OPPO, MANUELA
 Distribuzione geografica
Continente #
AS - Asia 127
NA - Nord America 90
SA - Sud America 39
EU - Europa 37
AF - Africa 1
Totale 294
Nazione #
US - Stati Uniti d'America 86
SG - Singapore 62
BR - Brasile 30
CN - Cina 19
VN - Vietnam 19
HK - Hong Kong 14
FR - Francia 10
IT - Italia 7
NL - Olanda 6
GB - Regno Unito 4
AR - Argentina 3
DE - Germania 3
KR - Corea 3
UZ - Uzbekistan 3
EC - Ecuador 2
SV - El Salvador 2
AE - Emirati Arabi Uniti 1
AZ - Azerbaigian 1
BE - Belgio 1
CA - Canada 1
CL - Cile 1
CO - Colombia 1
DK - Danimarca 1
FI - Finlandia 1
ID - Indonesia 1
IE - Irlanda 1
IQ - Iraq 1
JM - Giamaica 1
KG - Kirghizistan 1
LB - Libano 1
NP - Nepal 1
PE - Perù 1
PL - Polonia 1
PY - Paraguay 1
RU - Federazione Russa 1
SE - Svezia 1
ZA - Sudafrica 1
Totale 294
Città #
Singapore 36
Santa Clara 28
Hong Kong 14
San Jose 10
Ho Chi Minh City 9
Ashburn 7
Lauterbourg 6
Beijing 5
Hanoi 5
Los Angeles 4
Orem 4
Dallas 3
New York 3
Seoul 3
Assemini 2
Frankfurt am Main 2
Luziânia 2
Passo Fundo 2
San Salvador 2
Sorocaba 2
São Paulo 2
Tashkent 2
Ambato 1
Asunción 1
Baku 1
Belo Horizonte 1
Betim 1
Bishkek 1
Boa Esperança 1
Bogotá 1
Brooklyn 1
Brussels 1
Buffalo 1
Bình Dương Province 1
Bến Tre 1
Caieiras 1
Campina Grande 1
Conceição do Coité 1
Conceição do Jacuípe 1
Constantina 1
Da Nang 1
Denver 1
Dundalk 1
Eldorado do Sul 1
Franco da Rocha 1
Funes 1
Hefei 1
Helsinki 1
Houilles 1
Indaiatuba 1
Itapetininga 1
Johannesburg 1
Kansas City 1
Kingston 1
Kizilyurt 1
Le Havre 1
Lima 1
Maranguape 1
Maricá 1
Marlborough 1
Memphis 1
Montreal 1
Nasiriyah 1
Niterói 1
North Shields 1
Paris 1
Patos 1
Pharr 1
Poplar 1
Riachão 1
Rio de Janeiro 1
Samarkand 1
San Nicolás de los Arroyos 1
Santiago 1
Santo Domingo de los Colorados 1
Sertãozinho 1
Shanghai 1
South Lyon 1
Stockholm 1
Sumé 1
São Bernardo do Campo 1
Tallahassee 1
Tân An 1
Villa Eduardo Madero 1
Warsaw 1
Winchester 1
Totale 217
Nome #
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa 63
hole Genome Sequencing of 1000 Individuals in an Isolated Population. 45
Epileptic phenotypes related to the UNC79-UNC80-NALCN protein complex. 42
Likelihood Based Deletion Analysis in a Sample of Sequenced Sardinian Individuals. 41
Genetic Associations with the Variation in Aging from the SardiNIA/Progenia Project. 40
Unravelling the genetic causes of syndromic Intellectual Disability in the era of exome sequencing. 34
Buried in the Middle but Guilty: Intronic Mutations in the TCIRG1 Gene Cause Human Autosomal Recessive Osteopetrosis. 32
Totale 297
Categoria #
all - tutte 914
article - articoli 464
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 1.378


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/20243 0 0 0 0 0 0 0 0 0 0 3 0
2024/2025124 0 0 9 7 27 3 10 9 7 8 25 19
2025/2026170 3 13 11 30 47 8 19 6 9 15 9 0
Totale 297