CAPONE, GABRIELE LORENZO
 Distribuzione geografica
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Continente #
NA - Nord America 695
EU - Europa 495
AS - Asia 116
AF - Africa 1
Totale 1.307
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Nazione #
US - Stati Uniti d'America 694
PL - Polonia 279
IT - Italia 70
IE - Irlanda 49
CN - Cina 41
SE - Svezia 40
HK - Hong Kong 36
SG - Singapore 19
RU - Federazione Russa 17
DE - Germania 16
JO - Giordania 10
CH - Svizzera 8
VN - Vietnam 8
GB - Regno Unito 5
FI - Finlandia 3
AT - Austria 2
HR - Croazia 2
NL - Olanda 2
CA - Canada 1
GR - Grecia 1
JP - Giappone 1
KR - Corea 1
MU - Mauritius 1
UA - Ucraina 1
Totale 1.307
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Città #
Warsaw 279
Fairfield 123
Chandler 80
Ashburn 66
Woodbridge 65
Dublin 49
Seattle 43
Houston 40
Cambridge 34
Wilmington 33
Hong Kong 28
Altamura 22
Lawrence 22
Dearborn 18
Ann Arbor 17
Florence 16
Princeton 16
Beijing 15
Buffalo 13
Shanghai 12
Singapore 11
Boston 10
Bern 8
Dong Ket 8
Boardman 7
New York 6
Redwood City 6
Falls Church 5
Medford 5
Rome 4
San Diego 4
Hillsboro 3
Kent 3
Phoenix 3
Venezia 3
Amsterdam 2
Conversano 2
Kunming 2
Varaždin 2
Vienna 2
Washington 2
Acton 1
Anguillara Sabazia 1
Bremen 1
Böblingen 1
Castelliri 1
Chengdu 1
Correggio 1
Fremont 1
Fuzhou 1
Guangzhou 1
Köln 1
Laurel 1
London 1
Nanjing 1
Nantong 1
Redmond 1
Scafati 1
Seoul 1
Shenzhen 1
Stockholm 1
Tokyo 1
Torino 1
Toronto 1
Wuhan 1
Totale 1.113
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Nome #
A systematic assessment of accuracy in detecting somatic mosaic variants by deep amplicon sequencing: Application to NF2 gene 217
The Italian multiple sclerosis register. 161
Adjuvant chemotherapy in completely resected gastric cancer: A randomized phase III trial conducted by GOIRC 145
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification 139
Broadening the spectrum of SMARCB1-associated malignant tumors: A case of uterine leiomyosarcoma in a patient with schwannomatosis 124
Evaluation of a Next-Generation Sequencing Assay for BRCA1 and BRCA2 Mutation Detection 92
A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency 89
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas. 86
Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma 83
Retrospective analysis of 77 patients with ovarian cancer undergoing genetic testing for BRCA1 and BRCA2 mutations 65
Detection of BRCA1 and BRCA2 variants in circulating free DNA by using a commercial kit 52
Systematic Data Monitoring and Analysis of Cardiovascular Off-label Prescriptions in Pediatrics: Focus on Angiotensin-Converting Enzyme Inhibitors (ACE-I) and Beta Blockers 42
Schwannomatosis associated schwannomas show a different NF2 mutational spectrum compared to Neurofibromatosis type 2 patients 39
Totale 1.334
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Categoria #
all - tutte 4.156
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 4.156
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020359 0 18 8 26 43 53 55 45 40 34 31 6
2020/2021204 16 22 6 23 18 14 10 13 16 48 8 10
2021/2022113 10 8 9 6 1 3 3 8 5 6 26 28
2022/2023304 25 77 12 13 23 47 30 26 34 3 5 9
2023/2024112 5 9 14 6 8 16 6 29 5 3 4 7
2024/202532 21 11 0 0 0 0 0 0 0 0 0 0
Totale 1.334