BERNARDINI, Laura
 Distribuzione geografica
Continente #
NA - Nord America 303
EU - Europa 153
AS - Asia 68
AF - Africa 2
SA - Sud America 1
Totale 527
Nazione #
US - Stati Uniti d'America 298
IT - Italia 100
SG - Singapore 33
SE - Svezia 16
CN - Cina 14
DE - Germania 14
IN - India 10
FI - Finlandia 8
ID - Indonesia 8
CA - Canada 4
BG - Bulgaria 3
FR - Francia 2
RO - Romania 2
RU - Federazione Russa 2
UA - Ucraina 2
AZ - Azerbaigian 1
CH - Svizzera 1
CL - Cile 1
GB - Regno Unito 1
IE - Irlanda 1
KR - Corea 1
LA - Repubblica Popolare Democratica del Laos 1
MX - Messico 1
PL - Polonia 1
TG - Togo 1
ZA - Sudafrica 1
Totale 527
Città #
Fairfield 59
Rome 40
Wilmington 23
Ashburn 22
Singapore 22
Cambridge 21
Seattle 20
Woodbridge 20
Houston 19
Chandler 14
Jakarta 8
Princeton 8
Boston 6
Helsinki 6
San Diego 6
Bremen 5
Lawrence 5
Milan 5
Venezia 5
Phoenix 4
Plano 4
San Paolo di Civitate 4
Santa Clara 4
Ann Arbor 3
Beijing 3
Nuremberg 3
Sofia 3
Stuttgart 3
Toronto 3
Trento 3
Agliana 2
Bari 2
Bisceglie 2
Boardman 2
Des Moines 2
Fasano 2
Kuopio 2
Naples 2
Sant'Oreste 2
Siena 2
Tappahannock 2
Torre del Greco 2
Anagni 1
Baku 1
Bern 1
Cesana Brianza 1
Dearborn 1
Dong-gu 1
Dublin 1
Falkenstein 1
Grumolo delle Abbadesse 1
Guangzhou 1
Hebei 1
Hefei 1
Las Vegas 1
Latina 1
Lomé 1
London 1
Macerata 1
Mentana 1
Mexico City 1
Millbury 1
Moscow 1
Muizenberg 1
Nanjing 1
Nanning 1
New York 1
Newark 1
Pescara 1
Romola 1
San Francisco 1
Santiago 1
Shaoxing 1
Teramo 1
Vancouver 1
Vientiane 1
Warsaw 1
Totale 410
Nome #
Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stage 96
Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7 94
Epilepsy phenotype in patients with Xp22.31 microduplication 91
Production and characterization of CSSI003 (2961) human induced pluripotent stem cells (iPSCs) carrying a novel puntiform mutation in RAI1 gene, Causative of Smith–Magenis syndrome 79
Protein–protein interaction network analysis applied to DNA copy number profiling suggests new perspectives on the aetiology of Mayer–Rokitansky–Küster–Hauser syndrome 76
A novel developmental encephalopathy with epilepsy and hyperkinetic movement disorders associated with a deletion of the sodium channel gene cluster on chromosome 2q24.3 64
3-Methylglutaconic Aciduria Type I Due to AUH Defect: The Case Report of a Diagnostic Odyssey and a Review of the Literature 42
Array-comparative genomic hybridization analysis in a cohort of 130 children with Autism Spectrum Disorders: A single Center Italian Study 28
Totale 570
Categoria #
all - tutte 2.175
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 2.175


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202070 0 0 0 0 0 13 16 13 11 8 6 3
2020/202166 5 3 0 5 1 0 14 12 13 6 7 0
2021/202295 2 6 8 3 8 6 6 6 2 2 33 13
2022/202388 18 17 5 11 8 7 5 5 8 2 2 0
2023/202471 3 6 3 11 8 6 1 5 10 9 6 3
2024/202559 3 13 11 20 5 7 0 0 0 0 0 0
Totale 570