MAGI, ALBERTO
 Distribuzione geografica
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Continente #
EU - Europa 5.819
NA - Nord America 4.593
AS - Asia 822
AF - Africa 21
Continente sconosciuto - Info sul continente non disponibili 1
SA - Sud America 1
Totale 11.257
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Nazione #
US - Stati Uniti d'America 4.582
PL - Polonia 3.151
RU - Federazione Russa 1.163
IT - Italia 536
IE - Irlanda 363
SE - Svezia 277
CN - Cina 235
SG - Singapore 174
HK - Hong Kong 166
IN - India 84
CH - Svizzera 76
DE - Germania 76
JO - Giordania 67
VN - Vietnam 66
FI - Finlandia 49
GB - Regno Unito 44
UA - Ucraina 20
ES - Italia 18
CI - Costa d'Avorio 17
TR - Turchia 17
CA - Canada 11
KR - Corea 10
BE - Belgio 9
FR - Francia 9
NL - Olanda 8
AT - Austria 5
EE - Estonia 3
EG - Egitto 3
GR - Grecia 3
RO - Romania 3
MT - Malta 2
AE - Emirati Arabi Uniti 1
BG - Bulgaria 1
BR - Brasile 1
BY - Bielorussia 1
CZ - Repubblica Ceca 1
EU - Europa 1
IL - Israele 1
PT - Portogallo 1
SC - Seychelles 1
TH - Thailandia 1
Totale 11.257
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Città #
Warsaw 3.150
Fairfield 782
Chandler 410
Ashburn 407
Woodbridge 353
Dublin 350
Seattle 346
Cambridge 318
Houston 274
Wilmington 273
Florence 155
Singapore 146
Altamura 136
Lawrence 134
Ann Arbor 129
Hong Kong 101
Beijing 94
Princeton 93
Bern 75
Mumbai 70
Boston 61
San Diego 59
Boardman 55
Dong Ket 54
Shanghai 50
Buffalo 46
Jacksonville 36
New York 36
Medford 29
Moscow 27
Kent 24
Phoenix 20
Santa Clara 20
Barcelona 18
Abidjan 17
Bremen 17
Redwood City 17
Hillsboro 16
Izmir 16
Rome 14
Dearborn 13
Falls Church 13
Los Angeles 13
Siena 13
Norwalk 12
Andover 11
Fontebuona 11
Pune 10
Toronto 9
Brussels 8
Shenzhen 8
Tappahannock 8
Washington 8
Guangzhou 7
Pian di Scò 7
Seoul 7
Bologna 6
Fondi 6
Grafing 6
Helsinki 6
Milan 6
Fiesole 5
London 5
Munich 5
Vienna 5
Yubileyny 5
Padova 4
Prato 4
Verona 4
West Jordan 4
Zhengzhou 4
Cairo 3
Carrara 3
Chennai 3
Kilburn 3
Lappeenranta 3
Messina 3
Naaldwijk 3
Nanjing 3
Pavia 3
Pisa 3
Sesto Fiorentino 3
Tartu 3
Timisoara 3
Amsterdam 2
Arezzo 2
Arzachena 2
Auburn Hills 2
Castelliri 2
Cremona 2
Frankfurt am Main 2
Fuzhou 2
Hefei 2
Kunming 2
Lucca 2
Melita 2
Montepulciano 2
Paris 2
Redmond 2
San Mateo 2
Totale 8.732
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Nome #
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm. 283
Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2 271
Desmoglein-2-integrin Beta-8 interaction regulates actin assembly in endothelial cells: deregulation in systemic sclerosis 270
RNA sequencing reveals a distinct transcriptomic profile predictive of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 263
Sphingosine 1-phosphate induces differentiation of mesoangioblasts towards smooth muscle. A role for GATA6. 263
Characterization and identification of hidden rare variants in the human genome 260
Detection of Genomic Structural Variants from Next-Generation Sequencing Data 258
WNP: A Novel Algorithm for Gene Products Annotation from Weighted Functional Networks. 251
Carotid artery disease: Novel pathophysiological mechanisms identified by gene-expression profiling of peripheral blood 250
Moment estimation in discrete shifting level model applied to fast array-CGH segmentation 245
Gene expression profiling of peripheral blood in patients with abdominal aortic aneurysm 235
EXCAVATOR: detecting copy number variants from whole-exome sequencing data 235
High-throughput multiplex single-nucleotide polymorphism (SNP) analysis in genes involved in methionine metabolism 231
Gene expression profile of rat left ventricles reveals persisting changes following chronic mild exercise protocol: implications for cardioprotection 226
Editorial: Repetitive Structures in Biological Sequences: Algorithms and Applications 225
Using a calibration experiment to assess gene-specific information: full Bayesian and empirical Bayesian models for two-channel microarray data. 220
Early-onset ischaemic stroke: analysis of 58 polymorphisms in 17 genes involved in methionine metabolism 208
SLMSuite: a suite of algorithms for segmenting genomic profiles 208
A model of anti-angiogenesis: differential transcriptosome profiling of microvascular endothelial cells from diffuse systemic sclerosis patients. 205
Epilepsy with auditory features: A heterogeneous clinico-molecular disease 192
Apolipoprotein(a) kringle-IV type 2 copy number variation is associated with venous thromboembolism 190
Correction: Desmoglein-2-integrin Beta-8 interaction regulates actin assembly in endothelial cells: Deregulation in Systemic sclerosis (PLoS ONE (2013) 8, 7, (e68117) doi: 10.1371/journal.pone.0068117) 173
H3M2: Detection of runs of homozygosity from whole-exome sequencing data 170
Genetic bases of bicuspid aortic valve: The contribution of traditional and high-throughput sequencing approaches on research and diagnosis 155
Acute kidney injury promotes development of papillary renal cell adenoma and carcinoma from renal progenitor cells. 147
The ion channels and transporters gene expression profile indicates a shift in excitability and metabolisms during malignant progression of Follicular Lymphoma 146
Genome-wide copy number analysis in pediatric glioblastoma multiforme. 141
Nanopore sequencing data analysis: state of the art, applications and challenges 138
Read count approach for DNA copy number variants detection. 136
Bicuspid Aortic Valve: Role of Multiple Gene Variants in Influencing the Clinical Phenotype 135
A microRNA profile of pediatric glioblastoma: The role of NUCKS1 upregulation 125
Characterization of MinION nanopore data for resequencing analyses 125
A transcriptomic profile predicts clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 125
EX-HOM (EXome HOMozygosity): A Proof of Principle. 124
A very fast and accurate method for calling aberrations in array-CGH data. 121
372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment. 121
Nano-GLADIATOR: real-time detection of copy number alterations from nanopore sequencing data 119
RNA sequencing reveals PNN and KCNQ1OT1 as predictive biomarkers of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 117
The antiangiogenic tissue kallikrein pattern of endothelial cells in systemic sclerosis. 110
Involvement of RUNX1 Pathway Is a Common Event in the Leukemic Transformation of Chronic Myeloproliferative Neoplasms (MPNs) 107
A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria. 105
A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria. 103
D13Global gene expression profile reveals a distinct transcriptomic profile predictive of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 103
Abstract 2471: Pan-cancer catalog of Differentially Methylated Regions by Rocker-meth, a new computational method 102
Genetic analysis of 56 polymorphisms in 17 genes involved in methionine metabolism in patients with abdominal aortic aneurysm. 100
H3M2: detection of runs of homozygosity from whole-exome sequencing data. 100
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman 100
A new hybrid approach for MHC genotyping: high-throughput NGS and long read MinION nanopore sequencing, with application to the non-model vertebrate Alpine chamois (Rupicapra rupicapra) 99
Discovering chimeric transcripts in paired-end RNA-seq data by using EricScript. 98
Bioinformatics for Next Generation Sequencing Data 97
Long Reads, Short Time: Feasibility of Prenatal Sample Karyotyping by Nanopore Genome Sequencing 97
Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type i reveals candidate genes for cranio-facial development 97
Xome-Blender: A novel cancer genome simulator 95
The Coenzyme Q10 (CoQ10) as Countermeasure for Retinal Damage Onboard the International Space Station: the CORM Project 93
5Genome-wide identification of actionable copy number alterations from targeted sequencing panels with Excavator2 93
Differentiation of crescent-forming kidney progenitor cells into podocytes attenuates severe glomerulonephritis in mice 92
THIRD GENERATION SEQUENCING OF NORMAL KARYOTYPE ACUTE MYELOID LEUKEMIA: IMPLICATIONS FOR PROGNOSIS 89
Assessment of fibrinolytic activity by measuring the lysis time of a tissue-factor-induced clot: a feasibility evaluation. 89
Genetic and nutritional factors determining circulating levels of lipoprotein(a): results of the "Montignoso Study" 88
6Precision Trial Designer: A computational tool to assist in the design of genomics-driven trials in oncology 88
PyPore: a python toolbox for nanopore sequencing data handling 87
A shifting level model algorithm that identifies aberrations in array-CGH data 86
Using XCAVATOR and EXCAVATOR2 to Identify CNVs from WGS, WES, and TS Data 86
GENE-03. MICRORNAS PROFILE IN PAEDIATRIC GBMS 84
Sanger Validation of High-Throughput Sequencing in Genetic Diagnosis: Still the Best Practice? 83
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients 83
XCAVATOR: Accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experiments 82
Genetic polymorphisms of antioxidant enzymes as risk factors for oxidative stress-associated complications in preterm infants. 81
Versatile Quality Control Methods for Nanopore Sequencing 80
Global gene expression profile reveals a distinct transcriptomic profile predictive of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 76
3Precision systems medicine in urological Tumors – Molecular profiling and functional testing 75
Effect of space flight on the behavior of human retinal pigment epithelial ARPE-19 cells and evaluation of coenzyme Q10 treatment 75
VISOR: a versatile haplotype-aware structural variant simulator for short and long read sequencing 69
Heterogeneous magnitude of immunological memory to SARS-CoV-2 in recovered individuals 68
Precision Trial Drawer, a Computational Tool to Assist Planning of Genomics-Driven Trials in Oncology 67
Detection of runs of homozygosity from whole exome sequencing data: state of the art and perspectives for clinical, population and epidemiological studies. 66
AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics 65
NANOR: A user-friendly R package to analyze and compare nanopore sequencing data 62
Charting differentially methylated regions in cancer with Rocker-meth 59
Tubular cell polyploidy protects from lethal acute kidney injury but promotes consequent chronic kidney disease 59
TRPA1 mediates damage of the retina induced by ischemia and reperfusion in mice 57
TRiCoLOR: tandem repeat profiling using whole-genome long-read sequencing data 55
β3-adrenergic receptor on tumor-infiltrating lymphocytes sustains IFN-γ-dependent PD-L1 expression and impairs anti-tumor immunity in neuroblastoma 52
Evaluation of Germline Structural Variant Calling Methods for Nanopore Sequencing Data 48
Third-Generation Cytogenetic Analysis: Diagnostic Application of Long-Read Sequencing 45
From multitude to singularity: An up-to-date overview of scRNA-seq data generation and analysis 45
Clonally expanded PD-1-expressing T cells are enriched in synovial fluid of juvenile idiopathic arthritis patients 42
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization. 40
High-resolution Nanopore methylome-maps reveal random hyper-methylation at CpG-poor regions as driver of chemoresistance in leukemias 38
Polyploid tubular cells initiate a TGF-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury 35
Digital droplet PCR versus quantitative PCR for lipoprotein (a) kringle IV type 2 repeat polymorphism genetic characterization 26
Benzo[a]pyrene impairs the migratory ability of human GnRH neuroblasts through the inhibition of RhoA/ROCK pathway 22
GASOLINE: detecting germline and somatic structural variants from long-reads data 11
Totale 11.461
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Categoria #
all - tutte 30.690
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 30.690
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.044 0 0 0 145 257 335 278 320 268 195 202 44
2020/20211.691 122 172 95 249 90 134 107 147 138 279 63 95
2021/2022688 31 33 60 26 78 43 22 55 31 49 105 155
2022/20231.899 159 377 102 104 136 302 213 113 196 18 74 105
2023/2024716 37 57 99 45 55 108 44 131 17 30 47 46
2024/20251.559 152 496 297 614 0 0 0 0 0 0 0 0
Totale 11.461