IRIS
BENETTI, ELISA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 3.709
NA - Nord America 3.161
AS - Asia 1.735
SA - Sud America 303
Continente sconosciuto - Info sul continente non disponibili 202
AF - Africa 103
OC - Oceania 5
Totale 9.218
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 3.084
IT - Italia 1.344
RU - Federazione Russa 911
SG - Singapore 507
CN - Cina 383
DE - Germania 310
IE - Irlanda 270
BR - Brasile 267
VN - Vietnam 223
HK - Hong Kong 206
GB - Regno Unito 191
FI - Finlandia 164
FR - Francia 161
SE - Svezia 103
KR - Corea 90
BD - Bangladesh 81
NL - Olanda 78
IN - India 61
ZA - Sudafrica 46
CA - Canada 45
ES - Italia 32
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
UA - Ucraina 15
PK - Pakistan 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
EC - Ecuador 6
GR - Grecia 6
HN - Honduras 6
AZ - Azerbaigian 5
PE - Perù 5
PH - Filippine 5
RO - Romania 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
PT - Portogallo 4
TT - Trinidad e Tobago 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
BG - Bulgaria 2
BY - Bielorussia 2
CY - Cipro 2
DK - Danimarca 2
ET - Etiopia 2
JM - Giamaica 2
LB - Libano 2
PA - Panama 2
PY - Paraguay 2
QA - Qatar 2
TN - Tunisia 2
AL - Albania 1
AM - Armenia 1
AO - Angola 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
MQ - Martinica 1
NI - Nicaragua 1
NR - Nauru 1
OM - Oman 1
PR - Porto Rico 1
PS - Palestinian Territory 1
Totale 9.009
Salva come PNG Salva come JPEG
Città #
Dallas 965
Singapore 331
Moscow 307
Milan 294
Dublin 256
Ashburn 234
San Jose 228
Hong Kong 193
Santa Clara 188
Munich 183
Council Bluffs 158
Siena 155
Chandler 127
Hefei 126
Southend 119
Helsinki 113
Los Angeles 109
Rome 89
Seoul 89
New York 79
Ho Chi Minh City 75
Beijing 72
Florence 68
Lauterbourg 54
Hanoi 53
Fairfield 46
Johannesburg 41
São Paulo 37
The Dalles 37
Princeton 30
Brescia 29
Seattle 27
Ann Arbor 26
Chicago 26
Buffalo 25
Houston 25
Nuremberg 23
Turku 23
Wilmington 23
Naples 20
Bengaluru 19
Paris 19
Lappeenranta 18
Figino 17
Frankfurt am Main 17
London 17
Bologna 16
Cambridge 16
Orem 16
Abidjan 15
Düsseldorf 15
Fremont 15
Shanghai 15
Warsaw 15
Denver 14
Málaga 14
Washington 14
San Diego 13
Tokyo 13
Woodbridge 13
Haiphong 12
Portsmouth 12
Columbus 11
Dong Ket 11
Phoenix 11
Redondo Beach 11
Stockholm 11
Tashkent 11
Zurich 11
Aachen 10
Boardman 10
Boston 10
Brno 10
Comun Nuovo 10
Rio de Janeiro 10
Abuja 9
Atlanta 9
Baghdad 9
Charlotte 9
Chennai 9
Montreal 9
Newark 9
Toronto 9
Brooklyn 8
Carrara 8
Perugia 8
Turin 8
Da Nang 7
Hyderabad 7
Livorno 7
Mumbai 7
Amman 6
Amsterdam 6
Anagni 6
City of London 6
Istanbul 6
Napoli 6
Olomouc 6
Pisa 6
Salerno 6
Totale 5.761
Salva come PNG Salva come JPEG
Nome #
A first update on mapping the human genetic architecture of COVID-19 601
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population 592
Association of toll-like receptor 7 variants with life-threatening COVID-19 disease in males: Findings from a nested case-control study 508
Genetic mechanisms of critical illness in COVID-19 452
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males 440
An explainable model of host genetic interactions linked to COVID-19 severity 386
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity 382
Pathogen-sugar interactions revealed by universal saturation transfer analysis 373
Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males 355
Mapping the human genetic architecture of COVID-19 325
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients 313
C9orf72 intermediate repeats confer genetic risk for severe covid-19 pneumonia independently of age 284
AAV-mediated FOXG1 gene editing in human Rett primary cells 257
High rate of HDR in gene editing of p.(Thr158Met) MECP2 mutational hotspot 243
Whole-genome sequencing reveals host factors underlying critical COVID-19 218
WES profiling of COVID-19 215
Protective role of a TMPRSS2 variant on severe COVID-19 outcome in young males and elderly women 202
New candidates for autism/intellectual disability identified by whole-exome sequencing 198
Correction: New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells 196
Identifying host genetics risk factors for COVID-19 from Exome Sequencing 189
SELP Asp603Asn and severe thrombosis in COVID-19 males 179
Correction to: High rate of HDR in gene editing of p.(Thr158Met) MECP2 mutational hotspot 174
Exome sequencing in 200 intellectual disability/autistic patients: new candidates and atypical presentations 163
Corrigendum: Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes (Front. Oncol., (2021), 11, 10.3389/fonc.2021.649435) 160
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses 160
Correction: SELP Asp603Asn and severe thrombosis in COVID-19 males 159
New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells 158
Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders 133
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) 130
Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint 129
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14 128
Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant 120
Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases 114
A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis 107
Solving unsolved rare neurological diseases—a Solve-RD viewpoint 100
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases 99
Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data 98
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing 90
Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility 88
Totale 9.218
Salva come PNG Salva come JPEG
Categoria #
all - tutte 28.435
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 28.435
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022386 0 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
2025/20264.853 290 666 738 564 822 171 584 141 183 285 159 250
2026/2027347 222 125 0 0 0 0 0 0 0 0 0 0
Totale 9.218