IRIS
SOLDA', GIULIA MARIA EMILIA ANTONIETTA
 Distribuzione geografica
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Continente #
NA - Nord America 2.465
EU - Europa 571
AS - Asia 378
AF - Africa 88
SA - Sud America 23
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 3.530
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Nazione #
US - Stati Uniti d'America 2.448
SG - Singapore 230
FI - Finlandia 162
IE - Irlanda 112
CN - Cina 106
NG - Nigeria 83
IT - Italia 63
DE - Germania 60
FR - Francia 43
NL - Olanda 35
SE - Svezia 29
GB - Regno Unito 19
BE - Belgio 17
CA - Canada 16
BR - Brasile 14
HK - Hong Kong 8
IL - Israele 8
CH - Svizzera 7
IN - India 5
TR - Turchia 5
UA - Ucraina 5
CL - Cile 4
IR - Iran 4
AT - Austria 3
AU - Australia 3
DK - Danimarca 3
EG - Egitto 3
JP - Giappone 3
AR - Argentina 2
EC - Ecuador 2
GR - Grecia 2
NO - Norvegia 2
PK - Pakistan 2
RU - Federazione Russa 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
BD - Bangladesh 1
BH - Bahrain 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
ES - Italia 1
EU - Europa 1
IQ - Iraq 1
KZ - Kazakistan 1
MA - Marocco 1
MD - Moldavia 1
MK - Macedonia 1
MX - Messico 1
MY - Malesia 1
PE - Perù 1
PL - Polonia 1
RO - Romania 1
TH - Thailandia 1
UZ - Uzbekistan 1
Totale 3.530
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Città #
Chandler 484
Wilmington 444
San Mateo 190
Helsinki 162
Ann Arbor 160
Singapore 125
Dublin 112
New York 89
Shanghai 89
Lawrence 86
Princeton 86
Benin City 83
Leawood 83
Boardman 79
Fairfield 44
Paris 43
Woodbridge 41
Ashburn 40
Amsterdam 34
Milan 28
Seattle 23
Brussels 17
San Diego 15
London 13
Toronto 13
Abbiategrasso 11
Norwalk 9
Tempe 9
Hanover 8
Hong Kong 7
Houston 7
Monmouth Junction 6
Phoenix 6
Santa Clara 6
Falkenstein 5
Kocaeli 5
Des Moines 4
Gunzenhausen 4
Pune 4
Redmond 4
Tappahannock 4
Cologno Monzese 3
Falls Church 3
Guangzhou 3
Munich 3
Redwood City 3
Waxhaw 3
Winnipeg 3
Zurich 3
Bonn 2
Brierley Hill 2
Buenos Aires 2
Cambridge 2
Clearwater 2
Florence 2
Hialeah 2
Lecco 2
Los Angeles 2
Lugano 2
Lyngby 2
Monza 2
Raleigh 2
Shenzhen 2
São Paulo 2
Toba Tek Singh 2
Almaty 1
Athens 1
Basel 1
Belém 1
Bologna 1
Borås 1
Brasília 1
Brno 1
Brookings 1
Caieiras 1
Casablanca 1
Casalecchio di Reno 1
Causeway Bay 1
Chisinau 1
Chuoku 1
Council Bluffs 1
Cupertino 1
Feijó Municipality 1
Fuzhou 1
Gaylord 1
Greifswald 1
Guayaquil 1
Henderson 1
Ibarra 1
Iúna 1
Jena 1
Kemerovo 1
Kuala Lumpur 1
La Canada Flintridge 1
Lima 1
Linyi 1
Logan 1
Manama 1
Modesto 1
Muenster 1
Totale 2.773
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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 83
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 72
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 70
Glucocerebrosidase mutations in primary parkinsonism 70
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family 69
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis 66
Non-random retention of protein-coding overlapping genes in Metazoa. 66
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis. 62
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 61
Tumor-derived prostaglandin E2 promotes p50 NF-κB-dependent differentiation of monocytic MDSC 61
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 60
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 60
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 58
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis. *Shared first authorship 57
Expression of distinct RNAs from 3' untranslated regions. *Shared first authorship (TRM, DW,MED,GS). 2010 NAR Featured Article (top 5% of papers) 56
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes. *Corresponding author 55
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 52
The double-faced association of the PRKCA gene with multiple sclerosis 52
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 52
Response: Further thoughts on the "phantom" delta6/7 FXI isoform 51
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 51
4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy 51
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest. 51
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 50
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 50
DNAJC12 and dopa-responsive nonprogressive parkinsonism 49
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing. BMC Highly accessed paper 49
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 48
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years 48
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 46
LIQUID BIOPSY BY PROSTATE-DERIVED TUMOR CELLS ENRICHED FROM SEMINAL FLUID (SF): THE SEMEN PROSTATE CANCER TUMOR ELEMENTS (SPECTRE) PROJECT. 45
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy 44
Evolution, identification and expression of noncoding RNAs in animals 44
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 44
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 43
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs 43
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson's disease 42
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 42
Geni sovrapposti in eucarioti superiori 42
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 42
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 41
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation 40
In-depth characterization of breast cancer tumor-promoting cell transcriptome by RNA sequencing and microarrays 40
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency 40
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population 39
Characterization of Long Noncoding RNAs Associated with Developmental Genes in Vertebrates 39
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p. 38
Type II Mutation (Glu117stop) Causes Factor XI Deficiency By Inducing Allele Specific mRNA Degradation 38
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 37
Survival and dementia in GBA-associated Parkinson's disease: The mutation matters 37
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 37
X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases 37
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 36
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 36
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson disease 35
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 34
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 34
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 34
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). 33
First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features 33
No association of GBA mutations and multiple system atrophy 33
Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites 33
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 32
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 31
Improving mRNA 5′ coding sequence determination in the mouse genome 30
Regulated independent expression of 3' untranslated regions in mammals 30
Functional study of the tail-to-tail overlap between human neuronal nicotinic acetylcholine receptor CHRNA3 and CHRNA5 genes 28
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 28
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 27
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 27
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 27
MiR-634: a new player in the pathogenesis of multiple sclerosis? 26
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss 25
Search for novel deafness genes by exome sequencing of autosomal recessive NSHL families 25
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 25
Side-by-side comparison of next-generation sequencing, cytology, and histology in diagnosing locally advanced pancreatic adenocarcinoma 24
Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer 23
“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 22
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 21
Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer 20
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 19
Prospective evaluation of the role of imaging techniques and TMPRSS2:ERG mutation for the diagnosis of clinically significant prostate cancer 19
Massive Accumulation of Sphingomyelin Affects the Lysosomal and Mitochondria Compartments and Promotes Apoptosis in Niemann-Pick Disease Type A 18
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear 17
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD 17
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 15
SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa 15
How I faced my prostate cancer: a molecular biologist's perspective 15
Post-Biopsy Cell-Free DNA From Blood: An Open Window on Primary Prostate Cancer Genetics and Biology 14
Fine characterization of the recurrent c.1584 +18672 A>G deep-intronic mutation in the CFTR gene 12
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 12
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 12
Male awareness of prostate cancer risk remains poor in relatives of women with germline variants in DNA-repair genes 5
Totale 3.622
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Categoria #
all - tutte 30.799
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 30.799
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20207 0 0 0 0 0 0 0 0 0 0 0 7
2020/2021889 8 15 6 7 11 271 134 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
2024/2025212 45 44 23 36 64 0 0 0 0 0 0 0
Totale 3.622