IRIS
RICCI, CLAUDIA
 Distribuzione geografica
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Continente #
NA - Nord America 3.772
EU - Europa 3.335
AS - Asia 738
SA - Sud America 157
AF - Africa 31
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 4
Totale 8.045
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Nazione #
US - Stati Uniti d'America 3.754
GB - Regno Unito 1.073
IE - Irlanda 581
IT - Italia 362
CN - Cina 353
SE - Svezia 274
UA - Ucraina 259
RU - Federazione Russa 242
SG - Singapore 240
FR - Francia 154
DE - Germania 152
BR - Brasile 149
FI - Finlandia 114
TR - Turchia 75
NL - Olanda 28
ES - Italia 27
CI - Costa d'Avorio 23
BE - Belgio 19
VN - Vietnam 14
AT - Austria 13
CZ - Repubblica Ceca 13
CA - Canada 12
AU - Australia 8
HK - Hong Kong 6
IL - Israele 6
KR - Corea 6
IN - India 5
IR - Iran 5
IQ - Iraq 4
CH - Svizzera 3
EU - Europa 3
GR - Grecia 3
JP - Giappone 3
PH - Filippine 3
PK - Pakistan 3
SA - Arabia Saudita 3
TN - Tunisia 3
AR - Argentina 2
BD - Bangladesh 2
BO - Bolivia 2
DO - Repubblica Dominicana 2
EG - Egitto 2
JO - Giordania 2
LT - Lituania 2
MD - Moldavia 2
MK - Macedonia 2
MX - Messico 2
RO - Romania 2
ZA - Sudafrica 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
CR - Costa Rica 1
DK - Danimarca 1
EC - Ecuador 1
EE - Estonia 1
GE - Georgia 1
HR - Croazia 1
ID - Indonesia 1
JM - Giamaica 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LV - Lettonia 1
MA - Marocco 1
NO - Norvegia 1
OM - Oman 1
PE - Perù 1
PL - Polonia 1
PT - Portogallo 1
PY - Paraguay 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
UZ - Uzbekistan 1
VE - Venezuela 1
Totale 8.045
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Città #
Southend 1.007
Dublin 579
Fairfield 556
Chandler 319
Ashburn 298
Santa Clara 249
Wilmington 239
Jacksonville 212
Woodbridge 209
Seattle 204
Cambridge 196
Houston 189
Siena 153
Ann Arbor 136
Princeton 103
Singapore 97
Beijing 77
Nanjing 68
Izmir 59
New York 44
Helsinki 40
Menlo Park 40
Milan 40
Boardman 36
Council Bluffs 31
San Diego 31
The Dalles 30
Nanchang 29
Shanghai 29
Lappeenranta 28
San Mateo 28
Dearborn 27
Moscow 27
Abidjan 23
Málaga 22
Shenyang 22
Hebei 18
Los Angeles 18
Nuremberg 17
Fremont 16
Dong Ket 14
Florence 14
San Francisco 14
Brussels 12
Munich 12
Norwalk 12
Redwood City 10
Rome 10
São Paulo 10
Brno 9
Ningbo 9
Segrate 9
Changsha 8
Clifton 8
Dallas 8
London 8
Poggiomarino 8
Washington 8
Düsseldorf 7
Jiaxing 7
Kunming 7
Belo Horizonte 6
Guangzhou 6
Hong Kong 6
Lancaster 6
Tianjin 6
Turin 6
Vienna 6
Waanrode 6
Zhengzhou 6
Mestre 5
Toronto 5
Turku 5
Bonndorf 4
Curitiba 4
Hangzhou 4
Kocaeli 4
Lauterbourg 4
Misano Adriatico 4
Phoenix 4
Pontedera 4
Verona 4
Brasília 3
Brooklyn 3
Canberra 3
Edinburgh 3
Greifswald 3
Hefei 3
Jinan 3
Lodi 3
Maceió 3
Manaus 3
Manila 3
Montreal 3
Olomouc 3
Paris 3
Pisa 3
Pistoia 3
Portsmouth 3
Renton 3
Totale 5.909
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Nome #
C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease 257
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 243
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 215
MicroRNAs as Biomarkers in Amyotrophic Lateral Sclerosis 207
Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia 205
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 203
Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients 196
Genetic architecture of ALS in Sardinia 196
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 188
No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population 186
Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation 179
Impaired intracortical transmission in G2019S leucine rich-repeat kinase Parkinson patients 174
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 165
Antimicrobial activity of novel dendrimeric peptides obtained by phage display selection and rational modification. 164
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD 163
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 163
Variants in MCT10 protein do not affect FT3 levels in athyreotic patients 163
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype 154
Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene. 149
Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT5–8 Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC) 143
Biochemical filtering of a protein-protein docking simulation identifies the structure of a complex between a recombinant antibody fragment and alpha-bungarotoxin 142
D90A-SOD1 mutation in ALS: The first report of heterozigous Italian patients and unusual findings 138
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 135
Lack of association of PON polymorphisms with sporadic ALS in an Italian population 134
Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP Gene 129
null 128
A novel SOD1 gene mutation in a familial ALS patient 127
Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family. 127
null 124
Genetic Variations within Krit1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a Large Italian Family Harbouring a Krit1/CCM1 Mutation 123
Phage display and colony filter screening for high-throughput selection of antibody libraries 121
Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene 119
Strategies for the construction and use of peptide and antibody libraries displayed on phages. 119
Concern regarding classification of c.703G>A/p.Gly235Arg as a novel missense variant in KRIT1 gene 118
null 118
Analysis of regulatory regions of macrophage migration inhibitory factor (MIF) gene in Italian ALS patients 116
A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS 115
null 114
A new Krit1 gene mutation in a family with cerebral cavernous malformation (CCM) associated with intraorbital optic nerve and cutaneous cavernous angiomas 112
Paraoxonase gene polymorphisms and susceptibility to sporadic ALS in Italian population. Preliminary results. 110
Molecular genetic analysis of cerebral cavernous malformations: An update 108
Descrizione di una nuova mutazione del gene Krit1 in una forma familiare di angioma cavernoso cerebrale associata ad angioma ottico e ad angioma cutaneo 106
KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants 100
The” D90A” still an enigma among SOD1 gene mutations. Report of three italian cases. 97
Progestin regulation of 11beta-hydroxysteroid dehydrogenase expression in T-47D human breast cancer cells 94
Macrophage migration inhibitory factor inthe human endometrium: expression and localization during the menstrual cycle andearly pregnancy 94
Synthetic inhibitors of anthrax lethal toxin 93
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 92
A novel variant in superoxide dismutase 1 gene (P.V119M) in als patients with pure lower motor neuron presentation 90
Thr92Ala polymorphism in the type 2 deiodinase gene: an evolutionary perspective 87
Molecular genetic features of cerebral cavernous malformations (CCM) patients: An overall view from genes to endothelial cells 84
Proteomics Reveals How the Tardigrade Damage Suppressor Protein Teaches Transfected Human Cells to Survive UV-C Stress 82
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 82
STRONG SYNTHETIC INHIBITORS OF ANTHRAX LETHAL TOXIN 80
Phenotipic-genotypic study of amyothrophic lateral sclerosis Italian families with the G41S SOD1 gene mutation. 79
Mitigation of UV-B Radiation Stress in Tobacco Pollen by Expression of the Tardigrade Damage Suppressor Protein (Dsup) 77
miRNA Targets: From Prediction Tools to Experimental Validation 76
What's Wrong in a Jump? Prediction and Validation of Splice Site Variants 70
From Circulating Tumor Cells to Mirna: New Challenges in the Diagnosis and Prognosis of Medullary Thyroid Cancer 65
The tardigrade damage suppressor protein modulates transcription factor and DNA repair genes in human cells treated with hydroxyl radicals and UV-C 62
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 60
BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration 58
Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort 51
HFE p.H63D polymorphism does not influence ALS phenotype and survival 50
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations 46
Neurodegenerative Disease: From Molecular Basis to Therapy 23
Totale 8.188
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Categoria #
all - tutte 28.447
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 28.447
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020116 0 0 0 0 0 0 0 0 0 0 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
2024/20251.353 51 116 187 105 244 121 67 79 169 83 131 0
Totale 8.188