GOLDONI, MARINA
 Distribuzione geografica
Continente #
NA - Nord America 218
EU - Europa 138
AS - Asia 62
AF - Africa 2
Totale 420
Nazione #
US - Stati Uniti d'America 215
IT - Italia 103
SG - Singapore 39
SE - Svezia 10
IN - India 9
CN - Cina 8
FI - Finlandia 7
DE - Germania 6
ID - Indonesia 5
CA - Canada 3
RU - Federazione Russa 3
BE - Belgio 2
BG - Bulgaria 2
GB - Regno Unito 2
EE - Estonia 1
IE - Irlanda 1
IL - Israele 1
NL - Olanda 1
TG - Togo 1
ZA - Sudafrica 1
Totale 420
Città #
Rome 53
Fairfield 33
Singapore 29
Seattle 16
Ashburn 14
Cambridge 13
Wilmington 12
Woodbridge 12
Santa Clara 10
Chandler 9
Ann Arbor 8
Houston 7
Helsinki 6
San Diego 6
Bremen 5
Jakarta 5
Princeton 5
Lawrence 4
New York 4
San Paolo di Civitate 4
Millbury 3
Toronto 3
Bisceglie 2
Boston 2
Brussels 2
Des Moines 2
Evanston 2
Fasano 2
London 2
Marino 2
Milan 2
Perugia 2
Phoenix 2
Plano 2
Sofia 2
Tappahannock 2
Alfianello 1
Bari 1
Boardman 1
Bologna 1
Cagliari 1
Chicago 1
Chongqing 1
Cisterna di Latina 1
Dublin 1
Guangzhou 1
Hebei 1
Lappeenranta 1
Lecce 1
Lomé 1
Los Angeles 1
Macerata 1
Moscow 1
Muizenberg 1
Nanning 1
Newark 1
Norwalk 1
Pescara 1
San Mateo 1
San Maurizio d'Opaglio 1
Shanghai 1
Shaoxing 1
Tartu 1
Tel Aviv 1
Torre del Greco 1
Vasto 1
Venezia 1
Totale 320
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 94
Epilepsy phenotype in patients with Xp22.31 microduplication 91
Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene 51
Neurodevelopmental outcome of a child with UPD(16)mat: A case report 43
Neurodevelopmental Impairment As the Main Phenotypic Hallmark Associated with the Translocation t(7;10)(7p22.3;q26.11) 40
null 38
Complete pseudo-anodontia in an adult woman with pseudo-hypoparathyroidism type 1a: a new additional nonclassical feature? 36
Mosaic genome‐wide paternal uniparental disomy after discordant results from primary fetal samples and cultured cells 33
Copy number variation analysis implicates novel pathways in patients with oculo-auriculo-vertebral-spectrum and congenital heart defects 25
Duplication at 19q13.32q13.33 Segregating with Neuropsychiatric Phenotype in a Three-Generation Family: Towards the Definition of a Critical Region 18
Totale 469
Categoria #
all - tutte 2.063
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 2.063


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202032 0 0 0 0 0 0 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
2024/202593 10 20 19 19 12 11 2 0 0 0 0 0
Totale 469