IRIS
RICCI, CLAUDIA
 Distribuzione geografica
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Continente #
NA - Nord America 3.320
EU - Europa 2.831
AS - Asia 434
SA - Sud America 6
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 4
Totale 6.600
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Nazione #
US - Stati Uniti d'America 3.311
GB - Regno Unito 1.063
IE - Irlanda 578
CN - Cina 322
SE - Svezia 270
UA - Ucraina 259
IT - Italia 255
FR - Francia 146
DE - Germania 111
FI - Finlandia 79
TR - Turchia 71
ES - Italia 25
BE - Belgio 19
VN - Vietnam 14
NL - Olanda 11
CA - Canada 9
KR - Corea 6
AU - Australia 5
IL - Israele 5
IR - Iran 5
IN - India 4
BR - Brasile 3
EU - Europa 3
HK - Hong Kong 2
JP - Giappone 2
MD - Moldavia 2
MK - Macedonia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AT - Austria 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CH - Svizzera 1
DK - Danimarca 1
EC - Ecuador 1
GR - Grecia 1
HR - Croazia 1
KZ - Kazakistan 1
PE - Perù 1
PL - Polonia 1
PT - Portogallo 1
RO - Romania 1
RS - Serbia 1
RU - Federazione Russa 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 6.600
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Città #
Southend 1.007
Dublin 576
Fairfield 556
Chandler 319
Ashburn 288
Wilmington 239
Jacksonville 212
Woodbridge 209
Seattle 204
Cambridge 196
Houston 189
Siena 142
Ann Arbor 136
Princeton 103
Beijing 76
Nanjing 68
Izmir 58
Menlo Park 40
New York 36
Helsinki 35
Boardman 31
San Diego 31
Nanchang 29
San Mateo 28
Shanghai 28
Dearborn 27
Málaga 22
Shenyang 21
Hebei 18
Fremont 16
Dong Ket 14
San Francisco 13
Brussels 12
Florence 12
Norwalk 12
Redwood City 10
Milan 9
Segrate 9
Changsha 8
Ningbo 8
Jiaxing 7
Kunming 7
Los Angeles 7
Rome 7
Washington 7
Lancaster 6
Waanrode 6
Guangzhou 5
Mestre 5
Tianjin 5
Zhengzhou 5
Bonndorf 4
Hangzhou 4
Kocaeli 4
Misano Adriatico 4
Canberra 3
Council Bluffs 3
Düsseldorf 3
Edinburgh 3
Hefei 3
Jinan 3
Lappeenranta 3
London 3
Paris 3
Renton 3
San Antonio 3
Tappahannock 3
Toronto 3
Vancouver 3
Verona 3
Acton 2
Albignasego 2
Baotou 2
Barcelona 2
Bergamo 2
Boston 2
Bursa 2
Castelfiorentino 2
Fuzhou 2
Giessen 2
Haikou 2
Hong Kong 2
Lanzhou 2
Melbourne 2
Montreal 2
New Bedfont 2
Nuremberg 2
Phoenix 2
Prescot 2
Sinalunga 2
Skopje 2
Taizhou 2
Torino 2
Vinci 2
Zanjan 2
Alghero 1
Almada 1
Amsterdam 1
Auburn Hills 1
Aurora 1
Totale 5.230
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Nome #
C9ORF72 gene expansion in a patient with intellectual disability and psychiatric disease 235
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 220
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 194
Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia 179
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients 179
MicroRNAs as Biomarkers in Amyotrophic Lateral Sclerosis 178
Genetic architecture of ALS in Sardinia 177
Identification of miRNAs as Potential Biomarkers in Cerebrospinal Fluid from Amyotrophic Lateral Sclerosis Patients 175
No association of MTHFR c.677C>T variant with sporadic ALS in an Italian population 171
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 164
Genotype–phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G SOD1 mutation 163
Impaired intracortical transmission in G2019S leucine rich-repeat kinase Parkinson patients 160
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis 152
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 147
Antimicrobial activity of novel dendrimeric peptides obtained by phage display selection and rational modification. 140
Variants in MCT10 protein do not affect FT3 levels in athyreotic patients 134
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD 133
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype 131
Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene. 130
null 128
Genotyping of Macrophage Migration Inhibitory Factor (MIF) CATT5–8 Repeat Polymorphism by Denaturing High-Performance Liquid Chromatography (DHPLC) 126
null 124
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 122
Biochemical filtering of a protein-protein docking simulation identifies the structure of a complex between a recombinant antibody fragment and alpha-bungarotoxin 119
D90A-SOD1 mutation in ALS: The first report of heterozigous Italian patients and unusual findings 119
Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP Gene 118
null 118
Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family. 115
null 114
Lack of association of PON polymorphisms with sporadic ALS in an Italian population 113
Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene 111
Phage display and colony filter screening for high-throughput selection of antibody libraries 110
Genetic Variations within Krit1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a Large Italian Family Harbouring a Krit1/CCM1 Mutation 107
Strategies for the construction and use of peptide and antibody libraries displayed on phages. 106
A novel SOD1 gene mutation in a familial ALS patient 104
Concern regarding classification of c.703G>A/p.Gly235Arg as a novel missense variant in KRIT1 gene 97
Analysis of regulatory regions of macrophage migration inhibitory factor (MIF) gene in Italian ALS patients 94
Paraoxonase gene polymorphisms and susceptibility to sporadic ALS in Italian population. Preliminary results. 91
A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS 91
A new Krit1 gene mutation in a family with cerebral cavernous malformation (CCM) associated with intraorbital optic nerve and cutaneous cavernous angiomas 90
The” D90A” still an enigma among SOD1 gene mutations. Report of three italian cases. 87
Synthetic inhibitors of anthrax lethal toxin 82
Descrizione di una nuova mutazione del gene Krit1 in una forma familiare di angioma cavernoso cerebrale associata ad angioma ottico e ad angioma cutaneo 81
Macrophage migration inhibitory factor inthe human endometrium: expression and localization during the menstrual cycle andearly pregnancy 77
Progestin regulation of 11beta-hydroxysteroid dehydrogenase expression in T-47D human breast cancer cells 76
Phenotipic-genotypic study of amyothrophic lateral sclerosis Italian families with the G41S SOD1 gene mutation. 69
STRONG SYNTHETIC INHIBITORS OF ANTHRAX LETHAL TOXIN 64
Thr92Ala polymorphism in the type 2 deiodinase gene: an evolutionary perspective 60
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 59
Molecular genetic analysis of cerebral cavernous malformations: An update 58
A novel variant in superoxide dismutase 1 gene (P.V119M) in als patients with pure lower motor neuron presentation 57
KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants 55
Molecular genetic features of cerebral cavernous malformations (CCM) patients: An overall view from genes to endothelial cells 52
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 48
What's Wrong in a Jump? Prediction and Validation of Splice Site Variants. 44
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry 37
miRNA Targets: From Prediction Tools to Experimental Validation 36
Proteomics Reveals How the Tardigrade Damage Suppressor Protein Teaches Transfected Human Cells to Survive UV-C Stress 35
HFE p.H63D polymorphism does not influence ALS phenotype and survival 33
Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort 31
The Tardigrade Damage Suppressor Protein Modulates Transcription Factor and DNA Repair Genes in Human Cells Treated with Hydroxyl Radicals and UV-C 29
BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration 24
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations 20
From Circulating Tumor Cells to Mirna: New Challenges in the Diagnosis and Prognosis of Medullary Thyroid Cancer 20
Neurodegenerative Disease: From Molecular Basis to Therapy 7
Totale 6.720
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Categoria #
all - tutte 20.327
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 20.327
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019591 0 0 0 0 0 0 0 0 0 170 224 197
2019/20201.414 156 70 84 217 96 118 123 179 143 112 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
2023/2024851 22 22 87 68 28 238 324 35 6 21 0 0
Totale 6.720