FABBRO, Dora
 Distribuzione geografica
Continente #
NA - Nord America 849
EU - Europa 205
AS - Asia 77
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.133
Nazione #
US - Stati Uniti d'America 847
UA - Ucraina 61
IT - Italia 47
DE - Germania 36
SG - Singapore 35
CN - Cina 30
FI - Finlandia 24
IE - Irlanda 9
IN - India 8
SE - Svezia 8
BE - Belgio 4
GB - Regno Unito 4
TR - Turchia 4
CH - Svizzera 3
CA - Canada 2
CZ - Repubblica Ceca 2
PT - Portogallo 2
AT - Austria 1
EG - Egitto 1
ES - Italia 1
EU - Europa 1
HU - Ungheria 1
NL - Olanda 1
RS - Serbia 1
Totale 1.133
Città #
Fairfield 114
Woodbridge 111
Ann Arbor 69
Ashburn 66
Chandler 55
Houston 46
Seattle 45
Jacksonville 40
Wilmington 40
Singapore 31
Cambridge 28
Udine 23
Dearborn 20
New York 18
Boardman 13
Beijing 12
Trieste 11
Princeton 10
Dublin 9
Munich 9
San Diego 8
Helsinki 5
Brussels 4
Columbus 4
Frankfurt am Main 4
Izmir 4
Ogden 4
Santa Clara 4
Caserta 3
Des Moines 3
Guangzhou 3
Kunming 3
Los Angeles 3
Washington 3
Zurich 3
Augusta 2
Brno 2
Cabiate 2
Jinan 2
Leawood 2
Monmouth Junction 2
Nanjing 2
Naples 2
Ottawa 2
San Mateo 2
Amsterdam 1
Belgrade 1
Birmingham 1
Cairo 1
Dallas 1
Fuzhou 1
Grafing 1
Hefei 1
Hyderabad 1
Lisbon 1
Madrid 1
Malappuram 1
Mumbai 1
Nandyāl 1
Ponte di Piave 1
Sacramento 1
Shanghai 1
Shenyang 1
Venezia 1
Vienna 1
Wuhan 1
Totale 869
Nome #
Functional analysis of a novel RUNX2 missense mutation found in a family with cleidocranial dysplasia 194
BAALC overexpression retains its negative prognostic role across all cytogenetic risk groups in acute myeloid leukemia patients 180
null 136
Histone post-translational modifications associated to BAALC expression in leukemic cells. 127
FREQUENCY OF FACTOR V, PROTHROMBIN AND METHYLENETETRAHYDROFOLATE REDUCTASE GENE VARIANTS IN PREECLAMPSIA 113
Mutations R67X and W303X of the protein Z-dependent protease inhibitor gene and venous thromboembolic disease: a case-control study in Italian subjects 99
Investigation of endothelin-1 type A receptor gene polymorphism (-231 G>A) in preeclampsia susceptibility 86
A deletion 3' to the PAX6 gene in familial aniridia cases 63
Osteopontin expression is an independent factor for poor survival in oral squamous cell carcinoma: a computer-assisted analysis on TMA sections. 50
EGFR expression is linked to osteopontin and Nf-κB signaling in clear cell renal cell carcinoma. 45
A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutation 26
Using the AlphaFold system to the interpretation of variants of uncertain significance 15
Immunoglobulin K light chain deficiency: A rare, but probably underestimated, humoral immune defect 9
Totale 1.143
Categoria #
all - tutte 3.512
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 3.512


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020194 0 0 0 0 20 37 32 35 22 22 7 19
2020/2021184 2 18 7 25 11 23 10 31 18 8 22 9
2021/2022104 4 6 2 4 3 5 5 7 0 12 44 12
2022/2023112 11 15 5 13 10 25 0 11 10 3 6 3
2023/202470 4 3 5 6 11 23 1 4 5 2 0 6
2024/202597 8 14 32 28 15 0 0 0 0 0 0 0
Totale 1.143