GOLDONI, MARINA
 Distribuzione geografica
Continente #
NA - Nord America 190
EU - Europa 112
AS - Asia 32
AF - Africa 1
Totale 335
Nazione #
US - Stati Uniti d'America 188
IT - Italia 85
SG - Singapore 16
SE - Svezia 10
IN - India 9
CN - Cina 7
DE - Germania 6
FI - Finlandia 5
BE - Belgio 2
BG - Bulgaria 2
CA - Canada 2
EE - Estonia 1
GB - Regno Unito 1
ZA - Sudafrica 1
Totale 335
Città #
Rome 44
Fairfield 33
Seattle 16
Ashburn 14
Cambridge 13
Wilmington 12
Woodbridge 12
Chandler 9
Ann Arbor 8
Houston 7
San Diego 6
Singapore 6
Bremen 5
Princeton 5
Helsinki 4
Lawrence 4
New York 4
San Paolo di Civitate 4
Millbury 3
Bisceglie 2
Boston 2
Brussels 2
Des Moines 2
Evanston 2
Fasano 2
Milan 2
Perugia 2
Phoenix 2
Plano 2
Sofia 2
Tappahannock 2
Toronto 2
Alfianello 1
Bari 1
Bologna 1
Cagliari 1
Chicago 1
Chongqing 1
Cisterna di Latina 1
Guangzhou 1
Hebei 1
Lappeenranta 1
Lecce 1
London 1
Macerata 1
Muizenberg 1
Nanning 1
Norwalk 1
Pescara 1
San Mateo 1
San Maurizio d'Opaglio 1
Shanghai 1
Shaoxing 1
Tartu 1
Torre del Greco 1
Vasto 1
Venezia 1
Totale 260
Nome #
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 90
Epilepsy phenotype in patients with Xp22.31 microduplication 85
Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene 45
null 38
Neurodevelopmental Impairment As the Main Phenotypic Hallmark Associated with the Translocation t(7;10)(7p22.3;q26.11) 35
Mosaic genome‐wide paternal uniparental disomy after discordant results from primary fetal samples and cultured cells 27
Complete pseudo-anodontia in an adult woman with pseudo-hypoparathyroidism type 1a: a new additional nonclassical feature? 23
“Neurodevelopmental outcome of a child with UPD(16)mat: A case report” 17
Copy number variation analysis implicates novel pathways in patients with oculo-auriculo-vertebral-spectrum and congenital heart defects 16
Duplication at 19q13.32q13.33 Segregating with Neuropsychiatric Phenotype in a Three-Generation Family: Towards the Definition of a Critical Region 4
Totale 380
Categoria #
all - tutte 1.511
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 1.511


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202061 10 1 3 1 8 6 10 8 6 3 3 2
2020/202137 2 1 0 4 0 12 0 0 1 6 2 9
2021/202282 6 2 10 1 6 3 4 17 5 1 19 8
2022/202365 12 8 0 10 5 8 3 4 5 5 2 3
2023/202488 3 7 3 5 10 14 5 6 1 8 8 18
2024/20254 4 0 0 0 0 0 0 0 0 0 0 0
Totale 380