IRIS Institutional Research Information System - OPENBS Open Archive UniBS

TRAVERSA, Michele
 Distribuzione geografica
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Continente #
NA - Nord America 1.582
EU - Europa 1.561
AS - Asia 435
OC - Oceania 5
SA - Sud America 2
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 3.587
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Nazione #
US - Stati Uniti d'America 1.579
PL - Polonia 860
CN - Cina 304
UA - Ucraina 231
IT - Italia 172
DE - Germania 80
FI - Finlandia 67
GB - Regno Unito 50
HK - Hong Kong 45
FR - Francia 43
VN - Vietnam 32
IE - Irlanda 30
SG - Singapore 27
IN - India 19
BE - Belgio 16
AU - Australia 4
CZ - Repubblica Ceca 4
CA - Canada 3
SE - Svezia 3
TR - Turchia 3
JP - Giappone 2
NL - Olanda 2
AR - Argentina 1
BD - Bangladesh 1
BG - Bulgaria 1
EC - Ecuador 1
ES - Italia 1
EU - Europa 1
ID - Indonesia 1
MY - Malesia 1
NZ - Nuova Zelanda 1
RU - Federazione Russa 1
ZA - Sudafrica 1
Totale 3.587
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Città #
Warsaw 860
Fairfield 171
Jacksonville 153
Ann Arbor 145
Woodbridge 144
Ashburn 132
Chandler 122
Houston 111
Brescia 98
Cambridge 61
Princeton 60
New York 58
Seattle 54
Wilmington 52
Beijing 46
Nanjing 45
Hong Kong 44
Helsinki 43
Dearborn 37
Dong Ket 32
Dublin 30
Shenyang 28
Jinan 27
Nanchang 24
Hebei 22
Des Moines 19
Brussels 16
Shanghai 15
Singapore 15
Los Angeles 14
Washington 14
Lancaster 13
Boardman 12
Changsha 12
Tianjin 11
San Diego 10
Zhengzhou 10
Jiaxing 9
Verona 9
Hangzhou 8
Fuzhou 7
Lanzhou 7
Norwalk 7
San Francisco 7
Ningbo 6
Haikou 5
Leawood 5
Mantova 5
Milan 5
Phoenix 5
Brno 4
Kunming 4
Redwood City 4
Hefei 3
Napoli 3
Orange 3
Taizhou 3
Auburn Hills 2
Canberra 2
Castenedolo 2
Kocaeli 2
London 2
Melbourne 2
Mirano 2
Ottawa 2
San Mateo 2
Tappahannock 2
Tokyo 2
Treviglio 2
Augusta 1
Baotou 1
Buenos Aires 1
Centurion 1
Cerea 1
Changchun 1
Dhaka 1
Esslingen am Neckar 1
Guangzhou 1
Guayaquil 1
Izhevsk 1
Jakarta 1
New Bedfont 1
Nogara 1
Oceanside 1
Rome 1
Serra D'aiello 1
Sofia 1
Taiyuan 1
Torino 1
Toronto 1
Trento 1
Wandsworth 1
Totale 2.916
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Nome #
Sorafenib induces variations of the DNA methylome in HA22T/VGH human hepatocellular carcinoma-derived cells 277
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement 261
New Copy Number Variations in Schizophrenia 260
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways 257
Clinical and molecular characterization of 40 patients with classic Ehlers--Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations. 204
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 204
Molecular characterization and transcriptome-wide expression profiling of two patients affected with spondyloepimetaphyseal dysplasia with joint laxity type 180
Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia 172
Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional role. 147
De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay. 131
The GRM7 gene, early response to risperidone, and schizophrenia: a genome-wide association study and a confirmatory pharmacogenetic analysis 120
De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia 115
A genome-wide pharmacogenomic study of patients with schizophrenia suggests that GRM7 mediates the effects of risperidone on positive symptoms 96
Analysis of Copy Number Variations in Schizophrenia Italian Patients 91
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 88
New Copy Number Variations in Schizophrenia Italian Patients 85
RESEARCH OF THE DISEASE-GENE IN A FAMILY AFFECTED BY A TYPE OF CEREBELLAR ATAXIA WITH AN UNKNOWN MOLECULAR DEFECT 82
Identification and molecular characterization of cryptic chromosomal rearrangements in mental retardation patients. 81
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 79
Detection of high level of autozygosity in a group of Italian schizophrenia patients 76
The factor structure analysis for the positive and negative syndrome scale (PANSS) in pharmacogenetics and pharmacogenomics studies. 74
Whole exome sequencing of schizophrenia patients with high level of autozygosity. 73
Identification and characterization of an Xq26-27 duplication in a male with psycomotor retardation and craniofacial dysmorphisms 71
Genome wide study of Italian schizophrenia patients 68
Genes and MiRNAs in mental retardation patients with cryptic chromosome imbalances detected by SNP-based array analysis. 67
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shades light on the molecular origin of the rearrangement. 67
Ricerca del gene malattia in una famiglia affetta da una forma di atassia cerebellare a difetto molecolare sconosciuto 63
Application of SNP-Arrays, FISH and GenotypeColour in Molecular Diagnosis of Mental Retardation 60
Genome-Wide pharmacogenomics analysis of early antipsychotic (risperidone) response in patients with schizophrenia 60
Identificazione mediante exome sequencing di una variante del gene RBMXL1 in una famiglia affetta da atassia cerebellare pura 60
Application of SNP-arrays, FISH and genotypecolour in molecular diagnosis of mental retardation 55
Totale 3.724
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Categoria #
all - tutte 11.304
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 11.304
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.007 117 49 48 82 63 110 78 98 68 107 133 54
2020/2021627 22 64 19 66 34 67 20 70 95 78 52 40
2021/2022266 26 60 3 1 9 9 7 10 13 28 34 66
2022/2023293 34 6 8 34 36 69 0 42 43 3 7 11
2023/2024324 19 8 38 26 21 104 3 8 46 16 0 35
2024/20253 3 0 0 0 0 0 0 0 0 0 0 0
Totale 3.724