PASSON, Nadia
 Distribuzione geografica
Continente #
NA - Nord America 749
EU - Europa 192
AS - Asia 123
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 1.066
Nazione #
US - Stati Uniti d'America 745
SG - Singapore 52
UA - Ucraina 43
DE - Germania 39
IT - Italia 35
CN - Cina 32
SE - Svezia 28
TR - Turchia 14
IN - India 13
RU - Federazione Russa 11
IE - Irlanda 9
GB - Regno Unito 8
IR - Iran 7
BE - Belgio 5
CA - Canada 4
FI - Finlandia 4
NL - Olanda 3
AT - Austria 2
CZ - Repubblica Ceca 2
HK - Hong Kong 2
VN - Vietnam 2
BG - Bulgaria 1
ES - Italia 1
EU - Europa 1
HR - Croazia 1
JP - Giappone 1
NZ - Nuova Zelanda 1
Totale 1.066
Città #
Fairfield 106
Chandler 73
Ashburn 63
Woodbridge 57
Singapore 51
Houston 45
Seattle 44
Ann Arbor 40
Wilmington 40
Cambridge 33
Boardman 19
Jacksonville 17
Munich 16
Izmir 14
Columbus 13
Dearborn 12
New York 10
Beijing 9
Dublin 9
Princeton 9
Udine 8
Augusta 7
Ogden 7
Des Moines 6
Brussels 5
Washington 5
Cagliari 4
Hyderabad 4
Norwalk 4
Redmond 4
Trieste 4
Ardabil 3
Hangzhou 3
Leawood 3
Los Angeles 3
Portici 3
Brno 2
Cabiate 2
Chaoyang 2
Dong Ket 2
Genoa 2
Grafing 2
Guangzhou 2
Hong Kong 2
Kunming 2
Moscow 2
Naples 2
New Delhi 2
Rome 2
San Mateo 2
Shenzhen 2
Turin 2
Vienna 2
Amsterdam 1
Auckland 1
Dallas 1
Falkenstein 1
Frankfurt am Main 1
Grottaglie 1
Helsinki 1
Jinan 1
Lappeenranta 1
London 1
Madrid 1
Malappuram 1
Monmouth Junction 1
Montreal 1
Nandyāl 1
Newark 1
Nuremberg 1
Ottawa 1
Salzgitter 1
San Michele al Tagliamento 1
Santa Clara 1
Shenyang 1
Sofia 1
Toronto 1
Winnipeg 1
Yantai 1
Yokohama 1
Zagreb 1
Zanjan 1
Totale 816
Nome #
Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells 130
Histone post-translational modifications associated to BAALC expression in leukemic cells. 129
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder 129
Somatic amplifications and deletions in genome of papillary thyroid carcinomas 121
Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches 109
Microdeletion 15q26.2qter and Microduplication 18q23 in a patient with prader-willi-like syndrome: Clinical findings 106
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers 84
ANALISI DI CARCINOMI PAPILLIFERI TIROIDEI MEDIANTE CGH-ARRAY 78
null 65
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype 43
A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutation 28
Quantitative PCR evaluation of deletions/duplications identified by array CGH 28
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance 19
A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases 18
Using the AlphaFold system to the interpretation of variants of uncertain significance 17
Totale 1.104
Categoria #
all - tutte 4.180
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 4.180


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020121 0 0 0 0 0 0 23 37 26 14 4 17
2020/2021175 9 18 5 22 5 31 6 16 12 11 26 14
2021/2022129 6 6 9 7 4 6 7 3 3 15 49 14
2022/2023133 13 22 2 17 19 23 0 14 17 0 4 2
2023/2024133 8 5 8 5 29 30 2 8 15 3 1 19
2024/2025153 12 13 21 69 18 14 6 0 0 0 0 0
Totale 1.104