FERRARI, SIMONA
 Distribuzione geografica
Continente #
NA - Nord America 506
EU - Europa 315
AS - Asia 145
AF - Africa 27
Totale 993
Nazione #
US - Stati Uniti d'America 506
GB - Regno Unito 88
VN - Vietnam 76
IT - Italia 58
SE - Svezia 45
CN - Cina 32
DE - Germania 30
SG - Singapore 17
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
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 993
Città #
Fairfield 89
Southend 77
Ann Arbor 41
Chandler 40
Ashburn 39
Houston 31
Woodbridge 31
Wilmington 29
Seattle 26
Cambridge 19
Dong Ket 19
Princeton 16
Bologna 15
Singapore 15
Dublin 14
Jacksonville 11
Lomé 10
New York 10
Padova 8
Santa Clara 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
Boardman 2
Bremen 2
Des Moines 2
Hebei 2
Hyderabad 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
Haikou 1
Hefei 1
Jiaxing 1
Kuban 1
London 1
Loreto Aprutino 1
Mahé 1
Medford 1
Nanchang 1
Ningbo 1
Norwalk 1
Old Bridge 1
Paris 1
Phoenix 1
Redwood City 1
Sala Bolognese 1
San Venanzo 1
Seoul 1
Torino 1
Wuhan 1
Totale 689
Nome #
BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotype 182
Autosomal dominant partial epilepsy with auditory features: A new locus on chromosome 19q13.11-q13.31. 160
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration 128
Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes 128
An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene. 125
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN). 114
IGA DEFICIENCY: CASE REVIEW AND CORRELATION WITH DEFECTS OF THE TACI GENE. 95
null 91
Totale 1.023
Categoria #
all - tutte 2.253
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 2.253


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020237 0 0 2 22 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
2024/202537 6 25 6 0 0 0 0 0 0 0 0 0
Totale 1.023