IRIS
Paraboschi, Elvezia Maria
 Distribuzione geografica
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Continente #
NA - Nord America 2.189
AS - Asia 931
EU - Europa 464
SA - Sud America 168
AF - Africa 109
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 2
Totale 3.868
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Nazione #
US - Stati Uniti d'America 2.150
SG - Singapore 491
CN - Cina 305
BR - Brasile 143
FI - Finlandia 97
NG - Nigeria 97
IT - Italia 77
IE - Irlanda 63
HK - Hong Kong 48
DE - Germania 42
SE - Svezia 41
FR - Francia 30
GB - Regno Unito 28
NL - Olanda 25
CA - Canada 19
BE - Belgio 14
IN - India 14
MX - Messico 12
AR - Argentina 10
IQ - Iraq 9
VN - Vietnam 9
BD - Bangladesh 7
PL - Polonia 7
RU - Federazione Russa 6
VE - Venezuela 6
ZA - Sudafrica 6
ID - Indonesia 5
PK - Pakistan 5
UA - Ucraina 5
UZ - Uzbekistan 5
CH - Svizzera 4
IL - Israele 4
JP - Giappone 4
PH - Filippine 4
TR - Turchia 4
AU - Australia 3
ES - Italia 3
GR - Grecia 3
PE - Perù 3
RO - Romania 3
AE - Emirati Arabi Uniti 2
AM - Armenia 2
AT - Austria 2
DO - Repubblica Dominicana 2
IR - Iran 2
JM - Giamaica 2
JO - Giordania 2
KE - Kenya 2
KR - Corea 2
LV - Lettonia 2
MY - Malesia 2
NO - Norvegia 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
TN - Tunisia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BG - Bulgaria 1
BO - Bolivia 1
CL - Cile 1
CO - Colombia 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
EG - Egitto 1
EU - Europa 1
FM - Micronesia 1
HR - Croazia 1
HU - Ungheria 1
IS - Islanda 1
KZ - Kazakistan 1
LT - Lituania 1
MA - Marocco 1
MK - Macedonia 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PA - Panama 1
PT - Portogallo 1
PY - Paraguay 1
SA - Arabia Saudita 1
SV - El Salvador 1
TM - Turkmenistan 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
Totale 3.868
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Città #
Chandler 357
Wilmington 280
Singapore 177
Shanghai 158
Dallas 133
San Mateo 119
The Dalles 113
Benin City 97
Helsinki 97
Ann Arbor 96
New York 81
Beijing 80
Ashburn 77
Boardman 69
Dublin 62
Lawrence 52
Princeton 52
Leawood 49
Hong Kong 48
Milan 33
Paris 29
Fairfield 26
Los Angeles 22
Phoenix 22
Woodbridge 20
Seattle 19
Amsterdam 17
London 16
Brussels 14
Santa Clara 13
Columbus 12
Norwalk 10
San Diego 8
São Paulo 8
Toronto 7
Falkenstein 6
Monmouth Junction 6
Naples 6
Belo Horizonte 5
Charlotte 5
Chicago 5
Council Bluffs 5
Mumbai 5
Tashkent 5
Erbil 4
Hanover 4
Kocaeli 4
Pelotas 4
Petrópolis 4
San Francisco 4
Tokyo 4
Warsaw 4
Winnipeg 4
Zavalla 4
Atlanta 3
Baghdad 3
Brooklyn 3
Caracas 3
Falls Church 3
Frankfurt am Main 3
Ho Chi Minh City 3
Johannesburg 3
Manchester 3
Mexico City 3
Montreal 3
Orem 3
Pittsburgh 3
Rio de Janeiro 3
Rome 3
Santo André 3
São Bernardo do Campo 3
Vancouver 3
Amman 2
Andover 2
Arraial do Cabo 2
Athens 2
Belford Roxo 2
Brasília 2
Bratislava 2
Caxias do Sul 2
Chennai 2
Cologno Monzese 2
Curitiba 2
Des Moines 2
Desio 2
Eunápolis 2
Feira de Santana 2
Ferrandina 2
Goiânia 2
Guarulhos 2
Gunzenhausen 2
Islamabad 2
Jacksonville 2
Juneau 2
Lima 2
Lugano 2
Maricá 2
Nairobi 2
Nevada City 2
New Delhi 2
Totale 2.671
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Nome #
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains 106
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 106
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 105
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 98
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 96
ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy 96
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women. 92
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 92
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 92
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay. 91
MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity 91
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 87
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency 84
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 83
The double-faced association of the PRKCA gene with multiple sclerosis 83
Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe FV deficiency 80
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 78
Abiotic ligation of DNA oligomers templated by their liquid crystal ordering 75
Mapping the human genetic architecture of COVID-19 74
Phase behavior and critical activated dynamics of limited-valence DNA nanostars 73
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases 73
Identification and characterization of 6 novel genetic defects leading to factor V deficiency 73
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 73
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis 72
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 72
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 71
Nonenzymatic Polymerization into Long Linear RNA Templated by Liquid Crystal Self-Assembly 71
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease 69
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 68
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 68
Molecular characterization of six novel mutations causing factor V deficiency 66
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 65
Hereditary Hypofibrinogenemia with Hepatic Storage 64
Functional and clinical implications of genetic structure in 1686 Italian exomes 64
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency 63
The first case of the TARDBP p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS? 60
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 59
Sighting acute myocardial infarction through platelet gene expression 56
Mycobacterium tuberculosis Drives Expansion of Low-Density Neutrophils Equipped With Regulatory Activities 55
Profiling the mutational landscape of coagulation factor V deficiency. 54
Newtonian to non-newtonian fluid transition of a model transient network 54
Notch1 regulates chemotaxis and proliferation by controlling the CC-chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia 52
OxDNA to Study Species Interactions 51
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 51
Needles in Haystacks: Understanding the Success of Selective Pairing of Nucleic Acids 50
Molecular investigation of 41 patients affected by coagulation factor XI deficiency 49
Mutational screening of 25 unrelated FV-deficient patients from six countries 49
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 48
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules 46
Detailed stratified GWAS analysis for severe COVID-19 in four European populations 45
MiR-634: a new player in the pathogenesis of multiple sclerosis? 45
Identification and characterization of 6 novel genetics defects leading to factor V deficiency 43
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 41
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 40
Genetic susceptibility to severe COVID-19 31
Long-term outcomes of early-onset myocardial infarction with non-obstructive coronary artery disease (MINOCA) 30
The Role of Epigenetics in Primary Biliary Cholangitis 28
Sex-Related Differences in Long-Term Outcomes After Early-Onset Myocardial Infarction 26
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 25
Chemosensor receptors are lipid-detecting regulators of macrophage function in cancer 15
Totale 3.917
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Categoria #
all - tutte 28.275
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 28.275
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021494 0 0 0 0 0 141 80 44 105 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
2025/2026804 287 107 152 114 110 34 0 0 0 0 0 0
Totale 3.917