IRIS
SOLDA', GIULIA MARIA EMILIA ANTONIETTA
 Distribuzione geografica
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Continente #
NA - Nord America 2.426
EU - Europa 557
AS - Asia 260
AF - Africa 88
SA - Sud America 8
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 3.344
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Nazione #
US - Stati Uniti d'America 2.409
FI - Finlandia 161
SG - Singapore 136
IE - Irlanda 111
CN - Cina 92
NG - Nigeria 83
IT - Italia 58
DE - Germania 54
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
EG - Egitto 3
AR - Argentina 2
BR - Brasile 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
CZ - Repubblica Ceca 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
TH - Thailandia 1
Totale 3.344
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Città #
Chandler 484
Wilmington 444
San Mateo 190
Helsinki 161
Ann Arbor 160
Dublin 111
Shanghai 89
Singapore 89
New York 88
Lawrence 86
Princeton 86
Benin City 83
Leawood 83
Boardman 78
Fairfield 44
Paris 43
Woodbridge 41
Amsterdam 34
Ashburn 28
Milan 27
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
Santa Clara 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
Buenos Aires 2
Cambridge 2
Clearwater 2
Florence 2
Guangzhou 2
Hialeah 2
Lecco 2
Los Angeles 2
Lugano 2
Lyngby 2
Monza 2
Munich 2
Raleigh 2
Toba Tek Singh 2
Almaty 1
Athens 1
Basel 1
Bologna 1
Borås 1
Brno 1
Brookings 1
Casablanca 1
Casalecchio di Reno 1
Causeway Bay 1
Chisinau 1
Chuoku 1
Council Bluffs 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
Rome 1
Rotterdam 1
Saint Louis 1
Stanford 1
Vienna 1
Wantage 1
Zhengzhou 1
Totale 2.697
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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
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 66
Next-generation sequencing analysis of miRNA expression in control and FSHD myogenesis 66
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 65
Non-random retention of protein-coding overlapping genes in Metazoa. 62
Tumor-derived prostaglandin E2 promotes p50 NF-κB-dependent differentiation of monocytic MDSC 61
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 60
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 59
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 58
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 57
Expression of distinct RNAs from 3' untranslated regions. *Shared first authorship (TRM, DW,MED,GS). 2010 NAR Featured Article (top 5% of papers) 55
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis. *Shared first authorship 54
Response: Further thoughts on the "phantom" delta6/7 FXI isoform 51
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 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. 50
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 49
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 49
DNAJC12 and dopa-responsive nonprogressive parkinsonism 49
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing 49
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing. BMC Highly accessed paper 49
Glucocerebrosidase mutations in primary parkinsonism 48
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years 48
The double-faced association of the PRKCA gene with multiple sclerosis 47
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms 47
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis. 47
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
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
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy 43
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family 42
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes. *Corresponding author 42
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 42
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson's disease 41
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency 41
Geni sovrapposti in eucarioti superiori 41
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
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator gene 40
In-depth characterization of breast cancer tumor-promoting cell transcriptome by RNA sequencing and microarrays 40
Role of the microRNA-183 family in the pathogenesis of hereditary nonsyndromic hearing loss in the Italian population 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
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency 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
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
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 35
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 34
A new class of non-coding RNAs associated with 3’ untranslated regions of mRNAs 34
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 34
The Asp620Asn mutation in VPS35 is not a common cause of familial Parkinson disease 34
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 33
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
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 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
First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features 32
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing 31
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss 31
Improving mRNA 5′ coding sequence determination in the mouse genome 30
Regulated independent expression of 3' untranslated regions in mammals 29
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 26
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss 25
MiR-634: a new player in the pathogenesis of multiple sclerosis? 24
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 24
Search for novel deafness genes by exome sequencing of autosomal recessive NSHL families 24
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 24
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
Prospective evaluation of the role of imaging techniques and TMPRSS2:ERG mutation for the diagnosis of clinically significant prostate cancer 19
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema) 18
null 17
Massive Accumulation of Sphingomyelin Affects the Lysosomal and Mitochondria Compartments and Promotes Apoptosis in Niemann-Pick Disease Type A 17
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD 16
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
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear 12
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 12
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 11
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 11
Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer 1
Totale 3.429
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Categoria #
all - tutte 26.305
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 26.305
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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
2023/2024710 79 73 127 34 23 100 43 36 13 8 76 98
2024/202533 33 0 0 0 0 0 0 0 0 0 0 0
Totale 3.429