FORZAN, MONICA
 Distribuzione geografica
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Continente #
NA - Nord America 1.314
EU - Europa 348
AS - Asia 165
OC - Oceania 1
Totale 1.828
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Nazione #
US - Stati Uniti d'America 1.311
IT - Italia 196
CN - Cina 100
SG - Singapore 55
SE - Svezia 50
FI - Finlandia 32
DE - Germania 30
FR - Francia 14
GB - Regno Unito 10
HK - Hong Kong 7
IE - Irlanda 3
IN - India 3
PL - Polonia 3
UA - Ucraina 3
CZ - Repubblica Ceca 2
MX - Messico 2
NL - Olanda 2
RU - Federazione Russa 2
AU - Australia 1
CA - Canada 1
CH - Svizzera 1
Totale 1.828
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Città #
Fairfield 211
Houston 144
Chandler 127
Woodbridge 106
Ashburn 104
Ann Arbor 92
Cambridge 71
Seattle 65
Wilmington 63
Santa Clara 44
Singapore 39
Boardman 28
San Diego 26
Beijing 24
Helsinki 21
Padova 21
Des Moines 19
Princeton 17
Medford 15
Milan 14
Parma 14
Roxbury 13
Nanjing 12
Jacksonville 11
New York 9
Bologna 7
Cagliari 6
Guangzhou 6
Jinan 6
Rome 6
Bari 5
Turin 5
Hong Kong 4
Lappeenranta 4
Naples 4
Tianjin 4
Camisano 3
Dublin 3
Nanchang 3
Pune 3
Redmond 3
San Francisco 3
Shanghai 3
Shenyang 3
Trieste 3
Verona 3
Washington 3
Alezio 2
Castelraimondo 2
Castignano 2
Catania 2
Cento 2
Cosenza 2
Ferrara 2
Gießen 2
Grottaglie 2
Gustavo Adolfo Madero 2
Inverigo 2
Jiaxing 2
Las Vegas 2
Lestizza 2
Marana 2
Modena 2
Monza 2
Munich 2
Norwalk 2
Nuremberg 2
Ogden 2
Redwood City 2
Reggio Emilia 2
Romano d'Ezzelino 2
Seravezza 2
Taiyuan 2
Treviso 2
Warsaw 2
Augusta 1
Bergamo 1
Bielefeld 1
Brno 1
Busto Arsizio 1
Casalserugo 1
Cavarzere 1
Changsha 1
Changzhou 1
Curtarolo 1
Dallas 1
Deiva Marina 1
Falls Church 1
Florence 1
Garden Grove 1
Gorla Maggiore 1
Hefei 1
Hengshui 1
Indiana 1
Islington 1
Jianning 1
Kharkiv 1
Limena 1
Lodz 1
London 1
Totale 1.481
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Nome #
Functional Splicing Assay mediante l'utilizzo di minigeni plasmidici nel gene NF1 213
Is CFTR 621+3 A > G a cystic fibrosis causing mutation? 145
The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromas 144
Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches 133
CATECHOL-O-METHYLTRANSFERASE GENOTYPE MODIFIES EXECUTIVE FUNCTIONING AND PREFRONTAL FUNCTIONAL CONNECTIVITY IN WOMEN WITH ANOREXIA NERVOSA. 127
Catechol-O-Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta-Analysis of Previously Published Studies 127
A genome-wide association study of anorexia nervosa 126
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index 106
p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas. 103
Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa 99
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling 97
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies 83
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders 72
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease 72
null 71
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa 70
Setup and Validation of a Targeted Next-Generation Sequencing Approach for the Diagnosis of Lysosomal Storage Disorders 48
Using ancestry-informative markers to identify fine structure across 15 populations of European origin 21
Totale 1.857
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Categoria #
all - tutte 6.818
article - articoli 6.168
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 12.986
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020216 0 0 0 0 0 0 32 39 47 55 27 16
2020/2021197 18 20 19 8 9 7 1 24 35 22 25 9
2021/2022320 24 31 21 31 26 26 21 24 26 14 27 49
2022/2023272 38 24 10 35 35 40 3 21 32 6 21 7
2023/2024221 14 32 20 6 14 30 14 14 8 17 32 20
2024/2025204 21 23 17 39 71 31 2 0 0 0 0 0
Totale 1.857