IRIS
CORRADO, Lucia
 Distribuzione geografica
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Continente #
EU - Europa 3.444
NA - Nord America 2.558
AS - Asia 2.033
SA - Sud America 365
AF - Africa 89
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 2
Totale 8.496
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Nazione #
US - Stati Uniti d'America 2.476
RU - Federazione Russa 837
IE - Irlanda 639
SG - Singapore 606
CN - Cina 522
IT - Italia 463
DE - Germania 421
SE - Svezia 338
VN - Vietnam 311
BR - Brasile 273
HK - Hong Kong 273
UA - Ucraina 213
FI - Finlandia 128
FR - Francia 124
GB - Regno Unito 84
IN - India 72
KR - Corea 64
CA - Canada 47
BJ - Benin 40
AR - Argentina 39
NL - Olanda 35
PL - Polonia 30
MX - Messico 28
BE - Belgio 24
CZ - Repubblica Ceca 24
ID - Indonesia 24
JP - Giappone 23
BD - Bangladesh 21
ZA - Sudafrica 21
AT - Austria 19
IQ - Iraq 19
TR - Turchia 19
ES - Italia 17
IR - Iran 15
EE - Estonia 14
EC - Ecuador 11
CO - Colombia 10
PH - Filippine 10
LT - Lituania 9
DZ - Algeria 8
CL - Cile 7
PE - Perù 7
PY - Paraguay 7
AE - Emirati Arabi Uniti 6
SA - Arabia Saudita 6
TH - Thailandia 6
MA - Marocco 5
PK - Pakistan 5
BO - Bolivia 4
EU - Europa 4
JO - Giordania 4
RO - Romania 4
UZ - Uzbekistan 4
CH - Svizzera 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
EG - Egitto 3
GR - Grecia 3
IL - Israele 3
JM - Giamaica 3
MY - Malesia 3
UY - Uruguay 3
VE - Venezuela 3
AL - Albania 2
AO - Angola 2
AU - Australia 2
AZ - Azerbaigian 2
BY - Bielorussia 2
HR - Croazia 2
KG - Kirghizistan 2
LB - Libano 2
LK - Sri Lanka 2
SN - Senegal 2
SY - Repubblica araba siriana 2
TN - Tunisia 2
TW - Taiwan 2
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BW - Botswana 1
ET - Etiopia 1
GY - Guiana 1
HU - Ungheria 1
KE - Kenya 1
KH - Cambogia 1
KW - Kuwait 1
LV - Lettonia 1
LY - Libia 1
MD - Moldavia 1
NG - Nigeria 1
PA - Panama 1
QA - Qatar 1
RS - Serbia 1
SI - Slovenia 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZM - Zambia 1
Totale 8.496
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Città #
Dublin 638
Jacksonville 372
Hong Kong 272
Singapore 231
Beijing 184
San Jose 180
Dearborn 178
Ashburn 170
Chandler 125
Moscow 105
Ho Chi Minh City 87
Lauterbourg 81
Los Angeles 81
Wilmington 77
Piemonte 69
Lawrence 68
Princeton 68
Ann Arbor 64
Seoul 61
Hanoi 54
Bremen 53
Munich 52
San Mateo 49
New York 47
Novara 46
Buffalo 45
Cotonou 40
Rome 35
Orem 32
Boardman 31
Dallas 31
The Dalles 30
Warsaw 28
São Paulo 27
Houston 25
Andover 24
Helsinki 24
Brno 23
Turin 21
Milan 19
Guangzhou 18
Nanjing 18
Tokyo 18
Brooklyn 17
Santa Clara 17
Woodbridge 17
Brussels 16
Council Bluffs 16
Frankfurt am Main 16
Nuremberg 16
Chennai 15
Denver 15
Düsseldorf 15
Haiphong 15
Montreal 15
Tianjin 15
Redondo Beach 14
Falkenstein 13
Boston 12
Da Nang 12
Stockholm 12
Atlanta 11
Johannesburg 11
London 11
Mexico City 11
Poplar 11
Toronto 11
Villadossola 11
Hangzhou 10
Kunming 10
Leawood 10
Monmouth Junction 10
Mülheim 10
Rio de Janeiro 10
Vienna 10
Zanjan 10
Amsterdam 9
Borgomanero 9
Hefei 9
Hải Dương 9
Norwalk 9
Turku 9
Ankara 8
Phoenix 8
Shanghai 8
Waanrode 8
Baghdad 7
Biên Hòa 7
Jakarta 7
Kocaeli 7
Manchester 7
Mumbai 7
Nanchang 7
Omegna 7
Strasbourg 7
Brasília 6
Curitiba 6
Dong Ket 6
Ninh Bình 6
Ottawa 6
Totale 4.505
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Nome #
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 156
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 148
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 140
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 132
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 128
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 127
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 126
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 126
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 125
A recurrent signal peptide mutation in the growth hormone releasing hormone receptor with defective translocation to the cell surface and isolated growth hormone deficiency 125
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 124
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 124
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 123
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 121
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 120
Association of osteopontin regulatory polymorphisms with systemic sclerosis 120
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 119
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 117
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR 114
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 114
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 114
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 114
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 111
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 110
Extensive genetics of ALS: a population-based study in Italy. 109
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 107
The multistep hypothesis of ALS revisited: The role of genetic mutations 107
Mapping of genes and ESTs assigned to 17q11.2 to a YAC contig centered on the NF1 gene 106
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 106
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 106
null 105
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants 104
The case of the solitary sick kidney 104
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 104
A patient with a large 17p11.2 deletion presenting with Smith-Magenis (SMS) and Joubert syndromes (JS): a tool for mapping the JS gene?” 103
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes 100
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 100
Cognitive impairment across ALS clinical stages in a population-based cohort 98
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis 94
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS 94
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 93
High resolution FISH tools 93
Variations of the perforin gene in patients with multiple sclerosis 93
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 93
Predicting functional impairment trajectories in amyotrophic lateral sclerosis: a probabilistic, multifactorial model of disease progression 93
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 92
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 91
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease 89
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations 88
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriers 88
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. 88
A case of early-onset Parkinson's disease in a patient with KBG syndrome 87
FISH with locus-specific probes on stretched chromosomes: a useful tool for genome organization studies. 87
ATXN-2 CAG repeat expansions are interrupted in ALS patients 86
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 83
HLA-class I markers and multiple sclerosis susceptibility in the Italian population 82
Regional spreading of symptoms at diagnosis as a prognostic marker in amyotrophic lateral sclerosis: A population-based study 81
Parkinson's disease and chronic inflammatory demyelinating polyneuropathy: Broadening the clinical spectrum of VCP mutations 80
Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 region 80
SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS) 79
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect. 79
Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis 78
Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1) 78
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 77
No association of DPP6 with amyotrophic lateral sclerosis in an Italian population 76
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis 76
High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis 74
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia. 73
VPS54 genetic analysis in ALS Italian cohort 73
Variants in the 5′UTR reduce SHOX expression and contribute to SHOX haploinsufficiency 73
Parkinsonism in SCA19/22: Dopamine Transporter Imaging in an Italian Family Harboring a Novel Mutation 72
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis 71
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology 70
Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients 67
Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions 67
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 67
GBA variants influence cognitive status in amyotrophic lateral sclerosis 66
“Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population 65
Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis 64
Profiling cognition and brain metabolism in amyotrophic lateral sclerosis and frontotemporal dementia 64
Identification of duplicated genes in 17q11.2 by using FISH on stretched chromosomes and DNA fibers 63
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia. 63
A Novel GBF1 Variant in a Charcot-Marie-Tooth Type 2: Insights from Familial Analysis 62
Metal(loid)s role in the pathogenesis of amyotrophic lateral sclerosis: Environmental, epidemiological, and genetic data 60
Identification of Transcriptomic Differences in Induced Pluripotent Stem Cells and Neural Progenitors from Amyotrophic Lateral Sclerosis Patients Carrying Different Mutations: A Pilot Study 59
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS 59
Challenging the boundaries: c9orf72 mutation presenting as Alzheimer's disease 58
Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis 57
Exploring the phenotypic fingerprints of ANXA11 variants in ALS: a population-based study in an European cohort 57
Variability in Clinical Phenotype in TARDBP Mutations: Amyotrophic Lateral Sclerosis Case Description and Literature Review 56
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort 54
Myoclonus‐Dystonia plus Syndrome in a Patient Carrying a Novel TCF20 Variant 52
A case of late-onset OCD developing PLS and FTD 43
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data 35
A case of progressive non-fluent aphasia as onset of amyotrophic lateral sclerosis with frontotemporal dementia 31
A case of late-onset OCD developing PLS and FTD 28
Totale 8.638
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Categoria #
all - tutte 40.383
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 40.383
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021105 0 0 0 0 0 0 0 0 0 15 74 16
2021/2022586 33 6 66 91 28 1 38 8 32 19 149 115
2022/20231.261 79 69 47 21 104 95 34 64 672 7 52 17
2023/2024418 31 32 48 19 63 4 75 4 10 4 48 80
2024/20251.161 35 31 76 38 24 136 93 117 226 109 50 226
2025/20263.611 193 164 249 619 390 276 522 672 268 258 0 0
Totale 8.638