SORASIO, LORENA
 Distribuzione geografica
Continente #
NA - Nord America 417
EU - Europa 263
AS - Asia 109
SA - Sud America 2
Totale 791
Nazione #
US - Stati Uniti d'America 411
IT - Italia 69
CN - Cina 43
DE - Germania 41
SE - Svezia 40
SG - Singapore 38
IE - Irlanda 34
FR - Francia 23
FI - Finlandia 17
KR - Corea 12
UA - Ucraina 11
VN - Vietnam 10
DK - Danimarca 9
GB - Regno Unito 6
CA - Canada 4
PL - Polonia 4
NL - Olanda 3
HK - Hong Kong 2
IN - India 2
RO - Romania 2
AR - Argentina 1
BE - Belgio 1
BR - Brasile 1
CR - Costa Rica 1
ES - Italia 1
ID - Indonesia 1
JP - Giappone 1
LT - Lituania 1
MX - Messico 1
SI - Slovenia 1
Totale 791
Città #
Chandler 97
Ann Arbor 49
Singapore 33
Dublin 32
Beijing 27
Villeurbanne 19
Santa Clara 16
Torino 16
Princeton 14
Nyköping 13
Dearborn 11
Jacksonville 11
Boardman 10
Houston 10
Medford 10
Ashburn 9
Columbus 7
Dong Ket 7
Milan 5
New Milton 5
New York 5
Wilmington 5
Ziebice 4
Fremont 3
Helsinki 3
Munich 3
Nanjing 3
Redwood City 3
Rome 3
Turin 3
Asti 2
Boston 2
Cantù 2
Dallas 2
Fairfield 2
Falkenstein 2
Falls Church 2
Hebei 2
Legnano 2
Leiden 2
London 2
Los Angeles 2
Lyndhurst 2
Lübeck 2
Mountain View 2
Piemonte 2
Rochester 2
Blaine 1
Brussels 1
Cambridge 1
Central District 1
Chatsworth 1
Chengdu 1
Edemissen 1
Esslingen am Neckar 1
Fuzhou 1
Genova 1
Guangzhou 1
Guiyang 1
Hangzhou 1
Hefei 1
Hong Kong 1
Jakarta 1
Jinan 1
Ljubljana 1
Malagueno 1
Marsala 1
Mexico 1
North York 1
Norwalk 1
Ottawa 1
Pantigliate 1
Pulsano 1
Quzhou 1
Sacramento 1
Salt Lake City 1
San José 1
Shaoxing 1
Siena 1
Stockholm 1
São Paulo 1
Tokyo 1
Verona 1
Vilnius 1
Wuhan 1
Totale 508
Nome #
Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes 256
Family-based whole exome sequencing allows a 25% diagnostic yield in patients with autism spectrum disorder 81
Craniostenosi complessa da riarrangiamento cromosomico subtelomerico 78
Analisi molecolare Arrays-CGH in 36 pazienti con fenotipo sindromico complesso 74
le anomalie dei capelli come segno di malattia mitocondriale 70
Phenotype resembling Donnai-Barrow syndrome in a patient with 9qter;16qter unbalanced translocation 69
Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire 69
Cleft lip and palate associated with cervical aplasia cutis 67
Subtelomeric FISH analysis in 92 patoents with mental retardation 54
Skipping of Exon 20 in EP300: A Novel Variant Linked to Rubinstein-Taybi Syndrome With Atypical and Severe Clinical Manifestations 4
Totale 822
Categoria #
all - tutte 2.812
article - articoli 0
book - libri 0
conference - conferenze 1.316
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.128


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202023 0 0 0 0 0 0 4 3 2 6 2 6
2020/202162 10 3 2 0 5 2 6 0 4 7 3 20
2021/2022162 15 5 6 28 8 7 6 4 8 7 36 32
2022/2023204 28 27 11 22 14 46 8 11 15 1 15 6
2023/202458 7 15 3 4 4 5 0 0 0 4 5 11
2024/202583 1 6 3 13 49 5 6 0 0 0 0 0
Totale 822