MAGI, ALBERTO
 Distribuzione geografica
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Continente #
NA - Nord America 9.187
EU - Europa 7.925
AS - Asia 3.786
SA - Sud America 431
Continente sconosciuto - Info sul continente non disponibili 230
AF - Africa 98
OC - Oceania 44
Totale 21.701
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Nazione #
US - Stati Uniti d'America 9.007
PL - Polonia 3.170
RU - Federazione Russa 1.775
IT - Italia 1.389
SG - Singapore 1.105
CN - Cina 934
HK - Hong Kong 480
VN - Vietnam 402
IE - Irlanda 368
BR - Brasile 341
SE - Svezia 293
KR - Corea 261
DE - Germania 206
FR - Francia 169
IN - India 139
GB - Regno Unito 130
FI - Finlandia 126
CA - Canada 121
BD - Bangladesh 114
CH - Svizzera 81
NL - Olanda 75
ID - Indonesia 74
JO - Giordania 73
AU - Australia 41
AR - Argentina 39
JP - Giappone 39
ES - Italia 35
TR - Turchia 35
IQ - Iraq 33
UA - Ucraina 25
ZA - Sudafrica 24
MX - Messico 21
CI - Costa d'Avorio 20
BE - Belgio 19
PK - Pakistan 16
EC - Ecuador 13
NG - Nigeria 12
AT - Austria 10
UZ - Uzbekistan 10
EG - Egitto 9
PY - Paraguay 9
IL - Israele 8
MY - Malesia 8
TW - Taiwan 8
VE - Venezuela 8
AE - Emirati Arabi Uniti 7
CO - Colombia 7
RO - Romania 7
TH - Thailandia 7
CR - Costa Rica 6
GR - Grecia 6
KE - Kenya 6
PH - Filippine 6
CZ - Repubblica Ceca 5
EE - Estonia 5
GT - Guatemala 5
JM - Giamaica 5
PA - Panama 5
AZ - Azerbaigian 4
BJ - Benin 4
BY - Bielorussia 4
CL - Cile 4
ET - Etiopia 4
HN - Honduras 4
MA - Marocco 4
NI - Nicaragua 4
PE - Perù 4
PT - Portogallo 4
BG - Bulgaria 3
BO - Bolivia 3
DZ - Algeria 3
LB - Libano 3
LT - Lituania 3
MT - Malta 3
NZ - Nuova Zelanda 3
SA - Arabia Saudita 3
SC - Seychelles 3
SN - Senegal 3
TN - Tunisia 3
UY - Uruguay 3
BH - Bahrain 2
CW - ???statistics.table.value.countryCode.CW??? 2
DO - Repubblica Dominicana 2
GI - Gibilterra 2
HU - Ungheria 2
KH - Cambogia 2
KZ - Kazakistan 2
NP - Nepal 2
PR - Porto Rico 2
RS - Serbia 2
SI - Slovenia 2
SV - El Salvador 2
TT - Trinidad e Tobago 2
AL - Albania 1
AO - Angola 1
BF - Burkina Faso 1
BQ - ???statistics.table.value.countryCode.BQ??? 1
CY - Cipro 1
DK - Danimarca 1
EU - Europa 1
Totale 21.461
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Città #
Warsaw 3.164
Santa Clara 1.666
Ashburn 1.231
Singapore 808
Fairfield 783
Chandler 412
Hong Kong 406
San Jose 380
Dublin 355
Woodbridge 354
Seattle 353
Cambridge 319
Houston 283
Wilmington 274
Seoul 255
Florence 220
Beijing 218
Milan 203
Council Bluffs 156
Altamura 136
Hefei 136
Lawrence 134
Los Angeles 131
Ann Arbor 129
The Dalles 123
Ho Chi Minh City 117
Buffalo 108
Princeton 93
Rome 91
Lauterbourg 89
New York 85
Munich 78
Mumbai 77
Bern 75
Boston 72
Hanoi 72
Shanghai 65
Phoenix 63
Dallas 62
Moscow 62
San Diego 60
Boardman 59
Dong Ket 54
Jakarta 54
Paris 52
Helsinki 47
Melbourne 39
Tokyo 38
Jacksonville 37
Kent 37
Bologna 32
Medford 30
São Paulo 30
Turku 30
Naples 29
Toronto 26
Clifton 24
London 24
Guangzhou 22
Da Nang 21
Montreal 21
Abidjan 20
Barcelona 18
Brooklyn 18
Frankfurt am Main 18
Orem 18
Bremen 17
Redwood City 17
Chicago 16
Hillsboro 16
Izmir 16
Redondo Beach 16
Turin 16
Atlanta 14
Dearborn 14
Johannesburg 14
Shenzhen 14
Siena 14
Washington 14
Baghdad 13
Changsha 13
Falls Church 13
Palermo 13
Poplar 13
Abuja 12
Norwalk 12
Pune 12
Rio de Janeiro 12
Tianjin 12
Andover 11
Charlotte 11
Denver 11
Fontebuona 11
Stockholm 11
Verona 11
Bari 10
Brussels 10
Elk Grove Village 10
San Francisco 10
Amsterdam 9
Totale 15.134
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Nome #
High-throughput multiplex single-nucleotide polymorphism (SNP) analysis in genes involved in methionine metabolism 391
Desmoglein-2-integrin Beta-8 interaction regulates actin assembly in endothelial cells: deregulation in systemic sclerosis 385
Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2 381
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm. 376
Acute kidney injury promotes development of papillary renal cell adenoma and carcinoma from renal progenitor cells. 375
RNA sequencing reveals a distinct transcriptomic profile predictive of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 360
Moment estimation in discrete shifting level model applied to fast array-CGH segmentation 355
Detection of Genomic Structural Variants from Next-Generation Sequencing Data 347
Characterization and identification of hidden rare variants in the human genome 345
WNP: A Novel Algorithm for Gene Products Annotation from Weighted Functional Networks. 342
Sphingosine 1-phosphate induces differentiation of mesoangioblasts towards smooth muscle. A role for GATA6. 336
Carotid artery disease: Novel pathophysiological mechanisms identified by gene-expression profiling of peripheral blood 334
Using a calibration experiment to assess gene-specific information: full Bayesian and empirical Bayesian models for two-channel microarray data. 316
Gene expression profiling of peripheral blood in patients with abdominal aortic aneurysm 315
EXCAVATOR: detecting copy number variants from whole-exome sequencing data 314
A model of anti-angiogenesis: differential transcriptosome profiling of microvascular endothelial cells from diffuse systemic sclerosis patients. 310
Early-onset ischaemic stroke: analysis of 58 polymorphisms in 17 genes involved in methionine metabolism 298
SLMSuite: a suite of algorithms for segmenting genomic profiles 298
Apolipoprotein(a) kringle-IV type 2 copy number variation is associated with venous thromboembolism 287
Gene expression profile of rat left ventricles reveals persisting changes following chronic mild exercise protocol: implications for cardioprotection 281
Differentiation of crescent-forming kidney progenitor cells into podocytes attenuates severe glomerulonephritis in mice 274
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) 262
Bicuspid Aortic Valve: Role of Multiple Gene Variants in Influencing the Clinical Phenotype 259
Editorial: Repetitive Structures in Biological Sequences: Algorithms and Applications 257
Genetic bases of bicuspid aortic valve: The contribution of traditional and high-throughput sequencing approaches on research and diagnosis 256
Nanopore sequencing data analysis: state of the art, applications and challenges 252
RNA sequencing reveals PNN and KCNQ1OT1 as predictive biomarkers of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 244
The ion channels and transporters gene expression profile indicates a shift in excitability and metabolisms during malignant progression of Follicular Lymphoma 243
A transcriptomic profile predicts clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 242
A microRNA profile of pediatric glioblastoma: The role of NUCKS1 upregulation 239
Epilepsy with auditory features: A heterogeneous clinico-molecular disease 239
Genome-wide copy number analysis in pediatric glioblastoma multiforme. 235
Involvement of RUNX1 Pathway Is a Common Event in the Leukemic Transformation of Chronic Myeloproliferative Neoplasms (MPNs) 233
Characterization of MinION nanopore data for resequencing analyses 229
PoreMeth2: decoding the evolution of methylome alterations with Nanopore sequencing 224
372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment. 221
H3M2: Detection of runs of homozygosity from whole-exome sequencing data 220
AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics 217
A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria. 216
THIRD GENERATION SEQUENCING OF NORMAL KARYOTYPE ACUTE MYELOID LEUKEMIA: IMPLICATIONS FOR PROGNOSIS 213
D13Global gene expression profile reveals a distinct transcriptomic profile predictive of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 207
BaP inhibits human GnRH neuron migration by altering the RhoA pathway 205
Global gene expression profile reveals a distinct transcriptomic profile predictive of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 204
GENE-03. MICRORNAS PROFILE IN PAEDIATRIC GBMS 203
A very fast and accurate method for calling aberrations in array-CGH data. 202
Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type i reveals candidate genes for cranio-facial development 199
Xome-Blender: A novel cancer genome simulator 198
BPS2025 - Long-term effect of Mavacamten impact force and sarcomere density in a MYBPC3 iPSC-cardiomyocyte model of hypertrophic cardiomyopathy 196
The antiangiogenic tissue kallikrein pattern of endothelial cells in systemic sclerosis. 196
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients 196
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) 195
β3-adrenergic receptor on tumor-infiltrating lymphocytes sustains IFN-γ-dependent PD-L1 expression and impairs anti-tumor immunity in neuroblastoma 194
Nano-GLADIATOR: real-time detection of copy number alterations from nanopore sequencing data 193
Read count approach for DNA copy number variants detection. 192
5Genome-wide identification of actionable copy number alterations from targeted sequencing panels with Excavator2 191
Genetic and nutritional factors determining circulating levels of lipoprotein(a): results of the "Montignoso Study" 191
Clonally expanded PD-1-expressing T cells are enriched in synovial fluid of juvenile idiopathic arthritis patients 189
The Coenzyme Q10 (CoQ10) as Countermeasure for Retinal Damage Onboard the International Space Station: the CORM Project 189
A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria. 188
Abstract 2471: Pan-cancer catalog of Differentially Methylated Regions by Rocker-meth, a new computational method 188
Tubular cell polyploidy protects from lethal acute kidney injury but promotes consequent chronic kidney disease 185
Genetic analysis of 56 polymorphisms in 17 genes involved in methionine metabolism in patients with abdominal aortic aneurysm. 184
H3M2: detection of runs of homozygosity from whole-exome sequencing data. 183
EX-HOM (EXome HOMozygosity): A Proof of Principle. 182
Sanger Validation of High-Throughput Sequencing in Genetic Diagnosis: Still the Best Practice? 182
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman 179
Genetic polymorphisms of antioxidant enzymes as risk factors for oxidative stress-associated complications in preterm infants. 178
Effect of space flight on the behavior of human retinal pigment epithelial ARPE-19 cells and evaluation of coenzyme Q10 treatment 178
Long Reads, Short Time: Feasibility of Prenatal Sample Karyotyping by Nanopore Genome Sequencing 177
6Precision Trial Designer: A computational tool to assist in the design of genomics-driven trials in oncology 176
Using XCAVATOR and EXCAVATOR2 to Identify CNVs from WGS, WES, and TS Data 173
Third-Generation Cytogenetic Analysis: Diagnostic Application of Long-Read Sequencing 172
Evaluation of Germline Structural Variant Calling Methods for Nanopore Sequencing Data 172
Benzo[a]pyrene impairs the migratory ability of human GnRH neuroblasts through the inhibition of RhoA/ROCK pathway 171
A shifting level model algorithm that identifies aberrations in array-CGH data 171
XCAVATOR: Accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experiments 168
Assessment of fibrinolytic activity by measuring the lysis time of a tissue-factor-induced clot: a feasibility evaluation. 168
Bioinformatics for Next Generation Sequencing Data 167
Charting differentially methylated regions in cancer with Rocker-meth 167
TRPA1 mediates damage of the retina induced by ischemia and reperfusion in mice 166
Heterogeneous magnitude of immunological memory to SARS-CoV-2 in recovered individuals 166
High-resolution Nanopore methylome-maps reveal random hyper-methylation at CpG-poor regions as driver of chemoresistance in leukemias 161
TRiCoLOR: tandem repeat profiling using whole-genome long-read sequencing data 160
3Precision systems medicine in urological Tumors – Molecular profiling and functional testing 160
Discovering chimeric transcripts in paired-end RNA-seq data by using EricScript. 159
Polyploid tubular cells initiate a TGF-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury 157
From multitude to singularity: An up-to-date overview of scRNA-seq data generation and analysis 156
PyPore: a python toolbox for nanopore sequencing data handling 155
GASOLINE: detecting germline and somatic structural variants from long-reads data 148
NANOR: A user-friendly R package to analyze and compare nanopore sequencing data 142
Digital droplet PCR versus quantitative PCR for lipoprotein (a) kringle IV type 2 repeat polymorphism genetic characterization 141
Precision Trial Drawer, a Computational Tool to Assist Planning of Genomics-Driven Trials in Oncology 139
VISOR: a versatile haplotype-aware structural variant simulator for short and long read sequencing 136
Versatile Quality Control Methods for Nanopore Sequencing 134
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients 121
Detection of runs of homozygosity from whole exome sequencing data: state of the art and perspectives for clinical, population and epidemiological studies. 120
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization. 97
PHGDH drives 5-FU chemoresistance in colorectal cancer through the Hedgehog signaling 77
Benchmarking DNA Foundation Models for zero-shot variant effect prediction: the role of context, training, and architecture 68
PoreMeth2 for decoding the evolution of methylome alterations with nanopore sequencing 55
Totale 21.588
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Categoria #
all - tutte 57.132
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 57.132
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022624 0 0 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
2024/20255.041 152 496 297 769 1.419 657 87 339 213 162 219 231
2025/20266.096 601 758 436 483 764 255 737 277 404 443 223 715
2026/2027662 220 154 288 0 0 0 0 0 0 0 0 0
Totale 21.701