IRIS
CORRADO, Lucia
 Distribuzione geografica
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Continente #
EU - Europa 3.563
NA - Nord America 3.418
AS - Asia 2.197
SA - Sud America 371
Continente sconosciuto - Info sul continente non disponibili 151
AF - Africa 90
OC - Oceania 2
Totale 9.792
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Nazione #
US - Stati Uniti d'America 3.307
RU - Federazione Russa 837
SG - Singapore 657
IE - Irlanda 640
IT - Italia 566
CN - Cina 555
DE - Germania 422
SE - Svezia 338
VN - Vietnam 314
HK - Hong Kong 280
BR - Brasile 275
UA - Ucraina 213
FI - Finlandia 128
FR - Francia 125
GB - Regno Unito 86
BD - Bangladesh 82
IN - India 72
KR - Corea 66
CA - Canada 58
BJ - Benin 40
AR - Argentina 39
NL - Olanda 36
MX - Messico 32
PL - Polonia 30
ID - Indonesia 25
JP - Giappone 25
BE - Belgio 24
CZ - Repubblica Ceca 24
ZA - Sudafrica 21
AT - Austria 19
IQ - Iraq 19
TR - Turchia 19
ES - Italia 18
IR - Iran 15
EE - Estonia 14
CO - Colombia 12
EC - Ecuador 12
JM - Giamaica 12
PH - Filippine 11
LT - Lituania 9
CL - Cile 8
DZ - Algeria 8
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
RO - Romania 5
BO - Bolivia 4
EU - Europa 4
JO - Giordania 4
UZ - Uzbekistan 4
DK - Danimarca 3
DO - Repubblica Dominicana 3
EG - Egitto 3
GR - Grecia 3
IL - Israele 3
LV - Lettonia 3
RS - Serbia 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
QA - Qatar 2
SN - Senegal 2
SY - Repubblica araba siriana 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BS - Bahamas 1
BW - Botswana 1
CR - Costa Rica 1
ET - Etiopia 1
GY - Guiana 1
HN - Honduras 1
HU - Ungheria 1
KE - Kenya 1
KH - Cambogia 1
KW - Kuwait 1
LY - Libia 1
MD - Moldavia 1
MK - Macedonia 1
NG - Nigeria 1
PA - Panama 1
PT - Portogallo 1
SC - Seychelles 1
Totale 9.643
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Città #
Dublin 638
Jacksonville 373
San Jose 345
Hong Kong 279
Singapore 239
Council Bluffs 207
Ashburn 202
Beijing 188
Dearborn 178
Chandler 125
Columbus 109
Los Angeles 109
Moscow 105
Ho Chi Minh City 88
Lauterbourg 81
Wilmington 78
Piemonte 69
Lawrence 68
Princeton 68
Ann Arbor 64
Seoul 62
New York 61
Novara 61
Hanoi 54
Bremen 53
Munich 52
Buffalo 51
San Mateo 49
Santa Clara 43
Rome 41
Cotonou 40
Dallas 38
Orem 35
Milan 34
Houston 33
Boardman 31
The Dalles 30
Warsaw 28
São Paulo 27
Phoenix 25
Turin 25
Andover 24
Helsinki 24
Brno 23
Brooklyn 19
Denver 19
Guangzhou 19
Nanjing 18
Philadelphia 18
Tokyo 18
Woodbridge 17
Brussels 16
Frankfurt am Main 16
Haiphong 16
Montreal 16
Nuremberg 16
Chennai 15
Düsseldorf 15
Mexico City 15
Tianjin 15
Atlanta 14
Chicago 14
Redondo Beach 14
Boston 13
Falkenstein 13
Tornaco 13
Toronto 13
Da Nang 12
Hangzhou 12
London 12
Stockholm 12
Johannesburg 11
Poplar 11
Villadossola 11
Kunming 10
Leawood 10
Monmouth Junction 10
Mülheim 10
Norwalk 10
Rio de Janeiro 10
Vienna 10
Zanjan 10
Amsterdam 9
Borgomanero 9
Hefei 9
Hải Dương 9
Shanghai 9
Turku 9
Ankara 8
San Francisco 8
Seattle 8
Waanrode 8
Baghdad 7
Biên Hòa 7
Brasília 7
Jakarta 7
Kocaeli 7
Manchester 7
Mumbai 7
Nanchang 7
Totale 5.222
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Nome #
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 185
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 171
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 163
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 150
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 148
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 147
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 141
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 136
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 135
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 135
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 134
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 133
A recurrent signal peptide mutation in the growth hormone releasing hormone receptor with defective translocation to the cell surface and isolated growth hormone deficiency 133
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 132
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 131
Association of osteopontin regulatory polymorphisms with systemic sclerosis 129
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 126
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 126
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 126
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants 123
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 122
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 121
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 120
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 118
The multistep hypothesis of ALS revisited: The role of genetic mutations 118
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR 117
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 117
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 115
Extensive genetics of ALS: a population-based study in Italy. 113
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 113
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 112
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriers 111
Mapping of genes and ESTs assigned to 17q11.2 to a YAC contig centered on the NF1 gene 111
Cognitive impairment across ALS clinical stages in a population-based cohort 111
The case of the solitary sick kidney 108
A patient with a large 17p11.2 deletion presenting with Smith-Magenis (SMS) and Joubert syndromes (JS): a tool for mapping the JS gene?” 107
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes 106
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 106
Variations of the perforin gene in patients with multiple sclerosis 105
null 105
HLA-class I markers and multiple sclerosis susceptibility in the Italian population 104
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis 101
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 101
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS 100
Predicting functional impairment trajectories in amyotrophic lateral sclerosis: a probabilistic, multifactorial model of disease progression 100
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations 99
Regional spreading of symptoms at diagnosis as a prognostic marker in amyotrophic lateral sclerosis: A population-based study 98
High resolution FISH tools 97
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 97
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 97
A case of early-onset Parkinson's disease in a patient with KBG syndrome 96
FISH with locus-specific probes on stretched chromosomes: a useful tool for genome organization studies. 95
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 95
A Novel GBF1 Variant in a Charcot-Marie-Tooth Type 2: Insights from Familial Analysis 94
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease 94
ATXN-2 CAG repeat expansions are interrupted in ALS patients 94
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. 93
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 93
Challenging the boundaries: c9orf72 mutation presenting as Alzheimer's disease 90
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology 89
Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1) 89
Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients 87
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 87
Variants in the 5′UTR reduce SHOX expression and contribute to SHOX haploinsufficiency 87
Parkinson's disease and chronic inflammatory demyelinating polyneuropathy: Broadening the clinical spectrum of VCP mutations 86
Parkinsonism in SCA19/22: Dopamine Transporter Imaging in an Italian Family Harboring a Novel Mutation 85
Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis 85
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect. 85
Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 region 85
Profiling cognition and brain metabolism in amyotrophic lateral sclerosis and frontotemporal dementia 84
SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS) 83
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis 83
No association of DPP6 with amyotrophic lateral sclerosis in an Italian population 82
High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis 82
Identification of Transcriptomic Differences in Induced Pluripotent Stem Cells and Neural Progenitors from Amyotrophic Lateral Sclerosis Patients Carrying Different Mutations: A Pilot Study 81
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia. 81
Exploring the phenotypic fingerprints of ANXA11 variants in ALS: a population-based study in an European cohort 80
Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions 80
VPS54 genetic analysis in ALS Italian cohort 78
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 77
Metal(loid)s role in the pathogenesis of amyotrophic lateral sclerosis: Environmental, epidemiological, and genetic data 76
Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis 75
GBA variants influence cognitive status in amyotrophic lateral sclerosis 75
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis 75
Identification of duplicated genes in 17q11.2 by using FISH on stretched chromosomes and DNA fibers 70
Variability in Clinical Phenotype in TARDBP Mutations: Amyotrophic Lateral Sclerosis Case Description and Literature Review 70
“Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population 69
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia. 69
Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis 68
Myoclonus‐Dystonia plus Syndrome in a Patient Carrying a Novel TCF20 Variant 67
A case of late-onset OCD developing PLS and FTD 66
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS 64
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort 63
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data 51
A case of late-onset OCD developing PLS and FTD 47
A case of progressive non-fluent aphasia as onset of amyotrophic lateral sclerosis with frontotemporal dementia 43
Expanding the phenotypic spectrum of SOD1‑related ALS: upper motor neuron predominance in a p.D91A case. 34
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 28
DNA Methylation Episignature as a Novel Diagnostic Tool for Diamond‐Blackfan Anemia Syndrome 28
Totale 9.792
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Categoria #
all - tutte 47.170
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 47.170
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022547 0 0 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
2025/20264.098 193 164 249 619 390 276 522 672 268 334 294 117
2026/2027667 220 333 114 0 0 0 0 0 0 0 0 0
Totale 9.792