PASSON, Nadia
 Distribuzione geografica
Continente #
NA - Nord America 715
EU - Europa 142
AS - Asia 68
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 927
Nazione #
US - Stati Uniti d'America 712
UA - Ucraina 43
SE - Svezia 28
CN - Cina 20
DE - Germania 19
IT - Italia 19
TR - Turchia 14
IN - India 12
SG - Singapore 12
GB - Regno Unito 8
IE - Irlanda 8
IR - Iran 7
BE - Belgio 5
CA - Canada 3
CZ - Repubblica Ceca 2
FI - Finlandia 2
NL - Olanda 2
RU - Federazione Russa 2
VN - Vietnam 2
AT - Austria 1
BG - Bulgaria 1
ES - Italia 1
EU - Europa 1
HR - Croazia 1
JP - Giappone 1
NZ - Nuova Zelanda 1
Totale 927
Città #
Fairfield 106
Chandler 73
Ashburn 63
Woodbridge 57
Houston 45
Seattle 44
Ann Arbor 40
Wilmington 40
Cambridge 33
Jacksonville 17
Izmir 14
Dearborn 12
Singapore 12
New York 10
Beijing 9
Princeton 9
Dublin 8
Augusta 7
Boardman 7
Ogden 7
Des Moines 6
Brussels 5
Washington 5
Cagliari 4
Hyderabad 4
Norwalk 4
Redmond 4
Udine 4
Ardabil 3
Leawood 3
Los Angeles 3
Portici 3
Brno 2
Chaoyang 2
Dong Ket 2
Grafing 2
Kunming 2
Naples 2
New Delhi 2
San Mateo 2
Auckland 1
Grottaglie 1
Hangzhou 1
Jinan 1
London 1
Madrid 1
Monmouth Junction 1
Montreal 1
Nandyāl 1
Ottawa 1
Salzgitter 1
Shenyang 1
Sofia 1
Trieste 1
Vienna 1
Winnipeg 1
Yokohama 1
Zagreb 1
Zanjan 1
Totale 696
Nome #
Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells 121
Histone post-translational modifications associated to BAALC expression in leukemic cells. 119
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder 119
Somatic amplifications and deletions in genome of papillary thyroid carcinomas 113
Microdeletion 15q26.2qter and Microduplication 18q23 in a patient with prader-willi-like syndrome: Clinical findings 101
Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches 99
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers 77
ANALISI DI CARCINOMI PAPILLIFERI TIROIDEI MEDIANTE CGH-ARRAY 66
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 34
Quantitative PCR evaluation of deletions/duplications identified by array CGH 21
A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutation 18
A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases 6
Totale 959
Categoria #
all - tutte 3.195
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 3.195


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020247 12 13 13 40 21 27 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
2024/20258 8 0 0 0 0 0 0 0 0 0 0 0
Totale 959