IRIS
SOLDA', GIULIA MARIA EMILIA ANTONIETTA
 Distribuzione geografica
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Continente #
NA - Nord America 3.306
AS - Asia 1.458
EU - Europa 685
SA - Sud America 429
AF - Africa 113
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 3
AN - Antartide 1
Totale 6.000
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Nazione #
US - Stati Uniti d'America 3.249
SG - Singapore 877
BR - Brasile 367
CN - Cina 334
FI - Finlandia 164
IE - Irlanda 114
IT - Italia 89
NG - Nigeria 83
DE - Germania 64
HK - Hong Kong 59
FR - Francia 46
NL - Olanda 42
VN - Vietnam 38
GB - Regno Unito 37
CA - Canada 36
SE - Svezia 35
AR - Argentina 29
IN - India 25
BE - Belgio 17
RU - Federazione Russa 14
PK - Pakistan 13
BD - Bangladesh 12
IQ - Iraq 12
TR - Turchia 12
IL - Israele 11
MX - Messico 11
ZA - Sudafrica 11
CH - Svizzera 10
UA - Ucraina 10
ID - Indonesia 9
PL - Polonia 8
CO - Colombia 7
EG - Egitto 7
JP - Giappone 7
ES - Italia 6
AE - Emirati Arabi Uniti 5
EC - Ecuador 5
IR - Iran 5
JO - Giordania 5
KG - Kirghizistan 5
NO - Norvegia 5
NP - Nepal 5
UZ - Uzbekistan 5
VE - Venezuela 5
AU - Australia 4
CL - Cile 4
DO - Repubblica Dominicana 4
MA - Marocco 4
PY - Paraguay 4
AT - Austria 3
AZ - Azerbaigian 3
BO - Bolivia 3
DK - Danimarca 3
GR - Grecia 3
KR - Corea 3
PE - Perù 3
PH - Filippine 3
TN - Tunisia 3
BG - Bulgaria 2
CZ - Repubblica Ceca 2
DZ - Algeria 2
HU - Ungheria 2
JM - Giamaica 2
KZ - Kazakistan 2
MY - Malesia 2
PA - Panama 2
PT - Portogallo 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AM - Armenia 1
AQ - Antartide 1
BH - Bahrain 1
EU - Europa 1
KE - Kenya 1
LB - Libano 1
LT - Lituania 1
MD - Moldavia 1
MK - Macedonia 1
RO - Romania 1
SV - El Salvador 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
TV - Tuvalu 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 6.000
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Città #
Chandler 484
Wilmington 444
Singapore 314
Dallas 207
San Mateo 190
The Dalles 187
Shanghai 175
Helsinki 162
Ann Arbor 160
Dublin 113
New York 111
Ashburn 107
Lawrence 86
Princeton 86
Benin City 83
Leawood 83
Boardman 79
Beijing 78
Hong Kong 58
Fairfield 44
Paris 43
Woodbridge 41
Amsterdam 36
Milan 31
Columbus 30
São Paulo 27
Los Angeles 25
Seattle 25
Ho Chi Minh City 19
Santa Clara 19
Brussels 17
Council Bluffs 15
London 15
San Diego 15
Toronto 15
Abbiategrasso 11
Brooklyn 11
Rio de Janeiro 11
Curitiba 10
Belo Horizonte 9
Montreal 9
Naples 9
Norwalk 9
Tempe 9
Hanover 8
Houston 8
Phoenix 8
Chennai 7
Johannesburg 6
Monmouth Junction 6
Warsaw 6
Zurich 6
Amman 5
Atlanta 5
Bogotá 5
Brasília 5
Caxias do Sul 5
Falkenstein 5
Kocaeli 5
Stockholm 5
Tashkent 5
Baghdad 4
Bishkek 4
Buenos Aires 4
Cairo 4
Charlotte 4
Des Moines 4
Goiânia 4
Guangzhou 4
Gunzenhausen 4
Hanoi 4
Juiz de Fora 4
Munich 4
Oslo 4
Petrópolis 4
Pune 4
Redmond 4
San Francisco 4
Santo André 4
Tappahannock 4
Tokyo 4
Uberlândia 4
Zavalla 4
Abu Dhabi 3
Baku 3
Boston 3
Campo Largo 3
Cape Town 3
Caracas 3
Chicago 3
Cleveland 3
Cologno Monzese 3
Dhaka 3
Erbil 3
Falls Church 3
Guarulhos 3
Islamabad 3
Jakarta 3
Joinville 3
Karachi 3
Totale 3.951
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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 130
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis. 110
Glucocerebrosidase mutations in primary parkinsonism 108
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family 107
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 106
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 103
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes. *Corresponding author 100
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 98
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 97
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest. 97
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 96
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 92
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 92
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs 89
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency 89
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 88
Tumor-derived prostaglandin E2 promotes p50 NF-κB-dependent differentiation of monocytic MDSC 85
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis 84
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 84
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis. *Shared first authorship 83
Non-random retention of protein-coding overlapping genes in Metazoa. 82
The double-faced association of the PRKCA gene with multiple sclerosis 82
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 82
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing. BMC Highly accessed paper 82
4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy 81
Expression of distinct RNAs from 3' untranslated regions. *Shared first authorship (TRM, DW,MED,GS). 2010 NAR Featured Article (top 5% of papers) 78
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 78
DNAJC12 and dopa-responsive nonprogressive parkinsonism 78
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years 78
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 74
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 72
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 72
Response: Further thoughts on the "phantom" delta6/7 FXI isoform 69
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 68
Survival and dementia in GBA-associated Parkinson's disease: The mutation matters 68
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 68
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 68
Impact of prostate cancer screening in European ancestry un‐affected men with germline DNA repair pathogenic variants 67
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 67
Characterization of Long Noncoding RNAs Associated with Developmental Genes in Vertebrates 66
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 66
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 65
Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer 64
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy 62
In-depth characterization of breast cancer tumor-promoting cell transcriptome by RNA sequencing and microarrays 62
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 62
LIQUID BIOPSY BY PROSTATE-DERIVED TUMOR CELLS ENRICHED FROM SEMINAL FLUID (SF): THE SEMEN PROSTATE CANCER TUMOR ELEMENTS (SPECTRE) PROJECT. 61
Geni sovrapposti in eucarioti superiori 60
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation 59
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 59
X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases 59
Prospective evaluation of the role of imaging techniques and TMPRSS2:ERG mutation for the diagnosis of clinically significant prostate cancer 59
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population 58
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson's disease 58
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 58
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 58
Evolution, identification and expression of noncoding RNAs in animals 58
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 56
Type II Mutation (Glu117stop) Causes Factor XI Deficiency By Inducing Allele Specific mRNA Degradation 55
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p. 54
Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer 54
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 53
First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features 53
Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites 52
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson disease 52
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 51
Massive Accumulation of Sphingomyelin Affects the Lysosomal and Mitochondria Compartments and Promotes Apoptosis in Niemann-Pick Disease Type A 51
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). 50
Regulated independent expression of 3' untranslated regions in mammals 50
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 50
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 49
No association of GBA mutations and multiple system atrophy 49
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 48
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss 45
MiR-634: a new player in the pathogenesis of multiple sclerosis? 45
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 43
Search for novel deafness genes by exome sequencing of autosomal recessive NSHL families 43
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 42
Functional study of the tail-to-tail overlap between human neuronal nicotinic acetylcholine receptor CHRNA3 and CHRNA5 genes 42
Side-by-side comparison of next-generation sequencing, cytology, and histology in diagnosing locally advanced pancreatic adenocarcinoma 42
Improving mRNA 5′ coding sequence determination in the mouse genome 41
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD 41
Post-Biopsy Cell-Free DNA From Blood: An Open Window on Primary Prostate Cancer Genetics and Biology 41
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 41
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear 40
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 40
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 40
“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 39
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 37
Fine characterization of the recurrent c.1584 +18672 A>G deep-intronic mutation in the CFTR gene 34
Male awareness of prostate cancer risk remains poor in relatives of women with germline variants in DNA-repair genes 34
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 33
How I faced my prostate cancer: a molecular biologist's perspective 32
SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa 29
Totale 6.097
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Categoria #
all - tutte 44.676
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 44.676
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021842 0 0 0 0 0 271 134 67 170 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
2025/20261.212 449 167 220 186 144 46 0 0 0 0 0 0
Totale 6.097