IRIS
BENETTI, ELISA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 3.463
NA - Nord America 2.714
AS - Asia 1.665
SA - Sud America 302
AF - Africa 103
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 5
Totale 8.257
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 2.662
IT - Italia 1.111
RU - Federazione Russa 911
SG - Singapore 505
CN - Cina 378
DE - Germania 309
IE - Irlanda 270
BR - Brasile 267
VN - Vietnam 223
HK - Hong Kong 203
GB - Regno Unito 190
FI - Finlandia 164
FR - Francia 160
SE - Svezia 100
KR - Corea 90
NL - Olanda 74
IN - India 58
ZA - Sudafrica 46
ES - Italia 32
CA - Canada 28
BD - Bangladesh 25
IQ - Iraq 25
PL - Polonia 25
CZ - Repubblica Ceca 20
IR - Iran 19
JP - Giappone 19
AT - Austria 18
TR - Turchia 18
CH - Svizzera 16
CI - Costa d'Avorio 15
PK - Pakistan 14
UA - Ucraina 14
AR - Argentina 13
UZ - Uzbekistan 13
MX - Messico 11
MA - Marocco 10
NG - Nigeria 9
SA - Arabia Saudita 9
KE - Kenya 8
MY - Malesia 8
ID - Indonesia 7
JO - Giordania 7
GR - Grecia 6
AZ - Azerbaigian 5
EC - Ecuador 5
HN - Honduras 5
PE - Perù 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
AU - Australia 4
BE - Belgio 4
CL - Cile 4
EE - Estonia 4
EG - Egitto 4
EU - Europa 4
HU - Ungheria 4
MK - Macedonia 4
PH - Filippine 4
PT - Portogallo 4
RO - Romania 4
DZ - Algeria 3
GE - Georgia 3
IL - Israele 3
KG - Kirghizistan 3
KZ - Kazakistan 3
LV - Lettonia 3
NO - Norvegia 3
NP - Nepal 3
BY - Bielorussia 2
CY - Cipro 2
DK - Danimarca 2
ET - Etiopia 2
LB - Libano 2
PA - Panama 2
PY - Paraguay 2
QA - Qatar 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
BG - Bulgaria 1
BH - Bahrain 1
BW - Botswana 1
CO - Colombia 1
DO - Repubblica Dominicana 1
GT - Guatemala 1
HR - Croazia 1
IS - Islanda 1
LK - Sri Lanka 1
LT - Lituania 1
LU - Lussemburgo 1
ML - Mali 1
NI - Nicaragua 1
NR - Nauru 1
OM - Oman 1
PS - Palestinian Territory 1
RS - Serbia 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 8.249
Salva come PNG Salva come JPEG
Città #
Dallas 955
Singapore 329
Moscow 307
Dublin 256
Ashburn 210
Hong Kong 190
Milan 186
Munich 183
Santa Clara 165
San Jose 157
Siena 155
Chandler 127
Hefei 126
Southend 119
Helsinki 113
Council Bluffs 106
Los Angeles 94
Seoul 89
Ho Chi Minh City 75
Beijing 70
Florence 67
Rome 65
New York 62
Lauterbourg 54
Hanoi 53
Fairfield 46
Johannesburg 41
São Paulo 37
The Dalles 37
Princeton 30
Brescia 29
Ann Arbor 26
Chicago 25
Houston 23
Nuremberg 23
Turku 23
Wilmington 21
Bengaluru 19
Paris 19
Lappeenranta 18
Frankfurt am Main 17
Buffalo 16
Cambridge 16
London 16
Orem 16
Abidjan 15
Düsseldorf 15
Seattle 15
Warsaw 15
Denver 14
Fremont 14
Málaga 14
Shanghai 14
Washington 14
Naples 13
San Diego 13
Tokyo 13
Woodbridge 13
Haiphong 12
Dong Ket 11
Portsmouth 11
Redondo Beach 11
Stockholm 11
Tashkent 11
Zurich 11
Aachen 10
Boardman 10
Bologna 10
Brno 10
Comun Nuovo 10
Rio de Janeiro 10
Abuja 9
Atlanta 9
Baghdad 9
Chennai 9
Carrara 8
Montreal 8
Perugia 8
Brooklyn 7
Charlotte 7
Da Nang 7
Hyderabad 7
Phoenix 7
Amman 6
Amsterdam 6
Anagni 6
Boston 6
City of London 6
Istanbul 6
Livorno 6
Napoli 6
Olomouc 6
Pisa 6
Verona 6
Vienna 6
Ankara 5
Baku 5
Catanzaro 5
Grosseto 5
Guangzhou 5
Totale 5.323
Salva come PNG Salva come JPEG
Nome #
A first update on mapping the human genetic architecture of COVID-19 575
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population 574
Association of toll-like receptor 7 variants with life-threatening COVID-19 disease in males: Findings from a nested case-control study 499
Genetic mechanisms of critical illness in COVID-19 409
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males 387
An explainable model of host genetic interactions linked to COVID-19 severity 365
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity 337
Pathogen-sugar interactions revealed by universal saturation transfer analysis 323
null 320
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients 292
Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males 283
C9orf72 intermediate repeats confer genetic risk for severe covid-19 pneumonia independently of age 253
AAV-mediated FOXG1 gene editing in human Rett primary cells 248
High rate of HDR in gene editing of p.(Thr158Met) MECP2 mutational hotspot 232
WES profiling of COVID-19 204
Whole-genome sequencing reveals host factors underlying critical COVID-19 198
Protective role of a TMPRSS2 variant on severe COVID-19 outcome in young males and elderly women 189
Correction: New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells 180
Identifying host genetics risk factors for COVID-19 from Exome Sequencing 175
New candidates for autism/intellectual disability identified by whole-exome sequencing 171
SELP Asp603Asn and severe thrombosis in COVID-19 males 170
Correction to: High rate of HDR in gene editing of p.(Thr158Met) MECP2 mutational hotspot 162
Exome sequencing in 200 intellectual disability/autistic patients: new candidates and atypical presentations 157
Corrigendum: Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes (Front. Oncol., (2021), 11, 10.3389/fonc.2021.649435) 154
Correction: SELP Asp603Asn and severe thrombosis in COVID-19 males 148
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses 148
New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells 143
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) 122
Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders 119
Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant 107
Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases 106
A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis 99
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14 98
Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data 94
Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint 90
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases 87
Solving unsolved rare neurological diseases—a Solve-RD viewpoint 80
Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility 76
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing 72
Mapping the human genetic architecture of COVID-19 5
Totale 8.451
Salva come PNG Salva come JPEG
Categoria #
all - tutte 25.745
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 25.745
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021100 0 0 0 0 0 0 0 0 0 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
2025/20264.433 290 666 738 564 822 171 584 141 183 274 0 0
Totale 8.451