Mancano, Giorgia
 Distribuzione geografica
Continente #
NA - Nord America 361
EU - Europa 321
AS - Asia 139
SA - Sud America 21
AF - Africa 3
Totale 845
Nazione #
US - Stati Uniti d'America 356
DE - Germania 111
SE - Svezia 64
CN - Cina 62
IT - Italia 45
SG - Singapore 45
UA - Ucraina 29
BR - Brasile 19
GB - Regno Unito 18
FI - Finlandia 13
IE - Irlanda 11
FR - Francia 10
RU - Federazione Russa 9
TR - Turchia 9
ID - Indonesia 8
IN - India 7
CA - Canada 4
BE - Belgio 3
HK - Hong Kong 2
PL - Polonia 2
VN - Vietnam 2
AM - Armenia 1
AT - Austria 1
CI - Costa d'Avorio 1
CL - Cile 1
CM - Camerun 1
ES - Italia 1
GR - Grecia 1
IL - Israele 1
IQ - Iraq 1
IS - Islanda 1
KR - Corea 1
MX - Messico 1
NO - Norvegia 1
RO - Romania 1
UY - Uruguay 1
ZA - Sudafrica 1
Totale 845
Città #
Chandler 70
Ashburn 32
Singapore 22
Nanjing 17
Cattolica 16
Jacksonville 16
San Mateo 15
Wilmington 15
Ann Arbor 14
Woodbridge 14
New York 12
Redwood City 12
Dublin 11
Nürnberg 11
Boston 9
Frankfurt am Main 8
Jakarta 8
Moscow 8
Falls Church 7
Lawrence 7
Fremont 6
Helsinki 6
Izmir 6
Nanchang 6
Dearborn 5
Cambridge 4
Kunming 4
Leawood 4
Los Angeles 4
Marseille 4
Mountain View 4
Rome 4
Seattle 4
Shenyang 4
Toronto 4
Brussels 3
Fairfield 3
Lancaster 3
Norwalk 3
Zhengzhou 3
Augusta 2
Bari 2
Bexley 2
Binetto 2
Bremen 2
Changchun 2
Changsha 2
Düsseldorf 2
Guarulhos 2
Hebei 2
Hong Kong 2
Milan 2
San Salvatore Telesino 2
Shanghai 2
Tianjin 2
Warsaw 2
Abidjan 1
Acaraú 1
Araçatuba 1
Athens 1
Beijing 1
Belo Horizonte 1
Bend 1
Boardman 1
Bologna 1
Buffalo 1
Campinas 1
Charlotte 1
Contagem 1
Dois Vizinhos 1
Dong Ket 1
Easton 1
Gravataí 1
Hefei 1
Ho Chi Minh City 1
Houston 1
Indiana 1
Iowa City 1
Istanbul 1
Johannesburg 1
Konya 1
León 1
London 1
Macaé 1
Marliéria 1
Matelândia 1
Monmouth Junction 1
Mossoró 1
Mumbai 1
Munich 1
Newark 1
Ningbo 1
Nova Serrana 1
Palermo 1
Phoenix 1
Phoenixville 1
Ponta Grossa 1
Ramadi 1
Redmond 1
Renqiu 1
Totale 484
Nome #
Role of CTCF protein in regulating FMR1 locus transcription. 145
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 135
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells 129
An autosomal recessive DNASE1L3-related autoimmune disease with unusual clinical presentation mimicking systemic lupus erythematosus 122
Cardio-Facio-cutaneous syndrome: phenotypic variability and differential diagnosis in 3 cases with de novo BRAF mutations 113
Defining the role of the CGGBP1 protein in FMR1 gene expression 106
Interstitial deletion of 3p22.3p22.2 encompassing ARPP21 and CLASP2 is a potential pathogenic factor for a syndromic form of intellectual disability: a co-morbidity model with additional copy number variations in a large family 105
Totale 855
Categoria #
all - tutte 3.473
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 3.473


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20206 0 0 0 0 0 0 0 0 0 0 0 6
2020/202189 2 9 2 8 12 8 7 1 10 7 22 1
2021/202292 3 12 1 4 5 6 6 16 2 7 13 17
2022/2023172 30 27 12 31 7 21 9 11 17 2 2 3
2023/202477 3 20 2 7 2 14 8 0 1 3 10 7
2024/2025144 8 6 10 6 21 5 0 7 27 16 37 1
Totale 855