GIACOPUZZI, Edoardo
 Distribuzione geografica
Continente #
NA - Nord America 2.420
EU - Europa 2.225
AS - Asia 754
OC - Oceania 5
SA - Sud America 3
AF - Africa 2
Totale 5.409
Nazione #
US - Stati Uniti d'America 2.396
PL - Polonia 1.261
CN - Cina 402
UA - Ucraina 271
IT - Italia 236
DE - Germania 133
SG - Singapore 127
FR - Francia 86
FI - Finlandia 83
HK - Hong Kong 79
GB - Regno Unito 58
VN - Vietnam 56
IE - Irlanda 52
TR - Turchia 41
CA - Canada 24
IN - India 20
ID - Indonesia 17
BE - Belgio 15
CZ - Repubblica Ceca 14
RU - Federazione Russa 9
AU - Australia 4
KR - Corea 3
SA - Arabia Saudita 3
SE - Svezia 3
BR - Brasile 2
PK - Pakistan 2
AR - Argentina 1
BY - Bielorussia 1
EG - Egitto 1
ES - Italia 1
IR - Iran 1
JO - Giordania 1
KG - Kirghizistan 1
LT - Lituania 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
UZ - Uzbekistan 1
ZA - Sudafrica 1
Totale 5.409
Città #
Warsaw 1.261
Fairfield 348
Woodbridge 244
Jacksonville 209
Ann Arbor 184
Ashburn 173
Chandler 145
Houston 140
Cambridge 131
Brescia 123
Singapore 110
Wilmington 109
Seattle 104
Princeton 94
New York 80
Hong Kong 78
Nanjing 75
Helsinki 66
Beijing 61
Dearborn 61
Dong Ket 56
Dublin 52
Istanbul 39
Jinan 28
Shenyang 26
Des Moines 24
Shanghai 24
Changsha 23
Hebei 21
Nanchang 21
San Diego 18
Jakarta 16
Toronto 16
Brussels 15
Jiaxing 14
Munich 14
Hangzhou 13
Zhengzhou 13
Milan 12
Tianjin 12
Ningbo 10
Phoenix 10
Fuzhou 9
Haikou 9
Los Angeles 8
Olomouc 8
San Francisco 8
Boardman 7
Bolzano 6
Brno 6
Leawood 6
London 6
Québec 6
Lanzhou 5
Mantova 5
Augusta 4
Bologna 4
Gunzenhausen 4
Kunming 4
Orange 4
Pune 4
San Mateo 4
Taiyuan 4
Chiswick 3
Guangzhou 3
Jeddah 3
Lancaster 3
Pieve D'alpago 3
Redwood City 3
Canberra 2
Dong-gu 2
Düsseldorf 2
Hefei 2
Hounslow 2
Islamabad 2
Kilburn 2
Napoli 2
Norwalk 2
Qingdao 2
Quzhou 2
Rome 2
Sydney 2
Taizhou 2
Washington 2
Ahmedabad 1
Amman 1
Ardabil 1
Bangalore 1
Baoding 1
Baotou 1
Barcelona 1
Bishkek 1
Brierley Hill 1
Buffalo 1
Cairo 1
Casoria 1
Ceresara 1
Changchun 1
Falkenstein 1
Falls Church 1
Totale 4.458
Nome #
Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis 316
Mesenchymal stromal cells (MSCs) induce ex vivo proliferation and erythroid commitment of cord blood haematopoietic stem cells (CB-CD34+ cells) 265
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways 264
Differential Enzymatic Activity of Rat ADAR2 Splicing Variants Is Due to Altered Capability to Interact with RNA in the Deaminase Domain 228
The effect of childhood trauma on blood transcriptome expression in major depressive disorder 223
In silico identification of new putative pathogenic variants in the NEU1 sialidase gene affecting enzyme function and subcellular localization 205
Report on a patient with extremely fragile skin, dermatosparaxis, joint hypermobility, short stature, skeletal deformities, and lipomas: a new syndrome? 193
Genome-wide analysis of consistently RNA edited sites in human blood reveals interactions with mRNA processing genes and suggests correlations with cell types and biological variables 176
The impairment of GABAergic pathway as one of the driver forces in the etiopathogenesis of schizophrenia: evidence from functional studies and gene-set enrichment analyses 169
New biological pathways for major depression: gene expression decomposition in G x E components 161
Genomic restricted maximum likelihood (GREML) analysis to estimate the heritability of response/resistance in major depressive disorder (MDD) 146
Further defining the phenotypic spectrum of B3GAT3 mutations and literature review on linkeropathy syndromes 132
A recognizable systemic connective tissue disorder with polyvalvular heart dystrophy and dysmorphism associated with TAB2 mutations 131
A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme 128
Real-world clinical applicability of pathogenicity predictors assessed on SERPINA1 mutations in alpha-1-antitrypsin deficiency 127
slc7a6os Gene Plays a Critical Role in Defined Areas of the Developing CNS in Zebrafish 125
Characterization and expression analysis of mcoln1.1 and mcoln1.2, the putative zebrafish co-orthologs of the gene responsible for human mucolipidosis type IV. 123
Molecular cloning and knockdown of galactocerebrosidase in zebrafish: New insights into the pathogenesis of Krabbe's disease. 122
Amplicon-based semiconductor sequencing of human exomes: performance evaluation and optimization strategies 122
Gallus gallus NEU3 sialidase as model to study protein evolution mechanism based on rapid evolving loops 116
Genomic and biochemical characterization of sialic acid acetylesterase (siae) in zebrafish 116
Human sialic acid acetyl esterase: Towards a better understanding of a puzzling enzyme 112
The Role of Metabotropic Glutamate Receptor Genes in Schizophrenia 110
Computational and functional analysis of biopharmaceutical drugs in zebrafish: Erythropoietin as a test model 109
Functional study of a novel homozygous mutation in the GAD1 gene, detected in a patient with schizophrenia. 108
Treatment-Resistant Schizophrenia: Genetic and Neuroimaging Correlates 104
Clinical and molecular characterization of a 13-year-old Indian boy with cutis laxa type 2B: Identification of two novel PYCR1 mutations by amplicon-based semiconductor exome sequencing 102
New insights on the sialidase protein family revealed by a phylogenetic analysis in metazoa 101
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 93
Study of the genetic architecture behind mood disorders by whole exome sequencing on a large Italian pedigree 88
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 86
The effect of childhood trauma on blood transcriptome expression in major depressive disorder 84
Exome sequencing of schizophrenia patients with high level of homozygosity identifies a homozygous novel mutation that reduces the glutamate acid decarboxylase 67 (GAD67) activity 82
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 76
Substrate-immobilized HIV-1 Tat drives VEGFR2/αvβ3 integrin complex formation and polarization in endothelial cells 72
Analysis of human exome and genome using the Ion Proton platform 64
VEGFR2 and v3 recruitment and cross-talk at the basal aspect of HIV-1 Tat-adherent endothelial cells drives pp60src/ERK1/2 activation, cytoskeleton organization and pro-angiogenic activation 62
Flk-1/KDR and v3 recruitment and cross-talk at the basal aspect of HIV-1 Tat-adherent endothelial cells drives pp60src/ERK1/2 activation, cytoskeleton organization and pro-angiogenic activation 62
Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles 60
Analysis of Citalopram response heterogeneity among STAR*D patients using in-silico methods 60
Genome-wide analysis of RNA-editing levels in human blood identifies interactions with mRNA processing genes and suggests correlation with biological and drug-related variables 58
Genome-wide analysis of RNA-editing levels in human blood identified interactions with mRNA processing genes and suggested correlation with biological and drug-related variables 57
Ehlers-Danlos syndrome with lethal cardiac valvular dystrophy in males carrying a novel splice mutation in FLNA 54
GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS 51
Investigating an in silico approach for prioritizing antidepressant drug prescription based on drug-induced expression profiles and predicted gene expression 50
Genome-wide analysis of RNA editing levels in human blood identified interactions with mRNA processing genes and suggested correlations with biological and drug-related variables 46
Clinical validation of a combinatorial PharmAcogeNomic approach in major Depressive disorder: an Observational prospective RAndomized, participant and rater-blinded, controlled trial (PANDORA trial) 37
Genome-wide association studies on Northern Italy isolated populations provide further support concerning genetic susceptibility for major depressive disorder 17
Totale 5.593
Categoria #
all - tutte 21.094
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 21.094


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.211 0 0 0 0 115 197 184 177 137 193 127 81
2020/20211.023 45 104 57 112 53 87 38 96 115 133 106 77
2021/2022452 43 46 33 9 3 27 18 20 24 85 29 115
2022/2023397 60 5 22 36 34 108 2 32 61 6 15 16
2023/2024450 30 13 49 33 21 105 11 8 83 10 13 74
2024/2025241 7 10 4 135 85 0 0 0 0 0 0 0
Totale 5.593