IRIS
CORRADO, Lucia
 Distribuzione geografica
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Continente #
EU - Europa 2.553
NA - Nord America 2.174
AS - Asia 1.437
SA - Sud America 321
AF - Africa 65
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 1
Totale 6.556
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Nazione #
US - Stati Uniti d'America 2.107
IE - Irlanda 636
SG - Singapore 495
IT - Italia 421
DE - Germania 398
SE - Svezia 336
CN - Cina 312
HK - Hong Kong 259
BR - Brasile 247
UA - Ucraina 210
RU - Federazione Russa 151
VN - Vietnam 140
FI - Finlandia 125
GB - Regno Unito 72
KR - Corea 60
IN - India 52
CA - Canada 41
BJ - Benin 40
FR - Francia 33
AR - Argentina 31
NL - Olanda 30
BE - Belgio 24
CZ - Repubblica Ceca 24
PL - Polonia 24
MX - Messico 22
ID - Indonesia 21
AT - Austria 17
JP - Giappone 17
TR - Turchia 17
BD - Bangladesh 15
IR - Iran 15
ES - Italia 14
EE - Estonia 13
ZA - Sudafrica 13
EC - Ecuador 10
IQ - Iraq 10
CL - Cile 7
LT - Lituania 7
PE - Perù 7
PY - Paraguay 6
CO - Colombia 5
MA - Marocco 5
AE - Emirati Arabi Uniti 4
EU - Europa 4
DK - Danimarca 3
DO - Repubblica Dominicana 3
EG - Egitto 3
GR - Grecia 3
IL - Israele 3
RO - Romania 3
SA - Arabia Saudita 3
UY - Uruguay 3
VE - Venezuela 3
CH - Svizzera 2
DZ - Algeria 2
HR - Croazia 2
JO - Giordania 2
LK - Sri Lanka 2
PK - Pakistan 2
AU - Australia 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BO - Bolivia 1
BW - Botswana 1
BY - Bielorussia 1
ET - Etiopia 1
GY - Guiana 1
HU - Ungheria 1
JM - Giamaica 1
KG - Kirghizistan 1
KH - Cambogia 1
KW - Kuwait 1
MD - Moldavia 1
MY - Malesia 1
PH - Filippine 1
RS - Serbia 1
UZ - Uzbekistan 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 6.556
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Città #
Dublin 636
Jacksonville 372
Hong Kong 259
Dearborn 178
Beijing 177
Singapore 175
Chandler 125
Ashburn 115
Wilmington 77
Los Angeles 70
Piemonte 69
Lawrence 68
Princeton 68
Ann Arbor 64
Moscow 62
Seoul 60
Bremen 53
Munich 52
San Mateo 49
Novara 46
Buffalo 42
Ho Chi Minh City 42
Cotonou 40
New York 40
Boardman 31
Dallas 30
Rome 30
Andover 24
São Paulo 24
Brno 23
Hanoi 23
Houston 23
Warsaw 22
Helsinki 21
Turin 19
Milan 18
Woodbridge 17
Brussels 16
Düsseldorf 15
Nanjing 15
Tokyo 15
Denver 14
Nuremberg 14
Redondo Beach 14
Boston 12
Brooklyn 12
Montreal 12
Tianjin 12
Poplar 11
Santa Clara 11
The Dalles 11
Frankfurt am Main 10
Kunming 10
Leawood 10
Monmouth Junction 10
Mülheim 10
Stockholm 10
Toronto 10
Zanjan 10
Atlanta 9
Borgomanero 9
Chennai 9
Hefei 9
Norwalk 9
Orem 9
Turku 9
Vienna 9
Ankara 8
Mexico City 8
Phoenix 8
Waanrode 8
Jakarta 7
Kocaeli 7
Omegna 7
Rio de Janeiro 7
Strasbourg 7
Brasília 6
Curitiba 6
Dong Ket 6
London 6
Ottawa 6
Seattle 6
Vercelli 6
Amsterdam 5
Belo Horizonte 5
Biên Hòa 5
Buenos Aires 5
Chicago 5
Falkenstein 5
Haiphong 5
Johannesburg 5
Mumbai 5
Nanchang 5
Porto Alegre 5
Quận Bình Thạnh 5
Sacramento 5
Augusta 4
Baghdad 4
Council Bluffs 4
Dhaka 4
Totale 3.770
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Nome #
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 132
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 120
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 116
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 116
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 110
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 107
null 105
A recurrent signal peptide mutation in the growth hormone releasing hormone receptor with defective translocation to the cell surface and isolated growth hormone deficiency 104
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 103
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 102
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 102
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 101
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 101
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 99
Association of osteopontin regulatory polymorphisms with systemic sclerosis 98
Extensive genetics of ALS: a population-based study in Italy. 97
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 96
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 95
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR 94
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 94
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 93
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 90
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 90
A patient with a large 17p11.2 deletion presenting with Smith-Magenis (SMS) and Joubert syndromes (JS): a tool for mapping the JS gene?” 89
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 88
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 88
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 87
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 87
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 87
The multistep hypothesis of ALS revisited: The role of genetic mutations 86
The case of the solitary sick kidney 85
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes 84
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 84
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 83
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 82
Cognitive impairment across ALS clinical stages in a population-based cohort 82
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 82
Mapping of genes and ESTs assigned to 17q11.2 to a YAC contig centered on the NF1 gene 80
High resolution FISH tools 79
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 78
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. 76
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 76
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease 74
FISH with locus-specific probes on stretched chromosomes: a useful tool for genome organization studies. 73
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants 72
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS 71
SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS) 71
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect. 70
Variations of the perforin gene in patients with multiple sclerosis 69
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 69
ATXN-2 CAG repeat expansions are interrupted in ALS patients 69
Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 region 68
Regional spreading of symptoms at diagnosis as a prognostic marker in amyotrophic lateral sclerosis: A population-based study 67
Predicting functional impairment trajectories in amyotrophic lateral sclerosis: a probabilistic, multifactorial model of disease progression 67
HLA-class I markers and multiple sclerosis susceptibility in the Italian population 66
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 65
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis 65
Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis 64
High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis 64
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 63
VPS54 genetic analysis in ALS Italian cohort 63
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriers 62
Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1) 62
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis 61
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia. 61
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis 60
Variants in the 5′UTR reduce SHOX expression and contribute to SHOX haploinsufficiency 58
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 57
No association of DPP6 with amyotrophic lateral sclerosis in an Italian population 55
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations 54
A case of early-onset Parkinson's disease in a patient with KBG syndrome 53
Identification of duplicated genes in 17q11.2 by using FISH on stretched chromosomes and DNA fibers 52
“Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population 51
Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions 51
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS 51
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia. 50
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology 48
Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis 47
Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients 47
Parkinsonism in SCA19/22: Dopamine Transporter Imaging in an Italian Family Harboring a Novel Mutation 44
Parkinson's disease and chronic inflammatory demyelinating polyneuropathy: Broadening the clinical spectrum of VCP mutations 43
GBA variants influence cognitive status in amyotrophic lateral sclerosis 41
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort 41
Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis 39
Metal(loid)s role in the pathogenesis of amyotrophic lateral sclerosis: Environmental, epidemiological, and genetic data 39
Variability in Clinical Phenotype in TARDBP Mutations: Amyotrophic Lateral Sclerosis Case Description and Literature Review 31
Profiling cognition and brain metabolism in amyotrophic lateral sclerosis and frontotemporal dementia 28
Identification of Transcriptomic Differences in Induced Pluripotent Stem Cells and Neural Progenitors from Amyotrophic Lateral Sclerosis Patients Carrying Different Mutations: A Pilot Study 28
Challenging the boundaries: c9orf72 mutation presenting as Alzheimer's disease 27
A Novel GBF1 Variant in a Charcot-Marie-Tooth Type 2: Insights from Familial Analysis 26
Myoclonus‐Dystonia plus Syndrome in a Patient Carrying a Novel TCF20 Variant 25
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data 22
Exploring the phenotypic fingerprints of ANXA11 variants in ALS: a population-based study in an European cohort 21
A case of late-onset OCD developing PLS and FTD 12
A case of progressive non-fluent aphasia as onset of amyotrophic lateral sclerosis with frontotemporal dementia 8
A case of late-onset OCD developing PLS and FTD 5
Totale 6.698
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Categoria #
all - tutte 36.878
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 36.878
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021281 0 0 0 0 0 11 77 12 76 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
2025/20261.671 193 164 249 619 390 56 0 0 0 0 0 0
Totale 6.698