Asaro, Alessia
 Distribuzione geografica
Continente #
EU - Europa 361
NA - Nord America 307
AS - Asia 86
Totale 754
Nazione #
US - Stati Uniti d'America 303
DE - Germania 174
SE - Svezia 47
CN - Cina 39
UA - Ucraina 32
IT - Italia 31
SG - Singapore 28
FR - Francia 19
GB - Regno Unito 17
IE - Irlanda 11
PL - Polonia 9
RU - Federazione Russa 8
ID - Indonesia 7
IN - India 7
FI - Finlandia 6
BE - Belgio 4
CA - Canada 4
HK - Hong Kong 3
IR - Iran 2
AT - Austria 1
IS - Islanda 1
LV - Lettonia 1
Totale 754
Città #
Chandler 80
Ann Arbor 24
Jacksonville 22
Singapore 19
New York 17
Ashburn 16
San Mateo 14
Nürnberg 13
Cattolica 11
Dublin 11
Wilmington 11
Nanjing 9
Boston 7
Jakarta 7
Lancaster 7
Marseille 7
Dearborn 6
Lawrence 6
Nanchang 6
Boardman 5
Moscow 5
Seattle 5
Brussels 4
Fremont 4
Warsaw 4
Brescia 3
Guangzhou 3
Houston 3
Los Angeles 3
Mountain View 3
Munich 3
Norwalk 3
Rome 3
Tianjin 3
Toronto 3
Woodbridge 3
Bari 2
Bremen 2
Buffalo 2
Guidonia 2
Hong Kong 2
Polska 2
Pune 2
Redwood City 2
Romainville 2
San Giuliano Milanese 2
Shenyang 2
Simi Valley 2
University Park 2
Ardabil 1
Beijing 1
Changchun 1
Costa Mesa 1
Glossop 1
Ha Kwai Chung 1
Hebei 1
Hefei 1
Indiana 1
Kilburn 1
Kish 1
Kunming 1
Las Vegas 1
Leawood 1
Milan 1
Palermo 1
Paris 1
Phoenix 1
Princeton 1
Riga 1
San Diego 1
San Francisco 1
Taizhou 1
Tappahannock 1
Velikiy Novgorod 1
Verona 1
Vienna 1
Yellowknife 1
Totale 407
Nome #
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 148
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder 123
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome 122
Unique genomic profile associated with pediatric uveal melanoma 116
Variable expressivity of a familial 1.9 Mb microdeletion in 3q28 leading to haploinsufficiency of TP63: Refinement of the critical region for a new microdeletion phenotype 112
Variable expressivity of a familial 1.9 Mb microdeletion in 3q28 leading to haploinsufficiency of TP63: Refinement of the critical region for a new microdeletion phenotype. 82
Variable expressivity of a familial 1.9 Mb microdeletion in 3q28 leading to haploinsufficiency of TP63: Refinement of the critical region for a new microdeletion phenotype. 63
Totale 766
Categoria #
all - tutte 2.552
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 2.552


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202065 0 0 0 0 2 11 13 7 4 5 14 9
2020/202168 2 10 1 8 11 2 3 3 10 2 16 0
2021/202273 3 5 0 6 4 5 0 16 4 4 12 14
2022/2023188 30 26 15 30 8 27 9 16 15 2 6 4
2023/202478 3 14 1 9 2 21 3 0 0 2 11 12
2024/202535 4 7 7 4 13 0 0 0 0 0 0 0
Totale 766