IRIS
RICCI, CLAUDIA
 Distribuzione geografica
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Continente #
NA - Nord America 5.767
EU - Europa 4.743
AS - Asia 2.294
SA - Sud America 370
AF - Africa 148
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 5
Totale 13.335
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Nazione #
US - Stati Uniti d'America 5.683
GB - Regno Unito 1.133
RU - Federazione Russa 897
IT - Italia 763
CN - Cina 762
SG - Singapore 705
IE - Irlanda 585
BR - Brasile 314
SE - Svezia 286
UA - Ucraina 270
FR - Francia 233
VN - Vietnam 218
DE - Germania 216
HK - Hong Kong 188
FI - Finlandia 155
KR - Corea 95
TR - Turchia 90
ZA - Sudafrica 78
IN - India 60
NL - Olanda 54
CA - Canada 45
ES - Italia 40
BD - Bangladesh 32
CI - Costa d'Avorio 25
MX - Messico 23
JP - Giappone 22
PL - Polonia 22
BE - Belgio 20
PK - Pakistan 20
AR - Argentina 19
IQ - Iraq 18
AT - Austria 16
SA - Arabia Saudita 16
CZ - Repubblica Ceca 13
NG - Nigeria 13
TN - Tunisia 9
AU - Australia 8
CO - Colombia 8
EC - Ecuador 8
IL - Israele 8
JO - Giordania 8
UZ - Uzbekistan 8
VE - Venezuela 8
EG - Egitto 7
IR - Iran 7
CH - Svizzera 6
PH - Filippine 6
KE - Kenya 5
LT - Lituania 5
AL - Albania 4
CL - Cile 4
CR - Costa Rica 4
GR - Grecia 4
BO - Bolivia 3
EU - Europa 3
ID - Indonesia 3
KZ - Kazakistan 3
MD - Moldavia 3
MY - Malesia 3
PY - Paraguay 3
RO - Romania 3
TH - Thailandia 3
AZ - Azerbaigian 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GE - Georgia 2
HR - Croazia 2
LB - Libano 2
LY - Libia 2
MA - Marocco 2
MK - Macedonia 2
NP - Nepal 2
PE - Perù 2
RS - Serbia 2
SV - El Salvador 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AO - Angola 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BS - Bahamas 1
BY - Bielorussia 1
CG - Congo 1
DK - Danimarca 1
DM - Dominica 1
EE - Estonia 1
ET - Etiopia 1
GA - Gabon 1
GT - Guatemala 1
JM - Giamaica 1
KG - Kirghizistan 1
KH - Cambogia 1
LV - Lettonia 1
MM - Myanmar 1
MN - Mongolia 1
MT - Malta 1
NI - Nicaragua 1
NO - Norvegia 1
OM - Oman 1
Totale 13.324
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Città #
Southend 1.007
Dallas 634
Dublin 581
Fairfield 556
Ashburn 460
Singapore 385
Chandler 319
San Jose 295
Moscow 280
Santa Clara 270
Wilmington 239
Milan 218
Jacksonville 212
Woodbridge 209
Seattle 207
Houston 198
Cambridge 196
Beijing 183
Hong Kong 183
Siena 153
Ann Arbor 136
Hefei 118
Council Bluffs 106
Princeton 104
The Dalles 92
Seoul 88
Los Angeles 86
New York 79
Johannesburg 73
Nanjing 68
Izmir 59
Helsinki 57
Hanoi 54
Lauterbourg 54
Rome 54
Ho Chi Minh City 52
Munich 51
Menlo Park 40
Boardman 37
Buffalo 33
Shanghai 33
San Diego 32
Lappeenranta 30
Nanchang 29
San Mateo 28
Dearborn 27
São Paulo 27
Turku 27
Abidjan 25
San Francisco 24
Turin 24
Columbus 23
Málaga 23
Shenyang 23
Brooklyn 22
Orem 22
Florence 21
Warsaw 20
Atlanta 19
Frankfurt am Main 19
Montreal 19
Hebei 18
Nuremberg 18
Tokyo 18
Fremont 16
London 15
Changsha 14
Dong Ket 14
Figino 14
Naples 14
Abuja 13
Bengaluru 13
Chennai 13
Da Nang 13
Denver 13
Brussels 12
Chicago 12
Manchester 12
Norwalk 12
Amsterdam 11
Boston 11
Phoenix 11
Poplar 11
Redondo Beach 11
Stockholm 11
Belo Horizonte 10
Ningbo 10
Paris 10
Redwood City 10
Toronto 10
Brno 9
Kunming 9
Segrate 9
Tianjin 9
Amman 8
Bologna 8
Brasília 8
Clifton 8
Guangzhou 8
Hangzhou 8
Totale 9.197
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Nome #
The tardigrade damage suppressor protein modulates transcription factor and DNA repair genes in human cells treated with hydroxyl radicals and UV-C 349
C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease 344
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 333
Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia 323
MicroRNAs as Biomarkers in Amyotrophic Lateral Sclerosis 295
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 287
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD 285
Antimicrobial activity of novel dendrimeric peptides obtained by phage display selection and rational modification. 281
Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients 280
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 274
No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population 268
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype 263
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 256
Genetic architecture of ALS in Sardinia 248
A new Krit1 gene mutation in a family with cerebral cavernous malformation (CCM) associated with intraorbital optic nerve and cutaneous cavernous angiomas 233
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 233
Biochemical filtering of a protein-protein docking simulation identifies the structure of a complex between a recombinant antibody fragment and alpha-bungarotoxin 231
Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation 229
A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS 228
Analysis of regulatory regions of macrophage migration inhibitory factor (MIF) gene in Italian ALS patients 227
Variants in MCT10 protein do not affect FT3 levels in athyreotic patients 226
D90A-SOD1 mutation in ALS: The first report of heterozigous Italian patients and unusual findings 225
Impaired intracortical transmission in G2019S leucine rich-repeat kinase Parkinson patients 224
Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT5–8 Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC) 220
Lack of association of PON polymorphisms with sporadic ALS in an Italian population 217
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 217
Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene. 216
A novel SOD1 gene mutation in a familial ALS patient 215
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 211
KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants 209
A novel variant in superoxide dismutase 1 gene (P.V119M) in als patients with pure lower motor neuron presentation 208
Mitigation of UV-B Radiation Stress in Tobacco Pollen by Expression of the Tardigrade Damage Suppressor Protein (Dsup) 201
Phage display and colony filter screening for high-throughput selection of antibody libraries 198
Descrizione di una nuova mutazione del gene Krit1 in una forma familiare di angioma cavernoso cerebrale associata ad angioma ottico e ad angioma cutaneo 196
miRNA Targets: From Prediction Tools to Experimental Validation 195
BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration 194
Proteomics Reveals How the Tardigrade Damage Suppressor Protein Teaches Transfected Human Cells to Survive UV-C Stress 191
Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family. 191
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 190
Concern regarding classification of c.703G>A/p.Gly235Arg as a novel missense variant in KRIT1 gene 189
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 188
From Circulating Tumor Cells to Mirna: New Challenges in the Diagnosis and Prognosis of Medullary Thyroid Cancer 184
Molecular genetic analysis of cerebral cavernous malformations: An update 182
Molecular genetic features of cerebral cavernous malformations (CCM) patients: An overall view from genes to endothelial cells 179
Paraoxonase gene polymorphisms and susceptibility to sporadic ALS in Italian population. Preliminary results. 178
Genetic Variations within Krit1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a Large Italian Family Harbouring a Krit1/CCM1 Mutation 177
Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP Gene 175
Progestin regulation of 11beta-hydroxysteroid dehydrogenase expression in T-47D human breast cancer cells 168
Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene 166
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations 164
Strategies for the construction and use of peptide and antibody libraries displayed on phages. 159
The” D90A” still an enigma among SOD1 gene mutations. Report of three italian cases. 153
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 147
Synthetic inhibitors of anthrax lethal toxin 145
Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort 138
Macrophage migration inhibitory factor inthe human endometrium: expression and localization during the menstrual cycle andearly pregnancy 137
HFE p.H63D polymorphism does not influence ALS phenotype and survival 136
Phenotipic-genotypic study of amyothrophic lateral sclerosis Italian families with the G41S SOD1 gene mutation. 134
Thr92Ala polymorphism in the type 2 deiodinase gene: an evolutionary perspective 131
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Strong synthetic inhibitors of anthrax lethal toxin 127
What's Wrong in a Jump? Prediction and Validation of Splice Site Variants 126
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Neurodegenerative Disease: From Molecular Basis to Therapy 83
Investigating the Cytoprotective Mechanisms of the Tardigrade Damage Suppressor (Dsup) Protein in Human Cells Under Hypoxic Stress 20
Totale 13.481
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Categoria #
all - tutte 40.649
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 40.649
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2024/20251.863 51 116 187 105 244 121 67 79 169 83 233 408
2025/20264.655 351 603 501 509 823 166 529 136 184 240 113 500
2026/2027128 128 0 0 0 0 0 0 0 0 0 0 0
Totale 13.481