IRIS Institutional Research Information System - OPENBS Open Archive UniBS

MAGRI, Chiara
 Distribuzione geografica
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Continente #
NA - Nord America 4.559
EU - Europa 3.258
AS - Asia 2.438
SA - Sud America 486
AF - Africa 46
OC - Oceania 16
Continente sconosciuto - Info sul continente non disponibili 4
Totale 10.807
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Nazione #
US - Stati Uniti d'America 4.454
PL - Polonia 1.310
CN - Cina 885
SG - Singapore 743
UA - Ucraina 499
IT - Italia 453
BR - Brasile 417
DE - Germania 274
HK - Hong Kong 242
VN - Vietnam 235
FI - Finlandia 200
GB - Regno Unito 133
FR - Francia 92
TR - Turchia 87
RU - Federazione Russa 84
IN - India 82
IE - Irlanda 75
CA - Canada 65
BD - Bangladesh 34
ID - Indonesia 33
BE - Belgio 22
ZA - Sudafrica 21
AR - Argentina 20
MX - Messico 20
NL - Olanda 20
CZ - Repubblica Ceca 19
SE - Svezia 19
SA - Arabia Saudita 18
EC - Ecuador 17
AT - Austria 15
AU - Australia 15
ES - Italia 13
JP - Giappone 13
IQ - Iraq 11
KE - Kenya 9
CO - Colombia 8
VE - Venezuela 8
LT - Lituania 7
MA - Marocco 7
PK - Pakistan 6
UZ - Uzbekistan 6
CH - Svizzera 5
CL - Cile 5
PY - Paraguay 5
TW - Taiwan 5
AL - Albania 4
BG - Bulgaria 4
BH - Bahrain 4
IL - Israele 4
JM - Giamaica 4
KG - Kirghizistan 4
KR - Corea 4
PT - Portogallo 4
TT - Trinidad e Tobago 4
DO - Repubblica Dominicana 3
DZ - Algeria 3
EG - Egitto 3
EU - Europa 3
HN - Honduras 3
IR - Iran 3
PA - Panama 3
PE - Perù 3
PH - Filippine 3
AE - Emirati Arabi Uniti 2
JO - Giordania 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
NO - Norvegia 2
SI - Slovenia 2
UY - Uruguay 2
AM - Armenia 1
CR - Costa Rica 1
ET - Etiopia 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
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 10.807
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Città #
Warsaw 1.306
Fairfield 463
Ashburn 409
Singapore 359
Woodbridge 342
Jacksonville 335
Ann Arbor 258
Hong Kong 240
Chandler 226
Houston 225
Beijing 189
Brescia 184
Cambridge 182
Seattle 173
New York 166
Wilmington 162
Princeton 148
Helsinki 109
Nanjing 109
Los Angeles 108
Dearborn 91
Dublin 75
Istanbul 69
Dong Ket 68
Munich 66
Des Moines 63
Ho Chi Minh City 61
The Dalles 57
Nanchang 48
Jinan 45
São Paulo 43
Dallas 42
Shanghai 42
Shenyang 41
Turku 41
San Francisco 39
Buffalo 37
Hebei 36
Moscow 32
Hanoi 31
Chicago 26
Jakarta 26
Redondo Beach 26
Toronto 26
Changsha 25
Jiaxing 23
Milan 23
Brussels 22
Boardman 21
Rio de Janeiro 21
San Diego 21
Santa Clara 20
Tianjin 19
Phoenix 18
Hangzhou 17
Zhengzhou 17
Montreal 16
Brooklyn 15
Haikou 15
London 15
Washington 15
Rome 14
Lancaster 13
Bolzano 12
Lanzhou 12
Ningbo 12
Nuremberg 12
Tokyo 12
Brno 11
Chennai 11
Guangzhou 11
Orem 11
Verona 11
Atlanta 10
Council Bluffs 10
Denver 10
Johannesburg 10
Stockholm 10
Belo Horizonte 9
Frankfurt am Main 9
Naples 9
Da Nang 8
Fuzhou 8
Mexico City 8
Redwood City 8
Salvador 8
San Mateo 8
Düsseldorf 7
Guayaquil 7
Jeddah 7
Kunming 7
Mumbai 7
Nairobi 7
Ninh Bình 7
Norwalk 7
Orange 7
Porto Alegre 7
Vienna 7
Bela-Bela 6
Boston 6
Totale 7.503
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Nome #
"GenotypeColour": colour visualisation of SNPs and CNVs 318
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement 318
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways 311
New Copy Number Variations in Schizophrenia 304
ITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiency 293
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 275
The effect of childhood trauma on blood transcriptome expression in major depressive disorder 253
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 227
Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia 213
Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional role. 204
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 204
Genomic restricted maximum likelihood (GREML) analysis to estimate the heritability of response/resistance in major depressive disorder (MDD) 197
New biological pathways for major depression: gene expression decomposition in G x E components 195
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. 189
A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme 186
De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay. 183
Proteasome system dysregulation and treatment resistance mechanisms in major depressive disorder 176
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia 170
Gene per la neuregulina 1 e schizofrenia: ulteriori evidenze di associazione 170
Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder 163
Role of allelic variants of FK506-binding protein 51 (FKBP5) gene in the development of anxiety disorders. 157
Analysis of Copy Number Variations in Schizophrenia Italian Patients 154
The Role of allelic variants of FK506-binding protein 51 (FKBP5) gene in the development of anxiety disorders 154
The GRM7 gene, early response to risperidone, and schizophrenia: a genome-wide association study and a confirmatory pharmacogenetic analysis 151
A genome-wide pharmacogenomic study of patients with schizophrenia suggests that GRM7 mediates the effects of risperidone on positive symptoms 149
Functional study of a novel homozygous mutation in the GAD1 gene, detected in a patient with schizophrenia. 148
De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia 147
Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients 129
RESEARCH OF THE DISEASE-GENE IN A FAMILY AFFECTED BY A TYPE OF CEREBELLAR ATAXIA WITH AN UNKNOWN MOLECULAR DEFECT 128
Saami and Berbers--an unexpected mitochondrial DNA link 128
Identification and molecular characterization of cryptic chromosomal rearrangements in mental retardation patients. 123
Association study between schizophrenia and the AMPA genes GRIA1, GRIA2 AND GRIA4 122
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
Phylogeography of Y-chromosome haplogroup I reveals distinct domains of prehistoric gene flow in Europe 121
Exome sequencing of schizophrenia patients with high level of homozygosity identifies a homozygous novel mutation that reduces the glutamate acid decarboxylase 67 (GAD67) activity 120
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
Association study between HTR2A rs6313 polymorphism and early response to risperidone and olanzapine in schizophrenia patients 116
Detection of high level of autozygosity in a group of Italian schizophrenia patients 115
Genetic determinants of circulating VEGF levels in major depressive disorder and electroconvulsive therapy response 115
New Copy Number Variations in Schizophrenia Italian Patients 114
The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool 113
The factor structure analysis for the positive and negative syndrome scale (PANSS) in pharmacogenetics and pharmacogenomics studies. 113
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 112
Identification and characterization of an Xq26-27 duplication in a male with psycomotor retardation and craniofacial dysmorphisms 111
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shades light on the molecular origin of the rearrangement. 109
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 105
Application of SNP-arrays, FISH and genotypecolour in molecular diagnosis of mental retardation 103
Mitochondrial DNA haplogroups and age at onset of schizophrenia 102
Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles 102
The effect of childhood trauma on blood transcriptome expression in major depressive disorder 101
Rna editing and modifications in mood disorders 101
Analysis of Citalopram response heterogeneity among STAR*D patients using in-silico methods 101
Genes and MiRNAs in mental retardation patients with cryptic chromosome imbalances detected by SNP-based array analysis. 100
Identificazione mediante exome sequencing di una variante del gene RBMXL1 in una famiglia affetta da atassia cerebellare pura 98
Ricerca del gene malattia in una famiglia affetta da una forma di atassia cerebellare a difetto molecolare sconosciuto 97
Investigating an in silico approach for prioritizing antidepressant drug prescription based on drug-induced expression profiles and predicted gene expression 97
Genome-Wide pharmacogenomics analysis of early antipsychotic (risperidone) response in patients with schizophrenia 96
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections. 95
Long-term effects of HLA A*03:01 genotype on anti-SARS-CoV-2 Spike antibody levels following BNT162b2 vaccine 94
Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G Mutation 93
Y-chromosome and mtDNA polymorphisms in Iraq, a crossroad of the early human dispersal and of post-Neolithic migration 92
Application of SNP-Arrays, FISH and GenotypeColour in Molecular Diagnosis of Mental Retardation 91
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
GenotypeColour: a coloured way of visualising SNPs and CNVs 87
The 49af Haplotype 11 is a new marker of the Eu19 lineage which traces migrations from Northern regions of the Black Sea 84
From surnames to history of Y chromosomes: the Sardinian population as a case test 82
Assessment of haptoglobin alleles in autism spectrum disorders 82
GenotypeColour: un modo colorato di rappresentare SNP e CNV 79
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 79
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 78
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 75
Whole blood transcriptome characterization of 3xTg‐AD mouse and its modulation by transcranial direct current stimulation (TDCs) 75
Transcriptional Profiling of Rat Prefrontal Cortex after Acute Inescapable Footshock Stress 72
Clinical validation of a combinatorial PharmAcogeNomic approach in major Depressive disorder: an Observational prospective RAndomized, participant and rater-blinded, controlled trial (PANDORA trial) 70
A miR-137–Related Biological Pathway of Risk for Schizophrenia Is Associated With Human Brain Emotion Processing 66
Identificazione dei geni di suscettibilità per schizofrenia e disturbo bipolare in un selezionato campione di pazienti italiani 62
LRRK2 Kinase Inhibition Attenuates Astrocytic Activation in Response to Amyloid β1-42 Fibrils 61
Investigation on the high recurrence of the ATTRv-causing transthyretin variant Val142Ile in central Italy 58
The role of MED22 and its transcriptional interactions with childhood trauma and trauma-focused psychotherapy in patients with major depressive disorder 57
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. 39
The interplay of hypoxia, inflammation, and microbiota as indicators of malignant transformation in oral potentially malignant disorders 18
Totale 11.085
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Categoria #
all - tutte 46.951
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 46.951
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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
2025/20262.002 303 408 221 466 382 222 0 0 0 0 0 0
Totale 11.085