RUBINATO, ELISA
 Distribuzione geografica
Continente #
EU - Europa 498
NA - Nord America 485
AS - Asia 134
SA - Sud America 4
OC - Oceania 3
AF - Africa 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.127
Nazione #
US - Stati Uniti d'America 483
PL - Polonia 293
IT - Italia 78
CN - Cina 53
SE - Svezia 47
SG - Singapore 36
HK - Hong Kong 29
FI - Finlandia 17
UA - Ucraina 14
BE - Belgio 10
CH - Svizzera 7
IE - Irlanda 7
DE - Germania 6
BG - Bulgaria 5
TR - Turchia 5
CZ - Repubblica Ceca 4
VN - Vietnam 4
AU - Australia 3
CO - Colombia 3
DK - Danimarca 3
GB - Regno Unito 3
ES - Italia 2
FR - Francia 2
KR - Corea 2
SN - Senegal 2
BD - Bangladesh 1
BN - Brunei Darussalam 1
CA - Canada 1
EU - Europa 1
IN - India 1
IR - Iran 1
LK - Sri Lanka 1
MX - Messico 1
PE - Perù 1
Totale 1.127
Città #
Warsaw 292
Fairfield 62
Ann Arbor 48
Houston 47
Chandler 37
Trieste 37
Woodbridge 35
Singapore 32
Wilmington 32
Ashburn 29
Hong Kong 26
Cambridge 22
Seattle 22
Boardman 17
Jacksonville 13
Columbus 11
Helsinki 10
Princeton 10
Beijing 9
Brussels 9
Bern 7
Dublin 7
San Diego 6
Dearborn 5
Los Angeles 5
Sofia 5
Dong Ket 4
Hefei 4
Izmir 4
Redwood City 4
Santa Clara 4
Kunming 3
Turi 3
Barletta 2
Bogotá 2
Brno 2
Dakar 2
Düsseldorf 2
Florence 2
Fremont 2
Fuzhou 2
Horni Terlicko 2
Jinan 2
London 2
Melbourne 2
Mestre 2
Padova 2
Seoul 2
Triggiano 2
Vilanova i la Geltrú 2
Allentown 1
Bandar Seri Begawan 1
Bologna 1
Boston 1
Bremen 1
Brussel 1
Central 1
Changsha 1
Charlotte 1
Chicago 1
Colombo 1
Des Moines 1
Dhaka 1
Dongguan 1
Dormagen 1
Frankfurt am Main 1
Guangzhou 1
Hangzhou 1
Istanbul 1
Kashan 1
Lappeenranta 1
Lima 1
Lyon 1
Montpellier 1
Munich 1
Nanchang 1
Nanjing 1
New York 1
Phoenix 1
Pignone 1
Pune 1
Salt Lake City 1
San Francisco 1
Shenyang 1
Sparanise 1
Toronto 1
Treviglio 1
Wuhan 1
Xian 1
Totale 934
Nome #
PSIP1/LEDGF: A new gene likely involved in sensorineural progressive hearing loss 367
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 246
Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis 203
TBL1Y: a new gene involved in syndromic hearing loss 183
Pendred syndrome, or not pendred syndrome? That is the question 55
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 36
New insights on Noonan syndrome's clinical phenotype: a single center retrospective study 27
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population 25
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders 24
Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment 10
Totale 1.176
Categoria #
all - tutte 3.495
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 3.495


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020176 0 0 0 0 19 37 25 23 25 14 20 13
2020/2021175 19 14 12 17 27 14 19 11 17 10 9 6
2021/202277 6 2 6 2 11 6 2 4 8 7 6 17
2022/2023146 18 13 8 19 19 17 5 18 16 3 9 1
2023/2024146 13 4 4 21 8 8 30 20 1 7 24 6
2024/2025101 14 8 35 29 15 0 0 0 0 0 0 0
Totale 1.176