BREGANT, Elisa
 Distribuzione geografica
Continente #
NA - Nord America 316
EU - Europa 107
AS - Asia 98
SA - Sud America 12
Totale 533
Nazione #
US - Stati Uniti d'America 316
SG - Singapore 50
DE - Germania 28
CN - Cina 25
RU - Federazione Russa 22
IT - Italia 14
UA - Ucraina 13
BR - Brasile 9
SE - Svezia 8
FI - Finlandia 6
IN - India 5
VN - Vietnam 5
BE - Belgio 4
IE - Irlanda 4
HK - Hong Kong 3
IR - Iran 3
AR - Argentina 2
FR - Francia 2
GB - Regno Unito 2
KR - Corea 2
TR - Turchia 2
DK - Danimarca 1
ES - Italia 1
HR - Croazia 1
IQ - Iraq 1
LK - Sri Lanka 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
UY - Uruguay 1
Totale 533
Città #
Chandler 33
Ann Arbor 31
Fairfield 28
Singapore 28
Houston 24
Ashburn 19
Wilmington 19
Woodbridge 18
Seattle 16
Cambridge 15
Munich 15
Beijing 9
Boardman 8
Jacksonville 6
Brussels 4
Dong Ket 4
Dublin 4
New York 4
Princeton 4
Redmond 4
Shanghai 4
Columbus 3
Düsseldorf 3
Falls Church 3
Hefei 3
Hyderabad 3
San Diego 3
Turku 3
Udine 3
Augusta 2
Brooklyn 2
Buenos Aires 2
Curitiba 2
Des Moines 2
Guangzhou 2
Leawood 2
Los Angeles 2
New Delhi 2
Norwalk 2
San Mateo 2
Santa Clara 2
Seoul 2
Treviso 2
Washington 2
Ardabil 1
Belo Horizonte 1
Bratislava 1
Charlotte 1
Colombo 1
Dayton 1
Erbil 1
Frankfurt am Main 1
Garden City 1
Grafing 1
Grottaglie 1
Henderson 1
Hong Kong 1
Itumbiara 1
Izmir 1
Jaboticabal 1
Lappeenranta 1
Lauterbourg 1
Lincoln 1
Montevideo 1
Moscow 1
Newark 1
North Bergen 1
Nuremberg 1
Ogden 1
Rio Verde 1
Rio de Janeiro 1
Riyadh 1
Rozzano 1
San Michele al Tagliamento 1
Severínia 1
São Paulo 1
Tavagnacco 1
Trieste 1
Venezia 1
Yantai 1
Totale 387
Nome #
Evaluating the SERCA2 and VEGF mRNAs as Potential Molecular Biomarkers of the Onset and Progression in Huntington's Disease 162
Somatic amplifications and deletions in genome of papillary thyroid carcinomas 134
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers 100
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype 60
A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases 42
The molecular landscape of hereditary ataxia: a single-center study 30
The impact of the European Society of Cardiology guidelines and whole exome sequencing on genetic testing in hereditary cardiac diseases 27
Totale 555
Categoria #
all - tutte 2.221
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 2.221


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20207 0 0 0 0 0 0 0 0 0 0 0 7
2020/202178 4 8 1 10 2 16 3 6 3 3 12 10
2021/202253 0 3 3 1 3 5 2 3 4 3 21 5
2022/202357 4 8 1 11 7 13 0 2 7 0 2 2
2023/202434 3 0 2 0 4 8 0 1 7 3 0 6
2024/2025187 9 6 12 17 9 3 19 10 24 13 47 18
Totale 555