FERRARI, SIMONA
 Distribuzione geografica
Continente #
NA - Nord America 521
EU - Europa 315
AS - Asia 171
AF - Africa 27
Totale 1.034
Nazione #
US - Stati Uniti d'America 521
GB - Regno Unito 88
VN - Vietnam 76
IT - Italia 58
SE - Svezia 45
CN - Cina 42
SG - Singapore 31
DE - Germania 30
FR - Francia 16
IN - India 16
UA - Ucraina 16
RU - Federazione Russa 15
IE - Irlanda 14
TG - Togo 10
ZA - Sudafrica 8
BG - Bulgaria 7
EE - Estonia 7
CI - Costa d'Avorio 5
BE - Belgio 4
CH - Svizzera 4
AT - Austria 3
FI - Finlandia 3
PL - Polonia 3
ID - Indonesia 2
JO - Giordania 2
NG - Nigeria 2
GR - Grecia 1
HR - Croazia 1
KR - Corea 1
LB - Libano 1
MU - Mauritius 1
SC - Seychelles 1
Totale 1.034
Città #
Fairfield 89
Southend 77
Ann Arbor 41
Ashburn 40
Chandler 40
Houston 31
Woodbridge 31
Singapore 29
Wilmington 29
Seattle 26
Cambridge 19
Dong Ket 19
Princeton 16
Bologna 15
Dublin 14
Santa Clara 14
Jacksonville 11
Lomé 10
New York 10
Boardman 9
Padova 8
Westminster 8
Sofia 7
Nanjing 6
Abidjan 5
Jinan 5
Shenyang 5
Turin 5
Berlin 4
Bern 4
Brussels 4
Changsha 4
Florence 4
Saint Petersburg 4
San Diego 4
Beijing 3
Dearborn 3
Helsinki 3
Vienna 3
Abeokuta 2
Amman 2
Bremen 2
Des Moines 2
Hebei 2
Hyderabad 2
Jakarta 2
Los Angeles 2
Milan 2
Mountain View 2
Mülheim 2
Nonantola 2
Olalla 2
Reggio Nell'emilia 2
San Giovanni In Marignano 2
Tappahannock 2
Warsaw 2
Albany 1
Brooklyn 1
Castel Maggiore 1
Costa Mesa 1
Frankfurt am Main 1
Fremont 1
Guangzhou 1
Haikou 1
Hefei 1
Jiaxing 1
Kuban 1
London 1
Loreto Aprutino 1
Mahé 1
Medford 1
Nanchang 1
Nantong 1
Ningbo 1
Norwalk 1
Old Bridge 1
Paris 1
Phoenix 1
Qingdao 1
Redwood City 1
Sala Bolognese 1
San Venanzo 1
Seoul 1
Tianjin 1
Torino 1
Wuhan 1
Xi'an 1
Totale 724
Nome #
BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotype 187
Autosomal dominant partial epilepsy with auditory features: A new locus on chromosome 19q13.11-q13.31. 165
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration 136
Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes 133
An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene. 131
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN). 120
IGA DEFICIENCY: CASE REVIEW AND CORRELATION WITH DEFECTS OF THE TACI GENE. 101
null 91
Totale 1.064
Categoria #
all - tutte 2.388
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 2.388


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020213 0 0 0 0 33 31 34 37 43 15 9 11
2020/2021187 26 19 3 6 5 7 5 5 11 9 3 88
2021/2022176 10 5 9 16 16 10 3 9 8 14 52 24
2022/2023178 15 26 16 24 7 16 7 12 28 4 18 5
2023/202451 1 11 0 4 9 21 1 1 0 2 1 0
2024/202578 6 25 13 18 16 0 0 0 0 0 0 0
Totale 1.064