IRIS Institutional Research Information System - OPENBS Open Archive UniBS

MAGRI, Chiara
 Distribuzione geografica
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Continente #
NA - Nord America 3.497
EU - Europa 2.779
AS - Asia 852
OC - Oceania 13
SA - Sud America 5
Continente sconosciuto - Info sul continente non disponibili 3
AF - Africa 2
Totale 7.151
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Nazione #
US - Stati Uniti d'America 3.483
PL - Polonia 1.292
CN - Cina 572
UA - Ucraina 484
IT - Italia 391
DE - Germania 176
FI - Finlandia 142
HK - Hong Kong 137
GB - Regno Unito 88
FR - Francia 80
IE - Irlanda 75
VN - Vietnam 68
IN - India 41
BE - Belgio 22
CA - Canada 13
AU - Australia 12
SG - Singapore 12
TR - Turchia 10
SE - Svezia 9
NL - Olanda 6
RU - Federazione Russa 5
ES - Italia 3
EU - Europa 3
JP - Giappone 3
SA - Arabia Saudita 3
BG - Bulgaria 2
BR - Brasile 2
KR - Corea 2
AR - Argentina 1
CH - Svizzera 1
EC - Ecuador 1
FK - Isole Falkland (Malvinas) 1
GR - Grecia 1
ID - Indonesia 1
IQ - Iraq 1
KG - Kirghizistan 1
MU - Mauritius 1
MX - Messico 1
NZ - Nuova Zelanda 1
PK - Pakistan 1
PT - Portogallo 1
SI - Slovenia 1
ZA - Sudafrica 1
Totale 7.151
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Città #
Warsaw 1.291
Fairfield 463
Woodbridge 342
Jacksonville 334
Ashburn 262
Ann Arbor 256
Chandler 226
Houston 222
Cambridge 182
Seattle 169
Brescia 163
Wilmington 159
Princeton 148
Hong Kong 136
New York 129
Nanjing 109
Helsinki 93
Beijing 92
Dearborn 91
Dublin 75
Dong Ket 68
Nanchang 48
Jinan 44
Shenyang 41
Des Moines 39
Hebei 36
Changsha 23
Brussels 22
Jiaxing 22
Los Angeles 22
Shanghai 22
San Diego 21
Milan 17
Zhengzhou 16
Hangzhou 15
Tianjin 15
Boardman 14
Haikou 14
Washington 14
Lancaster 13
San Francisco 13
Bolzano 12
Ningbo 12
Lanzhou 11
Verona 11
Fuzhou 8
Redwood City 8
Rome 8
San Mateo 8
Kunming 7
Norwalk 7
Orange 7
Phoenix 7
Leawood 6
Québec 6
Canberra 5
Kocaeli 5
Mantova 5
Toronto 5
Guangzhou 4
Hefei 4
Kilburn 4
London 4
Pieve D'alpago 4
Auburn Hills 3
Changchun 3
Jeddah 3
Lappeenranta 3
Melbourne 3
Sydney 3
Taiyuan 3
Taizhou 3
Tokyo 3
Amsterdam 2
Augusta 2
Bergamo 2
Cagliari 2
Dong-gu 2
Esslingen am Neckar 2
Maccagno 2
Madrid 2
Mirano 2
Ottawa 2
Pignola 2
Pontassieve 2
Quzhou 2
Salerno 2
San Lazzaro di Savena 2
Sofia 2
São Paulo 2
Tappahannock 2
Taranto 2
Torino 2
Andover 1
Baotou 1
Bari 1
Bishkek 1
Brisbane 1
Buenos Aires 1
Castelvetrano 1
Totale 5.713
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Nome #
"GenotypeColour": colour visualisation of SNPs and CNVs 259
New Copy Number Variations in Schizophrenia 259
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement 259
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways 254
ITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiency 248
The effect of childhood trauma on blood transcriptome expression in major depressive disorder 217
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 203
Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia 171
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 171
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 163
New biological pathways for major depression: gene expression decomposition in G x E components 156
Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional role. 147
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. 144
Genomic restricted maximum likelihood (GREML) analysis to estimate the heritability of response/resistance in major depressive disorder (MDD) 137
De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay. 130
Proteasome system dysregulation and treatment resistance mechanisms in major depressive disorder 125
The GRM7 gene, early response to risperidone, and schizophrenia: a genome-wide association study and a confirmatory pharmacogenetic analysis 119
Gene per la neuregulina 1 e schizofrenia: ulteriori evidenze di associazione 118
A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme 118
Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder 117
De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia 113
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia 112
The Role of allelic variants of FK506-binding protein 51 (FKBP5) gene in the development of anxiety disorders 109
Role of allelic variants of FK506-binding protein 51 (FKBP5) gene in the development of anxiety disorders. 103
Origin, diffusion and differentiation of Y-chromosome haplogroups E and J: inferences on the Neolithization of Europe and later migratory events in the Mediterranean area 99
Functional study of a novel homozygous mutation in the GAD1 gene, detected in a patient with schizophrenia. 98
Saami and Berbers--an unexpected mitochondrial DNA link 97
Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM-IV-TR schizophrenia: a pilot case-control association study in an Italian sample 94
A genome-wide pharmacogenomic study of patients with schizophrenia suggests that GRM7 mediates the effects of risperidone on positive symptoms 94
Phylogeography of Y-chromosome haplogroup I reveals distinct domains of prehistoric gene flow in Europe 93
Analysis of Copy Number Variations in Schizophrenia Italian Patients 88
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 87
New Copy Number Variations in Schizophrenia Italian Patients 85
Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients 84
The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool 83
Study of the genetic architecture behind mood disorders by whole exome sequencing on a large Italian pedigree 83
Mitochondrial DNA haplogroups and age at onset of schizophrenia 81
RESEARCH OF THE DISEASE-GENE IN A FAMILY AFFECTED BY A TYPE OF CEREBELLAR ATAXIA WITH AN UNKNOWN MOLECULAR DEFECT 80
Identification and molecular characterization of cryptic chromosomal rearrangements in mental retardation patients. 80
The effect of childhood trauma on blood transcriptome expression in major depressive disorder 79
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 78
Detection of high level of autozygosity in a group of Italian schizophrenia patients 76
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 73
The factor structure analysis for the positive and negative syndrome scale (PANSS) in pharmacogenetics and pharmacogenomics studies. 72
Exome sequencing of schizophrenia patients with high level of homozygosity identifies a homozygous novel mutation that reduces the glutamate acid decarboxylase 67 (GAD67) activity 70
Identification and characterization of an Xq26-27 duplication in a male with psycomotor retardation and craniofacial dysmorphisms 69
Genetic determinants of circulating VEGF levels in major depressive disorder and electroconvulsive therapy response 68
Association study between schizophrenia and the AMPA genes GRIA1, GRIA2 AND GRIA4 67
Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G Mutation 67
Genome wide study of Italian schizophrenia patients 67
Genes and MiRNAs in mental retardation patients with cryptic chromosome imbalances detected by SNP-based array analysis. 66
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shades light on the molecular origin of the rearrangement. 66
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium 64
Ricerca del gene malattia in una famiglia affetta da una forma di atassia cerebellare a difetto molecolare sconosciuto 62
Y-chromosome and mtDNA polymorphisms in Iraq, a crossroad of the early human dispersal and of post-Neolithic migration 61
Application of SNP-Arrays, FISH and GenotypeColour in Molecular Diagnosis of Mental Retardation 59
Genome-Wide pharmacogenomics analysis of early antipsychotic (risperidone) response in patients with schizophrenia 59
GenotypeColour: a coloured way of visualising SNPs and CNVs 58
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections. 58
Identificazione mediante exome sequencing di una variante del gene RBMXL1 in una famiglia affetta da atassia cerebellare pura 58
GenotypeColour: un modo colorato di rappresentare SNP e CNV 57
Rna editing and modifications in mood disorders 57
Application of SNP-arrays, FISH and genotypecolour in molecular diagnosis of mental retardation 54
The 49af Haplotype 11 is a new marker of the Eu19 lineage which traces migrations from Northern regions of the Black Sea 53
Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles 53
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 51
Association study between HTR2A rs6313 polymorphism and early response to risperidone and olanzapine in schizophrenia patients 49
Assessment of haptoglobin alleles in autism spectrum disorders 48
From surnames to history of Y chromosomes: the Sardinian population as a case test 47
Investigating an in silico approach for prioritizing antidepressant drug prescription based on drug-induced expression profiles and predicted gene expression 46
Analysis of Citalopram response heterogeneity among STAR*D patients using in-silico methods 45
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 42
Identificazione dei geni di suscettibilità per schizofrenia e disturbo bipolare in un selezionato campione di pazienti italiani 38
Clinical validation of a combinatorial PharmAcogeNomic approach in major Depressive disorder: an Observational prospective RAndomized, participant and rater-blinded, controlled trial (PANDORA trial) 30
Evidence of an interaction between FXR1 and GSK3β polymorphisms on levels of Negative Symptoms of Schizophrenia and their response to antipsychotics 20
Whole blood transcriptome characterization of 3xTg‐AD mouse and its modulation by transcranial direct current stimulation (TDCs) 14
Transcriptional Profiling of Rat Prefrontal Cortex after Acute Inescapable Footshock Stress 14
Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele 10
LRRK2 Kinase Inhibition Attenuates Astrocytic Activation in Response to Amyloid β1-42 Fibrils 7
Investigation on the high recurrence of the ATTRv-causing transthyretin variant Val142Ile in central Italy 6
Totale 7.416
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Categoria #
all - tutte 27.007
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 27.007
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019263 0 0 0 0 0 0 0 0 0 0 141 122
2019/20202.045 237 90 80 168 132 242 183 207 148 234 209 115
2020/20211.456 44 145 58 154 60 150 67 149 185 198 142 104
2021/2022686 56 127 31 10 10 25 36 27 42 90 67 165
2022/2023608 89 8 23 61 60 163 3 68 86 11 17 19
2023/2024629 42 21 66 65 40 187 18 17 144 29 0 0
Totale 7.416