SCARPATO, MARGHERITA
 Distribuzione geografica
Continente #
EU - Europa 227
AS - Asia 159
NA - Nord America 54
SA - Sud America 26
Totale 466
Nazione #
RU - Federazione Russa 136
IT - Italia 56
US - Stati Uniti d'America 51
SG - Singapore 50
CN - Cina 40
BR - Brasile 22
HK - Hong Kong 22
KR - Corea 12
IE - Irlanda 11
VN - Vietnam 11
IN - India 8
DE - Germania 6
JP - Giappone 6
AT - Austria 4
GB - Regno Unito 4
EC - Ecuador 2
ID - Indonesia 2
NL - Olanda 2
SA - Arabia Saudita 2
TR - Turchia 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
BN - Brunei Darussalam 1
CA - Canada 1
CO - Colombia 1
CZ - Repubblica Ceca 1
ES - Italia 1
FI - Finlandia 1
FR - Francia 1
IQ - Iraq 1
JM - Giamaica 1
LT - Lituania 1
PA - Panama 1
PE - Perù 1
PL - Polonia 1
RO - Romania 1
UZ - Uzbekistan 1
Totale 466
Città #
Moscow 45
Hong Kong 22
Singapore 21
Hefei 15
Santa Clara 12
Seoul 12
Dublin 11
Naples 11
Ashburn 8
Bengaluru 6
Castellammare di Stabia 5
Caprecano 4
Dallas 4
Ho Chi Minh City 4
Munich 4
Viterbo 4
Beijing 3
Castelfranco Emilia 3
Ercolano 3
Hanoi 3
Milan 3
Aversa 2
Boardman 2
London 2
Los Angeles 2
Nuremberg 2
'Asir Region 1
Amsterdam 1
Ankara 1
Bandar Seri Begawan 1
Barra do Piraí 1
Belo Horizonte 1
Biên Hòa 1
Bologna 1
Boydton 1
Brno 1
Brooklyn 1
Caarapó 1
Campinas 1
Capâo Bonito 1
Cedar Knolls 1
Cezarina 1
Changchun 1
Cianorte 1
Cuenca 1
Da Nang 1
Denver 1
Dubai 1
Duque de Caxias 1
Garibaldi 1
Gaspar 1
Helena 1
Helsinki 1
Hưng Yên 1
Igarassu 1
Innisfil 1
Istanbul 1
Joinville 1
Lima 1
Limeira 1
Maceió 1
Machado 1
Manchester 1
Medellín 1
Medina 1
Mumbai 1
Olinda 1
Osasco 1
Paulista 1
Portici 1
Porto Alegre 1
Rio de Janeiro 1
San Giuseppe Vesuviano 1
Tashkent 1
Thanh Hóa 1
Tirana 1
Uberlândia 1
Vera 1
Vienna 1
Warsaw 1
Winder 1
Totale 268
Nome #
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy 108
A Novel Variant in TUBB4B Causes Progressive Cone‐Rod Dystrophy and Early Onset Sensorineural Hearing Loss 82
Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients 73
Nanopore Sequencing Solves an Elusive Case of Sotos Syndrome 72
Variants in the AGBL5 gene are responsible for autosomal recessive Retinitis pigmentosa with hearing loss 63
Late-onset mucopolysaccharidosis type IIIA mimicking Usher syndrome 53
Reanalysis of Undiagnosed Neurodevelopmental Disorder Cases: From RNU4-2 Variants to Clinical Phenotypes 27
Totale 478
Categoria #
all - tutte 1.451
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 1.451


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/202319 0 0 0 0 0 8 0 1 9 0 1 0
2023/202417 1 0 0 0 3 1 0 0 0 1 1 10
2024/2025130 8 1 0 3 12 10 9 27 14 18 9 19
2025/2026312 35 48 40 24 63 102 0 0 0 0 0 0
Totale 478