IRIS
CORRADO, Lucia
 Distribuzione geografica
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Continente #
EU - Europa 2.043
NA - Nord America 1.510
AS - Asia 382
Continente sconosciuto - Info sul continente non disponibili 4
SA - Sud America 3
AF - Africa 1
Totale 3.943
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Nazione #
US - Stati Uniti d'America 1.500
IE - Irlanda 636
DE - Germania 328
SE - Svezia 326
IT - Italia 323
UA - Ucraina 198
CN - Cina 126
SG - Singapore 118
FI - Finlandia 110
HK - Hong Kong 71
GB - Regno Unito 33
IN - India 30
CZ - Repubblica Ceca 24
NL - Olanda 24
BE - Belgio 21
IR - Iran 14
FR - Francia 12
CA - Canada 10
TR - Turchia 9
VN - Vietnam 6
EU - Europa 4
CH - Svizzera 2
CL - Cile 2
GR - Grecia 2
ID - Indonesia 2
AZ - Azerbaigian 1
BR - Brasile 1
BY - Bielorussia 1
EG - Egitto 1
HR - Croazia 1
IL - Israele 1
IQ - Iraq 1
KG - Kirghizistan 1
LK - Sri Lanka 1
PH - Filippine 1
PL - Polonia 1
RO - Romania 1
Totale 3.943
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Città #
Dublin 636
Jacksonville 372
Dearborn 178
Chandler 125
Singapore 79
Wilmington 77
Hong Kong 71
Piemonte 69
Lawrence 68
Princeton 68
Ann Arbor 64
Bremen 53
Beijing 52
San Mateo 49
Boardman 31
Munich 27
Andover 24
Ashburn 23
Brno 23
Turin 17
Woodbridge 17
Houston 16
Düsseldorf 15
Helsinki 15
Nanjing 14
Brussels 13
Dallas 13
Milan 13
Kunming 10
Leawood 10
Monmouth Junction 10
Mülheim 10
Novara 10
Zanjan 10
Borgomanero 9
Hefei 9
Norwalk 9
Rome 8
Waanrode 8
Kocaeli 7
Strasbourg 7
Dong Ket 6
Nanchang 5
Sacramento 5
Toronto 5
Dronten 4
Guangzhou 4
New York 4
Santa Clara 4
Seattle 4
Trieste 4
Vercelli 4
Alessandria 3
Ardabil 3
Augusta 3
Cassano Magnago 3
Frankfurt am Main 3
Jinan 3
Los Angeles 3
Philadelphia 3
Winnipeg 3
Wuhan 3
Albuzzano 2
Auburn Hills 2
Baotou 2
Bologna 2
Cascina 2
Changsha 2
Chengdu 2
Cologne 2
Concordia sulla Secchia 2
Espoo 2
Fairfield 2
Gunzenhausen 2
Hangzhou 2
Lissone 2
Mumbai 2
Ottawa 2
Pisa 2
Priocca 2
Savona 2
Torino 2
Washington 2
Zurich 2
Altamura 1
Amsterdam 1
Ariccia 1
Asti 1
Baghdad 1
Baku 1
Bangalore 1
Bari 1
Bishkek 1
Boston 1
Buffalo 1
Cairo 1
Cambridge 1
Carate Brianza 1
Chieti 1
Chongqing 1
Totale 2.478
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Nome #
Analysis of the GCG Repeat Length in NIPA1 Gene in C9orf72-mediated ALS in a Large Italian ALS Cohort 84
Extensive genetics of ALS: a population-based study in Italy. 82
Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR 80
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 79
Coeliac disease mimicking Amyotrophic Lateral Sclerosis. 79
ALS Phenotype Is Influenced by Age, Sex, and Genetics: A Population-Based Study 76
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes 74
A case of late-onset OCD developing PLS and FTD 70
Mapping of genes and ESTs assigned to 17q11.2 to a YAC contig centered on the NF1 gene 69
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 69
ATXN2 polyQ intermediate repeats are a modifier of ALS survival. 69
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population 69
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 68
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases 68
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 67
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies 67
A case of Progressive Non-Fluent Aphasia as onset of Amyotrophic Lateral Sclerosis with FrontoTemporal Dementia 67
Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. 66
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis 64
The case of the solitary sick kidney 62
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 62
High resolution FISH tools 61
Ptosis and bulbar onset: an unusual phenotype of familial ALS? 61
A patient with a large 17p11.2 deletion presenting with Smith-Magenis (SMS) and Joubert syndromes (JS): a tool for mapping the JS gene?” 61
The multistep hypothesis of ALS revisited: The role of genetic mutations 61
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 60
A recurrent signal peptide mutation in the growth hormone releasing hormone receptor with defective translocation to the cell surface and isolated growth hormone deficiency 60
A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 59
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study 59
Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects. 58
ATXN-2 CAG repeat expansions are interrupted in ALS patients 58
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 57
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect. 57
Association of osteopontin regulatory polymorphisms with systemic sclerosis 57
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 56
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. 56
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 55
The First Case of the TARDBP p.G294V Mutation in a Homozygous State: Is a Single Pathogenic Allele Sufficient to Cause ALS? 55
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 54
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering 53
FISH with locus-specific probes on stretched chromosomes: a useful tool for genome organization studies. 51
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 50
Variations of the perforin gene in patients with multiple sclerosis 48
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 48
HLA-class I markers and multiple sclerosis susceptibility in the Italian population 47
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 47
Cognitive impairment across ALS clinical stages in a population-based cohort 47
Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis 46
SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS) 46
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 44
Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 region 43
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia. 41
“Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population 40
High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis 40
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis 40
Regional spreading of symptoms at diagnosis as a prognostic marker in amyotrophic lateral sclerosis: A population-based study 40
Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1) 39
Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population 39
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease 38
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia. 38
No association of DPP6 with amyotrophic lateral sclerosis in an Italian population 37
Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions 37
VPS54 genetic analysis in ALS Italian cohort 37
Identification of duplicated genes in 17q11.2 by using FISH on stretched chromosomes and DNA fibers 36
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis 36
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS 35
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS 34
Predicting functional impairment trajectories in amyotrophic lateral sclerosis: a probabilistic, multifactorial model of disease progression 34
Variants in the 5′UTR reduce SHOX expression and contribute to SHOX haploinsufficiency 31
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis 30
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants 29
Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients 26
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriers 25
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 23
Metal(loid)s role in the pathogenesis of amyotrophic lateral sclerosis: Environmental, epidemiological, and genetic data 22
Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis 21
GBA variants influence cognitive status in amyotrophic lateral sclerosis 16
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology 15
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort 15
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis 14
Parkinsonism in SCA19/22: Dopamine Transporter Imaging in an Italian Family Harboring a Novel Mutation 12
A case of early-onset Parkinson's disease in a patient with KBG syndrome 12
Parkinson's disease and chronic inflammatory demyelinating polyneuropathy: Broadening the clinical spectrum of VCP mutations 11
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations 6
Variability in Clinical Phenotype in TARDBP Mutations: Amyotrophic Lateral Sclerosis Case Description and Literature Review 5
Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis 3
Totale 4.063
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Categoria #
all - tutte 23.822
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 23.822
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020640 0 0 0 0 108 122 145 34 78 63 86 4
2020/2021481 66 2 66 3 63 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
2024/2025197 35 31 76 38 17 0 0 0 0 0 0 0
Totale 4.063