TORRES, BARBARA
 Distribuzione geografica
Continente #
NA - Nord America 336
EU - Europa 219
AS - Asia 92
AF - Africa 3
Totale 650
Nazione #
US - Stati Uniti d'America 332
IT - Italia 130
SG - Singapore 58
SE - Svezia 27
DE - Germania 20
IN - India 15
CN - Cina 11
FI - Finlandia 10
BG - Bulgaria 7
ID - Indonesia 7
RO - Romania 5
CA - Canada 3
FR - Francia 3
GB - Regno Unito 3
PT - Portogallo 3
BE - Belgio 2
LT - Lituania 2
TG - Togo 2
UA - Ucraina 2
CH - Svizzera 1
IE - Irlanda 1
IR - Iran 1
MX - Messico 1
NL - Olanda 1
NO - Norvegia 1
RS - Serbia 1
ZA - Sudafrica 1
Totale 650
Città #
Rome 56
Fairfield 47
Singapore 41
Ashburn 24
Cambridge 19
Wilmington 17
Santa Clara 16
Chandler 15
Houston 15
Seattle 14
Woodbridge 13
Ann Arbor 10
Princeton 9
New York 8
Jakarta 7
San Paolo di Civitate 7
Sofia 7
Bremen 6
Helsinki 6
Millbury 6
San Diego 6
Lawrence 5
Tappahannock 4
Boston 3
Milan 3
Phoenix 3
Salerno 3
San Mateo 3
Stuttgart 3
Toronto 3
Torre del Greco 3
Agliana 2
Bari 2
Berlin 2
Bisceglie 2
Boardman 2
Bronx 2
Brussels 2
Buffalo 2
Bühl 2
Des Moines 2
Fasano 2
Florence 2
Grafing 2
Hamburg 2
Hyderabad 2
Kuopio 2
Lappeenranta 2
Lomé 2
London 2
Los Angeles 2
Palermo 2
Plano 2
Porto 2
Richmond 2
Sannois 2
Alfianello 1
Andover 1
Beijing 1
Bologna 1
Braga 1
Bromma 1
Cagliari 1
Cesana Brianza 1
Cisterna di Latina 1
Dallas 1
Dearborn 1
Dublin 1
Falkenstein 1
Fremont 1
Grumolo delle Abbadesse 1
Guangzhou 1
Hebei 1
Jacksonville 1
Macerata 1
Mexico City 1
Minturno 1
Muizenberg 1
Nanning 1
Newark 1
Norwalk 1
Nuremberg 1
Oslo 1
Pathanamthitta 1
Penne 1
Pescara 1
Prescot 1
Redwood City 1
Romola 1
San Francisco 1
Shanghai 1
Shaoxing 1
Trento 1
Zurich 1
Totale 470
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
Small 7p22.3 microdeletion: case report of Snx8 haploinsufficiency and neurological findings 88
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 77
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformation. 74
A new case of SMABF2 diagnosed in stillbirth expands the prenatal presentation and mutational spectrum of ASCC1 69
Expanding the phenotype of the rare neuronal ceroid lipofuscinoses (ncl) 10 42
3-Methylglutaconic Aciduria Type I Due to AUH Defect: The Case Report of a Diagnostic Odyssey and a Review of the Literature 42
Neurodevelopmental Impairment As the Main Phenotypic Hallmark Associated with the Translocation t(7;10)(7p22.3;q26.11) 38
Complete pseudo-anodontia in an adult woman with pseudo-hypoparathyroidism type 1a: a new additional nonclassical feature? 35
Retinoic acid-induced 1 gene haploinsufficiency alters lipid metabolism and causes autophagy defects in Smith-Magenis syndrome 34
Mosaic genome‐wide paternal uniparental disomy after discordant results from primary fetal samples and cultured cells 32
Clinical variability in DYNC2H1-related skeletal ciliopathies includes Ellis-van Creveld syndrome 28
Chromosomal Microarray Analysis in Fetuses Detected with Isolated Cardiovascular Malformation: A Multicenter Study, Systematic Review of the Literature and Meta-Analysis 19
Duplication at 19q13.32q13.33 Segregating with Neuropsychiatric Phenotype in a Three-Generation Family: Towards the Definition of a Critical Region 17
Prenatal CFAP53-related laterality defect: case report and review of the literature 10
Totale 699
Categoria #
all - tutte 3.114
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 3.114


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202063 0 0 0 0 5 6 18 9 10 5 6 4
2020/202175 13 4 4 5 10 2 2 6 8 3 18 0
2021/2022114 2 6 12 5 12 6 3 7 4 1 42 14
2022/2023126 22 21 4 14 15 10 3 5 15 6 4 7
2023/2024157 6 19 4 16 18 28 11 9 1 21 14 10
2024/2025109 12 31 17 21 28 0 0 0 0 0 0 0
Totale 699