TORRES, BARBARA
 Distribuzione geografica
Continente #
NA - Nord America 299
EU - Europa 200
AS - Asia 54
AF - Africa 2
Totale 555
Nazione #
US - Stati Uniti d'America 295
IT - Italia 117
SG - Singapore 30
SE - Svezia 27
DE - Germania 19
IN - India 15
FI - Finlandia 9
CN - Cina 8
BG - Bulgaria 7
RO - Romania 5
CA - Canada 3
FR - Francia 3
GB - Regno Unito 3
PT - Portogallo 3
BE - Belgio 2
UA - Ucraina 2
CH - Svizzera 1
IE - Irlanda 1
IR - Iran 1
MX - Messico 1
RS - Serbia 1
TG - Togo 1
ZA - Sudafrica 1
Totale 555
Città #
Rome 50
Fairfield 47
Ashburn 24
Cambridge 19
Wilmington 17
Chandler 15
Houston 15
Seattle 14
Singapore 13
Woodbridge 13
Ann Arbor 10
Princeton 9
New York 8
San Paolo di Civitate 7
Sofia 7
Bremen 6
Millbury 6
San Diego 6
Helsinki 5
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
Berlin 2
Bisceglie 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
London 2
Los Angeles 2
Palermo 2
Plano 2
Porto 2
Richmond 2
Sannois 2
Alfianello 1
Andover 1
Bari 1
Beijing 1
Bologna 1
Braga 1
Bromma 1
Cagliari 1
Cesana Brianza 1
Cisterna di Latina 1
Dearborn 1
Dublin 1
Fremont 1
Grumolo delle Abbadesse 1
Guangzhou 1
Hebei 1
Jacksonville 1
Lomé 1
Macerata 1
Mexico City 1
Minturno 1
Muizenberg 1
Nanning 1
Norwalk 1
Nuremberg 1
Pathanamthitta 1
Penne 1
Pescara 1
Prescot 1
Redwood City 1
Shanghai 1
Shaoxing 1
Trento 1
Zurich 1
Totale 402
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
Small 7p22.3 microdeletion: case report of Snx8 haploinsufficiency and neurological findings 82
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 73
Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformation. 68
A new case of SMABF2 diagnosed in stillbirth expands the prenatal presentation and mutational spectrum of ASCC1 61
Expanding the phenotype of the rare neuronal ceroid lipofuscinoses (ncl) 10 35
Neurodevelopmental Impairment As the Main Phenotypic Hallmark Associated with the Translocation t(7;10)(7p22.3;q26.11) 35
3-Methylglutaconic Aciduria Type I Due to AUH Defect: The Case Report of a Diagnostic Odyssey and a Review of the Literature 35
Retinoic acid-induced 1 gene haploinsufficiency alters lipid metabolism and causes autophagy defects in Smith-Magenis syndrome 29
Mosaic genome‐wide paternal uniparental disomy after discordant results from primary fetal samples and cultured cells 28
Complete pseudo-anodontia in an adult woman with pseudo-hypoparathyroidism type 1a: a new additional nonclassical feature? 25
Clinical variability in DYNC2H1-related skeletal ciliopathies includes Ellis-van Creveld syndrome 24
Chromosomal Microarray Analysis in Fetuses Detected with Isolated Cardiovascular Malformation: A Multicenter Study, Systematic Review of the Literature and Meta-Analysis 11
Duplication at 19q13.32q13.33 Segregating with Neuropsychiatric Phenotype in a Three-Generation Family: Towards the Definition of a Critical Region 4
Prenatal CFAP53-related laterality defect: case report and review of the literature 2
Totale 602
Categoria #
all - tutte 2.522
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 2.522


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202069 0 2 3 1 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
2024/202512 12 0 0 0 0 0 0 0 0 0 0 0
Totale 602