Mancano, Giorgia
 Distribuzione geografica
Continente #
NA - Nord America 340
EU - Europa 294
AS - Asia 77
AF - Africa 3
SA - Sud America 1
Totale 715
Nazione #
US - Stati Uniti d'America 339
DE - Germania 101
SE - Svezia 61
CN - Cina 53
IT - Italia 45
UA - Ucraina 29
GB - Regno Unito 15
IE - Irlanda 11
SG - Singapore 10
FI - Finlandia 9
RU - Federazione Russa 9
IN - India 7
FR - Francia 6
TR - Turchia 6
BE - Belgio 2
PL - Polonia 2
CA - Canada 1
CI - Costa d'Avorio 1
CL - Cile 1
CM - Camerun 1
ES - Italia 1
IS - Islanda 1
NO - Norvegia 1
RO - Romania 1
VN - Vietnam 1
ZA - Sudafrica 1
Totale 715
Città #
Chandler 70
Ashburn 29
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 8
Moscow 8
Falls Church 7
Lawrence 7
Fremont 6
Izmir 6
Nanchang 6
Dearborn 5
Singapore 5
Cambridge 4
Kunming 4
Leawood 4
Marseille 4
Mountain View 4
Rome 4
Seattle 4
Shenyang 4
Fairfield 3
Lancaster 3
Los Angeles 3
Norwalk 3
Zhengzhou 3
Augusta 2
Bari 2
Binetto 2
Bremen 2
Brussels 2
Changchun 2
Changsha 2
Hebei 2
Helsinki 2
Milan 2
San Salvatore Telesino 2
Warsaw 2
Abidjan 1
Bend 1
Boardman 1
Bologna 1
Buffalo 1
Dong Ket 1
Easton 1
Houston 1
Indiana 1
Iowa City 1
Johannesburg 1
Monmouth Junction 1
Mumbai 1
Munich 1
Ningbo 1
Palermo 1
Phoenix 1
Phoenixville 1
Redmond 1
Renqiu 1
Shanghai 1
Simi Valley 1
Tianjin 1
Toronto 1
Udine 1
Totale 406
Nome #
Role of CTCF protein in regulating FMR1 locus transcription. 127
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 118
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells 107
An autosomal recessive DNASE1L3-related autoimmune disease with unusual clinical presentation mimicking systemic lupus erythematosus 103
Cardio-Facio-cutaneous syndrome: phenotypic variability and differential diagnosis in 3 cases with de novo BRAF mutations 93
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 89
Defining the role of the CGGBP1 protein in FMR1 gene expression 88
Totale 725
Categoria #
all - tutte 2.697
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 2.697


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202056 0 0 2 0 6 10 9 5 2 4 12 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
2024/202514 8 6 0 0 0 0 0 0 0 0 0 0
Totale 725