IRIS
SOLDA', GIULIA MARIA EMILIA ANTONIETTA
 Distribuzione geografica
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Continente #
NA - Nord America 2.376
EU - Europa 551
AS - Asia 110
AF - Africa 87
SA - Sud America 6
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 3.135
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Nazione #
US - Stati Uniti d'America 2.359
FI - Finlandia 161
IE - Irlanda 111
NG - Nigeria 83
CN - Cina 77
IT - Italia 55
DE - Germania 52
FR - Francia 43
NL - Olanda 35
SE - Svezia 29
GB - Regno Unito 19
BE - Belgio 16
CA - Canada 16
HK - Hong Kong 8
IL - Israele 8
CH - Svizzera 7
IN - India 5
TR - Turchia 5
UA - Ucraina 5
CL - Cile 4
AT - Austria 3
AU - Australia 3
DK - Danimarca 3
BR - Brasile 2
EG - Egitto 2
GR - Grecia 2
JP - Giappone 2
NO - Norvegia 2
PK - Pakistan 2
RU - Federazione Russa 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
DZ - Algeria 1
ES - Italia 1
EU - Europa 1
KZ - Kazakistan 1
MA - Marocco 1
MD - Moldavia 1
MK - Macedonia 1
MX - Messico 1
PL - Polonia 1
RO - Romania 1
SG - Singapore 1
TH - Thailandia 1
Totale 3.135
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Città #
Chandler 484
Wilmington 444
San Mateo 190
Helsinki 161
Ann Arbor 160
Dublin 111
New York 88
Lawrence 86
Princeton 86
Benin City 83
Leawood 83
Shanghai 74
Boardman 67
Fairfield 44
Paris 43
Woodbridge 41
Amsterdam 34
Ashburn 28
Milan 26
Seattle 18
Brussels 16
San Diego 15
London 13
Toronto 13
Abbiategrasso 11
Norwalk 9
Hanover 8
Hong Kong 7
Houston 7
Monmouth Junction 6
Falkenstein 5
Kocaeli 5
Phoenix 5
Des Moines 4
Gunzenhausen 4
Pune 4
Redmond 4
Tappahannock 4
Falls Church 3
Redwood City 3
Waxhaw 3
Winnipeg 3
Zurich 3
Bonn 2
Brierley Hill 2
Cambridge 2
Clearwater 2
Florence 2
Guangzhou 2
Hialeah 2
Lecco 2
Lugano 2
Lyngby 2
Monza 2
Raleigh 2
Toba Tek Singh 2
Almaty 1
Athens 1
Basel 1
Bologna 1
Borås 1
Brookings 1
Casablanca 1
Causeway Bay 1
Chisinau 1
Chuoku 1
Cupertino 1
Gaylord 1
Greifswald 1
Henderson 1
Jena 1
Kemerovo 1
La Canada Flintridge 1
Logan 1
Modesto 1
Muenster 1
Mumbai 1
Newark 1
Ocala 1
Oslo 1
Oxford 1
Penrith 1
Reghin 1
Rotterdam 1
Saint Louis 1
Santa Clara 1
Stanford 1
Vienna 1
Wantage 1
Zhengzhou 1
Totale 2.566
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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 82
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis 64
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 58
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 58
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 57
Tumor-derived prostaglandin E2 promotes p50 NF-κB-dependent differentiation of monocytic MDSC 57
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 56
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 56
Non-random retention of protein-coding overlapping genes in Metazoa. 54
Expression of distinct RNAs from 3' untranslated regions. *Shared first authorship (TRM, DW,MED,GS). 2010 NAR Featured Article (top 5% of papers) 54
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 54
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis. *Shared first authorship 50
Response: Further thoughts on the "phantom" delta6/7 FXI isoform 49
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 49
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 48
DNAJC12 and dopa-responsive nonprogressive parkinsonism 48
4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy 48
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest. 48
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing. BMC Highly accessed paper 48
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 47
The double-faced association of the PRKCA gene with multiple sclerosis 46
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis. 46
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 45
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years 45
Glucocerebrosidase mutations in primary parkinsonism 44
Not only cancer: the long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis. 44
LIQUID BIOPSY BY PROSTATE-DERIVED TUMOR CELLS ENRICHED FROM SEMINAL FLUID (SF): THE SEMEN PROSTATE CANCER TUMOR ELEMENTS (SPECTRE) PROJECT. 43
Evolution, identification and expression of noncoding RNAs in animals 42
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 42
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family 41
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 41
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes. *Corresponding author 41
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 41
Geni sovrapposti in eucarioti superiori 40
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy 39
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson's disease 39
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 39
In-depth characterization of breast cancer tumor-promoting cell transcriptome by RNA sequencing and microarrays 39
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA 39
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation 38
Characterization of Long Noncoding RNAs Associated with Developmental Genes in Vertebrates 38
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 38
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population 36
Type II Mutation (Glu117stop) Causes Factor XI Deficiency By Inducing Allele Specific mRNA Degradation 36
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 36
Survival and dementia in GBA-associated Parkinson's disease: The mutation matters 36
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency 36
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p. 34
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 34
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 33
X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases 33
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 32
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 32
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). 32
First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features 32
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 32
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 32
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 32
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson disease 32
No association of GBA mutations and multiple system atrophy 31
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs 30
Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites 30
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 28
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 28
Improving mRNA 5′ coding sequence determination in the mouse genome 27
Regulated independent expression of 3' untranslated regions in mammals 27
Functional study of the tail-to-tail overlap between human neuronal nicotinic acetylcholine receptor CHRNA3 and CHRNA5 genes 26
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 26
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 25
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss 24
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 23
Side-by-side comparison of next-generation sequencing, cytology, and histology in diagnosing locally advanced pancreatic adenocarcinoma 23
MiR-634: a new player in the pathogenesis of multiple sclerosis? 22
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 22
Search for novel deafness genes by exome sequencing of autosomal recessive NSHL families 22
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 22
Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer 22
“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 20
null 17
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 17
Prospective evaluation of the role of imaging techniques and TMPRSS2:ERG mutation for the diagnosis of clinically significant prostate cancer 17
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 16
Massive Accumulation of Sphingomyelin Affects the Lysosomal and Mitochondria Compartments and Promotes Apoptosis in Niemann-Pick Disease Type A 16
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD 15
SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa 13
How I faced my prostate cancer: a molecular biologist's perspective 13
Post-Biopsy Cell-Free DNA From Blood: An Open Window on Primary Prostate Cancer Genetics and Biology 12
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 11
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 10
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 10
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear 9
Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer 1
Totale 3.220
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Categoria #
all - tutte 23.353
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 23.353
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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
2022/20231.312 195 68 106 159 126 109 3 110 213 103 98 22
2023/2024534 79 73 127 34 23 100 43 36 13 6 0 0
Totale 3.220