RICCIARDELLO, Arianna
 Distribuzione geografica
Continente #
EU - Europa 235
NA - Nord America 162
AS - Asia 58
SA - Sud America 7
OC - Oceania 4
Totale 466
Nazione #
US - Stati Uniti d'America 162
IT - Italia 84
IE - Irlanda 68
SE - Svezia 64
SG - Singapore 21
CN - Cina 19
IN - India 14
CO - Colombia 6
AU - Australia 4
BE - Belgio 4
DE - Germania 3
FR - Francia 3
GR - Grecia 3
TR - Turchia 3
UA - Ucraina 2
AT - Austria 1
FI - Finlandia 1
GB - Regno Unito 1
HU - Ungheria 1
ID - Indonesia 1
PE - Perù 1
Totale 466
Città #
Dublin 68
Chandler 51
Nyköping 28
Singapore 16
Ashburn 9
Hyderabad 9
Princeton 9
Medford 8
Beijing 7
Dearborn 7
Atena Lucana 6
Des Moines 6
Medellín 6
Desio 5
Messina 5
Pune 5
Alba 4
Brussels 4
Jacksonville 4
Los Angeles 4
Redwood City 4
Cagliari 3
Catania 3
Livorno 3
Trabzon 3
Upper Caboollure 3
Viagrande 3
Amandola 2
Bari 2
Faenza 2
Göttingen 2
Koropí 2
Modigliana 2
Naples 2
Parma 2
Pontirolo Nuovo 2
Reggio Emilia 2
Rocca San Felice 2
Rome 2
Trapani 2
Venice 2
Acquaviva delle Fonti 1
Ann Arbor 1
Boardman 1
Bologna 1
Budapest 1
Casoria 1
Changsha 1
Chengdu 1
Council Bluffs 1
Dalian 1
Espoo 1
Fairfield 1
Hangzhou 1
Hattiesburg 1
Hebei 1
Jakarta 1
Jiaxing 1
Jinan 1
Lima 1
Milan 1
Munich 1
New York 1
Paris 1
Piraeus 1
Prairie View 1
Rimini 1
Seattle 1
Shanghai 1
Shenyang 1
Sydney 1
Turin 1
Vienna 1
Wilmington 1
Xiangfen 1
Zhengzhou 1
Totale 346
Nome #
Terapia farmacologica personalizzata: basi genetiche e meccanismi d'azione 88
The pediatric psychopharmacology of autism spectrum disorder: A systematic review - Part I: The past and the present 72
The Psychopharmacology of Autism Spectrum Disorder and Rett syndrome 61
Autisms 56
FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family 54
Evidence that ITGB3 promoter variants increase serotonin blood levels by regulating platelet serotonin transporter trafficking 46
Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: a systematic review 45
Huntingtin gene CAG repeat size affects autism risk: Family-based and case–control association study 43
Genotype-phenotype correlation in Phelan-McDermid syndrome: A comprehensive review of chromosome 22q13 deleted genes 26
Totale 491
Categoria #
all - tutte 2.529
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 2.529


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202023 0 0 0 0 0 7 1 3 0 8 2 2
2020/202140 4 0 3 7 8 1 1 3 7 2 3 1
2021/202290 6 4 0 0 3 1 4 3 5 35 2 27
2022/2023196 11 28 6 13 9 18 1 13 82 2 10 3
2023/202478 3 5 1 6 3 11 8 2 2 12 7 18
2024/202552 1 9 4 20 14 4 0 0 0 0 0 0
Totale 491