ARTUSO, LUCIA
 Distribuzione geografica
Continente #
NA - Nord America 3.220
AS - Asia 2.031
EU - Europa 1.960
SA - Sud America 263
AF - Africa 73
OC - Oceania 37
Continente sconosciuto - Info sul continente non disponibili 6
Totale 7.590
Nazione #
US - Stati Uniti d'America 3.152
SG - Singapore 552
CN - Cina 532
GB - Regno Unito 500
IT - Italia 430
VN - Vietnam 264
DE - Germania 194
SE - Svezia 183
BR - Brasile 181
HK - Hong Kong 172
RU - Federazione Russa 105
FR - Francia 99
FI - Finlandia 89
IN - India 76
TR - Turchia 76
IE - Irlanda 73
KR - Corea 69
UA - Ucraina 53
ID - Indonesia 42
CA - Canada 40
BD - Bangladesh 39
AU - Australia 35
PK - Pakistan 31
ES - Italia 29
IQ - Iraq 29
JP - Giappone 29
NL - Olanda 29
BG - Bulgaria 22
AR - Argentina 20
MX - Messico 20
PL - Polonia 19
IR - Iran 18
ZA - Sudafrica 18
BE - Belgio 17
CO - Colombia 17
SI - Slovenia 17
TW - Taiwan 14
AE - Emirati Arabi Uniti 12
CL - Cile 12
EC - Ecuador 12
LT - Lituania 12
CZ - Repubblica Ceca 11
KE - Kenya 11
MY - Malesia 11
RO - Romania 11
HU - Ungheria 10
MA - Marocco 10
NO - Norvegia 10
PH - Filippine 9
PT - Portogallo 8
UZ - Uzbekistan 8
AT - Austria 7
CH - Svizzera 7
EG - Egitto 7
SA - Arabia Saudita 7
TN - Tunisia 7
IL - Israele 6
NP - Nepal 6
TH - Thailandia 6
VE - Venezuela 6
BO - Bolivia 5
GH - Ghana 4
MD - Moldavia 4
PE - Perù 4
RS - Serbia 4
AZ - Azerbaigian 3
DK - Danimarca 3
DZ - Algeria 3
IS - Islanda 3
KG - Kirghizistan 3
KZ - Kazakistan 3
OM - Oman 3
PY - Paraguay 3
UY - Uruguay 3
XK - ???statistics.table.value.countryCode.XK??? 3
AL - Albania 2
BH - Bahrain 2
BY - Bielorussia 2
CI - Costa d'Avorio 2
DO - Repubblica Dominicana 2
EU - Europa 2
GR - Grecia 2
HR - Croazia 2
JO - Giordania 2
LY - Libia 2
MO - Macao, regione amministrativa speciale della Cina 2
NZ - Nuova Zelanda 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AO - Angola 1
BJ - Benin 1
CD - Congo 1
CG - Congo 1
CR - Costa Rica 1
ET - Etiopia 1
GE - Georgia 1
HN - Honduras 1
JM - Giamaica 1
KW - Kuwait 1
LV - Lettonia 1
Totale 7.579
Città #
Ashburn 386
Singapore 333
Southend 329
Santa Clara 290
Fairfield 243
San Jose 210
Chandler 179
Woodbridge 177
Hong Kong 158
Ann Arbor 125
Hefei 121
Houston 119
Beijing 118
Seattle 93
Nyköping 80
Modena 78
Wilmington 78
Council Bluffs 76
Dearborn 74
Ho Chi Minh City 74
Jacksonville 74
Dublin 70
London 70
Cambridge 64
Seoul 60
Helsinki 56
Hanoi 54
Los Angeles 53
New York 52
Munich 39
The Dalles 38
Shanghai 31
Jakarta 30
Moscow 30
Lauterbourg 28
Bologna 27
Frankfurt am Main 27
Fremont 25
Chicago 22
Falls Church 22
Redwood City 22
Sofia 22
Izmir 21
Melbourne 20
Princeton 20
Bremen 19
Buffalo 19
Dong Ket 19
Turku 19
Dallas 18
Milan 18
São Paulo 18
Warsaw 17
Eugene 16
Tokyo 15
Baghdad 14
Florence 14
Orem 14
Barcelona 13
Brussels 13
Da Nang 12
Falkenstein 12
Montreal 12
Boardman 11
Hyderabad 11
San Diego 11
Sydney 11
Toronto 11
Lawrence 10
Paris 10
Phoenix 10
Rome 10
Alexandria 9
Denver 9
Haiphong 9
Salt Lake City 9
Amsterdam 8
Colorno 8
Columbus 8
Guangzhou 8
Islamabad 8
Johannesburg 8
Oslo 8
Reggio Emilia 8
San Giuliano Milanese 8
Ankara 7
Bắc Ninh 7
Genoa 7
Hải Dương 7
Kassel 7
Nuremberg 7
Basingstoke 6
Bogotá 6
Brasília 6
Brno 6
Istanbul 6
Kent 6
Lahore 6
Madrid 6
Nairobi 6
Totale 4.899
Nome #
Targeted cancer exome sequencing reveals recurrent mutations in myeloproliferative neoplasms 553
A Next Generation Sequencing amplicon-based strategy to explore Inherited Retinal Degeneration complexity 521
Implementation of an NGS-based workflow for BRCA1 and BRCA2 mutation screening 455
Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Hybrid Posters 397
Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing 391
ERBB2 mutations in hormone receptor positive primary breast cancers samples and in their matched endocrine-resistant recurrences. 378
Amplicon-based Next Generation Sequencing: an effective approach to molecular diagnosis of Epidermolysis Bullosa 360
Genomic alterations at the basis of treatment resistance in metastatic breast cancer: Clinical applications 358
Amplicon-based next-generation sequencing: an effective approach for the molecular diagnosis of epidermolysis bullosa 346
Impact of mutational status on outcomes in myelofibrosis patients treated with ruxolitinib in the COMFORT-II study 323
Hereditary pancreatic cancer: A retrospective single-center study of 5143 Italian families with history of BRCA-related malignancies 323
Impact Of Prognostically Detrimental Mutations (ASXL1, EZH2, SRSF2, IDH1/2) On Outcomes In Patients With Myelofibrosis Treated With Ruxolitinib In COMFORT-II 295
Homozygous familial hypobetalipoproteinemia: A Turkish case carrying a missense mutation in apolipoprotein B 283
AMPLICON-BASED NGS: AN EFFECTIVE APPROACH FOR THE MOLECULAR DIAGNOSIS OF EPIDERMOLYSIS BULLOSA 273
STRATEGIES TO PREDICT TREATMENT RESPONSE AND SELECT THERAPIES IN METASTATIC BREAST CANCER PATIENTS USING A NEXT GENERATION SEQUENCING MULTI-GENE PANEL 244
STRATEGIES TO PREDICT TREATMENT RESPONSE AND SELECT THERAPIES IN METASTATIC BREAST CANCER PATIENTS USING A NEXT GENERATION SEQUENCING (NGS) MULTI-GENE PANEL 242
Characterization of new ATM deletion associated with hereditary breast cancer 231
Clinical application of NGS in the diagnosis of iron overload disorders or hyperferritinemia of genetic origin 229
Pre-mir146a e FSHR sono marker di mosaicismo tiroideo nel carcinoma follicolare della tiroide 229
Automated capture-based NGS workflow: one thousand patients experience in a clinical routine framework 215
Ivar, an interpretation‐oriented tool to manage the update and revision of variant annotation and classification 201
Constitutional Mosaicism: A Critical Issue in the Definition of BRCA-Inherited Cancer Risk 181
LOW-FREQUENCY ALLELE VARIANTS IN NGS MULTI-GENE PANELS FOR HEREDITARY CANCER TESTING: ARTIFACTS, CHIP OR MOSAICS? MANAGING THE RESULTS IN THE LABORATORY ROUTINE 153
Automation of a capture-based NGS workflow: one thousand patients experience in a diagnostic clinical routine framework 151
Clinically relevant low-frequency Next Generation Sequencing variants in hereditary cancer patients: an operational multi-step algorithm for laboratory managing 148
Characterization of copy number variants in hereditary cancer patients through NGS shows a distinctive PALB2 contribution to the diagnostic yield 95
Diagnostic Yield and Clinical Impact of a Small Genetic Panel for Kidney Disease: A Multicenter, Retrospective European Study 88
Totale 7.663
Categoria #
all - tutte 23.639
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 23.639


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202194 0 0 0 0 0 0 0 0 0 0 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
2025/20262.523 228 139 195 214 335 212 433 178 274 315 0 0
Totale 7.663