BOCCIA, ANGELO
 Distribuzione geografica
Continente #
EU - Europa 348
NA - Nord America 242
AS - Asia 129
SA - Sud America 9
AF - Africa 3
Totale 731
Nazione #
US - Stati Uniti d'America 233
RU - Federazione Russa 155
IT - Italia 98
SG - Singapore 73
HK - Hong Kong 25
CN - Cina 24
NL - Olanda 24
DE - Germania 20
FI - Finlandia 11
UA - Ucraina 11
SE - Svezia 10
BR - Brasile 9
CA - Canada 9
IE - Irlanda 8
GB - Regno Unito 6
CI - Costa d'Avorio 3
IR - Iran 3
FR - Francia 2
PK - Pakistan 2
PL - Polonia 2
BE - Belgio 1
IN - India 1
IQ - Iraq 1
Totale 731
Città #
Moscow 40
Chandler 37
Singapore 32
Hong Kong 25
Naples 23
Santa Clara 23
Ashburn 21
Amsterdam 20
Jacksonville 12
Milan 8
Napoli 8
Los Angeles 7
Munich 7
Princeton 7
Ottawa 6
Ann Arbor 5
Beijing 5
Boston 5
Nanchang 5
Houston 4
Millbury 4
Düsseldorf 3
Kunming 3
London 3
Toronto 3
Wilmington 3
Boardman 2
Cava De' Tirreni 2
Dallas 2
Dublin 2
Falkenstein 2
Falls Church 2
Formia 2
Hefei 2
Lappeenranta 2
Osimo 2
Peshawar 2
Polska 2
Seattle 2
Washington 2
Baghdad 1
Boituva 1
Brussels 1
Buffalo 1
Bussolengo 1
Caserta 1
Castel Morrone 1
Changsha 1
Charlotte 1
Chengdu 1
Cincinnati 1
Cologne 1
Como 1
Des Moines 1
Fernandópolis 1
Fortaleza 1
Frankfurt am Main 1
Giugliano in Campania 1
Guarulhos 1
Guidonia 1
Hebei 1
Helsinki 1
Indiana 1
Kochi 1
Kronberg 1
Lauterbourg 1
Lawrence 1
Marabá 1
Marano Di Napoli 1
Marano di Napoli 1
Marcianise 1
Marigliano 1
Marsala 1
Mugnano di Napoli 1
New York 1
Norwalk 1
Nuremberg 1
Orange 1
Padova 1
Phoenix 1
Piacenza 1
Porto Franco 1
Rende 1
Rio de Janeiro 1
Rome 1
San Giuseppe Vesuviano 1
San Severo 1
Scafati 1
São Bento do Sul 1
São Luiz Gonzaga 1
The Dalles 1
Tianjin 1
Trentola-Ducenta 1
Turku 1
Vazzola 1
Vicenza 1
Xiaogan 1
Zhengzhou 1
Totale 405
Nome #
The complete 12 Mb genome and transcriptome of Nonomuraea gerenzanensis with new insights into its duplicated "magic" RNA polymerase 100
A novel mutation in RP1 is a major cause of autosomal dominant retinitis pigmentosa in Southern Italy. 95
Colon OCTN2 gene expression is up-regulated by peroxisome proliferator-activated receptor gamma in humans and mice and contributes to local and systemic carnitine homeostasis 82
DG-CST (Disease Gene Conserved Sequence Tags), a database of human�mouse conserved elements associated to disease genes 77
Systematic analysis of human kinase genes: a large number of genes and alternative splicing events result in functional and structural diversity 73
Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individuals 63
Targeting Group 3 Medulloblastoma by the Anti-PRUNE-1 and Anti-LSD1/KDM1A Epigenetic Molecules 56
DNA sequence capture and high-throughput sequencing technology: a novel approach to identify a large number of hypertrophic cardiomyopathy-causing genes 56
SARS-CoV-2 Pandemic Tracing in Italy Highlights Lineages with Mutational Burden in Growing Subsets 51
Inherited rare variants in homologous recombination and neurodevelopmental genes are associated with increased risk of neuroblastoma 50
Three novel CFTR polymorphic repeats improve segregation analysis for cystic fibrosis 49
Totale 752
Categoria #
all - tutte 3.021
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 3.021


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202013 0 0 0 0 0 0 0 0 0 0 8 5
2020/202136 0 2 6 3 6 5 2 3 3 1 3 2
2021/202255 2 0 0 1 2 2 0 1 6 6 22 13
2022/2023113 8 4 2 7 9 10 1 20 24 21 5 2
2023/202487 2 16 11 12 5 12 1 7 3 6 10 2
2024/2025375 11 10 2 19 32 16 39 31 41 33 141 0
Totale 752