CINECA IRIS Institutional Research Information System

BRUNETTI, Maura
 Distribuzione geografica
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Continente #
NA - Nord America 2.502
EU - Europa 1.866
AS - Asia 1.674
SA - Sud America 253
AF - Africa 31
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 1
Totale 6.347
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Nazione #
US - Stati Uniti d'America 2.440
SG - Singapore 762
IT - Italia 555
CN - Cina 532
DE - Germania 280
BR - Brasile 213
IE - Irlanda 212
FI - Finlandia 201
SE - Svezia 160
VN - Vietnam 104
AT - Austria 95
KR - Corea 77
FR - Francia 74
GB - Regno Unito 70
IN - India 53
NL - Olanda 48
HK - Hong Kong 45
CA - Canada 37
UA - Ucraina 35
PL - Polonia 27
JP - Giappone 22
BE - Belgio 21
ID - Indonesia 20
MX - Messico 19
AR - Argentina 17
AU - Australia 17
RU - Federazione Russa 17
ES - Italia 15
GR - Grecia 15
TR - Turchia 13
ZA - Sudafrica 11
BD - Bangladesh 9
CZ - Repubblica Ceca 9
UZ - Uzbekistan 8
BG - Bulgaria 7
EC - Ecuador 7
EG - Egitto 5
IQ - Iraq 5
CL - Cile 4
DK - Danimarca 4
HR - Croazia 4
MA - Marocco 4
PT - Portogallo 4
PY - Paraguay 4
PK - Pakistan 3
TH - Thailandia 3
AE - Emirati Arabi Uniti 2
CH - Svizzera 2
CO - Colombia 2
DZ - Algeria 2
IL - Israele 2
IR - Iran 2
JO - Giordania 2
KZ - Kazakistan 2
LT - Lituania 2
NP - Nepal 2
NZ - Nuova Zelanda 2
PE - Perù 2
RO - Romania 2
SN - Senegal 2
TN - Tunisia 2
TW - Taiwan 2
UY - Uruguay 2
BB - Barbados 1
BO - Bolivia 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
HN - Honduras 1
IS - Islanda 1
JM - Giamaica 1
KE - Kenya 1
LV - Lettonia 1
MT - Malta 1
NE - Niger 1
NO - Norvegia 1
OM - Oman 1
PH - Filippine 1
PR - Porto Rico 1
PS - Palestinian Territory 1
PW - Palau 1
RS - Serbia 1
SA - Arabia Saudita 1
SC - Seychelles 1
SI - Slovenia 1
TG - Togo 1
VE - Venezuela 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 6.347
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Città #
Singapore 397
Chandler 316
Beijing 241
Ashburn 232
Dublin 209
Santa Clara 169
Munich 154
Turin 130
Torino 106
Dallas 93
Houston 80
Fairfield 78
Vienna 74
Helsinki 69
Seoul 59
Hefei 58
Lappeenranta 57
Nyköping 54
Medford 53
Princeton 52
Columbus 51
Jacksonville 51
Los Angeles 49
Ann Arbor 47
Villeurbanne 43
Milan 41
Hong Kong 40
Seattle 35
Buffalo 34
Nuremberg 33
Wilmington 33
Fremont 31
Woodbridge 29
Dearborn 24
Redwood City 24
Turku 23
Cambridge 22
Ho Chi Minh City 21
Bengaluru 20
Warsaw 20
Boston 19
Jakarta 19
São Paulo 19
Dong Ket 18
Boardman 16
Hanoi 16
New York 16
Pisa 16
Amsterdam 15
Redondo Beach 15
Düsseldorf 14
Nanjing 14
Brussels 13
Norwalk 13
Toronto 13
Chengdu 11
Guangzhou 11
London 11
Agliè 9
Athens 9
Hangzhou 9
Hebei 9
Frankfurt am Main 8
Ottawa 8
Oxford 8
Silver Spring 8
Johannesburg 7
Jyväskylä 7
Mountain View 7
San Diego 7
Shanghai 7
Lauterbourg 6
Mexico City 6
Moncalieri 6
Montreal 6
Nürnberg 6
Rio de Janeiro 6
Rome 6
Stockholm 6
Sydney 6
Valencia 6
Belo Horizonte 5
Brooklyn 5
Changsha 5
Chicago 5
Curitiba 5
Falkenstein 5
Phoenix 5
San Francisco 5
San Mauro Torinese 5
Tokyo 5
Washington 5
Birmingham 4
Biên Hòa 4
Bologna 4
Dhaka 4
Genova 4
Istanbul 4
Mumbai 4
Novara 4
Totale 3.871
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Nome #
Parkinsonian traits in amyotrophic lateral sclerosis (ALS): a prospective population-based study 253
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia 216
A novel p.Ser108LeufsTer15 SOD1 mutation leading to the formation of a premature stop codon in an apparently sporadic ALS patient: insights into the underlying pathomechanisms 206
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 200
Correlation between Apolipoprotein E genotype and brain metabolism in amyotrophic lateral sclerosis 195
The multistep hypothesis of ALS revisited: The role of genetic mutations 192
Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP Gene 169
Cognitive impairment across ALS clinical stages in a population-based cohort 160
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis 154
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 145
NADPH oxidase (NOX2) activity is a modifier of survival in ALS 143
Regional spreading of symptoms at diagnosis as a prognostic marker in amyotrophic lateral sclerosis: A population-based study 141
HFE p.H63D polymorphism does not influence ALS phenotype and survival 140
Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes 129
NADPH oxidase (NOX2) activity is a modifier of survival in ALS. 125
Extensive genetics of ALS: A population-based study in Italy 124
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis 124
Common polymorphisms of chemokine (C-X3-C motif) receptor 1 gene modify amyotrophic lateral sclerosis outcome: A population-based study 121
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS 121
A cluster of ALS Cases in Sardinia due to a founder mutation of the TARDBP gene 118
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population 118
ALS phenotype is influenced by age, sex, and genetics: A population-based study 116
A patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTD 113
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 111
Differential neuropsychological profile of ALS patients with and without C9orf72 mutation 110
An ALS-FTD Patient Carrying a Double Pathogenetic Mutation of C9ORF72 and TARDBP: Case Report 108
A novel splice site FUS mutation in a familial ALS case: effects on protein expression 108
An ALS patient with a Homozygous A382T Missense Mutation of the TARDBP Gene 102
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 102
An ALS case with a novel D90N-SOD1 heterozygous missense mutation 101
Analysis of the GCG repeat length in NIPA1 gene in C9orf72-mediated ALS in a large Italian ALS cohort 100
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation 97
A familial amyotrophic lateral sclerosis pedigree discordant for a novel p.Glu46Asp heterozygous OPTN variant and the p.Ala5Val heterozygous SOD1 missense mutation 97
A de novo missense mutation of the FUS gene in a "true" sporadic ALS case 96
GBA variants influence cognitive status in amyotrophic lateral sclerosis 94
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 93
UNC13A influences survival in Italian amyotrophic lateral sclerosis patients: a population-based study 93
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort 92
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology 89
Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis 84
The role of APOE in the occurrence of frontotemporal dementia in amyotrophic lateral sclerosis 80
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 79
Systematic evaluation of genetic mutations in ALS: a population-based study 78
Factors predicting disease progression in C9ORF72 ALS patients 76
Broadening the clinical spectrum of FUS mutations: a case with monomelic amyotrophy with a late progression to amyotrophic lateral sclerosis 76
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis 74
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: A cross-sectional study 74
High Frequency of Cognitive and Behavioral Impairment in Amyotrophic Lateral Sclerosis Patients with SOD1 Pathogenic Variants 72
Exome sequencing reveals VCP mutations as a cause of familial ALS 71
Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral Sclerosis 67
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture 67
Cognitive and Behavioral Features of Patients With Amyotrophic Lateral Sclerosis Who Are Carriers of the TARDBP Pathogenic Variant 62
Predictors for progression in amyotrophic lateral sclerosis associated to SOD1 mutation: insight from two population-based registries 59
Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis 59
Brain Metabolic Features of FUS-ALS: A 2-[18F]FDG-PET Study 58
Frequency and Early Predictors of Cognitive Deterioration in Amyotrophic Lateral Sclerosis: A Longitudinal Population-Based Study 48
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations 46
KIF5A p.Pro986Leu Risk Variant and Accelerated Progression of Amyotrophic Lateral Sclerosis 41
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data 40
Novel compound heterozygous spatacsin mutations in a Greek kindred with hereditary spastic paraplegia SPG11 and dementia 40
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis 34
Totale 6.501
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Categoria #
all - tutte 24.320
article - articoli 0
book - libri 0
conference - conferenze 1.547
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 25.867
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021300 0 0 0 0 31 23 23 33 80 30 25 55
2021/2022612 14 13 23 51 39 54 33 25 33 61 150 116
2022/20231.006 109 88 20 89 95 239 59 56 133 30 51 37
2023/2024502 65 90 36 18 20 51 36 16 5 75 35 55
2024/20251.734 24 76 48 126 319 139 103 127 279 110 163 220
2025/20261.251 318 165 241 321 206 0 0 0 0 0 0 0
Totale 6.501