BRUNETTI, Maura
 Distribuzione geografica
Continente #
NA - Nord America 1219
EU - Europa 1007
AS - Asia 351
OC - Oceania 8
AF - Africa 6
SA - Sud America 1
Totale 2592
Nazione #
US - Stati Uniti d'America 1192
IT - Italia 327
CN - Cina 244
IE - Irlanda 171
SE - Svezia 136
AT - Austria 63
DE - Germania 56
FR - Francia 52
FI - Finlandia 45
GB - Regno Unito 43
VN - Vietnam 37
UA - Ucraina 31
KR - Corea 25
CA - Canada 23
BE - Belgio 21
IN - India 20
PL - Polonia 18
GR - Grecia 12
JP - Giappone 12
NL - Olanda 10
AU - Australia 8
UZ - Uzbekistan 7
HK - Hong Kong 4
MX - Messico 4
BG - Bulgaria 3
DK - Danimarca 3
HR - Croazia 3
ES - Italia 2
RO - Romania 2
RU - Federazione Russa 2
SN - Senegal 2
TN - Tunisia 2
BR - Brasile 1
BY - Bielorussia 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
EG - Egitto 1
ID - Indonesia 1
IS - Islanda 1
MT - Malta 1
NO - Norvegia 1
PT - Portogallo 1
SC - Seychelles 1
TR - Turchia 1
Totale 2592
Città #
Chandler 302
Dublin 170
Beijing 162
Torino 106
Houston 80
Fairfield 78
Vienna 63
Medford 53
Princeton 52
Jacksonville 51
Ann Arbor 47
Villeurbanne 43
Nyköping 37
Wilmington 33
Fremont 30
Woodbridge 29
Seattle 27
Dearborn 24
Turin 24
Redwood City 23
Ashburn 22
Cambridge 22
Milan 20
Dong Ket 18
Boston 16
Pisa 16
Warsaw 16
Brussels 13
Norwalk 13
Chengdu 11
Toronto 11
Boardman 10
Athens 9
Hangzhou 9
Hebei 9
Ottawa 8
Oxford 8
Hefei 7
Mountain View 7
San Diego 7
Seoul 7
Nürnberg 6
Nanjing 5
San Mauro Torinese 5
Bologna 4
Genova 4
London 4
Waanrode 4
Bethesda 3
Binasco 3
Cardiff 3
Guiyang 3
Jinan 3
Leawood 3
Modena 3
Reggio Emilia 3
Shenyang 3
Silver Spring 3
Southend 3
Amsterdam 2
Berlin 2
Birmingham 2
Brisbane 2
Buffalo 2
Central District 2
Clemmons 2
Des Moines 2
Falls Church 2
Ferrara di Monte Baldo 2
Florence 2
Gorizia 2
Guangzhou 2
Kunming 2
Leuven 2
Munich 2
Nanchang 2
Napoli 2
New York 2
Nijmegen 2
Pasadena 2
San Mateo 2
Sofia 2
Stockholm 2
Taranto 2
Tokyo 2
Trento 2
Vigevano 2
Xian 2
Aarhus 1
Aci Sant'antonio 1
Agugliano 1
Alessandria 1
Alghero 1
Atlanta 1
Aurora 1
Bari 1
Berkeley 1
Bozeman 1
Brescia 1
Brooklyn 1
Totale 1828
Nome #
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia 139
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion 122
Large Proportion of Amyotrophic Lateral Sclerosis Cases in Sardinia Due to a Single Founder Mutation of the TARDBP Gene 120
The multistep hypothesis of ALS revisited: The role of genetic mutations 112
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 100
Correlation between Apolipoprotein E genotype and brain metabolism in amyotrophic lateral sclerosis 98
Genetic counselling in ALS: facts, uncertainties and clinical suggestions 93
HFE p.H63D polymorphism does not influence ALS phenotype and survival 89
Extensive genetics of ALS: A population-based study in Italy 85
Cognitive impairment across ALS clinical stages in a population-based cohort 81
NADPH oxidase (NOX2) activity is a modifier of survival in ALS 80
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population 78
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis 75
NADPH oxidase (NOX2) activity is a modifier of survival in ALS. 73
A cluster of ALS Cases in Sardinia due to a founder mutation of the TARDBP gene 68
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation 67
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis 66
Common polymorphisms of chemokine (C-X3-C motif) receptor 1 gene modify amyotrophic lateral sclerosis outcome: A population-based study 66
An ALS patient with a Homozygous A382T Missense Mutation of the TARDBP Gene 62
A patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTD 61
An ALS-FTD Patient Carrying a Double Pathogenetic Mutation of C9ORF72 and TARDBP: Case Report 58
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 57
An ALS case with a novel D90N-SOD1 heterozygous missense mutation 51
The role of APOE in the occurrence of frontotemporal dementia in amyotrophic lateral sclerosis 48
ALS phenotype is influenced by age, sex, and genetics: A population-based study 48
Parkinsonian traits in amyotrophic lateral sclerosis (ALS): a prospective population-based study 48
UNC13A influences survival in Italian amyotrophic lateral sclerosis patients: a population-based study 47
A de novo missense mutation of the FUS gene in a "true" sporadic ALS case 44
TBK1 is associated with ALS and ALS-FTD in Sardinian patients 44
Regional spreading of symptoms at diagnosis as a prognostic marker in amyotrophic lateral sclerosis: A population-based study 43
Analysis of the GCG repeat length in NIPA1 gene in C9orf72-mediated ALS in a large Italian ALS cohort 41
Differential neuropsychological profile of ALS patients with and without C9orf72 mutation 40
Exome sequencing reveals VCP mutations as a cause of familial ALS 39
Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis 38
A familial amyotrophic lateral sclerosis pedigree discordant for a novel p.Glu46Asp heterozygous OPTN variant and the p.Ala5Val heterozygous SOD1 missense mutation 37
Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes 34
GBA variants influence cognitive status in amyotrophic lateral sclerosis 34
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort 30
A novel splice site FUS mutation in a familial ALS case: effects on protein expression 30
Broadening the clinical spectrum of FUS mutations: a case with monomelic amyotrophy with a late progression to amyotrophic lateral sclerosis 29
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture 28
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology 24
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS 20
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis 15
Novel compound heterozygous spatacsin mutations in a Greek kindred with hereditary spastic paraplegia SPG11 and dementia 13
Identifying and predicting amyotrophic lateral sclerosis clinical subgroups: a population-based machine-learning study 10
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: A cross-sectional study 9
Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral Sclerosis 7
Systematic evaluation of genetic mutations in ALS: a population-based study 7
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeats 5
Factors predicting disease progression in C9ORF72 ALS patients 5
Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis 4
Totale 2722
Categoria #
all - tutte 5419
article - articoli 0
book - libri 0
conference - conferenze 466
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 5885


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/2018179 0000 00 031 94291015
2018/2019200 51937 1417 1728 12223422
2019/2020351 69621 967 4930 47543023
2020/2021410 22382228 3123 2333 80302555
2021/2022612 14132351 3954 3325 3361150116
2022/2023714 109882089 95239 713 0000
Totale 2722