BELIGNI, GIADA
 Distribuzione geografica
Continente #
EU - Europa 860
NA - Nord America 269
AS - Asia 58
OC - Oceania 4
Totale 1.191
Nazione #
IT - Italia 466
US - Stati Uniti d'America 268
IE - Irlanda 175
GB - Regno Unito 41
SE - Svezia 38
DE - Germania 31
FI - Finlandia 28
FR - Francia 22
RU - Federazione Russa 19
ES - Italia 14
CN - Cina 11
TR - Turchia 11
IN - India 10
SG - Singapore 10
CZ - Repubblica Ceca 6
HK - Hong Kong 6
BG - Bulgaria 5
CH - Svizzera 5
AU - Australia 4
PL - Polonia 4
IR - Iran 3
KR - Corea 3
AL - Albania 1
AZ - Azerbaigian 1
BE - Belgio 1
CA - Canada 1
JP - Giappone 1
LV - Lettonia 1
NL - Olanda 1
PH - Filippine 1
RO - Romania 1
SK - Slovacchia (Repubblica Slovacca) 1
TW - Taiwan 1
Totale 1.191
Città #
Dublin 169
Siena 80
Florence 60
Ashburn 49
Chandler 36
Milan 31
Helsinki 27
Rome 27
New York 26
Southend 22
Fairfield 18
Chicago 15
Málaga 11
Comun Nuovo 10
Fremont 10
Istanbul 9
Princeton 8
Shanghai 8
Washington 8
Anagni 6
Boardman 6
Edinburgh 6
Hong Kong 6
Livorno 6
London 6
Moscow 6
Rubano 6
Singapore 6
Bari 5
Brescia 5
Grosseto 5
Migliarino 5
Padova 5
Sofia 5
Verona 5
Cagliari 4
Catania 4
Fiesole 4
Munich 4
Naples 4
Paris 4
Pontedera 4
Wilmington 4
Ann Arbor 3
Bergamo 3
Brno 3
Carrara 3
Delhi 3
Gdynia 3
Guagnano 3
Hyderabad 3
Los Angeles 3
Modugno 3
Pistoia 3
Rieti 3
Salerno 3
San Diego 3
Seattle 3
Tocco da Casauria 3
Venice 3
Berlin 2
Bologna 2
Bonndorf 2
Borgo Valsugana 2
Borgonovo Val Tidone 2
Cambridge 2
Campi Bisenzio 2
Carbonara di Nola 2
Clifton 2
Houston 2
Jinju 2
Kayseri 2
Melbourne 2
Noceto 2
Norwalk 2
Olomouc 2
Osimo 2
Palagonia 2
Palermo 2
Pedrengo 2
Poggibonsi 2
Pomarance 2
Prato 2
Reggio Calabria 2
Rimini 2
Saint-Fons 2
Santa Cruz de Tenerife 2
Santa Maria a Monte 2
Sinalunga 2
Trieste 2
Turin 2
Watford 2
Wettingen 2
Woodbridge 2
Zollikofen 2
Aachen 1
Amsterdam 1
Bacoli 1
Baku 1
Bangalore 1
Totale 871
Nome #
Application of the CRISPR-Cas9 genome editing approach for the correction of the p.Gly2019Ser (c.6055G>A) LRRK2 variant in Parkinson Disease. 142
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males 132
Association of toll-like receptor 7 variants with life-threatening COVID-19 disease in males: Findings from a nested case-control study 118
Pathogen-sugar interactions revealed by universal saturation transfer analysis 108
A first update on mapping the human genetic architecture of COVID-19 95
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients 94
An explainable model of host genetic interactions linked to COVID-19 severity 82
Carriers of ADAMTS13 Rare Variants Are at High Risk of Life-Threatening COVID-19 79
Severe COVID-19 in hospitalized carriers of single CFTR pathogenic variants 76
Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes 74
SELP Asp603Asn and severe thrombosis in COVID-19 males 69
C9orf72 intermediate repeats confer genetic risk for severe covid-19 pneumonia independently of age 51
Whole-genome sequencing reveals host factors underlying critical COVID-19 45
Detection of RSV Genome in Cerebrospinal Fluid of a Patient with Guillain Barrè Syndrome: A Case Report 27
null 24
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity 21
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity 17
Totale 1.254
Categoria #
all - tutte 6.685
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 6.685


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202116 0 0 0 0 0 0 0 0 6 3 5 2
2021/2022132 20 11 3 13 4 1 6 5 5 9 22 33
2022/2023391 12 14 23 32 19 49 83 51 33 26 36 13
2023/2024604 33 26 62 43 34 107 111 44 13 36 46 49
2024/2025111 79 32 0 0 0 0 0 0 0 0 0 0
Totale 1.254