Mancano, Giorgia
 Distribuzione geografica
Continente #
NA - Nord America 346
EU - Europa 304
AS - Asia 103
AF - Africa 3
SA - Sud America 1
Totale 757
Nazione #
US - Stati Uniti d'America 342
DE - Germania 103
SE - Svezia 62
CN - Cina 56
IT - Italia 45
UA - Ucraina 29
SG - Singapore 25
GB - Regno Unito 16
FI - Finlandia 13
IE - Irlanda 11
RU - Federazione Russa 9
ID - Indonesia 8
IN - India 7
FR - Francia 6
TR - Turchia 6
CA - Canada 4
BE - Belgio 3
PL - Polonia 2
AT - Austria 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 757
Città #
Chandler 70
Ashburn 30
Singapore 20
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
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
Marseille 4
Mountain View 4
Rome 4
Seattle 4
Shenyang 4
Toronto 4
Brussels 3
Fairfield 3
Lancaster 3
Los Angeles 3
Norwalk 3
Zhengzhou 3
Augusta 2
Bari 2
Binetto 2
Bremen 2
Changchun 2
Changsha 2
Frankfurt am Main 2
Hebei 2
Milan 2
San Salvatore Telesino 2
Shanghai 2
Tianjin 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
London 1
Monmouth Junction 1
Mumbai 1
Munich 1
Ningbo 1
Palermo 1
Phoenix 1
Phoenixville 1
Redmond 1
Renqiu 1
Santa Clara 1
Simi Valley 1
Udine 1
Vienna 1
Totale 445
Nome #
Role of CTCF protein in regulating FMR1 locus transcription. 132
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 124
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells 117
An autosomal recessive DNASE1L3-related autoimmune disease with unusual clinical presentation mimicking systemic lupus erythematosus 108
Cardio-Facio-cutaneous syndrome: phenotypic variability and differential diagnosis in 3 cases with de novo BRAF mutations 98
Defining the role of the CGGBP1 protein in FMR1 gene expression 96
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 92
Totale 767
Categoria #
all - tutte 3.020
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 3.020


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202048 0 0 0 0 0 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
2024/202556 8 6 10 6 21 5 0 0 0 0 0 0
Totale 767