TORRENTE, ISABELLA
 Distribuzione geografica
Continente #
NA - Nord America 283
EU - Europa 88
AS - Asia 28
AF - Africa 3
SA - Sud America 1
Totale 403
Nazione #
US - Stati Uniti d'America 277
IT - Italia 59
IN - India 12
CN - Cina 8
SE - Svezia 7
SG - Singapore 7
FI - Finlandia 5
CA - Canada 4
NL - Olanda 3
PT - Portogallo 3
TG - Togo 3
BE - Belgio 2
BG - Bulgaria 2
DE - Germania 2
FR - Francia 2
MX - Messico 2
BR - Brasile 1
GB - Regno Unito 1
PK - Pakistan 1
RS - Serbia 1
UA - Ucraina 1
Totale 403
Città #
Fairfield 48
Woodbridge 33
Rome 25
Houston 22
Ashburn 20
Chandler 19
Wilmington 17
Seattle 16
Des Moines 10
Ann Arbor 7
Beijing 7
Cambridge 6
Lawrence 5
Milan 5
Princeton 5
San Paolo di Civitate 5
Andover 4
Plano 4
Polignano a Mare 4
San Diego 4
Boston 3
Dearborn 3
Lomé 3
Boardman 2
Gatineau 2
Mexico City 2
Millbury 2
Montreal 2
New York 2
Porto 2
Sannois 2
Sofia 2
Waanrode 2
Alfianello 1
Amsterdam 1
Belgrade 1
Braga 1
Bremen 1
Bühl 1
Cisterna di Latina 1
Falls Church 1
Florence 1
Guidonia 1
Helsinki 1
Kunming 1
Lappeenranta 1
London 1
Los Angeles 1
Mumbai 1
Norwalk 1
Pune 1
Siena 1
Singapore 1
São Luís 1
Totale 316
Nome #
p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas 92
Bilateral (opercular and paracentral lobular) polymicrogyria and neurofibromatosis type 1 82
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome 78
Evaluation of a DHPLC-based assay for rapid detection of RET germline mutations in Italian patients with medullary thyroid carcinoma 66
Germline and mosaic variants in PRKACA and PRKACB cause a multiple congenital malformation syndrome 44
Generation of an induced pluripotent stem cell line CSSi015-A (9553), carrying a point mutation c.2915C > T in the human calcium sensing receptor (CasR) gene 30
Mosaic genome‐wide paternal uniparental disomy after discordant results from primary fetal samples and cultured cells 25
Clinical variability in DYNC2H1-related skeletal ciliopathies includes Ellis-van Creveld syndrome 16
Evaluation of TP53 mutations with the AmpliChip p53 research test in chronic lymphocytic leukemia: correlation with clinical outcome and gene expression profiling 1
Totale 434
Categoria #
all - tutte 1.144
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 1.144


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201933 0 0 0 0 0 0 0 0 0 0 18 15
2019/202077 9 4 0 2 8 9 8 10 9 12 6 0
2020/202143 4 2 4 0 0 2 5 1 9 10 2 4
2021/202284 18 5 5 2 11 3 0 14 6 2 6 12
2022/202395 9 17 4 11 3 15 4 5 9 2 11 5
2023/202469 4 9 3 15 10 10 2 4 1 11 0 0
Totale 434