IRIS
Paraboschi, Elvezia Maria
 Distribuzione geografica
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Continente #
NA - Nord America 2.491
AS - Asia 1.499
EU - Europa 546
SA - Sud America 199
AF - Africa 124
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 2
Totale 4.866
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Nazione #
US - Stati Uniti d'America 2.440
SG - Singapore 851
CN - Cina 342
BR - Brasile 162
VN - Vietnam 113
FI - Finlandia 98
IT - Italia 97
NG - Nigeria 97
IE - Irlanda 64
HK - Hong Kong 56
DE - Germania 54
GB - Regno Unito 43
FR - Francia 42
SE - Svezia 41
IN - India 27
NL - Olanda 25
CA - Canada 21
MX - Messico 18
IQ - Iraq 17
AR - Argentina 16
BE - Belgio 14
BD - Bangladesh 12
PH - Filippine 11
ZA - Sudafrica 11
PK - Pakistan 10
PL - Polonia 10
ES - Italia 9
UA - Ucraina 9
JP - Giappone 7
TR - Turchia 7
VE - Venezuela 7
ID - Indonesia 6
IL - Israele 6
RO - Romania 6
RU - Federazione Russa 6
UZ - Uzbekistan 6
KE - Kenya 5
CH - Svizzera 4
JO - Giordania 4
PE - Perù 4
AU - Australia 3
CL - Cile 3
DO - Repubblica Dominicana 3
GR - Grecia 3
JM - Giamaica 3
LT - Lituania 3
NP - Nepal 3
AE - Emirati Arabi Uniti 2
AM - Armenia 2
AT - Austria 2
CO - Colombia 2
DZ - Algeria 2
EC - Ecuador 2
IR - Iran 2
KR - Corea 2
KZ - Kazakistan 2
LB - Libano 2
LV - Lettonia 2
MA - Marocco 2
MY - Malesia 2
NO - Norvegia 2
PT - Portogallo 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
TN - Tunisia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BZ - Belize 1
CZ - Repubblica Ceca 1
EG - Egitto 1
ET - Etiopia 1
EU - Europa 1
FM - Micronesia 1
GE - Georgia 1
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
IS - Islanda 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 4.866
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Città #
Singapore 417
Chandler 357
Wilmington 280
Ashburn 160
Shanghai 158
San Jose 156
Dallas 133
The Dalles 120
San Mateo 119
Helsinki 98
Benin City 97
Ann Arbor 96
Beijing 94
New York 83
Boardman 69
Dublin 63
Hong Kong 55
Lawrence 52
Princeton 52
Leawood 49
Ho Chi Minh City 40
Milan 34
Paris 32
Fairfield 26
Hanoi 25
Los Angeles 24
Phoenix 22
London 21
Woodbridge 20
Orem 19
Seattle 19
Amsterdam 17
Falkenstein 16
Santa Clara 16
Brussels 14
Columbus 12
Manchester 10
Norwalk 10
Da Nang 9
São Paulo 9
Naples 8
San Diego 8
Johannesburg 7
Mumbai 7
Toronto 7
Charlotte 6
Monmouth Junction 6
Tashkent 6
Warsaw 6
Baghdad 5
Belo Horizonte 5
Chicago 5
Council Bluffs 5
Frankfurt am Main 5
Haiphong 5
Mexico City 5
Nairobi 5
Rome 5
Amman 4
Caracas 4
Erbil 4
Hanover 4
Kocaeli 4
Montreal 4
Pelotas 4
Petrópolis 4
Rio de Janeiro 4
San Francisco 4
Tokyo 4
Winnipeg 4
Zavalla 4
Atlanta 3
Brooklyn 3
Curitiba 3
Falls Church 3
Hillsboro 3
Islamabad 3
Lima 3
New Delhi 3
Pittsburgh 3
Santo André 3
Sorocaba 3
São Bernardo do Campo 3
Vancouver 3
Verona 3
Ahmedabad 2
Andover 2
Arraial do Cabo 2
Athens 2
Basra 2
Belford Roxo 2
Brasília 2
Bratislava 2
Cape Town 2
Caxias do Sul 2
Chennai 2
Cologno Monzese 2
Des Moines 2
Desio 2
Dhaka 2
Totale 3.333
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Nome #
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 136
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains 134
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 130
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 123
MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity 120
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 114
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 111
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay. 110
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency 108
ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy 108
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 106
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 106
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women. 105
Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe FV deficiency 102
The double-faced association of the PRKCA gene with multiple sclerosis 102
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 101
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 96
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease 95
Nonenzymatic Polymerization into Long Linear RNA Templated by Liquid Crystal Self-Assembly 89
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases 88
Mapping the human genetic architecture of COVID-19 88
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 87
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 87
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 86
Phase behavior and critical activated dynamics of limited-valence DNA nanostars 85
Abiotic ligation of DNA oligomers templated by their liquid crystal ordering 85
Identification and characterization of 6 novel genetic defects leading to factor V deficiency 83
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency 82
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis 82
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 82
Molecular characterization of six novel mutations causing factor V deficiency 80
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 79
Functional and clinical implications of genetic structure in 1686 Italian exomes 79
Mycobacterium tuberculosis Drives Expansion of Low-Density Neutrophils Equipped With Regulatory Activities 78
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 78
Hereditary Hypofibrinogenemia with Hepatic Storage 77
The first case of the TARDBP p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS? 76
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 76
Notch1 regulates chemotaxis and proliferation by controlling the CC-chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia 70
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 69
OxDNA to Study Species Interactions 68
Sighting acute myocardial infarction through platelet gene expression 68
Needles in Haystacks: Understanding the Success of Selective Pairing of Nucleic Acids 67
Profiling the mutational landscape of coagulation factor V deficiency. 67
Newtonian to non-newtonian fluid transition of a model transient network 66
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 66
Detailed stratified GWAS analysis for severe COVID-19 in four European populations 65
Molecular investigation of 41 patients affected by coagulation factor XI deficiency 62
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 60
Mutational screening of 25 unrelated FV-deficient patients from six countries 60
MiR-634: a new player in the pathogenesis of multiple sclerosis? 59
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules 57
Identification and characterization of 6 novel genetics defects leading to factor V deficiency 55
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 53
Genetic susceptibility to severe COVID-19 48
Sex-Related Differences in Long-Term Outcomes After Early-Onset Myocardial Infarction 46
Long-term outcomes of early-onset myocardial infarction with non-obstructive coronary artery disease (MINOCA) 42
The Role of Epigenetics in Primary Biliary Cholangitis 40
Chemosensor receptors are lipid-detecting regulators of macrophage function in cancer 37
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 36
Totale 4.915
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Categoria #
all - tutte 29.994
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 29.994
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021124 0 0 0 0 0 0 0 0 0 55 1 68
2021/2022293 11 1 5 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
2025/20261.802 287 107 152 114 110 88 631 95 111 107 0 0
Totale 4.915