IRIS
BENETTI, ELISA
 Distribuzione geografica
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Continente #
EU - Europa 1.406
NA - Nord America 807
AS - Asia 85
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
SA - Sud America 2
Totale 2.306
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Nazione #
US - Stati Uniti d'America 801
IT - Italia 491
IE - Irlanda 363
GB - Regno Unito 163
SE - Svezia 117
FR - Francia 76
DE - Germania 75
FI - Finlandia 52
CN - Cina 29
ES - Italia 29
IN - India 17
IR - Iran 11
VN - Vietnam 11
UA - Ucraina 8
CA - Canada 6
BG - Bulgaria 5
CH - Svizzera 5
EU - Europa 4
MK - Macedonia 4
PK - Pakistan 4
GR - Grecia 3
HK - Hong Kong 3
JP - Giappone 3
PL - Polonia 3
RU - Federazione Russa 3
AU - Australia 2
CL - Cile 2
NL - Olanda 2
PH - Filippine 2
PT - Portogallo 2
QA - Qatar 2
RO - Romania 2
AZ - Azerbaigian 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
EE - Estonia 1
JO - Giordania 1
TR - Turchia 1
Totale 2.306
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Città #
Dublin 350
Chandler 157
Southend 150
Ashburn 108
Siena 88
Fairfield 60
New York 51
Helsinki 50
Florence 49
Princeton 37
Milan 34
Ann Arbor 33
Wilmington 29
Rome 25
Houston 22
Málaga 22
Cambridge 20
Fremont 19
Shanghai 19
Washington 18
Woodbridge 17
Seattle 15
San Diego 13
Aachen 12
Dong Ket 11
Comun Nuovo 10
Hyderabad 8
Chicago 7
London 6
Los Angeles 6
Napoli 6
Zanjan 6
Brescia 5
Salerno 5
San Mateo 5
Sofia 5
Viterbo 5
Boardman 4
Brindisi 4
Cagliari 4
Carrara 4
Fiesole 4
Guangzhou 4
Naples 4
Noceto 4
Norwalk 4
Paris 4
Pisa 4
Redwood City 4
Rieti 4
Arese 3
Bologna 3
Empoli 3
Esslingen am Neckar 3
Gdynia 3
Guagnano 3
Lebanon 3
Lentate sul Seveso 3
Prato 3
Strada in Chianti 3
Thessaloniki 3
Torino 3
Toronto 3
Verona 3
Wettingen 3
Amsterdam 2
Barcelona 2
Basel 2
Bergamo 2
Berlin 2
Bonndorf 2
Borgonovo Val Tidone 2
Carbonara di Nola 2
Casale 2
Charlotte 2
Chieti 2
Dallas 2
Doha 2
Falkenstein 2
Genoa 2
Giugliano in Campania 2
Grosseto 2
Indore 2
Medicina 2
Osimo 2
Padova 2
Palermo 2
Pedrengo 2
Pleasanton 2
Poggibonsi 2
Pune 2
Rimini 2
Saint-Fons 2
San Francisco 2
Sevilla 2
Skopje 2
Uzzano 2
Winnipeg 2
Amman 1
Andover 1
Totale 1.648
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Nome #
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population 176
Genetic mechanisms of critical illness in COVID-19 171
null 134
High rate of HDR in gene editing of p.(Thr158Met) MECP2 mutational hotspot 126
AAV-mediated FOXG1 gene editing in human Rett primary cells 120
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity 119
null 114
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males. 110
New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells 98
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients 90
WES profiling of COVID-19 81
A first update on mapping the human genetic architecture of COVID-19 80
null 75
Whole Exome Sequencing in BRCA1-2 Candidate Families: The Contribution of Other Cancer Susceptibility Genes 75
Severe COVID-19 in hospitalized carriers of single CFTR pathogenic variants 72
Identifying host genetics risk factors for COVID-19 from Exome Sequencing 72
An explainable model of host genetic interactions linked to COVID-19 severity 68
SELP Asp603Asn and severe thrombosis in COVID-19 males 63
null 61
Exome sequencing in 200 intellectual disability/autistic patients: New candidates and atypical presentations 60
Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders 57
New Candidates for Autism/Intellectual Disability Identified by Whole-Exome Sequencing 51
null 48
Whole-genome sequencing reveals host factors underlying critical COVID-19 38
Corrigendum: Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes (Front. Oncol., (2021), 11, 10.3389/fonc.2021.649435) 35
Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males 32
Protective Role of a TMPRSS2 Variant on Severe COVID-19 Outcome in Young Males and Elderly Women 30
Exome sequencing in BRCA1-2 candidate familias: the contribution of other cancer susceptibility genes. 28
New Candidates for Autism/Intellectual Disability Identified by Whole-Exome Sequencing. 27
Exome Sequencing in 200 Intellectual Disability/Autistic Patients: New Candidates and Atypical Presentations. 27
Clinical and molecular characterization of COVID-19 hospitalized patients 26
null 23
New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells 17
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity 11
Employing a systematic approach to biobanking and analyzing clinical and genetic data for advancing COVID-19 research 4
Association of toll-like receptor 7 variants with life-threatening COVID-19 disease in males: Findings from a nested case-control study 3
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males 2
Totale 2.424
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Categoria #
all - tutte 11.039
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 11.039
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021329 17 4 20 11 32 36 15 30 46 35 42 41
2021/2022530 58 37 25 40 39 36 28 36 31 31 73 96
2022/2023765 46 77 75 80 51 109 87 75 67 37 39 22
2023/2024800 41 31 110 43 46 203 229 47 11 39 0 0
Totale 2.424