IRIS
CORRADO, Lucia
 Distribuzione geografica
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Continente #
EU - Europa 3.514
NA - Nord America 2.833
AS - Asia 2.156
SA - Sud America 365
AF - Africa 90
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 2
Totale 8.966
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Nazione #
US - Stati Uniti d'America 2.736
RU - Federazione Russa 837
SG - Singapore 650
IE - Irlanda 639
CN - Cina 552
IT - Italia 527
DE - Germania 421
SE - Svezia 338
VN - Vietnam 313
HK - Hong Kong 275
BR - Brasile 273
UA - Ucraina 213
FI - Finlandia 128
FR - Francia 124
GB - Regno Unito 86
IN - India 72
KR - Corea 64
BD - Bangladesh 62
CA - Canada 53
BJ - Benin 40
AR - Argentina 39
NL - Olanda 35
MX - Messico 31
PL - Polonia 30
JP - Giappone 25
BE - Belgio 24
CZ - Repubblica Ceca 24
ID - Indonesia 24
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
JM - Giamaica 8
CL - Cile 7
PE - Perù 7
PY - Paraguay 7
AE - Emirati Arabi Uniti 6
SA - Arabia Saudita 6
TH - Thailandia 6
CH - Svizzera 5
MA - Marocco 5
MY - Malesia 5
PK - Pakistan 5
BO - Bolivia 4
EU - Europa 4
JO - Giordania 4
RO - Romania 4
UZ - Uzbekistan 4
DK - Danimarca 3
DO - Repubblica Dominicana 3
EG - Egitto 3
GR - Grecia 3
IL - Israele 3
LV - Lettonia 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
LY - Libia 1
MD - Moldavia 1
NG - Nigeria 1
PA - Panama 1
QA - Qatar 1
RS - Serbia 1
SC - Seychelles 1
SI - Slovenia 1
SX - ???statistics.table.value.countryCode.SX??? 1
TT - Trinidad e Tobago 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZM - Zambia 1
Totale 8.966
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Città #
Dublin 638
Jacksonville 373
Hong Kong 274
San Jose 259
Singapore 233
Beijing 187
Ashburn 179
Dearborn 178
Chandler 125
Moscow 105
Los Angeles 104
Ho Chi Minh City 87
Lauterbourg 81
Wilmington 78
Council Bluffs 69
Piemonte 69
Lawrence 68
Princeton 68
Ann Arbor 64
Seoul 61
New York 56
Hanoi 54
Novara 54
Bremen 53
Munich 52
San Mateo 49
Buffalo 48
Cotonou 40
Rome 40
Dallas 35
Orem 35
Boardman 31
Milan 30
The Dalles 30
Warsaw 28
São Paulo 27
Houston 26
Andover 24
Helsinki 24
Santa Clara 24
Turin 24
Brno 23
Denver 19
Guangzhou 19
Nanjing 18
Tokyo 18
Brooklyn 17
Woodbridge 17
Brussels 16
Frankfurt am Main 16
Haiphong 16
Montreal 16
Nuremberg 16
Chennai 15
Düsseldorf 15
Tianjin 15
Mexico City 14
Redondo Beach 14
Falkenstein 13
Tornaco 13
Boston 12
Da Nang 12
Hangzhou 12
London 12
Stockholm 12
Toronto 12
Atlanta 11
Johannesburg 11
Poplar 11
Villadossola 11
Chicago 10
Kunming 10
Leawood 10
Monmouth Junction 10
Mülheim 10
Rio de Janeiro 10
Vienna 10
Zanjan 10
Amsterdam 9
Borgomanero 9
Columbus 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
Totale 4.760
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Nome #
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 178
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 161
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 158
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 141
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 141
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 141
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 133
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 131
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 131
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 130
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 128
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 128
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
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 124
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 123
Association of osteopontin regulatory polymorphisms with systemic sclerosis 123
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 122
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 122
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 120
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 117
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants 116
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 115
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 115
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR 114
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 112
Extensive genetics of ALS: a population-based study in Italy. 111
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 111
The multistep hypothesis of ALS revisited: The role of genetic mutations 111
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 109
Mapping of genes and ESTs assigned to 17q11.2 to a YAC contig centered on the NF1 gene 108
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 108
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 107
The case of the solitary sick kidney 105
null 105
A patient with a large 17p11.2 deletion presenting with Smith-Magenis (SMS) and Joubert syndromes (JS): a tool for mapping the JS gene?” 104
Cognitive impairment across ALS clinical stages in a population-based cohort 104
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes 101
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 101
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriers 100
HLA-class I markers and multiple sclerosis susceptibility in the Italian population 98
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis 96
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS 95
Variations of the perforin gene in patients with multiple sclerosis 95
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations 94
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 94
High resolution FISH tools 94
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 94
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 94
Predicting functional impairment trajectories in amyotrophic lateral sclerosis: a probabilistic, multifactorial model of disease progression 94
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 93
FISH with locus-specific probes on stretched chromosomes: a useful tool for genome organization studies. 91
A case of early-onset Parkinson's disease in a patient with KBG syndrome 90
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. 90
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease 89
ATXN-2 CAG repeat expansions are interrupted in ALS patients 89
Regional spreading of symptoms at diagnosis as a prognostic marker in amyotrophic lateral sclerosis: A population-based study 89
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 88
Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients 82
Parkinson's disease and chronic inflammatory demyelinating polyneuropathy: Broadening the clinical spectrum of VCP mutations 82
SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS) 81
Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 region 81
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect. 80
Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1) 80
Parkinsonism in SCA19/22: Dopamine Transporter Imaging in an Italian Family Harboring a Novel Mutation 79
Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis 79
Challenging the boundaries: c9orf72 mutation presenting as Alzheimer's disease 78
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia. 78
High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis 78
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology 77
No association of DPP6 with amyotrophic lateral sclerosis in an Italian population 77
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
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis 77
A Novel GBF1 Variant in a Charcot-Marie-Tooth Type 2: Insights from Familial Analysis 76
Variants in the 5′UTR reduce SHOX expression and contribute to SHOX haploinsufficiency 76
VPS54 genetic analysis in ALS Italian cohort 75
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis 72
Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions 72
Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis 71
Profiling cognition and brain metabolism in amyotrophic lateral sclerosis and frontotemporal dementia 71
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 71
Identification of Transcriptomic Differences in Induced Pluripotent Stem Cells and Neural Progenitors from Amyotrophic Lateral Sclerosis Patients Carrying Different Mutations: A Pilot Study 70
Metal(loid)s role in the pathogenesis of amyotrophic lateral sclerosis: Environmental, epidemiological, and genetic data 68
GBA variants influence cognitive status in amyotrophic lateral sclerosis 67
“Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population 66
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia. 65
Exploring the phenotypic fingerprints of ANXA11 variants in ALS: a population-based study in an European cohort 64
Identification of duplicated genes in 17q11.2 by using FISH on stretched chromosomes and DNA fibers 64
Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis 59
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS 59
Variability in Clinical Phenotype in TARDBP Mutations: Amyotrophic Lateral Sclerosis Case Description and Literature Review 58
Myoclonus‐Dystonia plus Syndrome in a Patient Carrying a Novel TCF20 Variant 56
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort 55
A case of late-onset OCD developing PLS and FTD 51
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data 42
A case of late-onset OCD developing PLS and FTD 33
A case of progressive non-fluent aphasia as onset of amyotrophic lateral sclerosis with frontotemporal dementia 32
Expanding the phenotypic spectrum of SOD1‑related ALS: upper motor neuron predominance in a p.D91A case. 15
A multi-omics study on monozygotic twins discordant for amyotrophic lateral sclerosis and literature review underline a potential role for innate immunity and epigenetic dysregulation in disease mechanisms 15
DNA Methylation Episignature as a Novel Diagnostic Tool for Diamond‐Blackfan Anemia Syndrome 1
Totale 9.111
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Categoria #
all - tutte 43.402
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 43.402
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202116 0 0 0 0 0 0 0 0 0 0 0 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
2025/20264.084 193 164 249 619 390 276 522 672 268 334 294 103
Totale 9.111