ARTUSO, LUCIA
 Distribuzione geografica
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Continente #
NA - Nord America 2.797
EU - Europa 1.802
AS - Asia 1.518
SA - Sud America 201
AF - Africa 40
OC - Oceania 27
Continente sconosciuto - Info sul continente non disponibili 5
Totale 6.390
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Nazione #
US - Stati Uniti d'America 2.758
CN - Cina 486
GB - Regno Unito 484
SG - Singapore 412
IT - Italia 383
DE - Germania 183
SE - Svezia 182
BR - Brasile 157
HK - Hong Kong 150
RU - Federazione Russa 100
VN - Vietnam 100
FI - Finlandia 76
IE - Irlanda 72
FR - Francia 71
TR - Turchia 65
IN - India 59
KR - Corea 49
UA - Ucraina 49
ID - Indonesia 39
ES - Italia 26
AU - Australia 25
PK - Pakistan 25
JP - Giappone 24
NL - Olanda 24
BG - Bulgaria 22
CA - Canada 22
BD - Bangladesh 20
IQ - Iraq 20
IR - Iran 18
BE - Belgio 17
PL - Polonia 17
SI - Slovenia 17
AR - Argentina 12
MX - Messico 12
ZA - Sudafrica 12
TW - Taiwan 11
LT - Lituania 10
NO - Norvegia 10
CO - Colombia 9
RO - Romania 9
CZ - Repubblica Ceca 8
EC - Ecuador 8
MY - Malesia 8
AT - Austria 7
CH - Svizzera 6
PT - Portogallo 6
CL - Cile 5
HU - Ungheria 5
IL - Israele 5
TH - Thailandia 5
UZ - Uzbekistan 5
EG - Egitto 4
GH - Ghana 4
KE - Kenya 4
MD - Moldavia 4
TN - Tunisia 4
IS - Islanda 3
MA - Marocco 3
PE - Perù 3
PH - Filippine 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
AZ - Azerbaigian 2
BO - Bolivia 2
CI - Costa d'Avorio 2
DK - Danimarca 2
EU - Europa 2
HR - Croazia 2
KZ - Kazakistan 2
MO - Macao, regione amministrativa speciale della Cina 2
NZ - Nuova Zelanda 2
RS - Serbia 2
XK - ???statistics.table.value.countryCode.XK??? 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
AM - Armenia 1
BH - Bahrain 1
BJ - Benin 1
CD - Congo 1
CG - Congo 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GE - Georgia 1
GR - Grecia 1
JM - Giamaica 1
KG - Kirghizistan 1
LV - Lettonia 1
LY - Libia 1
MK - Macedonia 1
PA - Panama 1
PR - Porto Rico 1
PY - Paraguay 1
QA - Qatar 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TG - Togo 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
Totale 6.390
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Città #
Southend 329
Ashburn 317
Santa Clara 278
Fairfield 243
Singapore 233
Chandler 179
Woodbridge 177
Hong Kong 139
Ann Arbor 125
Hefei 121
Houston 118
Beijing 96
Seattle 93
Nyköping 80
Wilmington 78
Modena 76
Dearborn 74
Jacksonville 74
Dublin 69
London 68
Cambridge 64
Council Bluffs 53
New York 47
Los Angeles 46
Helsinki 43
Seoul 40
Munich 39
Moscow 30
Jakarta 29
Shanghai 29
Fremont 25
Bologna 23
Ho Chi Minh City 23
Falls Church 22
Redwood City 22
Sofia 22
Izmir 21
Frankfurt am Main 20
Princeton 20
Bremen 19
Chicago 19
Dong Ket 19
Turku 19
Buffalo 18
Milan 17
Dallas 16
Eugene 16
São Paulo 16
Warsaw 16
Hanoi 15
Melbourne 15
San Jose 15
Florence 14
The Dalles 14
Barcelona 13
Brussels 13
Boardman 11
San Diego 11
Tokyo 11
Baghdad 10
Falkenstein 10
Hyderabad 10
Lawrence 10
Orem 10
Paris 10
Phoenix 10
Alexandria 9
Colorno 8
Columbus 8
Denver 8
Guangzhou 8
Oslo 8
Salt Lake City 8
San Giuliano Milanese 8
Toronto 8
Ankara 7
Islamabad 7
Kassel 7
Nuremberg 7
Reggio Emilia 7
Rome 7
Sydney 7
Brasília 6
Kent 6
Nanjing 6
New Taipei 6
Serra San Bruno 6
Stockholm 6
Verona 6
Absecon 5
Birigui 5
Brno 5
Da Nang 5
Genoa 5
Johannesburg 5
Kunming 5
Lauterbourg 5
Madrid 5
Maia 5
Montreal 5
Totale 4.181
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Nome #
Targeted cancer exome sequencing reveals recurrent mutations in myeloproliferative neoplasms 500
A Next Generation Sequencing amplicon-based strategy to explore Inherited Retinal Degeneration complexity 450
Implementation of an NGS-based workflow for BRCA1 and BRCA2 mutation screening 410
Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing 339
ERBB2 mutations in hormone receptor positive primary breast cancers samples and in their matched endocrine-resistant recurrences. 332
Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Hybrid Posters 322
Genomic alterations at the basis of treatment resistance in metastatic breast cancer: Clinical applications 314
Amplicon-based Next Generation Sequencing: an effective approach to molecular diagnosis of Epidermolysis Bullosa 310
Amplicon-based next-generation sequencing: an effective approach for the molecular diagnosis of epidermolysis bullosa 305
Hereditary pancreatic cancer: A retrospective single-center study of 5143 Italian families with history of BRCA-related malignancies 285
Impact of mutational status on outcomes in myelofibrosis patients treated with ruxolitinib in the COMFORT-II study 279
Impact Of Prognostically Detrimental Mutations (ASXL1, EZH2, SRSF2, IDH1/2) On Outcomes In Patients With Myelofibrosis Treated With Ruxolitinib In COMFORT-II 253
Homozygous familial hypobetalipoproteinemia: A Turkish case carrying a missense mutation in apolipoprotein B 246
STRATEGIES TO PREDICT TREATMENT RESPONSE AND SELECT THERAPIES IN METASTATIC BREAST CANCER PATIENTS USING A NEXT GENERATION SEQUENCING MULTI-GENE PANEL 220
AMPLICON-BASED NGS: AN EFFECTIVE APPROACH FOR THE MOLECULAR DIAGNOSIS OF EPIDERMOLYSIS BULLOSA 215
STRATEGIES TO PREDICT TREATMENT RESPONSE AND SELECT THERAPIES IN METASTATIC BREAST CANCER PATIENTS USING A NEXT GENERATION SEQUENCING (NGS) MULTI-GENE PANEL 206
Pre-mir146a e FSHR sono marker di mosaicismo tiroideo nel carcinoma follicolare della tiroide 200
Characterization of new ATM deletion associated with hereditary breast cancer 188
Clinical application of NGS in the diagnosis of iron overload disorders or hyperferritinemia of genetic origin 178
Automated capture-based NGS workflow: one thousand patients experience in a clinical routine framework 172
Ivar, an interpretation‐oriented tool to manage the update and revision of variant annotation and classification 165
Constitutional Mosaicism: A Critical Issue in the Definition of BRCA-Inherited Cancer Risk 137
LOW-FREQUENCY ALLELE VARIANTS IN NGS MULTI-GENE PANELS FOR HEREDITARY CANCER TESTING: ARTIFACTS, CHIP OR MOSAICS? MANAGING THE RESULTS IN THE LABORATORY ROUTINE 127
Clinically relevant low-frequency Next Generation Sequencing variants in hereditary cancer patients: an operational multi-step algorithm for laboratory managing 120
Automation of a capture-based NGS workflow: one thousand patients experience in a diagnostic clinical routine framework 119
Diagnostic Yield and Clinical Impact of a Small Genetic Panel for Kidney Disease: A Multicenter, Retrospective European Study 42
Characterization of copy number variants in hereditary cancer patients through NGS shows a distinctive PALB2 contribution to the diagnostic yield 29
Totale 6.463
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Categoria #
all - tutte 21.655
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 21.655
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021361 0 0 0 0 0 54 37 68 46 62 30 64
2021/2022400 21 24 13 25 24 37 24 11 46 49 76 50
2022/2023647 77 75 57 56 51 57 27 56 122 8 40 21
2023/2024544 14 21 40 34 64 66 71 79 19 29 46 61
2024/20251.550 50 41 52 94 251 210 115 115 172 94 165 191
2025/20261.323 228 139 195 214 335 212 0 0 0 0 0 0
Totale 6.463