IRIS
Paraboschi, Elvezia Maria
 Distribuzione geografica
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Continente #
NA - Nord America 2.651
AS - Asia 1.596
EU - Europa 548
SA - Sud America 199
AF - Africa 125
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 2
Totale 5.126
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Nazione #
US - Stati Uniti d'America 2.591
SG - Singapore 890
CN - Cina 386
BR - Brasile 162
VN - Vietnam 114
IT - Italia 99
FI - Finlandia 98
NG - Nigeria 97
IE - Irlanda 64
HK - Hong Kong 61
DE - Germania 54
GB - Regno Unito 43
FR - Francia 42
SE - Svezia 41
IN - India 27
CA - Canada 25
NL - Olanda 25
MX - Messico 19
IQ - Iraq 17
AR - Argentina 16
BE - Belgio 14
BD - Bangladesh 13
ZA - Sudafrica 12
PH - Filippine 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
NP - Nepal 5
CH - Svizzera 4
JO - Giordania 4
KR - Corea 4
MY - Malesia 4
PE - Perù 4
AE - Emirati Arabi Uniti 3
AU - Australia 3
CL - Cile 3
DO - Repubblica Dominicana 3
GR - Grecia 3
JM - Giamaica 3
LT - Lituania 3
AM - Armenia 2
AT - Austria 2
BS - Bahamas 2
CO - Colombia 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
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
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
PR - Porto Rico 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 5.126
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Città #
Singapore 419
Chandler 357
Wilmington 280
San Jose 191
Ashburn 187
Shanghai 160
Dallas 137
The Dalles 120
San Mateo 119
Beijing 98
Helsinki 98
Benin City 97
Ann Arbor 96
New York 94
Boardman 69
Dublin 63
Hong Kong 60
Lawrence 52
Princeton 52
Leawood 49
Ho Chi Minh City 40
Los Angeles 35
Milan 34
Paris 32
Santa Clara 29
Fairfield 26
Hanoi 26
Phoenix 22
London 21
Woodbridge 20
Orem 19
Seattle 19
Amsterdam 17
Falkenstein 16
Brussels 14
Columbus 12
Manchester 10
Norwalk 10
Chicago 9
Da Nang 9
São Paulo 9
Buffalo 8
Charlotte 8
Naples 8
San Diego 8
Toronto 8
Johannesburg 7
Mumbai 7
Mexico City 6
Monmouth Junction 6
Montreal 6
Tashkent 6
Warsaw 6
Baghdad 5
Belo Horizonte 5
Council Bluffs 5
Frankfurt am Main 5
Haiphong 5
Nairobi 5
Rome 5
Amman 4
Caracas 4
Erbil 4
Hanover 4
Hillsboro 4
Kocaeli 4
Newark 4
Pelotas 4
Petrópolis 4
Rio de Janeiro 4
San Francisco 4
Tokyo 4
Winnipeg 4
Zavalla 4
Atlanta 3
Brooklyn 3
Cape Town 3
Curitiba 3
Falls Church 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
Caxias do Sul 2
Changsha 2
Chennai 2
Cologno Monzese 2
Totale 3.468
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Nome #
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains 143
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 138
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 137
MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity 136
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 134
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 124
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease 117
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay. 115
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 115
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency 113
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 112
ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy 110
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 108
Mapping the human genetic architecture of COVID-19 107
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women. 106
The double-faced association of the PRKCA gene with multiple sclerosis 106
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 103
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 103
Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe FV deficiency 102
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 102
Nonenzymatic Polymerization into Long Linear RNA Templated by Liquid Crystal Self-Assembly 93
Phase behavior and critical activated dynamics of limited-valence DNA nanostars 91
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 90
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases 89
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 89
Abiotic ligation of DNA oligomers templated by their liquid crystal ordering 87
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency 86
Identification and characterization of 6 novel genetic defects leading to factor V deficiency 84
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis 84
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 84
Functional and clinical implications of genetic structure in 1686 Italian exomes 82
Molecular characterization of six novel mutations causing factor V deficiency 81
Hereditary Hypofibrinogenemia with Hepatic Storage 81
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 80
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 80
Mycobacterium tuberculosis Drives Expansion of Low-Density Neutrophils Equipped With Regulatory Activities 79
The first case of the TARDBP p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS? 79
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 79
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 73
Detailed stratified GWAS analysis for severe COVID-19 in four European populations 72
Notch1 regulates chemotaxis and proliferation by controlling the CC-chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia 72
OxDNA to Study Species Interactions 70
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 70
Needles in Haystacks: Understanding the Success of Selective Pairing of Nucleic Acids 69
Sighting acute myocardial infarction through platelet gene expression 68
Profiling the mutational landscape of coagulation factor V deficiency. 67
Newtonian to non-newtonian fluid transition of a model transient network 67
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 66
Molecular investigation of 41 patients affected by coagulation factor XI deficiency 63
Mutational screening of 25 unrelated FV-deficient patients from six countries 61
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules 60
MiR-634: a new player in the pathogenesis of multiple sclerosis? 59
Identification and characterization of 6 novel genetics defects leading to factor V deficiency 57
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 53
Sex-Related Differences in Long-Term Outcomes After Early-Onset Myocardial Infarction 52
Genetic susceptibility to severe COVID-19 51
Long-term outcomes of early-onset myocardial infarction with non-obstructive coronary artery disease (MINOCA) 47
The Role of Epigenetics in Primary Biliary Cholangitis 44
Chemosensor receptors are lipid-detecting regulators of macrophage function in cancer 41
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 38
Splicing-based biomarkers define a robust multigene classifier for relapsing-remitting multiple sclerosis 5
Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severity 3
Totale 5.177
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Categoria #
all - tutte 31.858
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 31.858
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202168 0 0 0 0 0 0 0 0 0 0 0 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
2025/20262.064 287 107 152 114 110 88 631 95 111 143 134 92
Totale 5.177