IRIS
SOLDA', GIULIA MARIA EMILIA ANTONIETTA
 Distribuzione geografica
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Continente #
NA - Nord America 4.293
AS - Asia 2.457
EU - Europa 891
SA - Sud America 486
AF - Africa 122
Continente sconosciuto - Info sul continente non disponibili 109
OC - Oceania 7
AN - Antartide 1
Totale 8.366
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Nazione #
US - Stati Uniti d'America 4.203
SG - Singapore 1.497
CN - Cina 448
BR - Brasile 398
IT - Italia 210
VN - Vietnam 201
FI - Finlandia 163
IE - Irlanda 111
DE - Germania 90
HK - Hong Kong 83
NG - Nigeria 81
FR - Francia 66
CA - Canada 52
NL - Olanda 47
GB - Regno Unito 46
IN - India 43
AR - Argentina 38
SE - Svezia 35
TR - Turchia 19
BD - Bangladesh 18
BE - Belgio 18
IQ - Iraq 17
PK - Pakistan 17
MX - Messico 16
PL - Polonia 16
RU - Federazione Russa 15
IL - Israele 14
CO - Colombia 13
ZA - Sudafrica 13
ID - Indonesia 12
JP - Giappone 12
CH - Svizzera 11
ES - Italia 11
PH - Filippine 9
UA - Ucraina 9
EC - Ecuador 8
VE - Venezuela 8
CL - Cile 7
EG - Egitto 7
MY - Malesia 7
AE - Emirati Arabi Uniti 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
JM - Giamaica 5
KE - Kenya 5
KG - Kirghizistan 5
NO - Norvegia 5
PT - Portogallo 5
PY - Paraguay 5
TN - Tunisia 5
AT - Austria 4
AZ - Azerbaigian 4
CZ - Repubblica Ceca 4
KR - Corea 4
SA - Arabia Saudita 4
DK - Danimarca 3
GR - Grecia 3
LB - Libano 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
PR - Porto Rico 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
LU - Lussemburgo 1
MK - Macedonia 1
RS - Serbia 1
TV - Tuvalu 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZW - Zimbabwe 1
Totale 8.260
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Città #
Singapore 716
Chandler 471
Wilmington 435
Ashburn 275
Dallas 220
San Jose 220
The Dalles 194
San Mateo 187
Shanghai 174
Helsinki 161
Ann Arbor 158
New York 127
Council Bluffs 119
Beijing 118
Dublin 109
Princeton 92
Milan 87
Lawrence 84
Benin City 81
Leawood 81
Boardman 79
Hong Kong 77
Ho Chi Minh City 69
Santa Clara 63
Paris 46
Fairfield 45
Hanoi 41
Los Angeles 40
Woodbridge 38
Amsterdam 37
Columbus 33
São Paulo 31
Seattle 28
Falkenstein 27
Rome 27
Orem 20
Toronto 20
Brussels 18
Buffalo 18
San Diego 17
Houston 16
Brooklyn 15
London 14
Montreal 14
Rio de Janeiro 13
Chennai 12
Da Nang 12
Phoenix 12
Warsaw 12
Abbiategrasso 11
Figino 11
Miami 11
Belo Horizonte 10
Cincinnati 10
Curitiba 10
Naples 10
Charlotte 9
Mumbai 9
Norwalk 9
Tempe 9
Chicago 8
Johannesburg 8
Philadelphia 8
Atlanta 7
Hanover 7
Manchester 7
Mexico City 7
Newark 7
Verona 7
Zurich 7
Amman 6
Brasília 6
Guangzhou 6
Monmouth Junction 6
South Bend 6
Tashkent 6
Austin 5
Baghdad 5
Biên Hòa 5
Bogotá 5
Cleveland 5
Dhaka 5
Haiphong 5
Hải Dương 5
Kocaeli 5
Lahore 5
Las Vegas 5
Quận Một 5
San Antonio 5
Stockholm 5
Tokyo 5
Uberlândia 5
Washington 5
Baku 4
Bishkek 4
Buenos Aires 4
Cairo 4
Caracas 4
Caxias do Sul 4
Des Moines 4
Totale 5.334
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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 167
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 146
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 139
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 138
Glucocerebrosidase mutations in primary parkinsonism 137
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest. 136
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs 135
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis. 135
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family 132
Tumor-derived prostaglandin E2 promotes p50 NF-κB-dependent differentiation of monocytic MDSC 130
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis. *Shared first authorship 128
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 125
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency 125
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 124
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes. *Corresponding author 123
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 119
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 118
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 118
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing. BMC Highly accessed paper 117
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 115
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 113
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 113
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years 113
The double-faced association of the PRKCA gene with multiple sclerosis 112
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 110
DNAJC12 and dopa-responsive nonprogressive parkinsonism 108
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 107
Survival and dementia in GBA-associated Parkinson's disease: The mutation matters 103
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis 101
4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy 101
Non-random retention of protein-coding overlapping genes in Metazoa. 99
Impact of prostate cancer screening in European ancestry un‐affected men with germline DNA repair pathogenic variants 96
Expression of distinct RNAs from 3' untranslated regions. *Shared first authorship (TRM, DW,MED,GS). 2010 NAR Featured Article (top 5% of papers) 95
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 95
X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases 94
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 93
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 93
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 92
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 91
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 91
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy 87
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 87
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 87
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 87
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 87
Response: Further thoughts on the "phantom" delta6/7 FXI isoform 86
In-depth characterization of breast cancer tumor-promoting cell transcriptome by RNA sequencing and microarrays 84
LIQUID BIOPSY BY PROSTATE-DERIVED TUMOR CELLS ENRICHED FROM SEMINAL FLUID (SF): THE SEMEN PROSTATE CANCER TUMOR ELEMENTS (SPECTRE) PROJECT. 84
Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer 82
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population 82
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 80
First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features 79
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson's disease 78
Geni sovrapposti in eucarioti superiori 78
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 76
Prospective evaluation of the role of imaging techniques and TMPRSS2:ERG mutation for the diagnosis of clinically significant prostate cancer 75
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation 74
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 74
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 73
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 72
Type II Mutation (Glu117stop) Causes Factor XI Deficiency By Inducing Allele Specific mRNA Degradation 72
Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer 72
Side-by-side comparison of next-generation sequencing, cytology, and histology in diagnosing locally advanced pancreatic adenocarcinoma 71
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 70
Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites 70
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 70
Evolution, identification and expression of noncoding RNAs in animals 69
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). 68
Massive Accumulation of Sphingomyelin Affects the Lysosomal and Mitochondria Compartments and Promotes Apoptosis in Niemann-Pick Disease Type A 68
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p. 67
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 67
Post-Biopsy Cell-Free DNA From Blood: An Open Window on Primary Prostate Cancer Genetics and Biology 65
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 65
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss 64
MiR-634: a new player in the pathogenesis of multiple sclerosis? 64
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson disease 64
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 64
Search for novel deafness genes by exome sequencing of autosomal recessive NSHL families 62
No association of GBA mutations and multiple system atrophy 61
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD 60
How I faced my prostate cancer: a molecular biologist's perspective 60
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 60
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear 59
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 59
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 58
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 56
Functional study of the tail-to-tail overlap between human neuronal nicotinic acetylcholine receptor CHRNA3 and CHRNA5 genes 54
Male awareness of prostate cancer risk remains poor in relatives of women with germline variants in DNA-repair genes 53
“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 52
Improving mRNA 5′ coding sequence determination in the mouse genome 50
SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa 49
Fine characterization of the recurrent c.1584 +18672 A>G deep-intronic mutation in the CFTR gene 47
Two novel splicing mutations in the OTUD6B gene associated with intellectual disability and seizures 32
Correcting CFTR mRNA splicing defects with the plant cytokine kinetin and its analogues 17
Applying artificial intelligence to uncover the genetic landscape of coagulation factors 16
Germline homologous recombination repair (gHRR) variants in bladder cancer: Preliminary evidence and clinical implications 13
Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severity 13
Functional characterisation of missense ceruloplasmin variants and real-world prevalence assessment of Aceruloplasminemia using population data 13
Genetics Influences Telomere Length in Parkinson's Disease: A Study in Monozygotic Discordant Twins 12
Lewy pathology formation in patient-derived GBA1 Parkinson’s disease midbrain organoids 11
Totale 8.356
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Categoria #
all - tutte 51.897
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 51.897
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022458 0 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
2024/20251.456 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
2026/2027503 270 233 0 0 0 0 0 0 0 0 0 0
Totale 8.366