Paraboschi, Elvezia Maria
 Distribuzione geografica
Continente #
NA - Nord America 3.306
AS - Asia 1.632
EU - Europa 578
SA - Sud America 206
AF - Africa 125
Continente sconosciuto - Info sul continente non disponibili 56
OC - Oceania 5
Totale 5.908
Nazione #
US - Stati Uniti d'America 3.229
SG - Singapore 902
CN - Cina 395
BR - Brasile 165
IT - Italia 121
VN - Vietnam 118
FI - Finlandia 98
NG - Nigeria 97
HK - Hong Kong 65
IE - Irlanda 64
DE - Germania 54
GB - Regno Unito 45
FR - Francia 43
SE - Svezia 41
CA - Canada 37
IN - India 28
NL - Olanda 26
MX - Messico 20
AR - Argentina 17
IQ - Iraq 17
BE - Belgio 15
BD - Bangladesh 14
PH - Filippine 14
ZA - Sudafrica 12
PL - Polonia 11
PK - Pakistan 10
ES - Italia 9
UA - Ucraina 9
JP - Giappone 8
TR - Turchia 8
VE - Venezuela 7
ID - Indonesia 6
IL - Israele 6
RO - Romania 6
RU - Federazione Russa 6
UZ - Uzbekistan 6
JM - Giamaica 5
KE - Kenya 5
NP - Nepal 5
CH - Svizzera 4
CL - Cile 4
CO - Colombia 4
JO - Giordania 4
KR - Corea 4
MY - Malesia 4
PE - Perù 4
AE - Emirati Arabi Uniti 3
AU - Australia 3
DO - Repubblica Dominicana 3
GR - Grecia 3
LT - Lituania 3
AM - Armenia 2
AT - Austria 2
BS - Bahamas 2
BZ - Belize 2
DZ - Algeria 2
EC - Ecuador 2
HN - Honduras 2
IR - Iran 2
KZ - Kazakistan 2
LB - Libano 2
LV - Lettonia 2
MA - Marocco 2
NO - Norvegia 2
PR - Porto Rico 2
PT - Portogallo 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
TN - Tunisia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
CZ - Repubblica Ceca 1
EG - Egitto 1
ET - Etiopia 1
EU - Europa 1
FM - Micronesia 1
GE - Georgia 1
HR - Croazia 1
HU - Ungheria 1
IS - Islanda 1
LU - Lussemburgo 1
LY - Libia 1
MD - Moldavia 1
MK - Macedonia 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PA - Panama 1
PY - Paraguay 1
RS - Serbia 1
SA - Arabia Saudita 1
SN - Senegal 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
TM - Turkmenistan 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
ZW - Zimbabwe 1
Totale 5.854
Città #
Singapore 425
Chandler 357
Wilmington 280
San Jose 233
Ashburn 214
Shanghai 160
Dallas 142
The Dalles 120
San Mateo 119
New York 104
Beijing 99
Helsinki 98
Benin City 97
Ann Arbor 96
Council Bluffs 72
Boardman 69
Hong Kong 64
Dublin 63
Princeton 58
Lawrence 52
Leawood 49
Santa Clara 46
Ho Chi Minh City 42
Los Angeles 41
Milan 40
Phoenix 34
Paris 33
Fairfield 26
Hanoi 26
London 22
Seattle 21
Woodbridge 20
Orem 19
Amsterdam 17
Chicago 16
Falkenstein 16
Brussels 15
Columbus 15
Charlotte 12
San Diego 11
São Paulo 11
Manchester 10
Miami 10
Norwalk 10
Toronto 10
Buffalo 9
Da Nang 9
Naples 9
Montreal 8
Rome 8
Dearborn 7
Johannesburg 7
Mumbai 7
Warsaw 7
Abbeville 6
Atlanta 6
Brooklyn 6
Houston 6
Mexico City 6
Monmouth Junction 6
Riverside 6
Tashkent 6
Baghdad 5
Belo Horizonte 5
Frankfurt am Main 5
Haiphong 5
Las Vegas 5
Nairobi 5
Queens 5
San Francisco 5
Tokyo 5
Amman 4
Caracas 4
Cincinnati 4
Erbil 4
Falls Church 4
Hanover 4
Hillsboro 4
Jacksonville 4
Kocaeli 4
Minneapolis 4
Newark 4
Pelotas 4
Petrópolis 4
Philadelphia 4
Pittsburgh 4
Rio de Janeiro 4
Winnipeg 4
Zavalla 4
Caloocan 3
Cape Town 3
Curitiba 3
Glendale 3
Islamabad 3
Lima 3
Milwaukee 3
New Delhi 3
North Charleston 3
Plymouth 3
Santo André 3
Totale 3.763
Nome #
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains 160
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 153
MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity 151
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 146
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 145
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease 140
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 137
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 131
Mapping the human genetic architecture of COVID-19 128
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 126
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 126
ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy 125
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency 124
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay. 123
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 121
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 118
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women. 117
The double-faced association of the PRKCA gene with multiple sclerosis 116
Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe FV deficiency 112
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 111
Abiotic ligation of DNA oligomers templated by their liquid crystal ordering 107
Nonenzymatic Polymerization into Long Linear RNA Templated by Liquid Crystal Self-Assembly 101
Phase behavior and critical activated dynamics of limited-valence DNA nanostars 100
Functional analysis of missense mutations in the Myocyte Enhancer Factor 2A (MEF2A) gene do not support their causal role in the pathogenesis of myocardial infarction 100
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 98
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 98
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency 97
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 97
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases 94
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 94
Functional and clinical implications of genetic structure in 1686 Italian exomes 94
Hereditary Hypofibrinogenemia with Hepatic Storage 93
Identification and characterization of 6 novel genetic defects leading to factor V deficiency 91
Molecular characterization of six novel mutations causing factor V deficiency 90
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis 90
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 89
The first case of the TARDBP p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS? 85
Mycobacterium tuberculosis Drives Expansion of Low-Density Neutrophils Equipped With Regulatory Activities 84
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 81
Detailed stratified GWAS analysis for severe COVID-19 in four European populations 81
OxDNA to Study Species Interactions 80
MiR-634: a new player in the pathogenesis of multiple sclerosis? 80
Notch1 regulates chemotaxis and proliferation by controlling the CC-chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia 79
Needles in Haystacks: Understanding the Success of Selective Pairing of Nucleic Acids 78
Sighting acute myocardial infarction through platelet gene expression 78
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 77
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 77
Profiling the mutational landscape of coagulation factor V deficiency. 74
Newtonian to non-newtonian fluid transition of a model transient network 73
Mutational screening of 25 unrelated FV-deficient patients from six countries 72
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules 71
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 70
Molecular investigation of 41 patients affected by coagulation factor XI deficiency 69
Sex-Related Differences in Long-Term Outcomes After Early-Onset Myocardial Infarction 63
Identification and characterization of 6 novel genetics defects leading to factor V deficiency 63
Long-term outcomes of early-onset myocardial infarction with non-obstructive coronary artery disease (MINOCA) 62
Genetic susceptibility to severe COVID-19 58
Chemosensor receptors are lipid-detecting regulators of macrophage function in cancer 55
The Role of Epigenetics in Primary Biliary Cholangitis 53
Reply to: Hultström et al., Genetic determinants of mannose-binding lectin activity predispose to thromboembolic complications in critical COVID-19. Mannose-binding lectin genetics in COVID-19 44
Splicing-based biomarkers define a robust multigene classifier for relapsing-remitting multiple sclerosis 18
Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severity 18
Factor XI Deficiency in apoE/FXI Double-Knockout Mice Decreases Atherosclerosis by Lowering MSR1 mRNA Expression Within the Plaque 9
Neutrophils restricted contribution of CCRL2 genetic variants to COVID-19 severity 7
Polygenic Prediction of Recurrent Events After Early-Onset Myocardial Infarction 6
Totale 5.908
Categoria #
all - tutte 35.205
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 35.205


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022276 0 0 0 62 3 5 10 35 34 46 62 19
2022/2023934 116 53 70 131 113 76 0 79 166 66 51 13
2023/2024568 44 48 84 34 22 87 51 53 10 7 64 64
2024/2025801 42 27 11 15 18 122 32 66 107 178 87 96
2025/20262.100 287 107 152 114 110 88 631 95 111 143 134 128
2026/2027695 128 144 352 71 0 0 0 0 0 0 0 0
Totale 5.908