Mancano, Giorgia
 Distribuzione geografica
Continente #
NA - Nord America 338
EU - Europa 283
AS - Asia 59
AF - Africa 3
SA - Sud America 1
Totale 684
Nazione #
US - Stati Uniti d'America 337
DE - Germania 101
SE - Svezia 61
CN - Cina 44
IT - Italia 42
UA - Ucraina 29
GB - Regno Unito 15
IE - Irlanda 11
FI - Finlandia 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
RU - Federazione Russa 1
SG - Singapore 1
VN - Vietnam 1
ZA - Sudafrica 1
Totale 684
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
Falls Church 7
Lawrence 7
Fremont 6
Izmir 6
Nanchang 6
Dearborn 5
Cambridge 4
Kunming 4
Leawood 4
Marseille 4
Mountain View 4
Rome 4
Seattle 4
Shenyang 4
Fairfield 3
Lancaster 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
Buffalo 1
Dong Ket 1
Easton 1
Houston 1
Indiana 1
Iowa City 1
Johannesburg 1
Los Angeles 1
Monmouth Junction 1
Moscow 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 391
Nome #
Role of CTCF protein in regulating FMR1 locus transcription. 122
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 112
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells 102
An autosomal recessive DNASE1L3-related autoimmune disease with unusual clinical presentation mimicking systemic lupus erythematosus 98
Cardio-Facio-cutaneous syndrome: phenotypic variability and differential diagnosis in 3 cases with de novo BRAF mutations 90
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 86
Defining the role of the CGGBP1 protein in FMR1 gene expression 84
Totale 694
Categoria #
all - tutte 2.291
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 2.291


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201919 0 0 0 0 0 0 0 0 0 0 14 5
2019/202087 21 10 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
2023/202460 3 20 2 7 2 14 8 0 1 3 0 0
Totale 694