ARTUSO, LUCIA
 Distribuzione geografica
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Continente #
NA - Nord America 3.628
AS - Asia 2.129
EU - Europa 2.034
SA - Sud America 269
Continente sconosciuto - Info sul continente non disponibili 79
AF - Africa 76
OC - Oceania 37
Totale 8.252
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Nazione #
US - Stati Uniti d'America 3.531
SG - Singapore 565
CN - Cina 546
GB - Regno Unito 501
IT - Italia 497
VN - Vietnam 266
DE - Germania 194
BR - Brasile 183
SE - Svezia 183
HK - Hong Kong 174
RU - Federazione Russa 105
FR - Francia 100
BD - Bangladesh 97
FI - Finlandia 89
IN - India 79
TR - Turchia 76
IE - Irlanda 73
KR - Corea 70
CA - Canada 59
UA - Ucraina 53
ID - Indonesia 42
AU - Australia 35
PK - Pakistan 32
ES - Italia 31
IQ - Iraq 29
JP - Giappone 29
NL - Olanda 29
BG - Bulgaria 22
AR - Argentina 21
IR - Iran 21
PL - Polonia 21
MX - Messico 20
ZA - Sudafrica 19
CO - Colombia 18
BE - Belgio 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
SA - Arabia Saudita 8
TN - Tunisia 8
UZ - Uzbekistan 8
AT - Austria 7
CH - Svizzera 7
EG - Egitto 7
VE - Venezuela 7
IL - Israele 6
NP - Nepal 6
TH - Thailandia 6
BO - Bolivia 5
GH - Ghana 5
CR - Costa Rica 4
MD - Moldavia 4
PE - Perù 4
PY - Paraguay 4
RS - Serbia 4
AZ - Azerbaigian 3
DK - Danimarca 3
DZ - Algeria 3
GR - Grecia 3
HN - Honduras 3
IS - Islanda 3
JM - Giamaica 3
KG - Kirghizistan 3
KZ - Kazakistan 3
OM - Oman 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
HR - Croazia 2
JO - Giordania 2
LY - Libia 2
MO - Macao, regione amministrativa speciale della Cina 2
NZ - Nuova Zelanda 2
PR - Porto Rico 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AO - Angola 1
BJ - Benin 1
CD - Congo 1
CG - Congo 1
ET - Etiopia 1
GE - Georgia 1
GT - Guatemala 1
Totale 8.166
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Città #
Ashburn 431
Singapore 338
Southend 329
Santa Clara 300
San Jose 254
Fairfield 243
Chandler 179
Woodbridge 177
Hong Kong 160
Council Bluffs 135
Ann Arbor 125
Beijing 125
Hefei 121
Houston 120
Seattle 95
Nyköping 80
Modena 79
Wilmington 79
Ho Chi Minh City 75
Dearborn 74
Jacksonville 74
London 71
Dublin 70
Cambridge 66
New York 63
Seoul 61
Los Angeles 60
Helsinki 56
Hanoi 55
Munich 39
The Dalles 38
Shanghai 31
Bologna 30
Jakarta 30
Moscow 30
Milan 29
Lauterbourg 28
Frankfurt am Main 27
Buffalo 26
Chicago 26
Fremont 25
Falls Church 22
Redwood City 22
Sofia 22
Dallas 21
Izmir 21
Melbourne 20
Princeton 20
Bremen 19
Dong Ket 19
Turku 19
Florence 18
São Paulo 18
Warsaw 17
Columbus 16
Eugene 16
Boardman 15
Orem 15
Tokyo 15
Baghdad 14
Montreal 14
Phoenix 14
Rome 14
Barcelona 13
Brussels 13
Toronto 13
Da Nang 12
Falkenstein 12
San Diego 12
Hyderabad 11
Paris 11
Sydney 11
Denver 10
Lawrence 10
Alexandria 9
Haiphong 9
Salt Lake City 9
Amsterdam 8
Colorno 8
Guangzhou 8
Islamabad 8
Johannesburg 8
Oslo 8
Philadelphia 8
Reggio Emilia 8
San Giuliano Milanese 8
Ankara 7
Bogotá 7
Bắc Ninh 7
Genoa 7
Hải Dương 7
Kassel 7
Nuremberg 7
Turin 7
Basingstoke 6
Boston 6
Brasília 6
Brno 6
Brooklyn 6
Istanbul 6
Totale 5.164
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Nome #
Targeted cancer exome sequencing reveals recurrent mutations in myeloproliferative neoplasms 576
A Next Generation Sequencing amplicon-based strategy to explore Inherited Retinal Degeneration complexity 571
Implementation of an NGS-based workflow for BRCA1 and BRCA2 mutation screening 473
ERBB2 mutations in hormone receptor positive primary breast cancers samples and in their matched endocrine-resistant recurrences. 432
Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Hybrid Posters 420
Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing 403
Amplicon-based Next Generation Sequencing: an effective approach to molecular diagnosis of Epidermolysis Bullosa 378
Amplicon-based next-generation sequencing: an effective approach for the molecular diagnosis of epidermolysis bullosa 376
Hereditary pancreatic cancer: A retrospective single-center study of 5143 Italian families with history of BRCA-related malignancies 376
Genomic alterations at the basis of treatment resistance in metastatic breast cancer: Clinical applications 374
Impact of mutational status on outcomes in myelofibrosis patients treated with ruxolitinib in the COMFORT-II study 344
Impact Of Prognostically Detrimental Mutations (ASXL1, EZH2, SRSF2, IDH1/2) On Outcomes In Patients With Myelofibrosis Treated With Ruxolitinib In COMFORT-II 314
Homozygous familial hypobetalipoproteinemia: A Turkish case carrying a missense mutation in apolipoprotein B 305
AMPLICON-BASED NGS: AN EFFECTIVE APPROACH FOR THE MOLECULAR DIAGNOSIS OF EPIDERMOLYSIS BULLOSA 293
STRATEGIES TO PREDICT TREATMENT RESPONSE AND SELECT THERAPIES IN METASTATIC BREAST CANCER PATIENTS USING A NEXT GENERATION SEQUENCING (NGS) MULTI-GENE PANEL 284
STRATEGIES TO PREDICT TREATMENT RESPONSE AND SELECT THERAPIES IN METASTATIC BREAST CANCER PATIENTS USING A NEXT GENERATION SEQUENCING MULTI-GENE PANEL 260
Characterization of new ATM deletion associated with hereditary breast cancer 254
Pre-mir146a e FSHR sono marker di mosaicismo tiroideo nel carcinoma follicolare della tiroide 239
Clinical application of NGS in the diagnosis of iron overload disorders or hyperferritinemia of genetic origin 236
Automated capture-based NGS workflow: one thousand patients experience in a clinical routine framework 235
Ivar, an interpretation‐oriented tool to manage the update and revision of variant annotation and classification 214
Constitutional Mosaicism: A Critical Issue in the Definition of BRCA-Inherited Cancer Risk 190
Automation of a capture-based NGS workflow: one thousand patients experience in a diagnostic clinical routine framework 164
Clinically relevant low-frequency Next Generation Sequencing variants in hereditary cancer patients: an operational multi-step algorithm for laboratory managing 164
LOW-FREQUENCY ALLELE VARIANTS IN NGS MULTI-GENE PANELS FOR HEREDITARY CANCER TESTING: ARTIFACTS, CHIP OR MOSAICS? MANAGING THE RESULTS IN THE LABORATORY ROUTINE 162
Characterization of copy number variants in hereditary cancer patients through NGS shows a distinctive PALB2 contribution to the diagnostic yield 110
Diagnostic Yield and Clinical Impact of a Small Genetic Panel for Kidney Disease: A Multicenter, Retrospective European Study 105
Totale 8.252
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Categoria #
all - tutte 26.867
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 26.867
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022355 0 0 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
2025/20262.860 228 139 195 214 335 212 433 178 274 315 196 141
2026/2027252 85 122 45 0 0 0 0 0 0 0 0 0
Totale 8.252