CRIS Current Research Information System

MARASCO, ELENA
 Distribuzione geografica
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Continente #
NA - Nord America 3.053
AS - Asia 2.585
EU - Europa 2.449
AF - Africa 200
SA - Sud America 144
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.442
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Nazione #
US - Stati Uniti d'America 3.008
VN - Vietnam 707
SG - Singapore 696
IT - Italia 624
CN - Cina 614
GB - Regno Unito 530
SE - Svezia 295
DE - Germania 244
HK - Hong Kong 159
FR - Francia 123
IN - India 120
NL - Olanda 107
RU - Federazione Russa 100
BR - Brasile 91
IE - Irlanda 84
FI - Finlandia 61
ZA - Sudafrica 58
UA - Ucraina 56
CI - Costa d'Avorio 48
KR - Corea 48
JP - Giappone 43
TG - Togo 43
BG - Bulgaria 35
JO - Giordania 35
CH - Svizzera 32
EE - Estonia 32
GR - Grecia 27
CA - Canada 26
PH - Filippine 26
ID - Indonesia 23
BE - Belgio 22
SC - Seychelles 21
AT - Austria 19
AR - Argentina 18
UZ - Uzbekistan 16
TH - Thailandia 15
TR - Turchia 15
MX - Messico 14
NG - Nigeria 14
CL - Cile 11
IR - Iran 11
IQ - Iraq 10
LT - Lituania 10
PL - Polonia 10
AU - Australia 9
BD - Bangladesh 9
PK - Pakistan 8
EC - Ecuador 7
ES - Italia 7
RO - Romania 7
AL - Albania 5
PE - Perù 5
PY - Paraguay 5
TW - Taiwan 5
EG - Egitto 4
SK - Slovacchia (Repubblica Slovacca) 4
CO - Colombia 3
CZ - Repubblica Ceca 3
ET - Etiopia 3
HR - Croazia 3
KE - Kenya 3
KZ - Kazakistan 3
PS - Palestinian Territory 3
SA - Arabia Saudita 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
AM - Armenia 2
DK - Danimarca 2
HU - Ungheria 2
JM - Giamaica 2
KH - Cambogia 2
LB - Libano 2
LU - Lussemburgo 2
MA - Marocco 2
NO - Norvegia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AO - Angola 1
AZ - Azerbaigian 1
BH - Bahrain 1
BO - Bolivia 1
CG - Congo 1
CY - Cipro 1
DZ - Algeria 1
GE - Georgia 1
IL - Israele 1
MQ - Martinica 1
NI - Nicaragua 1
OM - Oman 1
RS - Serbia 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
TJ - Tagikistan 1
TN - Tunisia 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 8.442
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Città #
Singapore 502
Southend 454
Ashburn 341
Fairfield 307
Chandler 274
Bologna 200
Hong Kong 155
Houston 143
Ann Arbor 135
San Jose 135
Seattle 133
Ho Chi Minh City 131
Hanoi 126
Woodbridge 126
Wilmington 114
Beijing 111
Dong Ket 105
Cambridge 102
Princeton 86
Dublin 84
Santa Clara 81
Los Angeles 64
Hefei 62
Boardman 59
Helsinki 54
Abidjan 48
Nanjing 47
Lomé 43
Westminster 42
Amman 35
Lauterbourg 35
Sofia 35
Padova 34
New York 30
Tokyo 30
Council Bluffs 29
Seoul 28
Munich 27
Berlin 26
Bern 26
Milan 26
Guangzhou 23
Jacksonville 23
Saint Petersburg 22
Falls Church 21
Brussels 20
Jinan 19
Buffalo 18
Da Nang 18
Hebei 18
London 18
Redmond 18
São Paulo 18
Phoenix 16
Cento 15
Florence 15
Haiphong 15
Jakarta 15
Redondo Beach 15
Shenyang 15
Changsha 14
Dallas 14
Nanchang 14
Turin 14
Bremen 13
Frankfurt am Main 13
San Diego 13
Tianjin 13
Dearborn 12
Hangzhou 12
Shanghai 12
Abeokuta 11
Johannesburg 11
Paris 11
Vienna 11
Zhengzhou 11
Medford 10
Norwalk 10
Olalla 10
Shenzhen 10
Des Moines 9
Falkenstein 9
Nashville 9
Redwood City 9
Rome 9
Amsterdam 8
Ningbo 8
Warsaw 8
Montreal 7
Nuremberg 7
Orem 7
Athens 6
Atlanta 6
Boston 6
Brooklyn 6
Chennai 6
Mountain View 6
Mumbai 6
Poplar 6
Rimini 6
Totale 5.350
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Nome #
Acceleration of leukocytes' epigenetic age as an early tumorand sex-specific marker of breast and colorectal cancer 378
Genomic history of the Italian population recapitulates key evolutionary dynamics of both Continental and Southern Europeans 375
A POLYMORPHISM IN THE CHROMOSOME 9P21 ANRIL LOCUS IS ASSOCIATED TO PHILADELPHIA POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA SUSCEPTIBILITY 347
A polymorphism in the chromosome 9p21 ANRIL locus is associated to Philadelphia positive acute lymphoblastic leukemia 302
Decreased epigenetic age of PBMCs from Italian semi-supercentenarians and their offspring 297
The epigenetic landscape of age-related diseases: the geroscience perspective 276
Molecular Aging of Human Liver: An Epigenetic/Transcriptomic Signature 273
Impact of demography and population dynamics on the genetic architecture of human longevity 256
Whole-genome sequencing analysis of semi-supercentenarians 251
Susceptibility to Philadelphia-Positive acute Lymphoblastic Leukemia (ALL) Is Associated with a Germline Polymorphism In the ANRIL (CDKN2BAS) Locus. 244
Epigenetically induced ectopic expression of uncx impairs the proliferation and differentiation of myeloid cells 235
Interazione uomo-ambiente: contaminazione da SOlventi Clorurati e Impatto sui profili Epigenetici (metilazione del DNA) nella popolazione ITaliana [SOCIE-IT] 232
Double-heterozygous mutations involving both HNF1A (MODY3) and HNF4A (MODY1) genes: a case report 231
Genomic stability, anti-inflammatory phenotype, and up-regulation of the RNAseH2 in cells from centenarians 224
Distinct Viral and Mutational Spectrum of Endemic Burkitt Lymphoma 220
Glutathione transferase-A2 S112T polymorphism predicts survival, transplant-related mortality, busulfan and bilirubin blood levels after allogeneic stem cell transplantation 217
Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients. 211
Systemic Age-Associated DNA Hypermethylation of ELOVL2 Gene: In Vivo and In Vitro Evidences of a Cell Replication Process 211
A germline polymorphism in the ANRIL (CDKN2BAS) locus is associated with susceptibility to Philadelphia-positive acute lymphoblastic leukemia (ALL) 200
Inferring the genetic history of lactase persistence along the Italian peninsula from a large genomic interval surrounding the LCT gene 197
In hepatocellular carcinoma miR-519d is up-regulated by p53 and DNA hypomethylation and targets CDKN1A/p21, PTEN, AKT3 and TIMP2. 185
First evidence of association between past environmental exposure to dioxin and DNA methylation of CYP1A1 and IGF2 genes in present day Vietnamese population 185
Space/Population and Time/Age in DNA methylation variability in humans: a study on IGF2/H19 locus in different Italian populations and in mono- and di-zygotic twins of different age 183
High-throughput genotyping of high-risk Human Papillomavirus by MALDI-TOF Mass Spectrometry-based method. 175
A New Entity of Acute Myeloid Leukemia Driven By Epigenetic and Somatic Dis-Regulation of Uncx, a Novel Homeobox Transcription Factor Gene 174
p53/mdm2 feedback loop sustains miR-221 expression and dictates the response to anticancer treatments in hepatocellular carcinoma 172
Epigenetic Variability across Human Populations: A Focus on DNA Methylation Profiles of the KRTCAP3, MAD1L1 and BRSK2 Genes 171
Genes associated with Type 2 Diabetes and vascular complications 168
Genetic variants of the NMDA receptor influence cortical excitability and plasticity in humans 166
dHPLC efficiency for semi-automated cDNA-AFLP analyses and fragment collection in the apple scab resistance gene model 162
THE RS564398, A POLYMORPHISM IN “THE ANTISENSE NON-CODING RNA IN THE INK4 LOCUS”, ANRIL, IS ASSOCIATED TO PHILADELPHIA POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA (ALL) SUSCEPTIBILITY 161
The methylation of nuclear and mitochondrial DNA in ageing phenotypes and longevity 161
You have accessA New Entity of Acute Myeloid Leukemia Driven By Epigenetic and Somatic Dis-Regulation of Uncx, a Novel Homeobox Transcription Factor Gene 154
Bile salt export pump deficiency disease: Two novel, late onset, ABCB11 mutations identified by next generation sequencing 149
Sviluppo di un saggio di spettrometria di massa, ad elevata processività, per la ricerca e genotipizzazione di 12 HPV ad alto rischio oncogeno 147
Erythropoietin (EPO) haplotype associated with all-cause mortality in a cohort of Italian patients with Type-2 Diabetes 143
High-throughput type-specific detection of HPV using MassARRAY technology 142
Identification and validation of loss of function variants in clinical contexts 138
TRPV1 channels regulate cortical excitability in humans 126
Quantitative methylation analysis of HOXA3, 7, 9, and 10 genes in glioma: association with tumor WHO grade and clinical outcome 122
Risk of acute promyelocytic leukemia in multiple sclerosis: coding variants of DNA repair genes. Neurology. 95
Erratum: Author Correction: Erythropoietin (EPO) haplotype associated with all-cause mortality in a cohort of Italian patients with Type-2 Diabetes (Scientific reports (2019) 9 1 (10395)) 83
Corrigendum: Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients(EMBO Mol Med, (2014), 6, (795–809), 10.1002/emmm.201303235) 69
Totale 8.608
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Categoria #
all - tutte 21.209
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 21.209
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021299 0 0 0 0 0 0 0 0 0 63 42 194
2021/20221.119 173 54 84 78 100 72 25 62 54 76 197 144
2022/20231.150 135 178 54 141 72 90 32 84 195 30 74 65
2023/2024313 14 47 21 26 17 53 28 25 14 24 14 30
2024/20251.203 36 139 91 113 182 86 105 72 19 101 47 212
2025/20262.363 212 191 165 172 309 185 267 93 560 209 0 0
Totale 8.608