sudafrica 13
JP - Giappone 12
MX - Messico 12
CH - Svizzera 11
CO - Colombia 11
ID - Indonesia 11
UA - Ucraina 11
ES - Italia 9
PH - Filippine 9
EC - Ecuador 8
EG - Egitto 7
VE - Venezuela 7
AE - Emirati Arabi Uniti 6
CL - Cile 6
JO - Giordania 6
MA - Marocco 6
NP - Nepal 6
UZ - Uzbekistan 6
AU - Australia 5
BO - Bolivia 5
DO - Repubblica Dominicana 5
IR - Iran 5
KG - Kirghizistan 5
MY - Malesia 5
NO - Norvegia 5
PY - Paraguay 5
TN - Tunisia 5
AT - Austria 4
AZ - Azerbaigian 4
KE - Kenya 4
SA - Arabia Saudita 4
CZ - Repubblica Ceca 3
DK - Danimarca 3
GR - Grecia 3
JM - Giamaica 3
KR - Corea 3
LB - Libano 3
PE - Perù 3
PT - Portogallo 3
AL - Albania 2
BG - Bulgaria 2
BH - Bahrain 2
BY - Bielorussia 2
DZ - Algeria 2
HU - Ungheria 2
KZ - Kazakistan 2
MD - Moldavia 2
PA - Panama 2
QA - Qatar 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
SY - Repubblica araba siriana 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AQ - Antartide 1
CR - Costa Rica 1
EU - Europa 1
FJ - Figi 1
HR - Croazia 1
LT - Lituania 1
MK - Macedonia 1
RS - Serbia 1
SV - El Salvador 1
TH - Thailandia 1
TV - Tuvalu 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZW - Zimbabwe 1
Totale 7.465
Salva come PNG Salva come JPEG
Città #
Singapore 712
Chandler 484
Wilmington 444
Ashburn 240
Dallas 208
The Dalles 196
San Mateo 190
Shanghai 175
San Jose 168
Helsinki 164
Ann Arbor 160
New York 114
Dublin 113
Beijing 96
Lawrence 86
Princeton 86
Benin City 83
Leawood 83
Boardman 79
Ho Chi Minh City 70
Hong Kong 67
Paris 46
Fairfield 44
Woodbridge 41
Hanoi 40
Amsterdam 37
Milan 35
São Paulo 31
Columbus 30
Los Angeles 29
Santa Clara 29
Falkenstein 28
Seattle 25
Brussels 18
Orem 18
London 17
Council Bluffs 16
San Diego 15
Toronto 15
Da Nang 13
Rio de Janeiro 13
Brooklyn 12
Chennai 12
Houston 12
Montreal 12
Abbiategrasso 11
Curitiba 11
Warsaw 11
Belo Horizonte 10
Naples 9
Norwalk 9
Tempe 9
Hanover 8
Johannesburg 8
Mumbai 8
Phoenix 8
Zurich 7
Amman 6
Brasília 6
Manchester 6
Monmouth Junction 6
Tashkent 6
Verona 6
Atlanta 5
Baghdad 5
Biên Hòa 5
Bogotá 5
Caxias do Sul 5
Charlotte 5
Guangzhou 5
Haiphong 5
Hải Dương 5
Kocaeli 5
Lahore 5
Quận Một 5
Stockholm 5
Tokyo 5
Uberlândia 5
Baku 4
Bishkek 4
Buenos Aires 4
Buffalo 4
Bến Tre 4
Cairo 4
Caracas 4
Des Moines 4
Dhaka 4
Frankfurt am Main 4
Goiânia 4
Gunzenhausen 4
Jakarta 4
Juiz de Fora 4
Karachi 4
Munich 4
Nairobi 4
New Delhi 4
Oslo 4
Petrópolis 4
Pune 4
Redmond 4
Totale 4.914
Salva come PNG Salva come JPEG
Nome #
Dual Role of G-runs and hnRNP F in the Regulation of a Mutation-Activated Pseudoexon in the Fibrinogen Gamma-Chain Transcript 147
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 136
Glucocerebrosidase mutations in primary parkinsonism 131
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 130
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis. 124
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family 122
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 120
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes. *Corresponding author 119
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 117
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 116
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis. *Shared first authorship 116
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest. 116
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs 114
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 114
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency 112
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 111
Tumor-derived prostaglandin E2 promotes p50 NF-κB-dependent differentiation of monocytic MDSC 110
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 106
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 106
The double-faced association of the PRKCA gene with multiple sclerosis 102
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing. BMC Highly accessed paper 102
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 101
DNAJC12 and dopa-responsive nonprogressive parkinsonism 101
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis 97
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 96
4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy 95
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years 95
Non-random retention of protein-coding overlapping genes in Metazoa. 93
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 92
Expression of distinct RNAs from 3' untranslated regions. *Shared first authorship (TRM, DW,MED,GS). 2010 NAR Featured Article (top 5% of papers) 91
Survival and dementia in GBA-associated Parkinson's disease: The mutation matters 89
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 87
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 87
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 86
Response: Further thoughts on the "phantom" delta6/7 FXI isoform 84
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 83
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 83
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy 82
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 82
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 82
A novel mutation within the MIR96 gene causes nonsyndromic inherited hearing loss in an Italian family by altering pre-microRNA processing to its mature forms 80
In-depth characterization of breast cancer tumor-promoting cell transcriptome by RNA sequencing and microarrays 79
Characterization of Long Noncoding RNAs Associated with Developmental Genes in Vertebrates 79
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 78
Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer 77
X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases 77
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 76
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 76
Impact of prostate cancer screening in European ancestry un‐affected men with germline DNA repair pathogenic variants 75
Geni sovrapposti in eucarioti superiori 74
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population 73
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson's disease 73
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 73
LIQUID BIOPSY BY PROSTATE-DERIVED TUMOR CELLS ENRICHED FROM SEMINAL FLUID (SF): THE SEMEN PROSTATE CANCER TUMOR ELEMENTS (SPECTRE) PROJECT. 72
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation 71
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 69
First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features 69
Type II Mutation (Glu117stop) Causes Factor XI Deficiency By Inducing Allele Specific mRNA Degradation 69
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 69
Evolution, identification and expression of noncoding RNAs in animals 68
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 67
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 66
Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer 66
Prospective evaluation of the role of imaging techniques and TMPRSS2:ERG mutation for the diagnosis of clinically significant prostate cancer 66
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p. 64
Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites 64
POSITIVE PROSTATE 68GAPSMA-PET/CT CORRELATES WITH DETECTION OF CD45-/PSMA(+) NON-SPERM EPITHELIAL CELLS OBTAINED BY LIQUID BIOPSY OF SEMINAL FLUID IN PATIENTS WITH PROSTATE CANCER (PCA). 63
Il cluster genico CHRNA5/A3/B4: la presenza di una regione di sovrapposizione genica suggerisce l’esistenza di meccanismi post-trascrizionali nel controllo dell’espressione delle subunità alfa3 e alfa5 del recettore nicotinico neuronale 63
Massive Accumulation of Sphingomyelin Affects the Lysosomal and Mitochondria Compartments and Promotes Apoptosis in Niemann-Pick Disease Type A 63
Regulated independent expression of 3' untranslated regions in mammals 62
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 62
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 60
MiR-634: a new player in the pathogenesis of multiple sclerosis? 59
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson disease 59
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 57
No association of GBA mutations and multiple system atrophy 57
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear 56
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss 56
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD 55
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 54
Post-Biopsy Cell-Free DNA From Blood: An Open Window on Primary Prostate Cancer Genetics and Biology 54
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 53
Search for novel deafness genes by exome sequencing of autosomal recessive NSHL families 53
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 53
Side-by-side comparison of next-generation sequencing, cytology, and histology in diagnosing locally advanced pancreatic adenocarcinoma 52
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 51
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 51
“Trascritti che si prendono per la coda”: la sovrapposizione tail-to-tail tra i geni umani CHRNA3 e CHRNA5 genera RNA-RNA duplex in vivo 50
Functional study of the tail-to-tail overlap between human neuronal nicotinic acetylcholine receptor CHRNA3 and CHRNA5 genes 49
Improving mRNA 5′ coding sequence determination in the mouse genome 48
How I faced my prostate cancer: a molecular biologist's perspective 47
Fine characterization of the recurrent c.1584 +18672 A>G deep-intronic mutation in the CFTR gene 44
SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa 43
Male awareness of prostate cancer risk remains poor in relatives of women with germline variants in DNA-repair genes 41
Totale 7.562
Salva come PNG Salva come JPEG
Categoria #
all - tutte 47.189
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 47.189
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021200 0 0 0 0 0 0 0 0 0 91 3 106
2021/2022478 13 4 5 99 9 9 22 67 58 67 86 39
2022/20231.313 195 68 106 159 126 109 3 110 213 103 99 22
2023/2024723 80 73 129 35 24 103 43 37 13 8 78 100
2024/20251.475 45 44 23 36 87 236 103 133 164 252 183 169
2025/20262.677 449 167 220 186 144 153 932 120 160 146 0 0
Totale 7.562