FORZAN, MONICA
 Distribuzione geografica
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Continente #
NA - Nord America 1.239
EU - Europa 253
AS - Asia 80
Totale 1.572
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Nazione #
US - Stati Uniti d'America 1.237
IT - Italia 122
CN - Cina 72
SE - Svezia 50
FI - Finlandia 29
DE - Germania 26
GB - Regno Unito 9
FR - Francia 7
HK - Hong Kong 5
IE - Irlanda 3
IN - India 3
PL - Polonia 3
UA - Ucraina 3
MX - Messico 2
CZ - Repubblica Ceca 1
Totale 1.572
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Città #
Fairfield 211
Houston 144
Chandler 127
Woodbridge 106
Ashburn 103
Ann Arbor 92
Cambridge 71
Seattle 65
Wilmington 63
San Diego 26
Beijing 23
Helsinki 20
Des Moines 19
Padova 17
Princeton 17
Medford 15
Roxbury 13
Nanjing 12
Parma 12
Boardman 11
Jacksonville 11
Milan 10
New York 9
Bologna 6
Cagliari 6
Guangzhou 6
Jinan 6
Bari 5
Rome 4
Tianjin 4
Camisano 3
Dublin 3
Nanchang 3
Pune 3
Redmond 3
Shanghai 3
Shenyang 3
Turin 3
Verona 3
Washington 3
Castelraimondo 2
Castignano 2
Ferrara 2
Gießen 2
Gustavo Adolfo Madero 2
Hong Kong 2
Inverigo 2
Jiaxing 2
Lappeenranta 2
Las Vegas 2
Lestizza 2
Naples 2
Norwalk 2
Ogden 2
Redwood City 2
Reggio Emilia 2
Romano d'Ezzelino 2
Taiyuan 2
Treviso 2
Warsaw 2
Augusta 1
Bergamo 1
Bielefeld 1
Busto Arsizio 1
Casalserugo 1
Cavarzere 1
Falls Church 1
Garden Grove 1
Gorla Maggiore 1
Hefei 1
Indiana 1
Islington 1
Kharkiv 1
Lodz 1
London 1
Marigliano 1
Palma Campania 1
Quzhou 1
Rockville 1
Rouen 1
San Francisco 1
Sant'Agata Bolognese 1
Siena 1
Taizhou 1
Tappahannock 1
Tettnang 1
Trieste 1
Venice 1
Wuhan 1
Totale 1.333
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Nome #
The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromas 134
Is CFTR 621+3 A > G a cystic fibrosis causing mutation? 133
Functional Splicing Assay mediante l'utilizzo di minigeni plasmidici nel gene NF1 131
Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches 125
CATECHOL-O-METHYLTRANSFERASE GENOTYPE MODIFIES EXECUTIVE FUNCTIONING AND PREFRONTAL FUNCTIONAL CONNECTIVITY IN WOMEN WITH ANOREXIA NERVOSA. 116
Catechol-O-Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta-Analysis of Previously Published Studies 114
A genome-wide association study of anorexia nervosa 108
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index 98
p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas. 93
Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa 86
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling 82
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies 74
null 71
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders 64
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa 62
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease 61
Setup and Validation of a Targeted Next-Generation Sequencing Approach for the Diagnosis of Lysosomal Storage Disorders 36
Using ancestry-informative markers to identify fine structure across 15 populations of European origin 13
Totale 1.601
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Categoria #
all - tutte 5.161
article - articoli 4.750
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.911
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019117 0 0 0 0 0 0 0 0 0 25 50 42
2019/2020358 39 16 10 30 30 17 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
2023/2024169 14 32 20 6 14 30 14 14 8 17 0 0
Totale 1.601