PASSON, Nadia
 Distribuzione geografica
Continente #
NA - Nord America 748
EU - Europa 180
AS - Asia 111
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 1.041
Nazione #
US - Stati Uniti d'America 745
SG - Singapore 44
UA - Ucraina 43
DE - Germania 38
IT - Italia 34
CN - Cina 28
SE - Svezia 28
TR - Turchia 14
IN - India 13
IE - Irlanda 9
GB - Regno Unito 8
IR - Iran 7
BE - Belgio 5
FI - Finlandia 4
CA - Canada 3
NL - Olanda 3
CZ - Repubblica Ceca 2
HK - Hong Kong 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 1.041
Città #
Fairfield 106
Chandler 73
Ashburn 63
Woodbridge 57
Houston 45
Seattle 44
Singapore 43
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
Hong Kong 2
Kunming 2
Naples 2
New Delhi 2
Rome 2
San Mateo 2
Shenzhen 2
Turin 2
Amsterdam 1
Auckland 1
Dallas 1
Falkenstein 1
Grottaglie 1
Guangzhou 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
Santa Clara 1
Shenyang 1
Sofia 1
Vienna 1
Winnipeg 1
Yantai 1
Yokohama 1
Zagreb 1
Zanjan 1
Totale 801
Nome #
Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells 128
Histone post-translational modifications associated to BAALC expression in leukemic cells. 127
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder 127
Somatic amplifications and deletions in genome of papillary thyroid carcinomas 120
Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches 107
Microdeletion 15q26.2qter and Microduplication 18q23 in a patient with prader-willi-like syndrome: Clinical findings 105
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers 83
ANALISI DI CARCINOMI PAPILLIFERI TIROIDEI MEDIANTE CGH-ARRAY 75
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 41
Quantitative PCR evaluation of deletions/duplications identified by array CGH 27
A case of familial brain-lung-thyroid syndrome due to a NKX2.1 run-on mutation 26
Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance 17
A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases 16
Using the AlphaFold system to the interpretation of variants of uncertain significance 15
Totale 1.079
Categoria #
all - tutte 3.855
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 3.855


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020169 0 0 0 0 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
2024/2025128 12 13 21 69 13 0 0 0 0 0 0 0
Totale 1.079