IRIS
Soldà, Giulia Maria Emilia Antonietta
 Distribuzione geografica
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Continente #
NA - Nord America 5.018
AS - Asia 2.478
EU - Europa 914
SA - Sud America 494
AF - Africa 122
Continente sconosciuto - Info sul continente non disponibili 109
OC - Oceania 7
AN - Antartide 1
Totale 9.143
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Nazione #
US - Stati Uniti d'America 4.891
SG - Singapore 1.501
CN - Cina 454
BR - Brasile 402
IT - Italia 221
VN - Vietnam 201
FI - Finlandia 163
IE - Irlanda 111
DE - Germania 92
HK - Hong Kong 85
NG - Nigeria 81
CA - Canada 70
FR - Francia 66
GB - Regno Unito 55
NL - Olanda 48
IN - India 43
AR - Argentina 38
SE - Svezia 35
BD - Bangladesh 20
TR - Turchia 19
BE - Belgio 18
IQ - Iraq 17
PK - Pakistan 17
MX - Messico 16
PL - Polonia 16
RU - Federazione Russa 15
CO - Colombia 14
IL - Israele 14
ID - Indonesia 13
JP - Giappone 13
ZA - Sudafrica 13
PH - Filippine 12
CH - Svizzera 11
ES - Italia 11
EC - Ecuador 9
UA - Ucraina 9
VE - Venezuela 9
CL - Cile 8
GT - Guatemala 8
AE - Emirati Arabi Uniti 7
EG - Egitto 7
MY - Malesia 7
JO - Giordania 6
MA - Marocco 6
NP - Nepal 6
UZ - Uzbekistan 6
AU - Australia 5
BO - Bolivia 5
CR - Costa Rica 5
DO - Repubblica Dominicana 5
IR - Iran 5
JM - Giamaica 5
KE - Kenya 5
KG - Kirghizistan 5
NO - Norvegia 5
PT - Portogallo 5
PY - Paraguay 5
SA - Arabia Saudita 5
TN - Tunisia 5
AT - Austria 4
AZ - Azerbaigian 4
CZ - Repubblica Ceca 4
KR - Corea 4
SV - El Salvador 4
BS - Bahamas 3
DK - Danimarca 3
GR - Grecia 3
HN - Honduras 3
LB - Libano 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
PE - Perù 2
PR - Porto Rico 2
QA - Qatar 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 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
EU - Europa 1
FJ - Figi 1
HR - Croazia 1
LC - Santa Lucia 1
LT - Lituania 1
LU - Lussemburgo 1
MK - Macedonia 1
NI - Nicaragua 1
RS - Serbia 1
Totale 9.034
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Città #
Singapore 716
Chandler 471
Wilmington 435
Ashburn 377
San Jose 279
Dallas 224
The Dalles 194
San Mateo 187
Shanghai 174
Helsinki 161
Ann Arbor 158
New York 130
Beijing 121
Council Bluffs 119
Dublin 109
Princeton 94
Milan 88
Santa Clara 88
Lawrence 86
Benin City 81
Leawood 81
Boardman 80
Hong Kong 78
Ho Chi Minh City 69
Los Angeles 52
Fairfield 46
Paris 46
Hanoi 41
Woodbridge 38
Amsterdam 37
Columbus 36
São Paulo 35
Seattle 29
Falkenstein 27
Rome 27
Phoenix 26
Toronto 22
San Diego 21
Montreal 20
Orem 20
Brooklyn 19
Buffalo 19
Chicago 19
Brussels 18
Houston 17
Atlanta 14
London 14
Miami 14
Cincinnati 13
Naples 13
Rio de Janeiro 13
Chennai 12
Da Nang 12
Warsaw 12
Abbiategrasso 11
Figino 11
Norwalk 11
Philadelphia 11
Belo Horizonte 10
Charlotte 10
Curitiba 10
Mumbai 9
Newark 9
Tempe 9
Johannesburg 8
Las Vegas 8
Hanover 7
Kansas City 7
Manchester 7
Mexico City 7
San Antonio 7
Verona 7
Zurich 7
Amman 6
Brasília 6
Cleveland 6
Dhaka 6
Fayetteville 6
Guangzhou 6
Lawrenceville 6
Monmouth Junction 6
Pasadena 6
Riverside 6
South Bend 6
Tashkent 6
Tokyo 6
Austin 5
Baghdad 5
Biên Hòa 5
Bogotá 5
Haiphong 5
Hải Dương 5
Indianapolis 5
Kocaeli 5
Lahore 5
Queens 5
Quận Một 5
San Francisco 5
Stockholm 5
Uberlândia 5
Totale 5.646
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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 170
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 154
Glucocerebrosidase mutations in primary parkinsonism 147
Tumor-derived prostaglandin E2 promotes p50 NF-κB-dependent differentiation of monocytic MDSC 147
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 145
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs 144
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 143
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis. 143
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest. 140
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family 138
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 138
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis. *Shared first authorship 134
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 132
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 131
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency 131
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes. *Corresponding author 129
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 127
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 126
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing. BMC Highly accessed paper 124
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 121
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 119
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years 119
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 118
The double-faced association of the PRKCA gene with multiple sclerosis 116
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 115
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 115
Survival and dementia in GBA-associated Parkinson's disease: The mutation matters 112
DNAJC12 and dopa-responsive nonprogressive parkinsonism 111
LIQUID BIOPSY BY PROSTATE-DERIVED TUMOR CELLS ENRICHED FROM SEMINAL FLUID (SF): THE SEMEN PROSTATE CANCER TUMOR ELEMENTS (SPECTRE) PROJECT. 109
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 109
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis 107
Non-random retention of protein-coding overlapping genes in Metazoa. 106
4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy 106
Impact of prostate cancer screening in European ancestry un‐affected men with germline DNA repair pathogenic variants 104
X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases 104
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 100
Expression of distinct RNAs from 3' untranslated regions. *Shared first authorship (TRM, DW,MED,GS). 2010 NAR Featured Article (top 5% of papers) 100
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 100
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 99
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 99
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 98
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 97
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 96
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 95
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy 91
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 91
Response: Further thoughts on the "phantom" delta6/7 FXI isoform 90
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 90
In-depth characterization of breast cancer tumor-promoting cell transcriptome by RNA sequencing and microarrays 88
Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer 87
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population 87
MiR-634: a new player in the pathogenesis of multiple sclerosis? 86
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson's disease 85
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 84
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 83
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation 83
First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features 83
Geni sovrapposti in eucarioti superiori 83
Massive Accumulation of Sphingomyelin Affects the Lysosomal and Mitochondria Compartments and Promotes Apoptosis in Niemann-Pick Disease Type A 83
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 82
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 82
Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer 82
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 79
Prospective evaluation of the role of imaging techniques and TMPRSS2:ERG mutation for the diagnosis of clinically significant prostate cancer 79
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 78
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 77
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 76
Type II Mutation (Glu117stop) Causes Factor XI Deficiency By Inducing Allele Specific mRNA Degradation 76
Search for novel deafness genes by exome sequencing of autosomal recessive NSHL families 76
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson disease 76
Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites 75
Side-by-side comparison of next-generation sequencing, cytology, and histology in diagnosing locally advanced pancreatic adenocarcinoma 74
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). 73
Evolution, identification and expression of noncoding RNAs in animals 73
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p. 72
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 71
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 71
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 71
Post-Biopsy Cell-Free DNA From Blood: An Open Window on Primary Prostate Cancer Genetics and Biology 70
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss 69
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear 68
No association of GBA mutations and multiple system atrophy 67
How I faced my prostate cancer: a molecular biologist's perspective 66
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 65
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 64
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD 64
Functional study of the tail-to-tail overlap between human neuronal nicotinic acetylcholine receptor CHRNA3 and CHRNA5 genes 60
Male awareness of prostate cancer risk remains poor in relatives of women with germline variants in DNA-repair genes 58
SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa 57
Improving mRNA 5′ coding sequence determination in the mouse genome 56
“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 56
Fine characterization of the recurrent c.1584 +18672 A>G deep-intronic mutation in the CFTR gene 51
Two novel splicing mutations in the OTUD6B gene associated with intellectual disability and seizures 39
Correcting CFTR mRNA splicing defects with the plant cytokine kinetin and its analogues 27
Germline homologous recombination repair (gHRR) variants in bladder cancer: Preliminary evidence and clinical implications 27
Applying artificial intelligence to uncover the genetic landscape of coagulation factors 26
Lewy pathology formation in patient-derived GBA1 Parkinson’s disease midbrain organoids 21
Splicing-based biomarkers define a robust multigene classifier for relapsing-remitting multiple sclerosis 20
Functional characterisation of missense ceruloplasmin variants and real-world prevalence assessment of Aceruloplasminemia using population data 20
Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severity 19
Totale 9.125
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Categoria #
all - tutte 55.369
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 55.369
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022449 0 0 0 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
2024/20251.456 44 43 23 38 87 234 100 132 158 250 181 166
2025/20263.064 449 167 215 186 145 151 921 117 163 215 154 181
2026/20271.280 270 261 499 250 0 0 0 0 0 0 0 0
Totale 9.143