IRIS
SOLDA', GIULIA MARIA EMILIA ANTONIETTA
 Distribuzione geografica
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Continente #
NA - Nord America 3.870
AS - Asia 2.392
EU - Europa 773
SA - Sud America 476
AF - Africa 121
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 3
AN - Antartide 1
Totale 7.643
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Nazione #
US - Stati Uniti d'America 3.788
SG - Singapore 1.472
CN - Cina 421
BR - Brasile 392
VN - Vietnam 199
FI - Finlandia 163
IE - Irlanda 110
IT - Italia 104
DE - Germania 90
NG - Nigeria 81
HK - Hong Kong 76
FR - Francia 65
CA - Canada 48
NL - Olanda 47
GB - Regno Unito 45
IN - India 42
AR - Argentina 38
SE - Svezia 35
BE - Belgio 18
TR - Turchia 18
BD - Bangladesh 17
IQ - Iraq 17
PK - Pakistan 17
MX - Messico 15
RU - Federazione Russa 15
IL - Israele 14
PL - Polonia 14
ZA - Sudafrica 13
JP - Giappone 12
CH - Svizzera 11
CO - Colombia 11
ID - Indonesia 11
PH - Filippine 9
UA - Ucraina 9
EC - Ecuador 8
ES - Italia 8
EG - Egitto 7
MY - Malesia 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
NO - Norvegia 5
PY - Paraguay 5
TN - Tunisia 5
AT - Austria 4
AZ - Azerbaigian 4
JM - Giamaica 4
KE - Kenya 4
KR - Corea 4
SA - Arabia Saudita 4
CZ - Repubblica Ceca 3
DK - Danimarca 3
GR - Grecia 3
LB - Libano 3
PT - Portogallo 3
AL - Albania 2
BG - Bulgaria 2
BH - Bahrain 2
BS - Bahamas 2
BY - Bielorussia 2
DZ - Algeria 2
HU - Ungheria 2
KZ - Kazakistan 2
MD - Moldavia 2
PA - Panama 2
PE - Perù 2
QA - Qatar 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
SV - El Salvador 2
SY - Repubblica araba siriana 2
TH - Thailandia 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
HN - Honduras 1
HR - Croazia 1
LT - Lituania 1
MK - Macedonia 1
RS - Serbia 1
TV - Tuvalu 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZW - Zimbabwe 1
Totale 7.643
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Città #
Singapore 703
Chandler 471
Wilmington 435
Ashburn 254
San Jose 217
Dallas 212
The Dalles 193
San Mateo 187
Shanghai 172
Helsinki 161
Ann Arbor 158
New York 121
Dublin 109
Beijing 107
Lawrence 84
Princeton 84
Benin City 81
Leawood 81
Boardman 79
Hong Kong 70
Ho Chi Minh City 69
Santa Clara 47
Paris 46
Fairfield 44
Hanoi 41
Los Angeles 38
Amsterdam 37
Woodbridge 37
Milan 34
São Paulo 31
Columbus 30
Falkenstein 27
Seattle 25
Toronto 20
Orem 19
Brussels 18
Council Bluffs 16
Buffalo 15
London 14
Montreal 14
San Diego 14
Brooklyn 13
Rio de Janeiro 13
Chennai 12
Da Nang 12
Houston 12
Abbiategrasso 11
Warsaw 11
Belo Horizonte 10
Curitiba 10
Naples 9
Norwalk 9
Tempe 9
Charlotte 8
Johannesburg 8
Mumbai 8
Phoenix 8
Atlanta 7
Hanover 7
Zurich 7
Amman 6
Brasília 6
Guangzhou 6
Manchester 6
Mexico City 6
Monmouth Junction 6
Tashkent 6
Verona 6
Baghdad 5
Biên Hòa 5
Bogotá 5
Chicago 5
Haiphong 5
Hải Dương 5
Kocaeli 5
Lahore 5
Quận Một 5
Rome 5
Stockholm 5
Tokyo 5
Uberlândia 5
Baku 4
Bishkek 4
Buenos Aires 4
Cairo 4
Caracas 4
Caxias do Sul 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
Newark 4
Oslo 4
Totale 4.988
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Nome #
Dual Role of G-runs and hnRNP F in the Regulation of a Mutation-Activated Pseudoexon in the Fibrinogen Gamma-Chain Transcript 150
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 138
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 134
Glucocerebrosidase mutations in primary parkinsonism 134
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 129
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis. 128
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family 125
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 122
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis. *Shared first authorship 122
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest. 121
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes. *Corresponding author 120
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 119
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency 119
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs 118
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 115
Tumor-derived prostaglandin E2 promotes p50 NF-κB-dependent differentiation of monocytic MDSC 112
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 112
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing. BMC Highly accessed paper 109
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 108
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 107
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years 107
The double-faced association of the PRKCA gene with multiple sclerosis 106
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 104
DNAJC12 and dopa-responsive nonprogressive parkinsonism 104
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 103
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 102
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis 99
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 98
4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy 98
Non-random retention of protein-coding overlapping genes in Metazoa. 95
Survival and dementia in GBA-associated Parkinson's disease: The mutation matters 94
Expression of distinct RNAs from 3' untranslated regions. *Shared first authorship (TRM, DW,MED,GS). 2010 NAR Featured Article (top 5% of papers) 93
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 90
Impact of prostate cancer screening in European ancestry un‐affected men with germline DNA repair pathogenic variants 89
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 89
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 87
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 85
Response: Further thoughts on the "phantom" delta6/7 FXI isoform 84
X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases 84
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 84
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy 83
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 83
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 82
In-depth characterization of breast cancer tumor-promoting cell transcriptome by RNA sequencing and microarrays 81
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 80
Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer 79
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 79
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 78
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population 77
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 77
Geni sovrapposti in eucarioti superiori 76
LIQUID BIOPSY BY PROSTATE-DERIVED TUMOR CELLS ENRICHED FROM SEMINAL FLUID (SF): THE SEMEN PROSTATE CANCER TUMOR ELEMENTS (SPECTRE) PROJECT. 74
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 73
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson's disease 73
First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features 73
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation 72
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 70
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 70
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 70
Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer 70
Type II Mutation (Glu117stop) Causes Factor XI Deficiency By Inducing Allele Specific mRNA Degradation 69
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 68
Evolution, identification and expression of noncoding RNAs in animals 68
Prospective evaluation of the role of imaging techniques and TMPRSS2:ERG mutation for the diagnosis of clinically significant prostate cancer 68
Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites 67
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 66
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p. 65
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). 65
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 65
Massive Accumulation of Sphingomyelin Affects the Lysosomal and Mitochondria Compartments and Promotes Apoptosis in Niemann-Pick Disease Type A 63
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson disease 61
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss 60
MiR-634: a new player in the pathogenesis of multiple sclerosis? 59
Post-Biopsy Cell-Free DNA From Blood: An Open Window on Primary Prostate Cancer Genetics and Biology 59
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 59
Side-by-side comparison of next-generation sequencing, cytology, and histology in diagnosing locally advanced pancreatic adenocarcinoma 58
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear 57
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
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 57
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD 57
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 54
Functional study of the tail-to-tail overlap between human neuronal nicotinic acetylcholine receptor CHRNA3 and CHRNA5 genes 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
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 52
“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 51
Improving mRNA 5′ coding sequence determination in the mouse genome 48
How I faced my prostate cancer: a molecular biologist's perspective 48
Fine characterization of the recurrent c.1584 +18672 A>G deep-intronic mutation in the CFTR gene 46
SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa 46
Male awareness of prostate cancer risk remains poor in relatives of women with germline variants in DNA-repair genes 44
Applying artificial intelligence to uncover the genetic landscape of coagulation factors 7
Functional characterisation of missense ceruloplasmin variants and real-world prevalence assessment of Aceruloplasminemia using population data 7
Correcting CFTR mRNA splicing defects with the plant cytokine kinetin and its analogues 6
Genetics Influences Telomere Length in Parkinson's Disease: A Study in Monozygotic Discordant Twins 5
Splicing-based biomarkers define a robust multigene classifier for relapsing-remitting multiple sclerosis 5
Lewy pathology formation in patient-derived GBA1 Parkinson’s disease midbrain organoids 4
Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severity 3
Totale 7.747
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Categoria #
all - tutte 49.152
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 49.152
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021103 0 0 0 0 0 0 0 0 0 0 0 103
2021/2022471 13 4 5 97 9 9 22 66 57 67 84 38
2022/20231.285 191 66 104 155 124 107 3 107 211 100 96 21
2023/2024711 78 72 127 34 24 101 42 36 13 8 77 99
2024/20251.447 44 43 23 36 87 232 100 132 157 248 179 166
2025/20262.957 441 166 214 184 141 151 912 116 160 212 152 108
Totale 7.747