IRIS
Paraboschi, Elvezia Maria
 Distribuzione geografica
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Continente #
NA - Nord America 1.647
EU - Europa 362
AS - Asia 114
AF - Africa 101
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
SA - Sud America 2
Totale 2.231
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Nazione #
US - Stati Uniti d'America 1.637
NG - Nigeria 101
FI - Finlandia 100
CN - Cina 94
IE - Irlanda 64
SE - Svezia 40
IT - Italia 38
DE - Germania 35
FR - Francia 27
NL - Olanda 15
GB - Regno Unito 14
BE - Belgio 13
CA - Canada 10
IL - Israele 4
IN - India 4
TR - Turchia 4
IR - Iran 3
RO - Romania 3
AT - Austria 2
AU - Australia 2
CH - Svizzera 2
GR - Grecia 2
PL - Polonia 2
RU - Federazione Russa 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
BR - Brasile 1
CL - Cile 1
CZ - Repubblica Ceca 1
EU - Europa 1
JP - Giappone 1
MK - Macedonia 1
MY - Malesia 1
NZ - Nuova Zelanda 1
SG - Singapore 1
TH - Thailandia 1
UA - Ucraina 1
Totale 2.231
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Città #
Chandler 366
Wilmington 289
San Mateo 121
Benin City 101
Helsinki 100
Ann Arbor 96
Shanghai 93
New York 75
Dublin 64
Boardman 56
Lawrence 54
Princeton 54
Leawood 50
Ashburn 33
Paris 27
Fairfield 26
Milan 24
Woodbridge 20
Phoenix 19
Amsterdam 15
Brussels 13
London 13
Norwalk 10
Seattle 9
San Diego 7
Falkenstein 6
Monmouth Junction 6
Toronto 5
Hanover 4
Kocaeli 4
Winnipeg 4
Andover 3
Falls Church 3
Frankfurt am Main 3
Los Angeles 3
Des Moines 2
Gunzenhausen 2
Houston 2
Lugano 2
Mumbai 2
Piemonte 2
Sacramento 2
Vienna 2
Athens 1
Auckland 1
Brookings 1
Cambridge 1
Clearwater 1
Fremont 1
Guangzhou 1
Haifa 1
Henderson 1
Jacksonville 1
Kashan 1
Kuala Lumpur 1
Logan 1
Ludlow 1
Ottawa 1
Penrith 1
Prague 1
Redwood City 1
Reghin 1
Saint Paul 1
Saratov 1
Segonzano 1
São Paulo 1
Tappahannock 1
Tokyo 1
Vallendar 1
Warsaw 1
Washington 1
Yerevan 1
Totale 1.821
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Nome #
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 66
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women. 63
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 60
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 59
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 58
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 56
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 56
Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe FV deficiency 55
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains 55
Genomewide Association Study of Severe Covid-19 with Respiratory Failure 55
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 54
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 54
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay. 53
ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy 51
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 50
Nonenzymatic Polymerization into Long Linear RNA Templated by Liquid Crystal Self-Assembly 50
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 49
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency 49
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 48
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases 48
Abiotic ligation of DNA oligomers templated by their liquid crystal ordering 48
Molecular characterization of six novel mutations causing factor V deficiency 46
The double-faced association of the PRKCA gene with multiple sclerosis 46
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis 45
Not only cancer: the long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis. 44
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 44
Identification and characterization of 6 novel genetic defects leading to factor V deficiency 43
The first case of the TARDBP p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS? 43
Phase behavior and critical activated dynamics of limited-valence DNA nanostars 42
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 42
Hereditary Hypofibrinogenemia with Hepatic Storage 39
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 38
Profiling the mutational landscape of coagulation factor V deficiency. 35
Newtonian to non-newtonian fluid transition of a model transient network 35
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 34
Molecular investigation of 41 patients affected by coagulation factor XI deficiency 33
Sighting acute myocardial infarction through platelet gene expression. 33
Mycobacterium tuberculosis Drives Expansion of Low-Density Neutrophils Equipped With Regulatory Activities 33
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency 33
Notch1 regulates chemotaxis and proliferation by controlling the CC-chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia 33
Functional and clinical implications of genetic structure in 1686 Italian exomes 33
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease 30
Mutational screening of 25 unrelated FV-deficient patients from six countries 27
Mapping the human genetic architecture of COVID-19 27
OxDNA to Study Species Interactions 26
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 26
MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity 26
X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis 25
Identification and characterization of 6 novel genetics defects leading to factor V deficiency 24
MiR-634: a new player in the pathogenesis of multiple sclerosis? 22
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 22
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 17
Needles in Haystacks: Understanding the Success of Selective Pairing of Nucleic Acids 16
Detailed stratified GWAS analysis for severe COVID-19 in four European populations 15
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules 14
Impact of chronic exposure to 5-alpha reductase inhibitors on the risk of hospitalization for COVID-19: a case-control study in male population from two COVID-19 regional centers of Lombardy, Italy 14
Long-term outcomes of early-onset myocardial infarction with non-obstructive coronary artery disease (MINOCA) 13
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 10
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 6
Sex-Related Differences in Long-Term Outcomes After Early-Onset Myocardial Infarction 3
Genetic susceptibility to severe COVID-19 2
The Role of Epigenetics in Primary Biliary Cholangitis 2
Totale 2.278
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Categoria #
all - tutte 15.337
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 15.337
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20206 0 0 0 0 0 0 0 0 0 0 0 6
2020/2021533 10 4 8 4 1 143 83 45 108 56 1 70
2021/2022308 11 2 6 63 3 5 10 36 36 48 68 20
2022/2023960 121 55 74 133 117 77 0 80 170 68 52 13
2023/2024471 46 49 90 38 22 95 56 55 11 9 0 0
Totale 2.278