IRIS
BENETTI, ELISA
 Distribuzione geografica
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Continente #
EU - Europa 2.690
NA - Nord America 2.167
AS - Asia 1.096
SA - Sud America 224
AF - Africa 33
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 3
Totale 6.218
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Nazione #
US - Stati Uniti d'America 2.139
IT - Italia 977
RU - Federazione Russa 449
SG - Singapore 351
CN - Cina 326
DE - Germania 289
IE - Irlanda 266
BR - Brasile 211
GB - Regno Unito 169
FI - Finlandia 152
HK - Hong Kong 141
FR - Francia 101
SE - Svezia 98
KR - Corea 89
NL - Olanda 60
IN - India 42
VN - Vietnam 36
ES - Italia 29
CZ - Repubblica Ceca 19
IR - Iran 19
CA - Canada 16
PL - Polonia 16
AT - Austria 15
CI - Costa d'Avorio 15
JP - Giappone 12
PK - Pakistan 11
BD - Bangladesh 10
TR - Turchia 10
UA - Ucraina 9
CH - Svizzera 8
IQ - Iraq 8
MA - Marocco 8
JO - Giordania 5
MX - Messico 5
PE - Perù 5
SA - Arabia Saudita 5
ZA - Sudafrica 5
BE - Belgio 4
EE - Estonia 4
EU - Europa 4
GR - Grecia 4
MK - Macedonia 4
AZ - Azerbaigian 3
KG - Kirghizistan 3
LV - Lettonia 3
PH - Filippine 3
PT - Portogallo 3
UZ - Uzbekistan 3
AR - Argentina 2
AU - Australia 2
CL - Cile 2
DK - Danimarca 2
EC - Ecuador 2
GE - Georgia 2
HN - Honduras 2
KE - Kenya 2
NO - Norvegia 2
PY - Paraguay 2
QA - Qatar 2
TT - Trinidad e Tobago 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
BH - Bahrain 1
BY - Bielorussia 1
CY - Cipro 1
DZ - Algeria 1
GT - Guatemala 1
HR - Croazia 1
ID - Indonesia 1
IL - Israele 1
IS - Islanda 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LT - Lituania 1
LU - Lussemburgo 1
ML - Mali 1
MY - Malesia 1
NI - Nicaragua 1
NP - Nepal 1
NR - Nauru 1
PA - Panama 1
PS - Palestinian Territory 1
RO - Romania 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
TL - Timor Orientale 1
TN - Tunisia 1
TW - Taiwan 1
XK - ???statistics.table.value.countryCode.XK??? 1
YE - Yemen 1
Totale 6.218
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Città #
Dallas 953
Dublin 253
Singapore 218
Munich 183
Milan 168
Santa Clara 163
Ashburn 156
Siena 155
Hong Kong 138
Moscow 130
Chandler 127
Southend 119
Hefei 107
Helsinki 101
Seoul 89
Beijing 69
Florence 66
Rome 58
New York 51
Fairfield 46
Los Angeles 44
São Paulo 33
Princeton 30
Brescia 29
Ann Arbor 26
Turku 23
Houston 22
Nuremberg 22
Wilmington 21
Lauterbourg 20
Bengaluru 19
Chicago 19
Lappeenranta 18
Cambridge 16
Abidjan 15
Düsseldorf 15
Fremont 14
Málaga 14
Seattle 14
Buffalo 13
Shanghai 13
Washington 13
Woodbridge 13
San Diego 12
Dong Ket 11
London 11
Portsmouth 11
Redondo Beach 11
Aachen 10
Boardman 10
Comun Nuovo 10
Naples 10
Paris 10
Tokyo 10
Bologna 9
Brno 9
Council Bluffs 9
Denver 9
Stockholm 9
Carrara 8
Rio de Janeiro 8
Warsaw 8
Atlanta 7
Frankfurt am Main 7
Hanoi 7
Hyderabad 7
Phoenix 7
Anagni 6
Brooklyn 6
Charlotte 6
Ho Chi Minh City 6
Livorno 6
Napoli 6
Olomouc 6
Pisa 6
Amman 5
Amsterdam 5
Catanzaro 5
Grosseto 5
Guangzhou 5
Lima 5
Salerno 5
Tehran 5
Verona 5
Vienna 5
Viterbo 5
Zanjan 5
Brussels 4
Cagliari 4
Espoo 4
Fiesole 4
Newark 4
Norwalk 4
Perugia 4
Portico di Caserta 4
Redwood City 4
Saint-Fons 4
Ankara 3
Baghdad 3
Baku 3
Totale 4.193
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Nome #
A first update on mapping the human genetic architecture of COVID-19 507
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population 494
Association of toll-like receptor 7 variants with life-threatening COVID-19 disease in males: Findings from a nested case-control study 435
Genetic mechanisms of critical illness in COVID-19 306
An explainable model of host genetic interactions linked to COVID-19 severity 299
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males 292
Pathogen-sugar interactions revealed by universal saturation transfer analysis 247
Mapping the human genetic architecture of COVID-19 237
Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males 225
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity 222
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients 208
AAV-mediated FOXG1 gene editing in human Rett primary cells 192
High rate of HDR in gene editing of p.(Thr158Met) MECP2 mutational hotspot 190
C9orf72 intermediate repeats confer genetic risk for severe covid-19 pneumonia independently of age 163
WES profiling of COVID-19 163
Identifying host genetics risk factors for COVID-19 from Exome Sequencing 146
Protective role of a TMPRSS2 variant on severe COVID-19 outcome in young males and elderly women 138
New candidates for autism/intellectual disability identified by whole-exome sequencing 127
SELP Asp603Asn and severe thrombosis in COVID-19 males 126
Exome sequencing in 200 intellectual disability/autistic patients: new candidates and atypical presentations 126
Corrigendum: Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes (Front. Oncol., (2021), 11, 10.3389/fonc.2021.649435) 119
Whole-genome sequencing reveals host factors underlying critical COVID-19 119
Correction: New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells 115
Correction to: High rate of HDR in gene editing of p.(Thr158Met) MECP2 mutational hotspot 110
New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells 107
Correction: SELP Asp603Asn and severe thrombosis in COVID-19 males 102
Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders 101
Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2) 93
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses 84
Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases 76
Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant 75
A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis 66
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14 65
Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint 63
Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data 58
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases 57
Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility 56
Solving unsolved rare neurological diseases—a Solve-RD viewpoint 53
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing 50
Totale 6.412
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Categoria #
all - tutte 22.298
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 22.298
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021230 0 0 0 0 31 25 13 21 40 24 40 36
2021/2022440 54 31 21 32 36 28 21 28 26 23 52 88
2022/2023630 35 58 56 60 45 100 69 77 41 31 36 22
2023/2024668 38 37 82 36 33 140 164 37 4 23 36 38
2024/20252.014 83 62 181 146 247 171 213 124 158 109 160 360
2025/20262.394 290 666 738 564 136 0 0 0 0 0 0 0
Totale 6.412