IRIS Institutional Research Information System - OPENBS Open Archive UniBS

MAGRI, Chiara
 Distribuzione geografica
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Continente #
NA - Nord America 4.469
EU - Europa 3.250
AS - Asia 2.365
SA - Sud America 477
AF - Africa 45
OC - Oceania 16
Continente sconosciuto - Info sul continente non disponibili 4
Totale 10.626
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Nazione #
US - Stati Uniti d'America 4.370
PL - Polonia 1.309
CN - Cina 876
SG - Singapore 728
UA - Ucraina 499
IT - Italia 450
BR - Brasile 412
DE - Germania 274
HK - Hong Kong 240
FI - Finlandia 200
VN - Vietnam 199
GB - Regno Unito 132
FR - Francia 92
TR - Turchia 87
RU - Federazione Russa 82
IN - India 78
IE - Irlanda 75
CA - Canada 63
ID - Indonesia 32
BD - Bangladesh 31
BE - Belgio 22
ZA - Sudafrica 21
NL - Olanda 20
CZ - Repubblica Ceca 19
MX - Messico 19
AR - Argentina 18
SA - Arabia Saudita 18
SE - Svezia 18
EC - Ecuador 17
AT - Austria 15
AU - Australia 15
ES - Italia 13
JP - Giappone 13
IQ - Iraq 10
KE - Kenya 9
CO - Colombia 8
LT - Lituania 7
MA - Marocco 7
VE - Venezuela 7
PK - Pakistan 6
CH - Svizzera 5
CL - Cile 5
PY - Paraguay 5
TW - Taiwan 5
UZ - Uzbekistan 5
AL - Albania 4
BG - Bulgaria 4
IL - Israele 4
JM - Giamaica 4
KG - Kirghizistan 4
KR - Corea 4
PT - Portogallo 4
TT - Trinidad e Tobago 4
BH - Bahrain 3
DZ - Algeria 3
EG - Egitto 3
EU - Europa 3
HN - Honduras 3
IR - Iran 3
PE - Perù 3
PH - Filippine 3
AE - Emirati Arabi Uniti 2
DO - Repubblica Dominicana 2
JO - Giordania 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
NO - Norvegia 2
PA - Panama 2
SI - Slovenia 2
AM - Armenia 1
FK - Isole Falkland (Malvinas) 1
GE - Georgia 1
GR - Grecia 1
GT - Guatemala 1
HU - Ungheria 1
MU - Mauritius 1
NG - Nigeria 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PS - Palestinian Territory 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
TJ - Tagikistan 1
UY - Uruguay 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 10.626
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Città #
Warsaw 1.305
Fairfield 463
Ashburn 390
Singapore 344
Woodbridge 342
Jacksonville 335
Ann Arbor 258
Hong Kong 238
Chandler 226
Houston 225
Beijing 189
Brescia 183
Cambridge 182
Seattle 173
New York 162
Wilmington 162
Princeton 148
Helsinki 109
Nanjing 109
Los Angeles 104
Dearborn 91
Dublin 75
Istanbul 69
Dong Ket 68
Munich 66
Des Moines 63
Ho Chi Minh City 55
Nanchang 48
Jinan 45
Dallas 42
Shanghai 42
Shenyang 41
Turku 41
São Paulo 40
San Francisco 39
Buffalo 37
Hebei 36
Moscow 31
The Dalles 29
Chicago 26
Hanoi 26
Redondo Beach 26
Toronto 26
Changsha 25
Jakarta 25
Jiaxing 23
Milan 23
Brussels 22
Boardman 21
Rio de Janeiro 21
San Diego 21
Santa Clara 19
Tianjin 19
Hangzhou 17
Phoenix 17
Zhengzhou 17
Haikou 15
London 15
Washington 15
Brooklyn 14
Montreal 14
Rome 14
Lancaster 13
Bolzano 12
Lanzhou 12
Ningbo 12
Nuremberg 12
Tokyo 12
Brno 11
Guangzhou 11
Verona 11
Denver 10
Johannesburg 10
Belo Horizonte 9
Chennai 9
Frankfurt am Main 9
Naples 9
Orem 9
Stockholm 9
Fuzhou 8
Mexico City 8
Redwood City 8
Salvador 8
San Mateo 8
Atlanta 7
Düsseldorf 7
Guayaquil 7
Jeddah 7
Kunming 7
Mumbai 7
Nairobi 7
Norwalk 7
Orange 7
Porto Alegre 7
Vienna 7
Bela-Bela 6
Brasília 6
Charlotte 6
Curitiba 6
Kyiv 6
Totale 7.393
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Nome #
"GenotypeColour": colour visualisation of SNPs and CNVs 316
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement 314
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways 309
New Copy Number Variations in Schizophrenia 302
ITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiency 292
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 269
The effect of childhood trauma on blood transcriptome expression in major depressive disorder 252
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 224
Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia 212
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 201
Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional role. 198
Genomic restricted maximum likelihood (GREML) analysis to estimate the heritability of response/resistance in major depressive disorder (MDD) 195
New biological pathways for major depression: gene expression decomposition in G x E components 191
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. 187
A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme 184
De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay. 181
Proteasome system dysregulation and treatment resistance mechanisms in major depressive disorder 172
Gene per la neuregulina 1 e schizofrenia: ulteriori evidenze di associazione 169
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia 168
Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder 162
Role of allelic variants of FK506-binding protein 51 (FKBP5) gene in the development of anxiety disorders. 154
The Role of allelic variants of FK506-binding protein 51 (FKBP5) gene in the development of anxiety disorders 151
Analysis of Copy Number Variations in Schizophrenia Italian Patients 150
The GRM7 gene, early response to risperidone, and schizophrenia: a genome-wide association study and a confirmatory pharmacogenetic analysis 149
A genome-wide pharmacogenomic study of patients with schizophrenia suggests that GRM7 mediates the effects of risperidone on positive symptoms 148
De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia 146
Functional study of a novel homozygous mutation in the GAD1 gene, detected in a patient with schizophrenia. 146
Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients 128
Saami and Berbers--an unexpected mitochondrial DNA link 125
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 122
RESEARCH OF THE DISEASE-GENE IN A FAMILY AFFECTED BY A TYPE OF CEREBELLAR ATAXIA WITH AN UNKNOWN MOLECULAR DEFECT 121
Association study between schizophrenia and the AMPA genes GRIA1, GRIA2 AND GRIA4 119
Phylogeography of Y-chromosome haplogroup I reveals distinct domains of prehistoric gene flow in Europe 119
Exome sequencing of schizophrenia patients with high level of homozygosity identifies a homozygous novel mutation that reduces the glutamate acid decarboxylase 67 (GAD67) activity 119
Identification and molecular characterization of cryptic chromosomal rearrangements in mental retardation patients. 118
Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM-IV-TR schizophrenia: a pilot case-control association study in an Italian sample 117
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 117
New Copy Number Variations in Schizophrenia Italian Patients 113
Detection of high level of autozygosity in a group of Italian schizophrenia patients 113
Association study between HTR2A rs6313 polymorphism and early response to risperidone and olanzapine in schizophrenia patients 113
The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool 112
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 112
Genetic determinants of circulating VEGF levels in major depressive disorder and electroconvulsive therapy response 112
The factor structure analysis for the positive and negative syndrome scale (PANSS) in pharmacogenetics and pharmacogenomics studies. 111
Identification and characterization of an Xq26-27 duplication in a male with psycomotor retardation and craniofacial dysmorphisms 109
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shades light on the molecular origin of the rearrangement. 107
Study of the genetic architecture behind mood disorders by whole exome sequencing on a large Italian pedigree 106
Genome wide study of Italian schizophrenia patients 103
Application of SNP-arrays, FISH and genotypecolour in molecular diagnosis of mental retardation 101
The effect of childhood trauma on blood transcriptome expression in major depressive disorder 101
Mitochondrial DNA haplogroups and age at onset of schizophrenia 101
Genes and MiRNAs in mental retardation patients with cryptic chromosome imbalances detected by SNP-based array analysis. 99
Analysis of Citalopram response heterogeneity among STAR*D patients using in-silico methods 99
Identificazione mediante exome sequencing di una variante del gene RBMXL1 in una famiglia affetta da atassia cerebellare pura 97
Rna editing and modifications in mood disorders 97
Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles 97
Investigating an in silico approach for prioritizing antidepressant drug prescription based on drug-induced expression profiles and predicted gene expression 96
Ricerca del gene malattia in una famiglia affetta da una forma di atassia cerebellare a difetto molecolare sconosciuto 95
Genome-Wide pharmacogenomics analysis of early antipsychotic (risperidone) response in patients with schizophrenia 95
Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G Mutation 93
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections. 93
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 91
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium 91
Y-chromosome and mtDNA polymorphisms in Iraq, a crossroad of the early human dispersal and of post-Neolithic migration 91
Application of SNP-Arrays, FISH and GenotypeColour in Molecular Diagnosis of Mental Retardation 90
Long-term effects of HLA A*03:01 genotype on anti-SARS-CoV-2 Spike antibody levels following BNT162b2 vaccine 87
GenotypeColour: a coloured way of visualising SNPs and CNVs 86
The 49af Haplotype 11 is a new marker of the Eu19 lineage which traces migrations from Northern regions of the Black Sea 84
Assessment of haptoglobin alleles in autism spectrum disorders 81
From surnames to history of Y chromosomes: the Sardinian population as a case test 80
GenotypeColour: un modo colorato di rappresentare SNP e CNV 78
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 78
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 77
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 72
Whole blood transcriptome characterization of 3xTg‐AD mouse and its modulation by transcranial direct current stimulation (TDCs) 71
Clinical validation of a combinatorial PharmAcogeNomic approach in major Depressive disorder: an Observational prospective RAndomized, participant and rater-blinded, controlled trial (PANDORA trial) 68
Transcriptional Profiling of Rat Prefrontal Cortex after Acute Inescapable Footshock Stress 68
Identificazione dei geni di suscettibilità per schizofrenia e disturbo bipolare in un selezionato campione di pazienti italiani 62
Investigation on the high recurrence of the ATTRv-causing transthyretin variant Val142Ile in central Italy 58
LRRK2 Kinase Inhibition Attenuates Astrocytic Activation in Response to Amyloid β1-42 Fibrils 57
A miR-137–Related Biological Pathway of Risk for Schizophrenia Is Associated With Human Brain Emotion Processing 57
The role of MED22 and its transcriptional interactions with childhood trauma and trauma-focused psychotherapy in patients with major depressive disorder 55
Evidence of an interaction between FXR1 and GSK3β polymorphisms on levels of Negative Symptoms of Schizophrenia and their response to antipsychotics 51
Profiling of miR-98-5p, miR-130a-3p, and miR-1246 levels in tissue and liquid biopsies of patients with hepatocellular carcinoma. 34
The interplay of hypoxia, inflammation, and microbiota as indicators of malignant transformation in oral potentially malignant disorders 15
Totale 10.904
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Categoria #
all - tutte 46.390
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 46.390
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021995 0 0 0 0 0 150 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
2023/2024744 42 21 66 65 40 187 18 17 144 29 9 106
2024/20251.552 13 25 12 210 148 128 108 58 168 126 308 248
2025/20261.821 303 408 221 466 382 41 0 0 0 0 0 0
Totale 10.904