Doronzio, Paolo Niccolo'
 Distribuzione geografica
Continente #
NA - Nord America 302
EU - Europa 242
AS - Asia 105
AF - Africa 3
SA - Sud America 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 655
Nazione #
US - Stati Uniti d'America 301
SE - Svezia 81
IT - Italia 65
CN - Cina 52
SG - Singapore 30
DE - Germania 26
IE - Irlanda 20
GB - Regno Unito 14
FR - Francia 13
ID - Indonesia 10
RU - Federazione Russa 5
TR - Turchia 5
BE - Belgio 3
ES - Italia 3
FI - Finlandia 3
KR - Corea 3
NL - Olanda 3
CI - Costa d'Avorio 2
GR - Grecia 2
HK - Hong Kong 2
IN - India 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
BR - Brasile 1
CA - Canada 1
CH - Svizzera 1
CL - Cile 1
CZ - Repubblica Ceca 1
LT - Lituania 1
PL - Polonia 1
TN - Tunisia 1
Totale 655
Città #
Chandler 93
Ashburn 54
New York 22
Dublin 20
Singapore 19
Hangzhou 15
Cattolica 14
Beijing 10
Jakarta 10
Los Angeles 9
Marseille 8
Milan 8
Dearborn 7
Princeton 7
San Mateo 7
Trieste 7
Wilmington 7
Bremen 6
Boston 4
Izmir 4
Rome 4
Tianjin 4
Tower Hamlets 4
Brugherio 3
Brussels 3
London 3
Moscow 3
Seoul 3
Abidjan 2
Augusta 2
Busto Arsizio 2
Central 2
Changsha 2
Chengdu 2
Helsinki 2
Houston 2
Nanjing 2
Nuremberg 2
Oshkosh 2
Redwood City 2
Shenyang 2
Wadgassen 2
Washington 2
Ann Arbor 1
Bochum 1
Botzingen 1
Brindisi 1
Brno 1
Camden 1
Canale Monterano 1
Chiswick 1
Clearwater 1
Dubai 1
Fairfield 1
Ferrara 1
Frankfurt am Main 1
Greenwich 1
Hebei 1
Hounslow 1
Lawrence 1
Mountain View 1
Mumbai 1
Naaldwijk 1
Nanchang 1
Napoli 1
Orangeburg 1
Ottawa 1
Pioltello 1
Piraeus 1
Pordenone 1
Provo 1
Pune 1
Reus 1
Riano 1
San Francisco 1
Sant'antimo 1
Santa Clara 1
Santiago 1
Seattle 1
Siena 1
São Paulo 1
Taranto 1
Trento 1
Valladolid 1
Verona 1
Totale 430
Nome #
Matrin 3 variants are frequent in Italian ALS patients 103
Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome 90
A novel truncating variant within exon 7 of KAT6B associated with features of both Say–Barber–Bieseker–Young–Simpson syndrome and genitopatellar syndrome: Further evidence of a continuum in the clinical spectrum of KAT6B-related disorders 89
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS 84
Novel variants and cellular studies on patients' primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesis 71
High-throughput genetic testing in ALS: The challenging path of variant classification considering the acmg guidelines 59
Syndromic craniosynostosis can define new candidate genes for suture development or result from the non-specifc effects of pleiotropic genes: Rasopathies and chromatinopathies as examples 47
LETM1 couples mitochondrial DNA metabolism and nutrient preference 47
Analysis of STMN2 CA repeats in italian ALS patients shows no association 30
Generation of an induced pluripotent stem cell line (UCSCi002-A) from a patient with a variant in TARDBP gene associated with familial amyotrophic lateral sclerosis and frontotemporal dementia 29
Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variant 26
Totale 675
Categoria #
all - tutte 3.935
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 3.935


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202022 0 0 0 0 5 1 6 3 4 1 1 1
2020/202126 2 0 0 0 1 1 10 0 1 6 4 1
2021/202289 3 0 3 19 0 1 1 10 3 4 21 24
2022/2023237 33 44 25 39 6 27 12 18 17 6 4 6
2023/2024181 6 33 5 15 8 33 18 13 2 10 19 19
2024/202549 4 7 12 2 24 0 0 0 0 0 0 0
Totale 675