IRIS
Paraboschi, Elvezia Maria
 Distribuzione geografica
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Continente #
NA - Nord America 2.825
AS - Asia 1.615
EU - Europa 569
SA - Sud America 203
AF - Africa 125
Continente sconosciuto - Info sul continente non disponibili 53
OC - Oceania 5
Totale 5.395
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Nazione #
US - Stati Uniti d'America 2.759
SG - Singapore 894
CN - Cina 394
BR - Brasile 162
VN - Vietnam 118
IT - Italia 116
FI - Finlandia 98
NG - Nigeria 97
IE - Irlanda 64
HK - Hong Kong 62
DE - Germania 54
FR - Francia 43
GB - Regno Unito 43
SE - Svezia 41
CA - Canada 29
IN - India 27
NL - Olanda 25
MX - Messico 19
AR - Argentina 17
IQ - Iraq 17
BE - Belgio 15
BD - Bangladesh 14
ZA - Sudafrica 12
PH - Filippine 11
PL - Polonia 11
PK - Pakistan 10
ES - Italia 9
UA - Ucraina 9
TR - Turchia 8
JP - Giappone 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
CL - Cile 4
CO - Colombia 4
JM - Giamaica 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
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
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
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 5.344
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Città #
Singapore 421
Chandler 357
Wilmington 280
Ashburn 198
San Jose 193
Shanghai 160
Dallas 142
The Dalles 120
San Mateo 119
Beijing 98
Helsinki 98
New York 98
Benin City 97
Ann Arbor 96
Boardman 69
Dublin 63
Hong Kong 61
Princeton 54
Lawrence 52
Leawood 49
Ho Chi Minh City 42
Milan 40
Santa Clara 37
Los Angeles 36
Paris 33
Fairfield 26
Hanoi 26
Phoenix 23
London 21
Seattle 21
Woodbridge 20
Orem 19
Amsterdam 17
Falkenstein 16
Brussels 15
Columbus 14
Chicago 12
Charlotte 11
Manchester 10
Norwalk 10
Da Nang 9
São Paulo 9
Toronto 9
Buffalo 8
Miami 8
Naples 8
Rome 8
San Diego 8
Dearborn 7
Johannesburg 7
Mumbai 7
Warsaw 7
Mexico City 6
Monmouth Junction 6
Montreal 6
Tashkent 6
Atlanta 5
Baghdad 5
Belo Horizonte 5
Council Bluffs 5
Frankfurt am Main 5
Haiphong 5
Houston 5
Nairobi 5
Amman 4
Caracas 4
Cincinnati 4
Erbil 4
Hanover 4
Hillsboro 4
Kocaeli 4
Newark 4
Pelotas 4
Petrópolis 4
Rio de Janeiro 4
Riverside 4
San Francisco 4
Tokyo 4
Winnipeg 4
Zavalla 4
Brooklyn 3
Cape Town 3
Curitiba 3
Falls Church 3
Islamabad 3
Jacksonville 3
Lima 3
Milwaukee 3
New Delhi 3
Pittsburgh 3
Plymouth 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
Totale 3.553
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Nome #
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains 150
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 145
MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity 144
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 140
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 138
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 130
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease 119
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency 119
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 118
Mapping the human genetic architecture of COVID-19 117
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay. 116
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 116
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 114
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 113
ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy 113
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 112
The double-faced association of the PRKCA gene with multiple sclerosis 110
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women. 108
Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe FV deficiency 105
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 105
Nonenzymatic Polymerization into Long Linear RNA Templated by Liquid Crystal Self-Assembly 95
Phase behavior and critical activated dynamics of limited-valence DNA nanostars 94
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 92
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 91
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency 91
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 90
Abiotic ligation of DNA oligomers templated by their liquid crystal ordering 90
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases 89
Functional and clinical implications of genetic structure in 1686 Italian exomes 88
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 87
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 86
Identification and characterization of 6 novel genetic defects leading to factor V deficiency 85
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis 85
Hereditary Hypofibrinogenemia with Hepatic Storage 84
Molecular characterization of six novel mutations causing factor V deficiency 82
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 82
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 circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 74
OxDNA to Study Species Interactions 73
Detailed stratified GWAS analysis for severe COVID-19 in four European populations 73
Notch1 regulates chemotaxis and proliferation by controlling the CC-chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia 73
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 73
Needles in Haystacks: Understanding the Success of Selective Pairing of Nucleic Acids 72
Sighting acute myocardial infarction through platelet gene expression 70
Profiling the mutational landscape of coagulation factor V deficiency. 69
Newtonian to non-newtonian fluid transition of a model transient network 69
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 69
Mutational screening of 25 unrelated FV-deficient patients from six countries 67
Molecular investigation of 41 patients affected by coagulation factor XI deficiency 63
MiR-634: a new player in the pathogenesis of multiple sclerosis? 63
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules 63
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 59
Identification and characterization of 6 novel genetics defects leading to factor V deficiency 58
Sex-Related Differences in Long-Term Outcomes After Early-Onset Myocardial Infarction 55
Long-term outcomes of early-onset myocardial infarction with non-obstructive coronary artery disease (MINOCA) 52
Genetic susceptibility to severe COVID-19 51
Chemosensor receptors are lipid-detecting regulators of macrophage function in cancer 46
The Role of Epigenetics in Primary Biliary Cholangitis 45
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
Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severity 11
Splicing-based biomarkers define a robust multigene classifier for relapsing-remitting multiple sclerosis 8
Totale 5.395
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Categoria #
all - tutte 33.046
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 33.046
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022282 0 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
2025/20262.100 287 107 152 114 110 88 631 95 111 143 134 128
2026/2027182 128 54 0 0 0 0 0 0 0 0 0 0
Totale 5.395