ARTUSO, LUCIA
 Distribuzione geografica
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Continente #
NA - Nord America 3.921
AS - Asia 2.134
EU - Europa 2.065
SA - Sud America 276
AF - Africa 80
Continente sconosciuto - Info sul continente non disponibili 79
OC - Oceania 37
Totale 8.592
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Nazione #
US - Stati Uniti d'America 3.810
SG - Singapore 566
CN - Cina 546
IT - Italia 516
GB - Regno Unito 506
VN - Vietnam 266
DE - Germania 195
BR - Brasile 188
SE - Svezia 183
HK - Hong Kong 174
RU - Federazione Russa 107
FR - Francia 100
BD - Bangladesh 97
FI - Finlandia 89
IN - India 80
TR - Turchia 76
IE - Irlanda 73
KR - Corea 70
CA - Canada 69
UA - Ucraina 53
ID - Indonesia 42
AU - Australia 35
PK - Pakistan 33
ES - Italia 31
JP - Giappone 30
IQ - Iraq 29
NL - Olanda 29
BG - Bulgaria 25
ZA - Sudafrica 22
AR - Argentina 21
IR - Iran 21
MX - Messico 21
PL - Polonia 21
CO - Colombia 19
BE - Belgio 17
SI - Slovenia 17
TW - Taiwan 14
CL - Cile 13
AE - Emirati Arabi Uniti 12
EC - Ecuador 12
KE - Kenya 12
LT - Lituania 12
CZ - Repubblica Ceca 11
MY - Malesia 11
RO - Romania 11
HU - Ungheria 10
MA - Marocco 10
NO - Norvegia 10
PH - Filippine 9
UZ - Uzbekistan 9
PT - Portogallo 8
SA - Arabia Saudita 8
TN - Tunisia 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
CR - Costa Rica 5
GH - Ghana 5
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
PR - Porto Rico 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
SV - El Salvador 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AO - Angola 1
BJ - Benin 1
CD - Congo 1
CG - Congo 1
EE - Estonia 1
ET - Etiopia 1
Totale 8.505
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Città #
Ashburn 504
Singapore 338
Southend 329
Santa Clara 304
San Jose 265
Fairfield 243
Chandler 179
Woodbridge 177
Council Bluffs 162
Hong Kong 160
Ann Arbor 125
Beijing 125
Hefei 121
Houston 121
Seattle 95
Nyköping 80
Modena 79
Wilmington 79
Ho Chi Minh City 75
Jacksonville 75
Dearborn 74
London 71
Dublin 70
Cambridge 66
New York 66
Los Angeles 62
Seoul 61
Helsinki 56
Hanoi 55
Munich 39
The Dalles 38
Chicago 34
Milan 32
Shanghai 31
Bologna 30
Buffalo 30
Jakarta 30
Moscow 30
Lauterbourg 28
Frankfurt am Main 27
Dallas 25
Fremont 25
Boardman 23
Falls Church 22
Redwood City 22
Sofia 22
São Paulo 22
Izmir 21
Melbourne 20
Princeton 20
Bremen 19
Dong Ket 19
Florence 19
Turku 19
Rome 18
Warsaw 17
Columbus 16
Eugene 16
Tokyo 16
Orem 15
Toronto 15
Baghdad 14
Montreal 14
Phoenix 14
Barcelona 13
Brussels 13
San Diego 13
Da Nang 12
Falkenstein 12
Hyderabad 11
Johannesburg 11
Paris 11
Sydney 11
Denver 10
Lawrence 10
Springfield 10
Alexandria 9
Haiphong 9
Salt Lake City 9
Amsterdam 8
Boston 8
Brooklyn 8
Colorno 8
Guangzhou 8
Islamabad 8
Oslo 8
Philadelphia 8
Reggio Emilia 8
San Giuliano Milanese 8
Ankara 7
Bogotá 7
Brasília 7
Bắc Ninh 7
Genoa 7
Hải Dương 7
Kassel 7
Miami 7
Nairobi 7
Nuremberg 7
Tashkent 7
Totale 5.340
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Nome #
A Next Generation Sequencing amplicon-based strategy to explore Inherited Retinal Degeneration complexity 602
Targeted cancer exome sequencing reveals recurrent mutations in myeloproliferative neoplasms 586
Implementation of an NGS-based workflow for BRCA1 and BRCA2 mutation screening 484
ERBB2 mutations in hormone receptor positive primary breast cancers samples and in their matched endocrine-resistant recurrences. 451
Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Hybrid Posters 440
Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing 411
Amplicon-based next-generation sequencing: an effective approach for the molecular diagnosis of epidermolysis bullosa 387
Amplicon-based Next Generation Sequencing: an effective approach to molecular diagnosis of Epidermolysis Bullosa 386
Genomic alterations at the basis of treatment resistance in metastatic breast cancer: Clinical applications 380
Hereditary pancreatic cancer: A retrospective single-center study of 5143 Italian families with history of BRCA-related malignancies 380
Impact of mutational status on outcomes in myelofibrosis patients treated with ruxolitinib in the COMFORT-II study 364
Impact Of Prognostically Detrimental Mutations (ASXL1, EZH2, SRSF2, IDH1/2) On Outcomes In Patients With Myelofibrosis Treated With Ruxolitinib In COMFORT-II 338
Homozygous familial hypobetalipoproteinemia: A Turkish case carrying a missense mutation in apolipoprotein B 314
AMPLICON-BASED NGS: AN EFFECTIVE APPROACH FOR THE MOLECULAR DIAGNOSIS OF EPIDERMOLYSIS BULLOSA 306
STRATEGIES TO PREDICT TREATMENT RESPONSE AND SELECT THERAPIES IN METASTATIC BREAST CANCER PATIENTS USING A NEXT GENERATION SEQUENCING (NGS) MULTI-GENE PANEL 288
STRATEGIES TO PREDICT TREATMENT RESPONSE AND SELECT THERAPIES IN METASTATIC BREAST CANCER PATIENTS USING A NEXT GENERATION SEQUENCING MULTI-GENE PANEL 268
Characterization of new ATM deletion associated with hereditary breast cancer 266
Pre-mir146a e FSHR sono marker di mosaicismo tiroideo nel carcinoma follicolare della tiroide 261
Automated capture-based NGS workflow: one thousand patients experience in a clinical routine framework 251
Clinical application of NGS in the diagnosis of iron overload disorders or hyperferritinemia of genetic origin 249
Ivar, an interpretation‐oriented tool to manage the update and revision of variant annotation and classification 227
Constitutional Mosaicism: A Critical Issue in the Definition of BRCA-Inherited Cancer Risk 200
Automation of a capture-based NGS workflow: one thousand patients experience in a diagnostic clinical routine framework 175
Clinically relevant low-frequency Next Generation Sequencing variants in hereditary cancer patients: an operational multi-step algorithm for laboratory managing 172
LOW-FREQUENCY ALLELE VARIANTS IN NGS MULTI-GENE PANELS FOR HEREDITARY CANCER TESTING: ARTIFACTS, CHIP OR MOSAICS? MANAGING THE RESULTS IN THE LABORATORY ROUTINE 167
Characterization of copy number variants in hereditary cancer patients through NGS shows a distinctive PALB2 contribution to the diagnostic yield 126
Diagnostic Yield and Clinical Impact of a Small Genetic Panel for Kidney Disease: A Multicenter, Retrospective European Study 113
Totale 8.592
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Categoria #
all - tutte 28.203
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 28.203
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022342 0 0 0 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
2026/2027592 85 122 191 194 0 0 0 0 0 0 0 0
Totale 8.592