BOCCIA, ANGELO
 Distribuzione geografica
Continente #
NA - Nord America 232
EU - Europa 154
AS - Asia 56
AF - Africa 3
Totale 445
Nazione #
US - Stati Uniti d'America 223
IT - Italia 75
SG - Singapore 31
CN - Cina 22
NL - Olanda 20
DE - Germania 12
SE - Svezia 10
UA - Ucraina 10
CA - Canada 9
FI - Finlandia 9
IE - Irlanda 8
GB - Regno Unito 6
CI - Costa d'Avorio 3
IR - Iran 3
PL - Polonia 2
FR - Francia 1
RU - Federazione Russa 1
Totale 445
Città #
Chandler 37
Singapore 26
Santa Clara 23
Ashburn 21
Amsterdam 20
Naples 20
Jacksonville 12
Napoli 8
Munich 7
Princeton 7
Los Angeles 6
Ottawa 6
Ann Arbor 5
Beijing 5
Boston 5
Nanchang 5
Houston 4
Millbury 4
Kunming 3
London 3
Milan 3
Toronto 3
Wilmington 3
Boardman 2
Cava De' Tirreni 2
Dallas 2
Dublin 2
Falls Church 2
Formia 2
Lappeenranta 2
Osimo 2
Polska 2
Washington 2
Buffalo 1
Bussolengo 1
Caserta 1
Castel Morrone 1
Changsha 1
Charlotte 1
Chengdu 1
Cincinnati 1
Cologne 1
Como 1
Des Moines 1
Falkenstein 1
Giugliano in Campania 1
Guidonia 1
Hebei 1
Indiana 1
Kronberg 1
Lawrence 1
Marano Di Napoli 1
Marano di Napoli 1
Marcianise 1
Marigliano 1
Marsala 1
Mugnano di Napoli 1
New York 1
Norwalk 1
Orange 1
Phoenix 1
Rende 1
San Severo 1
Scafati 1
Seattle 1
Tianjin 1
Trentola-Ducenta 1
Vazzola 1
Vicenza 1
Xiaogan 1
Zhengzhou 1
Totale 294
Nome #
The complete 12 Mb genome and transcriptome of Nonomuraea gerenzanensis with new insights into its duplicated "magic" RNA polymerase 77
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 58
DG-CST (Disease Gene Conserved Sequence Tags), a database of human�mouse conserved elements associated to disease genes 55
A novel mutation in RP1 is a major cause of autosomal dominant retinitis pigmentosa in Southern Italy. 55
Systematic analysis of human kinase genes: a large number of genes and alternative splicing events result in functional and structural diversity 52
DNA sequence capture and high-throughput sequencing technology: a novel approach to identify a large number of hypertrophic cardiomyopathy-causing genes 40
Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individuals 34
Inherited rare variants in homologous recombination and neurodevelopmental genes are associated with increased risk of neuroblastoma 30
SARS-CoV-2 Pandemic Tracing in Italy Highlights Lineages with Mutational Burden in Growing Subsets 26
Three novel CFTR polymorphic repeats improve segregation analysis for cystic fibrosis 24
Targeting Group 3 Medulloblastoma by the Anti-PRUNE-1 and Anti-LSD1/KDM1A Epigenetic Molecules 15
Totale 466
Categoria #
all - tutte 2.258
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 2.258


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202014 0 0 0 0 0 0 1 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
2024/202589 11 10 2 19 32 15 0 0 0 0 0 0
Totale 466