IRIS
RICCI, CLAUDIA
 Distribuzione geografica
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Continente #
NA - Nord America 3.350
EU - Europa 2.990
AS - Asia 492
AF - Africa 24
OC - Oceania 8
SA - Sud America 6
Continente sconosciuto - Info sul continente non disponibili 4
Totale 6.874
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Nazione #
US - Stati Uniti d'America 3.341
GB - Regno Unito 1.063
IE - Irlanda 580
CN - Cina 325
IT - Italia 289
SE - Svezia 270
UA - Ucraina 259
FR - Francia 146
DE - Germania 117
FI - Finlandia 100
RU - Federazione Russa 84
TR - Turchia 71
SG - Singapore 52
ES - Italia 25
CI - Costa d'Avorio 23
BE - Belgio 19
VN - Vietnam 14
NL - Olanda 12
CZ - Repubblica Ceca 11
CA - Canada 9
AU - Australia 8
IL - Israele 6
KR - Corea 6
IR - Iran 5
IN - India 4
BR - Brasile 3
EU - Europa 3
SA - Arabia Saudita 3
GR - Grecia 2
HK - Hong Kong 2
JP - Giappone 2
MD - Moldavia 2
MK - Macedonia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AT - Austria 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CH - Svizzera 1
DK - Danimarca 1
EC - Ecuador 1
HR - Croazia 1
KZ - Kazakistan 1
PE - Perù 1
PL - Polonia 1
PT - Portogallo 1
RO - Romania 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
TN - Tunisia 1
Totale 6.874
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Città #
Southend 1.007
Dublin 578
Fairfield 556
Chandler 319
Ashburn 292
Wilmington 239
Jacksonville 212
Woodbridge 209
Seattle 204
Cambridge 196
Houston 189
Siena 145
Ann Arbor 136
Princeton 103
Beijing 76
Nanjing 68
Izmir 58
Menlo Park 40
Helsinki 36
New York 36
Boardman 35
Singapore 32
San Diego 31
Nanchang 29
Shanghai 29
San Mateo 28
Dearborn 27
Moscow 26
Abidjan 23
Lappeenranta 23
Málaga 22
Shenyang 21
Hebei 18
Fremont 16
Dong Ket 14
Florence 14
San Francisco 14
Brussels 12
Milan 12
Norwalk 12
Redwood City 10
Brno 9
Segrate 9
Changsha 8
Dallas 8
Ningbo 8
Rome 8
Jiaxing 7
Kunming 7
Los Angeles 7
Washington 7
Lancaster 6
Waanrode 6
Guangzhou 5
Mestre 5
Munich 5
Tianjin 5
Zhengzhou 5
Bonndorf 4
Clifton 4
Hangzhou 4
Kocaeli 4
Misano Adriatico 4
Canberra 3
Council Bluffs 3
Düsseldorf 3
Edinburgh 3
Hefei 3
Jinan 3
Lodi 3
London 3
Nuremberg 3
Paris 3
Pisa 3
Renton 3
San Antonio 3
Sydney 3
Tappahannock 3
Toronto 3
Vancouver 3
Verona 3
Acton 2
Albignasego 2
Amsterdam 2
Atlanta 2
Baotou 2
Barcelona 2
Bergamo 2
Boston 2
Bursa 2
Castelfiorentino 2
Chicago 2
Corridonia 2
Fuzhou 2
Giessen 2
Haikou 2
Hong Kong 2
Jeddah 2
Lanzhou 2
Melbourne 2
Totale 5.374
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Nome #
C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease 238
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 229
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 203
MicroRNAs as Biomarkers in Amyotrophic Lateral Sclerosis 184
Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia 183
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 182
Genetic architecture of ALS in Sardinia 182
Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients 181
No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population 174
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 168
Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation 167
Impaired intracortical transmission in G2019S leucine rich-repeat kinase Parkinson patients 161
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 157
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 151
Antimicrobial activity of novel dendrimeric peptides obtained by phage display selection and rational modification. 143
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD 142
Variants in MCT10 protein do not affect FT3 levels in athyreotic patients 137
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype 135
Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene. 133
null 128
Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT5–8 Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC) 127
D90A-SOD1 mutation in ALS: The first report of heterozigous Italian patients and unusual findings 127
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 124
null 124
Biochemical filtering of a protein-protein docking simulation identifies the structure of a complex between a recombinant antibody fragment and alpha-bungarotoxin 122
Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP Gene 120
null 118
Lack of association of PON polymorphisms with sporadic ALS in an Italian population 116
Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family. 116
null 114
Phage display and colony filter screening for high-throughput selection of antibody libraries 112
Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene 111
Genetic Variations within Krit1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a Large Italian Family Harbouring a Krit1/CCM1 Mutation 110
A novel SOD1 gene mutation in a familial ALS patient 109
Strategies for the construction and use of peptide and antibody libraries displayed on phages. 108
Concern regarding classification of c.703G>A/p.Gly235Arg as a novel missense variant in KRIT1 gene 104
Analysis of regulatory regions of macrophage migration inhibitory factor (MIF) gene in Italian ALS patients 99
Paraoxonase gene polymorphisms and susceptibility to sporadic ALS in Italian population. Preliminary results. 97
A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS 95
A new Krit1 gene mutation in a family with cerebral cavernous malformation (CCM) associated with intraorbital optic nerve and cutaneous cavernous angiomas 93
The” D90A” still an enigma among SOD1 gene mutations. Report of three italian cases. 88
Descrizione di una nuova mutazione del gene Krit1 in una forma familiare di angioma cavernoso cerebrale associata ad angioma ottico e ad angioma cutaneo 85
Synthetic inhibitors of anthrax lethal toxin 84
Progestin regulation of 11beta-hydroxysteroid dehydrogenase expression in T-47D human breast cancer cells 81
Macrophage migration inhibitory factor inthe human endometrium: expression and localization during the menstrual cycle andearly pregnancy 79
Phenotipic-genotypic study of amyothrophic lateral sclerosis Italian families with the G41S SOD1 gene mutation. 72
Molecular genetic analysis of cerebral cavernous malformations: An update 68
STRONG SYNTHETIC INHIBITORS OF ANTHRAX LETHAL TOXIN 67
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 66
Thr92Ala polymorphism in the type 2 deiodinase gene: an evolutionary perspective 64
A novel variant in superoxide dismutase 1 gene (P.V119M) in als patients with pure lower motor neuron presentation 62
KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants 62
Molecular genetic features of cerebral cavernous malformations (CCM) patients: An overall view from genes to endothelial cells 56
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 54
What's Wrong in a Jump? Prediction and Validation of Splice Site Variants. 48
Proteomics Reveals How the Tardigrade Damage Suppressor Protein Teaches Transfected Human Cells to Survive UV-C Stress 45
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 42
miRNA Targets: From Prediction Tools to Experimental Validation 41
HFE p.H63D polymorphism does not influence ALS phenotype and survival 36
The tardigrade damage suppressor protein modulates transcription factor and DNA repair genes in human cells treated with hydroxyl radicals and UV-C 34
Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort 34
From Circulating Tumor Cells to Mirna: New Challenges in the Diagnosis and Prognosis of Medullary Thyroid Cancer 33
BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration 31
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations 24
Mitigation of UV-B Radiation Stress in Tobacco Pollen by Expression of the Tardigrade Damage Suppressor Protein (Dsup) 13
Neurodegenerative Disease: From Molecular Basis to Therapy 10
Totale 7.003
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Categoria #
all - tutte 22.613
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 22.613
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.188 0 0 84 217 96 118 123 179 143 112 31 85
2020/20211.198 65 154 41 109 71 109 79 217 134 83 81 55
2021/2022783 49 73 44 56 26 35 71 41 31 80 104 173
2022/20231.084 68 102 163 140 111 213 7 91 99 26 36 28
2023/2024966 22 22 87 68 28 238 324 35 6 37 17 82
2024/2025168 51 116 1 0 0 0 0 0 0 0 0 0
Totale 7.003