IRIS
RICCI, CLAUDIA
 Distribuzione geografica
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Continente #
NA - Nord America 3.669
EU - Europa 3.207
AS - Asia 598
AF - Africa 26
OC - Oceania 8
SA - Sud America 7
Continente sconosciuto - Info sul continente non disponibili 4
Totale 7.519
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Nazione #
US - Stati Uniti d'America 3.657
GB - Regno Unito 1.067
IE - Irlanda 581
CN - Cina 352
IT - Italia 321
SE - Svezia 272
UA - Ucraina 259
RU - Federazione Russa 239
FR - Francia 146
DE - Germania 125
SG - Singapore 124
FI - Finlandia 109
TR - Turchia 71
ES - Italia 26
CI - Costa d'Avorio 23
BE - Belgio 19
VN - Vietnam 14
NL - Olanda 13
CA - Canada 11
CZ - Repubblica Ceca 11
AU - Australia 8
IL - Israele 6
KR - Corea 6
IR - Iran 5
IN - India 4
BR - Brasile 3
EU - Europa 3
JP - Giappone 3
SA - Arabia Saudita 3
BO - Bolivia 2
CH - Svizzera 2
EG - Egitto 2
GR - Grecia 2
HK - Hong Kong 2
LT - Lituania 2
MD - Moldavia 2
MK - Macedonia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AT - Austria 1
BN - Brunei Darussalam 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EC - Ecuador 1
HR - Croazia 1
ID - Indonesia 1
KG - Kirghizistan 1
KZ - Kazakistan 1
NO - Norvegia 1
PE - Perù 1
PH - Filippine 1
PK - Pakistan 1
PL - Polonia 1
PT - Portogallo 1
RO - Romania 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
TN - Tunisia 1
UZ - Uzbekistan 1
Totale 7.519
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Città #
Southend 1.007
Dublin 579
Fairfield 556
Chandler 319
Ashburn 297
Santa Clara 249
Wilmington 239
Jacksonville 212
Woodbridge 209
Seattle 204
Cambridge 196
Houston 189
Siena 153
Ann Arbor 136
Princeton 103
Singapore 94
Beijing 77
Nanjing 68
Izmir 58
New York 41
Helsinki 40
Menlo Park 40
Boardman 35
San Diego 31
Nanchang 29
Shanghai 29
Lappeenranta 28
San Mateo 28
Dearborn 27
Moscow 26
Abidjan 23
Málaga 22
Shenyang 22
Milan 21
Hebei 18
Fremont 16
Dong Ket 14
Florence 14
San Francisco 14
Los Angeles 13
Brussels 12
Norwalk 12
Redwood City 10
Brno 9
Ningbo 9
Segrate 9
Changsha 8
Clifton 8
Dallas 8
Munich 8
Rome 8
Jiaxing 7
Kunming 7
Washington 7
Guangzhou 6
Lancaster 6
London 6
Tianjin 6
Turin 6
Waanrode 6
Council Bluffs 5
Mestre 5
Toronto 5
Zhengzhou 5
Bonndorf 4
Hangzhou 4
Kocaeli 4
Misano Adriatico 4
Pontedera 4
Canberra 3
Düsseldorf 3
Edinburgh 3
Hefei 3
Jinan 3
Lodi 3
Nuremberg 3
Paris 3
Pisa 3
Renton 3
San Antonio 3
Sydney 3
Tappahannock 3
Vancouver 3
Verona 3
Acton 2
Albignasego 2
Amsterdam 2
Atlanta 2
Baoding 2
Baotou 2
Barcelona 2
Bergamo 2
Boston 2
Brooklyn 2
Bursa 2
Cairo 2
Castelfiorentino 2
Chicago 2
Columbus 2
Corridonia 2
Totale 5.751
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Nome #
C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease 247
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 237
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 210
MicroRNAs as Biomarkers in Amyotrophic Lateral Sclerosis 198
Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia 193
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 190
Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients 189
Genetic architecture of ALS in Sardinia 187
No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population 183
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 178
Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation 172
Impaired intracortical transmission in G2019S leucine rich-repeat kinase Parkinson patients 168
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 162
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 159
Antimicrobial activity of novel dendrimeric peptides obtained by phage display selection and rational modification. 156
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD 152
Variants in MCT10 protein do not affect FT3 levels in athyreotic patients 151
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype 145
Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene. 142
Biochemical filtering of a protein-protein docking simulation identifies the structure of a complex between a recombinant antibody fragment and alpha-bungarotoxin 135
Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT5–8 Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC) 135
D90A-SOD1 mutation in ALS: The first report of heterozigous Italian patients and unusual findings 133
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 131
null 128
Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP Gene 126
Lack of association of PON polymorphisms with sporadic ALS in an Italian population 125
null 124
Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family. 123
A novel SOD1 gene mutation in a familial ALS patient 121
Phage display and colony filter screening for high-throughput selection of antibody libraries 118
null 118
Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene 117
Genetic Variations within Krit1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a Large Italian Family Harbouring a Krit1/CCM1 Mutation 116
null 114
Strategies for the construction and use of peptide and antibody libraries displayed on phages. 114
Concern regarding classification of c.703G>A/p.Gly235Arg as a novel missense variant in KRIT1 gene 112
Analysis of regulatory regions of macrophage migration inhibitory factor (MIF) gene in Italian ALS patients 110
A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS 106
Paraoxonase gene polymorphisms and susceptibility to sporadic ALS in Italian population. Preliminary results. 105
A new Krit1 gene mutation in a family with cerebral cavernous malformation (CCM) associated with intraorbital optic nerve and cutaneous cavernous angiomas 104
The” D90A” still an enigma among SOD1 gene mutations. Report of three italian cases. 96
Descrizione di una nuova mutazione del gene Krit1 in una forma familiare di angioma cavernoso cerebrale associata ad angioma ottico e ad angioma cutaneo 95
Synthetic inhibitors of anthrax lethal toxin 91
Progestin regulation of 11beta-hydroxysteroid dehydrogenase expression in T-47D human breast cancer cells 89
Macrophage migration inhibitory factor inthe human endometrium: expression and localization during the menstrual cycle andearly pregnancy 88
Molecular genetic analysis of cerebral cavernous malformations: An update 86
Thr92Ala polymorphism in the type 2 deiodinase gene: an evolutionary perspective 81
KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants 79
Phenotipic-genotypic study of amyothrophic lateral sclerosis Italian families with the G41S SOD1 gene mutation. 78
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 78
A novel variant in superoxide dismutase 1 gene (P.V119M) in als patients with pure lower motor neuron presentation 74
STRONG SYNTHETIC INHIBITORS OF ANTHRAX LETHAL TOXIN 73
Molecular genetic features of cerebral cavernous malformations (CCM) patients: An overall view from genes to endothelial cells 70
miRNA Targets: From Prediction Tools to Experimental Validation 68
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 67
Proteomics Reveals How the Tardigrade Damage Suppressor Protein Teaches Transfected Human Cells to Survive UV-C Stress 66
What's Wrong in a Jump? Prediction and Validation of Splice Site Variants 63
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 52
BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration 47
From Circulating Tumor Cells to Mirna: New Challenges in the Diagnosis and Prognosis of Medullary Thyroid Cancer 47
Mitigation of UV-B Radiation Stress in Tobacco Pollen by Expression of the Tardigrade Damage Suppressor Protein (Dsup) 47
The tardigrade damage suppressor protein modulates transcription factor and DNA repair genes in human cells treated with hydroxyl radicals and UV-C 46
HFE p.H63D polymorphism does not influence ALS phenotype and survival 45
Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort 42
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations 36
Neurodegenerative Disease: From Molecular Basis to Therapy 18
Totale 7.656
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Categoria #
all - tutte 25.213
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 25.213
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020791 0 0 0 0 0 118 123 179 143 112 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
2024/2025821 51 116 187 105 244 118 0 0 0 0 0 0
Totale 7.656