IRIS
Paraboschi, Elvezia Maria
 Distribuzione geografica
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Continente #
NA - Nord America 1.690
EU - Europa 372
AS - Asia 268
AF - Africa 100
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
SA - Sud America 1
Totale 2.436
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Nazione #
US - Stati Uniti d'America 1.680
CN - Cina 131
SG - Singapore 118
NG - Nigeria 99
FI - Finlandia 98
IE - Irlanda 61
IT - Italia 49
SE - Svezia 39
DE - Germania 38
FR - Francia 28
NL - Olanda 16
GB - Regno Unito 14
BE - Belgio 13
CA - Canada 10
IL - Israele 4
IN - India 4
TR - Turchia 4
RO - Romania 3
AT - Austria 2
AU - Australia 2
CH - Svizzera 2
GR - Grecia 2
IR - Iran 2
PL - Polonia 2
RU - Federazione Russa 2
TH - Thailandia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
CL - Cile 1
CZ - Repubblica Ceca 1
EG - Egitto 1
EU - Europa 1
JP - Giappone 1
MK - Macedonia 1
NZ - Nuova Zelanda 1
PK - Pakistan 1
UA - Ucraina 1
Totale 2.436
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Città #
Chandler 365
Wilmington 289
San Mateo 121
Shanghai 109
Benin City 99
Helsinki 98
Ann Arbor 96
Singapore 80
Boardman 71
New York 71
Dublin 61
Lawrence 53
Princeton 53
Leawood 50
Ashburn 35
Paris 28
Fairfield 26
Milan 25
Woodbridge 20
Phoenix 19
Seattle 18
Amsterdam 15
Brussels 13
London 12
Norwalk 10
San Diego 7
Beijing 6
Falkenstein 6
Monmouth Junction 6
Toronto 5
Hanover 4
Kocaeli 4
Winnipeg 4
Andover 3
Cologno Monzese 3
Falls Church 3
Frankfurt am Main 3
Santa Clara 3
Des Moines 2
Gunzenhausen 2
Houston 2
Los Angeles 2
Lugano 2
Mumbai 2
Piemonte 2
Sacramento 2
Trezzo sull'Adda 2
Vienna 2
Athens 1
Auckland 1
Bangkok 1
Brookings 1
Cambridge 1
Changsha 1
Clearwater 1
Council Bluffs 1
Eygelshoven 1
Guangzhou 1
Haifa 1
Harbin 1
Henderson 1
Jacksonville 1
Logan 1
Ludlow 1
Ottawa 1
Penrith 1
Prague 1
Redwood City 1
Reghin 1
Saint Paul 1
Saratov 1
Segonzano 1
Tangshan 1
Tappahannock 1
Tokyo 1
Vallendar 1
Warsaw 1
Washington 1
Yerevan 1
Totale 1.945
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Nome #
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains 75
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients 72
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 71
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients 70
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women. 66
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 63
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay. 61
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients 60
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis 60
Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe FV deficiency 59
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency 59
Genomewide Association Study of Severe Covid-19 with Respiratory Failure 59
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 58
Exploring the global landscape of genetic variation in coagulation factor XI deficiency 58
Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease 53
ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy 53
The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis 52
Nonenzymatic Polymerization into Long Linear RNA Templated by Liquid Crystal Self-Assembly 52
The double-faced association of the PRKCA gene with multiple sclerosis 52
Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions. 50
Abiotic ligation of DNA oligomers templated by their liquid crystal ordering 50
Molecular characterization of six novel mutations causing factor V deficiency 49
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases 49
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis 49
Not only cancer: The long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis 46
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 46
Identification and characterization of 6 novel genetic defects leading to factor V deficiency 45
Phase behavior and critical activated dynamics of limited-valence DNA nanostars 44
The first case of the TARDBP p.G294V mutation in a homozygous state: is a single pathogenic allele sufficient to cause ALS? 44
miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA 44
Meta-analysis of Multiple Sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes 42
Hereditary Hypofibrinogenemia with Hepatic Storage 41
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency 39
Newtonian to non-newtonian fluid transition of a model transient network 38
MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity 38
Profiling the mutational landscape of coagulation factor V deficiency. 37
Notch1 regulates chemotaxis and proliferation by controlling the CC-chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia 37
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 37
Sighting acute myocardial infarction through platelet gene expression 36
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease 35
Molecular investigation of 41 patients affected by coagulation factor XI deficiency 35
Mycobacterium tuberculosis Drives Expansion of Low-Density Neutrophils Equipped With Regulatory Activities 35
Functional and clinical implications of genetic structure in 1686 Italian exomes 34
Mapping the human genetic architecture of COVID-19 31
OxDNA to Study Species Interactions 29
Mutational screening of 25 unrelated FV-deficient patients from six countries 29
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 28
The microRNA miR-634: molecular characterization and potential relevance for multiple sclerosis 27
Identification and characterization of 6 novel genetics defects leading to factor V deficiency 26
MiR-634: a new player in the pathogenesis of multiple sclerosis? 26
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion 21
Needles in Haystacks: Understanding the Success of Selective Pairing of Nucleic Acids 19
Detailed stratified GWAS analysis for severe COVID-19 in four European populations 19
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules 18
The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile 15
Long-term outcomes of early-onset myocardial infarction with non-obstructive coronary artery disease (MINOCA) 15
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 8
Sex-Related Differences in Long-Term Outcomes After Early-Onset Myocardial Infarction 7
The Role of Epigenetics in Primary Biliary Cholangitis 6
Genetic susceptibility to severe COVID-19 5
Totale 2.482
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Categoria #
all - tutte 19.839
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 19.839
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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
2021/2022301 11 2 6 63 3 5 10 36 34 48 63 20
2022/2023950 118 54 72 133 116 77 0 80 169 67 51 13
2023/2024580 45 49 84 35 22 90 53 54 10 7 65 66
2024/2025112 42 27 11 15 17 0 0 0 0 0 0 0
Totale 2.482