PAGANINI, IRENE
 Distribuzione geografica
Continente #
NA - Nord America 865
EU - Europa 487
AS - Asia 142
OC - Oceania 3
AF - Africa 2
Totale 1.499
Nazione #
US - Stati Uniti d'America 864
RU - Federazione Russa 177
PL - Polonia 128
IT - Italia 65
CN - Cina 44
SG - Singapore 39
IE - Irlanda 38
HK - Hong Kong 36
SE - Svezia 35
DE - Germania 16
FI - Finlandia 15
IN - India 12
JO - Giordania 6
GB - Regno Unito 5
AU - Australia 3
AT - Austria 2
ES - Italia 2
FR - Francia 2
ID - Indonesia 2
VN - Vietnam 2
CA - Canada 1
CH - Svizzera 1
CI - Costa d'Avorio 1
KR - Corea 1
MU - Mauritius 1
UA - Ucraina 1
Totale 1.499
Città #
Santa Clara 227
Warsaw 128
Fairfield 106
Chandler 65
Ashburn 58
Woodbridge 50
Seattle 45
Dublin 38
Singapore 34
Cambridge 33
Houston 31
Wilmington 31
Hong Kong 28
Dearborn 22
Altamura 16
Lawrence 16
Florence 15
Princeton 15
Ann Arbor 14
Buffalo 11
Mumbai 11
Helsinki 10
Shanghai 9
Boston 8
Beijing 7
New York 6
Falls Church 5
Medford 5
Boardman 4
Moscow 4
Guangzhou 3
Melbourne 3
Redwood City 3
Rome 3
Venezia 3
Anguillara Sabazia 2
Barcelona 2
Brescia 2
Dong Ket 2
Jakarta 2
Kansas City 2
Kunming 2
London 2
San Diego 2
San Floriano del Collio 2
Udine 2
Vienna 2
Abidjan 1
Acton 1
Alessandria 1
Arezzo 1
Bern 1
Böblingen 1
Castelfranco Di Sopra 1
Castelliri 1
Chengdu 1
Correggio 1
Falkenstein 1
Fuzhou 1
Hefei 1
Hillsboro 1
Kent 1
Kilburn 1
Laurel 1
Nanchang 1
Nanjing 1
Nantong 1
Norwalk 1
Phoenix 1
Scafati 1
Shenzhen 1
Torino 1
Toronto 1
Washington 1
Wuhan 1
Xi'an 1
Xiaogan 1
Yubileyny 1
Totale 1.122
Nome #
A systematic assessment of accuracy in detecting somatic mosaic variants by deep amplicon sequencing: Application to NF2 gene 255
Broadening the spectrum of SMARCB1-associated malignant tumors: A case of uterine leiomyosarcoma in a patient with schwannomatosis 166
Expanding the mutational spectrum of LZTR1 in schwannomatosis. 145
Evaluation of a Next-Generation Sequencing Assay for BRCA1 and BRCA2 Mutation Detection 140
Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism. 138
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas. 130
A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency 129
Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma 125
Epigenomic, genomic, and transcriptomic landscape of schwannomatosis 111
Detection of BRCA1 and BRCA2 variants in circulating free DNA by using a commercial kit 99
Schwannomatosis associated schwannomas show a different NF2 mutational spectrum compared to Neurofibromatosis type 2 patients 87
Totale 1.525
Categoria #
all - tutte 4.292
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 4.292


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020132 0 0 0 0 0 0 44 28 25 15 16 4
2020/2021117 7 8 7 26 5 5 4 7 9 28 7 4
2021/202282 9 2 4 4 0 6 1 6 3 4 18 25
2022/2023250 19 62 11 15 16 39 25 19 33 3 3 5
2023/202496 5 8 12 4 3 12 5 29 7 1 6 4
2024/2025515 21 59 47 115 192 81 0 0 0 0 0 0
Totale 1.525