IRIS
RICCI, CLAUDIA
 Distribuzione geografica
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Continente #
NA - Nord America 5.353
EU - Europa 4.400
AS - Asia 2.277
SA - Sud America 365
AF - Africa 147
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 5
Totale 12.555
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Nazione #
US - Stati Uniti d'America 5.280
GB - Regno Unito 1.125
RU - Federazione Russa 897
CN - Cina 757
SG - Singapore 696
IE - Irlanda 585
IT - Italia 440
BR - Brasile 312
SE - Svezia 282
UA - Ucraina 270
FR - Francia 231
VN - Vietnam 217
DE - Germania 216
HK - Hong Kong 188
FI - Finlandia 155
KR - Corea 95
TR - Turchia 90
ZA - Sudafrica 78
IN - India 60
NL - Olanda 49
CA - Canada 40
ES - Italia 40
BD - Bangladesh 30
CI - Costa d'Avorio 25
JP - Giappone 22
MX - Messico 22
PL - Polonia 21
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
IL - Israele 8
JO - Giordania 8
UZ - Uzbekistan 8
VE - Venezuela 8
EG - Egitto 7
IR - Iran 7
CH - Svizzera 6
EC - Ecuador 6
PH - Filippine 6
LT - Lituania 5
AL - Albania 4
CL - Cile 4
GR - Grecia 4
KE - Kenya 4
BO - Bolivia 3
CR - Costa Rica 3
EU - Europa 3
ID - Indonesia 3
KZ - Kazakistan 3
MD - Moldavia 3
MY - Malesia 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
PY - Paraguay 2
RS - Serbia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AO - Angola 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 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
PA - Panama 1
PS - Palestinian Territory 1
Totale 12.547
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Città #
Southend 1.007
Dallas 627
Dublin 581
Fairfield 556
Ashburn 439
Singapore 385
Chandler 319
Moscow 280
Santa Clara 260
Wilmington 239
Jacksonville 212
Woodbridge 209
Seattle 206
Cambridge 196
Houston 196
San Jose 184
Beijing 183
Hong Kong 183
Siena 153
Ann Arbor 136
Hefei 118
Princeton 103
The Dalles 90
Seoul 88
Los Angeles 81
Council Bluffs 80
New York 74
Johannesburg 73
Nanjing 68
Izmir 59
Helsinki 57
Hanoi 54
Lauterbourg 54
Ho Chi Minh City 52
Munich 51
Milan 43
Menlo Park 40
Boardman 37
Shanghai 33
San Diego 32
Buffalo 31
Lappeenranta 30
Nanchang 29
San Mateo 28
Dearborn 27
São Paulo 27
Turku 27
Abidjan 25
Columbus 23
Málaga 23
Shenyang 23
Orem 21
San Francisco 21
Brooklyn 20
Frankfurt am Main 19
Montreal 19
Warsaw 19
Hebei 18
Nuremberg 18
Rome 18
Tokyo 18
Florence 17
Fremont 16
London 15
Atlanta 14
Dong Ket 14
Abuja 13
Bengaluru 13
Changsha 13
Chennai 13
Da Nang 13
Brussels 12
Denver 12
Manchester 12
Norwalk 12
Boston 11
Phoenix 11
Poplar 11
Redondo Beach 11
Belo Horizonte 10
Ningbo 10
Paris 10
Redwood City 10
Stockholm 10
Amsterdam 9
Brno 9
Chicago 9
Kunming 9
Segrate 9
Tianjin 9
Amman 8
Brasília 8
Clifton 8
Guangzhou 8
Hangzhou 8
Mexico City 8
Poggiomarino 8
Riyadh 8
Toronto 8
Washington 8
Totale 8.739
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Nome #
C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease 341
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 322
Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia 309
MicroRNAs as Biomarkers in Amyotrophic Lateral Sclerosis 282
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 278
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD 275
Antimicrobial activity of novel dendrimeric peptides obtained by phage display selection and rational modification. 274
Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients 272
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 266
No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population 259
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype 252
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 247
Genetic architecture of ALS in Sardinia 240
Biochemical filtering of a protein-protein docking simulation identifies the structure of a complex between a recombinant antibody fragment and alpha-bungarotoxin 226
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 226
A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS 222
Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation 221
A new Krit1 gene mutation in a family with cerebral cavernous malformation (CCM) associated with intraorbital optic nerve and cutaneous cavernous angiomas 220
Impaired intracortical transmission in G2019S leucine rich-repeat kinase Parkinson patients 220
D90A-SOD1 mutation in ALS: The first report of heterozigous Italian patients and unusual findings 215
Analysis of regulatory regions of macrophage migration inhibitory factor (MIF) gene in Italian ALS patients 214
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 214
Variants in MCT10 protein do not affect FT3 levels in athyreotic patients 213
Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT5–8 Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC) 212
A novel SOD1 gene mutation in a familial ALS patient 212
Lack of association of PON polymorphisms with sporadic ALS in an Italian population 205
Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene. 204
A novel variant in superoxide dismutase 1 gene (P.V119M) in als patients with pure lower motor neuron presentation 201
KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants 197
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 194
Descrizione di una nuova mutazione del gene Krit1 in una forma familiare di angioma cavernoso cerebrale associata ad angioma ottico e ad angioma cutaneo 188
Mitigation of UV-B Radiation Stress in Tobacco Pollen by Expression of the Tardigrade Damage Suppressor Protein (Dsup) 186
Phage display and colony filter screening for high-throughput selection of antibody libraries 185
BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration 181
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 181
Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family. 181
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 180
Proteomics Reveals How the Tardigrade Damage Suppressor Protein Teaches Transfected Human Cells to Survive UV-C Stress 179
Concern regarding classification of c.703G>A/p.Gly235Arg as a novel missense variant in KRIT1 gene 178
Molecular genetic analysis of cerebral cavernous malformations: An update 177
miRNA Targets: From Prediction Tools to Experimental Validation 177
Paraoxonase gene polymorphisms and susceptibility to sporadic ALS in Italian population. Preliminary results. 175
From Circulating Tumor Cells to Mirna: New Challenges in the Diagnosis and Prognosis of Medullary Thyroid Cancer 174
Molecular genetic features of cerebral cavernous malformations (CCM) patients: An overall view from genes to endothelial cells 168
Genetic Variations within Krit1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a Large Italian Family Harbouring a Krit1/CCM1 Mutation 167
The tardigrade damage suppressor protein modulates transcription factor and DNA repair genes in human cells treated with hydroxyl radicals and UV-C 163
Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP Gene 162
Progestin regulation of 11beta-hydroxysteroid dehydrogenase expression in T-47D human breast cancer cells 157
Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene 153
Strategies for the construction and use of peptide and antibody libraries displayed on phages. 153
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations 149
The” D90A” still an enigma among SOD1 gene mutations. Report of three italian cases. 146
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 141
Synthetic inhibitors of anthrax lethal toxin 139
Macrophage migration inhibitory factor inthe human endometrium: expression and localization during the menstrual cycle andearly pregnancy 133
null 128
Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort 128
HFE p.H63D polymorphism does not influence ALS phenotype and survival 127
null 124
Phenotipic-genotypic study of amyothrophic lateral sclerosis Italian families with the G41S SOD1 gene mutation. 123
Thr92Ala polymorphism in the type 2 deiodinase gene: an evolutionary perspective 121
null 118
STRONG SYNTHETIC INHIBITORS OF ANTHRAX LETHAL TOXIN 117
What's Wrong in a Jump? Prediction and Validation of Splice Site Variants 115
null 114
Neurodegenerative Disease: From Molecular Basis to Therapy 77
Totale 12.698
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Categoria #
all - tutte 37.821
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 37.821
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021219 0 0 0 0 0 0 0 0 0 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
2024/20251.863 51 116 187 105 244 121 67 79 169 83 233 408
2025/20264.000 351 603 501 509 823 166 529 136 184 198 0 0
Totale 12.698