CNR Institutional Research Information System

VITALE, EMILIA
 Distribuzione geografica
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Continente #
AS - Asia 1.306
NA - Nord America 717
EU - Europa 397
SA - Sud America 237
AF - Africa 25
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.686
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Nazione #
US - Stati Uniti d'America 677
SG - Singapore 554
CN - Cina 306
BR - Brasile 189
VN - Vietnam 141
IT - Italia 140
HK - Hong Kong 131
FR - Francia 98
KR - Corea 55
DE - Germania 37
BD - Bangladesh 33
NL - Olanda 25
GB - Regno Unito 19
CA - Canada 18
FI - Finlandia 18
JP - Giappone 17
AR - Argentina 15
IN - India 13
AT - Austria 12
PL - Polonia 10
EC - Ecuador 8
IL - Israele 8
IQ - Iraq 8
ES - Italia 7
ID - Indonesia 7
MX - Messico 7
PK - Pakistan 7
ZA - Sudafrica 7
CO - Colombia 6
MA - Marocco 6
SA - Arabia Saudita 6
IE - Irlanda 5
PE - Perù 5
SE - Svezia 5
VE - Venezuela 5
KE - Kenya 4
PY - Paraguay 4
UA - Ucraina 4
BE - Belgio 3
CR - Costa Rica 3
PH - Filippine 3
RU - Federazione Russa 3
TR - Turchia 3
UZ - Uzbekistan 3
AZ - Azerbaigian 2
EG - Egitto 2
ET - Etiopia 2
HN - Honduras 2
HR - Croazia 2
JM - Giamaica 2
LT - Lituania 2
NZ - Nuova Zelanda 2
RS - Serbia 2
TN - Tunisia 2
UY - Uruguay 2
AM - Armenia 1
AU - Australia 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BS - Bahamas 1
BW - Botswana 1
CH - Svizzera 1
CI - Costa d'Avorio 1
CL - Cile 1
DO - Repubblica Dominicana 1
GE - Georgia 1
GI - Gibilterra 1
GT - Guatemala 1
GY - Guiana 1
HT - Haiti 1
JO - Giordania 1
LB - Libano 1
ME - Montenegro 1
MM - Myanmar 1
NI - Nicaragua 1
NP - Nepal 1
PA - Panama 1
PS - Palestinian Territory 1
SI - Slovenia 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
VC - Saint Vincent e Grenadine 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 2.686
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Città #
Singapore 323
Santa Clara 208
San Jose 131
Hong Kong 129
Hefei 108
Beijing 85
Lauterbourg 71
Seoul 52
Ashburn 51
Ho Chi Minh City 48
Hanoi 35
Los Angeles 30
Naples 29
Rome 23
Dallas 21
São Paulo 18
Marigliano 13
Buffalo 12
Düsseldorf 11
New York 11
Nuremberg 11
Tokyo 11
Helsinki 9
Milan 9
Haiphong 7
Rio de Janeiro 7
Belo Horizonte 6
Brasília 6
Da Nang 6
Lappeenranta 6
Montreal 6
Warsaw 6
Dublin 5
Frankfurt am Main 5
Jeddah 5
Minamishinagawa 5
Baghdad 4
Chennai 4
Chicago 4
Goiânia 4
Jacksonville 4
Johannesburg 4
Medellín 4
Orem 4
Phoenix 4
Poplar 4
Thái Bình 4
Amsterdam 3
Asunción 3
Bắc Giang 3
Cagliari 3
Dhaka 3
Florence 3
Guangzhou 3
Guarulhos 3
Houston 3
Lahore 3
Lima 3
Mogi das Cruzes 3
Nairobi 3
New Delhi 3
Ninh Bình 3
Ribeirão Preto 3
Roubaix 3
San Antonio 3
Seattle 3
Stockholm 3
Tashkent 3
Taubaté 3
Turku 3
Wroclaw 3
Addis Ababa 2
An Giang Province 2
Ankara 2
Atlanta 2
Avellino 2
Baku 2
Belgrade 2
Bengaluru 2
Boardman 2
Bologna 2
Brussels 2
Cairo 2
Can Tho 2
Cape Town 2
Catania 2
Caxias do Sul 2
Charlotte 2
City of London 2
Contagem 2
Council Bluffs 2
Denver 2
Durham 2
Embu das Artes 2
Falkenstein 2
Fayetteville 2
Geneva 2
Genoa 2
Guayaquil 2
Hampstead 2
Totale 1.693
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Nome #
Sustained Depolarization Induces Gene Expression Pattern Changes Related to Synaptic Plasticity in a Human Cholinergic Cellular Model 93
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts 85
Give a selfie for women @CNR 75
300x100: Protagoniste per la ricerca 71
CD33 rs2455069 SNP: Correlation with Alzheimer’s Disease and Hypothesis of Functional Role 71
Gold nanoparticles (AuNPs) cause variation in the level of methylation in H3K4 and H3K9 59
Variants of ST8SIA1 are associated with risk of developing multiple sclerosis 59
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia 59
Loss-of-function mutations of progranulin (PGRN) in siblings with familial FTLD 58
Molecular responses of cells to 2-mercapto-1-methylimidazole gold nanoparticles (AuNPs)-mmi: investigations of histone methylation changes 58
GRN deletion in Familial Fronto-Temporal Dementia showing Association with clinical Variability in three familial cases 58
Uncommon PGRN deletion and FTD responsible for phenotype variability in three familial cases. 58
Fertility in a case of isochromosome Xq Klinefelter Syndrome (KS) 55
Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 55
CD33 and SIGLECL1 Immunoglobulin Superfamily Involved in Dementia 55
Identification, Characterization, and Regulatory Mechanisms of a Novel EGR1 Splicing Isoform 55
Clinical and Molecular Characterization of a Novel Progranulin Deletion Associated with Different Phenotypes 54
Circulating levels of IL-1 family cytokines and receptors in Alzheimer's disease: new markers of disease progression? 54
Imidazole-stabilized gold nanoparticles induce neuronal apoptosis: An in vitro and in vivo study 50
Metabolic response of SH-SY5Y cells to gold nanoparticles by NMR-based metabolomics analyses 50
Imidazole-stabilized gold nanoparticles induce neuronal apoptosis: An in vitro and in vivo study 49
Donor splice-site mutation in CUL4B is likely cause of X-linked intellectual disability 47
Imidazole-stabilized gold nanoparticles induce neuronal apoptosis: an in vitro and in vivo study. 47
Linc00473 as an immediate early gene under the control of the egr1 transcription factor 45
Early molecular and cellular characterization of extraocular phototransductive elements in Hydra (Cnidraria, Hydrozoa) 44
Loss-of-function mutations of progranulin (PGRN) in a familial FTLD 44
Loss-of-function mutation of progranulin (PGRN) in a familial FTLD 44
SH-imi-goldnanoparticles a possible drug target carrier: an evaluation using epigenetic histone dimethylation levels 43
Assignment of human aldolase C gene to chromosome 17, region cen→q21.1 43
Role of cytosolic calcium-dependent phospholipase A2 in Alzheimer's disease pathogenesis 41
Gold nanoparticles (AuNPs) in vivo and in vitro neuronal interaction 36
Non visual photoreception in Hydra: Molecular and morpho-functional correlates of the signal transduction cascade, 34
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene 32
Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12. 32
Microarray analysis identifies up-regulation of CD36 in human PBMC treated with endocannabinoids. 31
Rs34424835 PGRN gene variation a possible modifier in Frontotemporal lobar degeneration (FTLD) 31
Characterization of a type II collagen gene (COL2A1) mutation identified in cultured chondrocytes from human hypochondrogenesis 30
Early molecular and cellular characterization of extraocular phototransductive elements in Hydra 30
Cortical Metabolic Deficits in a Rat Model of Cholinergic Basal Forebrain Degeneration 30
Clinical and genetic associations in Marfan syndrome and related disorders 30
Impaired Ganglioside synthesis involved with pathogenic mechanism in a familial form of multiple sclerosis. 29
PGRN exon 6 deletion G.101349_101355delCTGCTGT associated with Nonfluent primary progressive aphasia in a familial form of FTLD 29
Second family with hearing impairment linked to 19q13 and refined DFNA4 localization. 28
Genetic linkage of the marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5 27
A second Middle Eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9 27
Arvanil and anandamide up-regulate CD36 expression in human peripheral blood mononuclear cells 27
Potential fertility in a case of isochromosome Xq Klinefelter syndrome (KS) due to maternal meiotic error:review of the i (Xq) KS casuistry. 26
Arvanil and anandamide up-regulate CD36 expression in human peripheral blood mononuclear cells. 26
Role of Cytosolic Calcium-Dependent Phospholipase A2 in Alzheimer's Disease Pathogenesis. 25
Genome Mapping of Multiple Sclerosis in alarge American pedigree. 25
Novel X-Linked mental retardation syndrome with short stature maps to Xq24. 24
Influence of Variations in Two Serotonin Genes and Gender Differences on Learning and Memory. 24
Linkage studies of non syndromic recessive deafness in a Turkishkindred which segregates DFNB9. 24
Gold nanoparticles (AuNPs) cross the BBB and induce cytotoxicity in SH-SY5Y cells 24
Paraparesi spastica complicata da epilessia in due fratelli 24
ST8SIA1 gene variants associated with risk of developing multiple sclerosis 24
Gold nanoparticles (AuNPs) cross the blood brain barrier and induce cytotoxicity in human neuroblastoma cells SH-SY5Y: an in vivo and in vitro study 23
Crossing of BBB using gold nanoparticles (AuNPs) 23
Variants of Risk of ST8SIA1 are associated with the risk of developing multiple sclerosis 23
A novel frameshift mutation of FOXC2gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitus 23
A familial form of multiple sclerosis showing impaired ganglioside synthesis. 22
Structural chromosomal variations in neurological diseases 22
Arvanil and anandamide up-regulate CD36 expression in human peripheral blood mononuclear cells 22
Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes 22
Genomic cloning and characterization of the human thrombin receptor gene: Structural similarity to the proteinase activated receptor-2 gene 21
Arvanil and anandamideup-regulate CD36 expression in human peripheral blood mononuclearcells. 21
A previously unreportedsyndrome of X-linked mental retardation with short stature maps toXq24 20
Risk of developing multiple sclerosis is associated with variants in the ST8SIA1 gene 19
Crossing of BBB using gold nanoparticles (AuNPS) 19
Repating developmental expression of G-Hox 7, a novel homeobox-containing gene in the chicken 19
Suggestive linkage of situs inversusand other left-right abnormalities to chromosome 6p. 18
Characterization of the human MSX-1 promoter and an enhancer responsible for retinoic acid induction 17
Totale 2.742
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Categoria #
all - tutte 8.938
article - articoli 5.809
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 14.747
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202412 0 0 0 0 0 0 0 0 2 4 4 2
2024/20251.049 3 3 67 35 198 78 13 67 49 39 262 235
2025/20261.627 109 139 152 249 267 81 243 108 92 92 63 32
2026/202754 54 0 0 0 0 0 0 0 0 0 0 0
Totale 2.742