IRIS
RICCI, CLAUDIA
 Distribuzione geografica
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Continente #
NA - Nord America 4.936
EU - Europa 4.190
AS - Asia 1.883
SA - Sud America 323
AF - Africa 51
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 5
Totale 11.396
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Nazione #
US - Stati Uniti d'America 4.882
GB - Regno Unito 1.104
RU - Federazione Russa 895
CN - Cina 711
SG - Singapore 601
IE - Irlanda 581
IT - Italia 390
BR - Brasile 290
SE - Svezia 282
UA - Ucraina 266
DE - Germania 202
FR - Francia 166
HK - Hong Kong 164
FI - Finlandia 140
KR - Corea 95
TR - Turchia 86
VN - Vietnam 81
IN - India 37
NL - Olanda 36
ES - Italia 35
CA - Canada 30
CI - Costa d'Avorio 24
BD - Bangladesh 19
BE - Belgio 19
JP - Giappone 18
AT - Austria 16
AR - Argentina 15
MX - Messico 15
PL - Polonia 15
CZ - Repubblica Ceca 13
PK - Pakistan 11
ZA - Sudafrica 11
AU - Australia 8
SA - Arabia Saudita 8
IQ - Iraq 7
IR - Iran 7
EC - Ecuador 6
IL - Israele 6
TN - Tunisia 6
PH - Filippine 5
CO - Colombia 4
EG - Egitto 4
GR - Grecia 4
AL - Albania 3
CH - Svizzera 3
EU - Europa 3
ID - Indonesia 3
JO - Giordania 3
KZ - Kazakistan 3
LT - Lituania 3
UZ - Uzbekistan 3
BO - Bolivia 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
GE - Georgia 2
KE - Kenya 2
LB - Libano 2
MD - Moldavia 2
MK - Macedonia 2
PE - Perù 2
RO - Romania 2
RS - Serbia 2
TH - Thailandia 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BY - Bielorussia 1
DK - Danimarca 1
DM - Dominica 1
EE - Estonia 1
ET - Etiopia 1
GT - Guatemala 1
HR - Croazia 1
JM - Giamaica 1
KG - Kirghizistan 1
LV - Lettonia 1
LY - Libia 1
MA - Marocco 1
MM - Myanmar 1
MN - Mongolia 1
NO - Norvegia 1
OM - Oman 1
PA - Panama 1
PS - Palestinian Territory 1
PT - Portogallo 1
PY - Paraguay 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 11.396
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Città #
Southend 1.007
Dallas 624
Dublin 579
Fairfield 556
Ashburn 400
Singapore 334
Chandler 319
Moscow 280
Santa Clara 257
Wilmington 239
Jacksonville 212
Woodbridge 209
Seattle 206
Cambridge 196
Houston 194
Beijing 182
Hong Kong 163
Siena 153
Ann Arbor 136
Princeton 103
Hefei 99
Seoul 88
Los Angeles 68
Nanjing 68
New York 68
Izmir 59
The Dalles 54
Munich 51
Helsinki 42
Milan 42
Menlo Park 40
Boardman 37
Council Bluffs 32
San Diego 32
Shanghai 32
Lappeenranta 30
Nanchang 29
Buffalo 28
San Mateo 28
Dearborn 27
Turku 27
São Paulo 25
Abidjan 24
Columbus 23
Málaga 23
Shenyang 23
Ho Chi Minh City 22
San Francisco 21
Brooklyn 20
Hebei 18
Nuremberg 18
Fremont 16
Hanoi 16
Rome 16
Florence 15
Tokyo 15
Dong Ket 14
Warsaw 14
Changsha 13
Montreal 13
Bengaluru 12
Brussels 12
Denver 12
Norwalk 12
Boston 11
Frankfurt am Main 11
London 11
Redondo Beach 11
Atlanta 10
Ningbo 10
Redwood City 10
Stockholm 10
Belo Horizonte 9
Brno 9
Chicago 9
Johannesburg 9
Kunming 9
Poplar 9
Segrate 9
Tianjin 9
Clifton 8
Guangzhou 8
Phoenix 8
Poggiomarino 8
Toronto 8
Washington 8
Düsseldorf 7
Hangzhou 7
Jiaxing 7
Lancaster 7
Orem 7
Vienna 7
Zhengzhou 7
Brasília 6
Mexico City 6
Naples 6
Turin 6
Waanrode 6
Chennai 5
Manchester 5
Totale 8.020
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Nome #
C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease 331
Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia 293
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 291
MicroRNAs as Biomarkers in Amyotrophic Lateral Sclerosis 264
Antimicrobial activity of novel dendrimeric peptides obtained by phage display selection and rational modification. 257
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 254
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD 253
No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population 249
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 248
Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients 247
Genetic architecture of ALS in Sardinia 231
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype 230
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 227
Biochemical filtering of a protein-protein docking simulation identifies the structure of a complex between a recombinant antibody fragment and alpha-bungarotoxin 215
A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS 205
Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation 205
Variants in MCT10 protein do not affect FT3 levels in athyreotic patients 203
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 202
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 201
A new Krit1 gene mutation in a family with cerebral cavernous malformation (CCM) associated with intraorbital optic nerve and cutaneous cavernous angiomas 200
Impaired intracortical transmission in G2019S leucine rich-repeat kinase Parkinson patients 198
D90A-SOD1 mutation in ALS: The first report of heterozigous Italian patients and unusual findings 196
Analysis of regulatory regions of macrophage migration inhibitory factor (MIF) gene in Italian ALS patients 195
A novel SOD1 gene mutation in a familial ALS patient 195
Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT5–8 Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC) 191
Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene. 191
Lack of association of PON polymorphisms with sporadic ALS in an Italian population 188
A novel variant in superoxide dismutase 1 gene (P.V119M) in als patients with pure lower motor neuron presentation 178
Descrizione di una nuova mutazione del gene Krit1 in una forma familiare di angioma cavernoso cerebrale associata ad angioma ottico e ad angioma cutaneo 173
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 171
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 170
KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants 170
Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family. 168
Concern regarding classification of c.703G>A/p.Gly235Arg as a novel missense variant in KRIT1 gene 168
Phage display and colony filter screening for high-throughput selection of antibody libraries 167
Paraoxonase gene polymorphisms and susceptibility to sporadic ALS in Italian population. Preliminary results. 161
Molecular genetic analysis of cerebral cavernous malformations: An update 156
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 155
Genetic Variations within Krit1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a Large Italian Family Harbouring a Krit1/CCM1 Mutation 151
Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP Gene 151
Mitigation of UV-B Radiation Stress in Tobacco Pollen by Expression of the Tardigrade Damage Suppressor Protein (Dsup) 151
Proteomics Reveals How the Tardigrade Damage Suppressor Protein Teaches Transfected Human Cells to Survive UV-C Stress 149
From Circulating Tumor Cells to Mirna: New Challenges in the Diagnosis and Prognosis of Medullary Thyroid Cancer 149
Progestin regulation of 11beta-hydroxysteroid dehydrogenase expression in T-47D human breast cancer cells 143
Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene 143
Strategies for the construction and use of peptide and antibody libraries displayed on phages. 143
BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration 142
miRNA Targets: From Prediction Tools to Experimental Validation 141
Molecular genetic features of cerebral cavernous malformations (CCM) patients: An overall view from genes to endothelial cells 134
The” D90A” still an enigma among SOD1 gene mutations. Report of three italian cases. 132
Synthetic inhibitors of anthrax lethal toxin 128
null 128
The tardigrade damage suppressor protein modulates transcription factor and DNA repair genes in human cells treated with hydroxyl radicals and UV-C 127
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 126
null 124
Macrophage migration inhibitory factor inthe human endometrium: expression and localization during the menstrual cycle andearly pregnancy 119
null 118
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations 117
Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort 117
null 114
STRONG SYNTHETIC INHIBITORS OF ANTHRAX LETHAL TOXIN 110
Phenotipic-genotypic study of amyothrophic lateral sclerosis Italian families with the G41S SOD1 gene mutation. 110
Thr92Ala polymorphism in the type 2 deiodinase gene: an evolutionary perspective 108
HFE p.H63D polymorphism does not influence ALS phenotype and survival 107
What's Wrong in a Jump? Prediction and Validation of Splice Site Variants 96
Neurodegenerative Disease: From Molecular Basis to Therapy 64
Totale 11.539
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Categoria #
all - tutte 35.648
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 35.648
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021758 0 0 0 0 0 109 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
2024/20251.863 51 116 187 105 244 121 67 79 169 83 233 408
2025/20262.841 351 603 501 509 823 54 0 0 0 0 0 0
Totale 11.539