MAGI, ALBERTO
 Distribuzione geografica
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Continente #
NA - Nord America 8.751
EU - Europa 7.861
AS - Asia 3.769
SA - Sud America 423
AF - Africa 94
OC - Oceania 44
Continente sconosciuto - Info sul continente non disponibili 3
Totale 20.945
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Nazione #
US - Stati Uniti d'America 8.617
PL - Polonia 3.170
RU - Federazione Russa 1.774
IT - Italia 1.346
SG - Singapore 1.104
CN - Cina 932
HK - Hong Kong 478
VN - Vietnam 399
IE - Irlanda 368
BR - Brasile 339
SE - Svezia 289
KR - Corea 261
DE - Germania 203
FR - Francia 168
IN - India 139
FI - Finlandia 126
GB - Regno Unito 126
BD - Bangladesh 114
CA - Canada 89
CH - Svizzera 78
NL - Olanda 74
JO - Giordania 73
ID - Indonesia 71
AU - Australia 41
JP - Giappone 39
AR - Argentina 38
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 15
NG - Nigeria 12
EC - Ecuador 11
AT - Austria 10
UZ - Uzbekistan 10
EG - Egitto 9
PY - Paraguay 9
IL - Israele 8
TW - Taiwan 8
VE - Venezuela 8
RO - Romania 7
AE - Emirati Arabi Uniti 6
GR - Grecia 6
MY - Malesia 6
PH - Filippine 6
TH - Thailandia 6
CO - Colombia 5
KE - Kenya 5
PA - Panama 5
AZ - Azerbaigian 4
BJ - Benin 4
BY - Bielorussia 4
CL - Cile 4
CZ - Repubblica Ceca 4
EE - Estonia 4
ET - Etiopia 4
GT - Guatemala 4
MA - Marocco 4
PT - Portogallo 4
BG - Bulgaria 3
BO - Bolivia 3
DZ - Algeria 3
HN - Honduras 3
JM - Giamaica 3
LT - Lituania 3
MT - Malta 3
NZ - Nuova Zelanda 3
PE - Perù 3
SA - Arabia Saudita 3
SN - Senegal 3
UY - Uruguay 3
BH - Bahrain 2
CR - Costa Rica 2
DO - Repubblica Dominicana 2
GI - Gibilterra 2
HU - Ungheria 2
KH - Cambogia 2
KZ - Kazakistan 2
LB - Libano 2
NP - Nepal 2
RS - Serbia 2
SC - Seychelles 2
SI - Slovenia 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
AL - Albania 1
AO - Angola 1
CW - ???statistics.table.value.countryCode.CW??? 1
CY - Cipro 1
DK - Danimarca 1
EU - Europa 1
IR - Iran 1
KG - Kirghizistan 1
KN - Saint Kitts e Nevis 1
LK - Sri Lanka 1
MD - Moldavia 1
Totale 20.935
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Città #
Warsaw 3.164
Santa Clara 1.657
Ashburn 1.201
Singapore 807
Fairfield 782
Chandler 410
Hong Kong 404
Dublin 355
Seattle 353
Woodbridge 353
Cambridge 319
San Jose 288
Houston 280
Wilmington 274
Seoul 255
Beijing 217
Florence 214
Milan 198
Altamura 136
Hefei 136
Lawrence 134
Ann Arbor 129
Los Angeles 123
The Dalles 122
Ho Chi Minh City 116
Buffalo 107
Princeton 93
Council Bluffs 92
Lauterbourg 89
Rome 89
New York 82
Munich 78
Mumbai 77
Bern 75
Boston 72
Hanoi 71
Shanghai 64
Moscow 62
Dallas 61
San Diego 60
Boardman 59
Dong Ket 54
Jakarta 54
Paris 52
Helsinki 47
Melbourne 39
Tokyo 38
Jacksonville 37
Kent 37
Phoenix 32
Bologna 31
Medford 30
São Paulo 30
Turku 30
Clifton 24
Naples 24
London 23
Guangzhou 22
Toronto 22
Da Nang 21
Abidjan 20
Barcelona 18
Frankfurt am Main 18
Montreal 18
Orem 18
Bremen 17
Redwood City 17
Hillsboro 16
Izmir 16
Redondo Beach 16
Turin 16
Brooklyn 15
Dearborn 14
Johannesburg 14
Shenzhen 14
Siena 14
Atlanta 13
Baghdad 13
Changsha 13
Falls Church 13
Palermo 13
Poplar 13
Washington 13
Abuja 12
Norwalk 12
Pune 12
Tianjin 12
Andover 11
Chicago 11
Denver 11
Fontebuona 11
Rio de Janeiro 11
Stockholm 11
Brussels 10
Charlotte 10
Verona 10
Amsterdam 9
Bari 9
Bengaluru 9
Catania 9
Totale 14.837
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Nome #
High-throughput multiplex single-nucleotide polymorphism (SNP) analysis in genes involved in methionine metabolism 387
Desmoglein-2-integrin Beta-8 interaction regulates actin assembly in endothelial cells: deregulation in systemic sclerosis 380
Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2 377
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm. 372
RNA sequencing reveals a distinct transcriptomic profile predictive of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 354
Acute kidney injury promotes development of papillary renal cell adenoma and carcinoma from renal progenitor cells. 350
Moment estimation in discrete shifting level model applied to fast array-CGH segmentation 349
Detection of Genomic Structural Variants from Next-Generation Sequencing Data 344
Characterization and identification of hidden rare variants in the human genome 338
WNP: A Novel Algorithm for Gene Products Annotation from Weighted Functional Networks. 336
Carotid artery disease: Novel pathophysiological mechanisms identified by gene-expression profiling of peripheral blood 333
Sphingosine 1-phosphate induces differentiation of mesoangioblasts towards smooth muscle. A role for GATA6. 332
Gene expression profiling of peripheral blood in patients with abdominal aortic aneurysm 312
EXCAVATOR: detecting copy number variants from whole-exome sequencing data 311
Using a calibration experiment to assess gene-specific information: full Bayesian and empirical Bayesian models for two-channel microarray data. 310
A model of anti-angiogenesis: differential transcriptosome profiling of microvascular endothelial cells from diffuse systemic sclerosis patients. 304
SLMSuite: a suite of algorithms for segmenting genomic profiles 294
Early-onset ischaemic stroke: analysis of 58 polymorphisms in 17 genes involved in methionine metabolism 291
Apolipoprotein(a) kringle-IV type 2 copy number variation is associated with venous thromboembolism 285
Gene expression profile of rat left ventricles reveals persisting changes following chronic mild exercise protocol: implications for cardioprotection 279
Differentiation of crescent-forming kidney progenitor cells into podocytes attenuates severe glomerulonephritis in mice 265
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) 259
Bicuspid Aortic Valve: Role of Multiple Gene Variants in Influencing the Clinical Phenotype 253
Editorial: Repetitive Structures in Biological Sequences: Algorithms and Applications 253
Genetic bases of bicuspid aortic valve: The contribution of traditional and high-throughput sequencing approaches on research and diagnosis 249
Nanopore sequencing data analysis: state of the art, applications and challenges 246
RNA sequencing reveals PNN and KCNQ1OT1 as predictive biomarkers of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 240
The ion channels and transporters gene expression profile indicates a shift in excitability and metabolisms during malignant progression of Follicular Lymphoma 239
A transcriptomic profile predicts clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 237
Epilepsy with auditory features: A heterogeneous clinico-molecular disease 236
A microRNA profile of pediatric glioblastoma: The role of NUCKS1 upregulation 234
Genome-wide copy number analysis in pediatric glioblastoma multiforme. 230
Involvement of RUNX1 Pathway Is a Common Event in the Leukemic Transformation of Chronic Myeloproliferative Neoplasms (MPNs) 227
Characterization of MinION nanopore data for resequencing analyses 221
H3M2: Detection of runs of homozygosity from whole-exome sequencing data 219
PoreMeth2: decoding the evolution of methylome alterations with Nanopore sequencing 215
372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment. 212
AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics 211
A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria. 210
D13Global gene expression profile reveals a distinct transcriptomic profile predictive of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 207
GENE-03. MICRORNAS PROFILE IN PAEDIATRIC GBMS 201
A very fast and accurate method for calling aberrations in array-CGH data. 200
THIRD GENERATION SEQUENCING OF NORMAL KARYOTYPE ACUTE MYELOID LEUKEMIA: IMPLICATIONS FOR PROGNOSIS 200
Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type i reveals candidate genes for cranio-facial development 196
BaP inhibits human GnRH neuron migration by altering the RhoA pathway 194
Global gene expression profile reveals a distinct transcriptomic profile predictive of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy 194
Xome-Blender: A novel cancer genome simulator 193
β3-adrenergic receptor on tumor-infiltrating lymphocytes sustains IFN-γ-dependent PD-L1 expression and impairs anti-tumor immunity in neuroblastoma 190
The antiangiogenic tissue kallikrein pattern of endothelial cells in systemic sclerosis. 190
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients 190
5Genome-wide identification of actionable copy number alterations from targeted sequencing panels with Excavator2 189
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) 189
Genetic and nutritional factors determining circulating levels of lipoprotein(a): results of the "Montignoso Study" 188
Read count approach for DNA copy number variants detection. 188
BPS2025 - Long-term effect of Mavacamten impact force and sarcomere density in a MYBPC3 iPSC-cardiomyocyte model of hypertrophic cardiomyopathy 187
Abstract 2471: Pan-cancer catalog of Differentially Methylated Regions by Rocker-meth, a new computational method 187
A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria. 186
Nano-GLADIATOR: real-time detection of copy number alterations from nanopore sequencing data 186
The Coenzyme Q10 (CoQ10) as Countermeasure for Retinal Damage Onboard the International Space Station: the CORM Project 185
Clonally expanded PD-1-expressing T cells are enriched in synovial fluid of juvenile idiopathic arthritis patients 183
H3M2: detection of runs of homozygosity from whole-exome sequencing data. 182
EX-HOM (EXome HOMozygosity): A Proof of Principle. 179
Genetic analysis of 56 polymorphisms in 17 genes involved in methionine metabolism in patients with abdominal aortic aneurysm. 178
Sanger Validation of High-Throughput Sequencing in Genetic Diagnosis: Still the Best Practice? 177
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman 176
Tubular cell polyploidy protects from lethal acute kidney injury but promotes consequent chronic kidney disease 176
6Precision Trial Designer: A computational tool to assist in the design of genomics-driven trials in oncology 175
Effect of space flight on the behavior of human retinal pigment epithelial ARPE-19 cells and evaluation of coenzyme Q10 treatment 174
Genetic polymorphisms of antioxidant enzymes as risk factors for oxidative stress-associated complications in preterm infants. 172
Long Reads, Short Time: Feasibility of Prenatal Sample Karyotyping by Nanopore Genome Sequencing 172
Third-Generation Cytogenetic Analysis: Diagnostic Application of Long-Read Sequencing 171
A shifting level model algorithm that identifies aberrations in array-CGH data 167
Using XCAVATOR and EXCAVATOR2 to Identify CNVs from WGS, WES, and TS Data 167
XCAVATOR: Accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experiments 166
Evaluation of Germline Structural Variant Calling Methods for Nanopore Sequencing Data 166
Charting differentially methylated regions in cancer with Rocker-meth 166
Assessment of fibrinolytic activity by measuring the lysis time of a tissue-factor-induced clot: a feasibility evaluation. 165
Heterogeneous magnitude of immunological memory to SARS-CoV-2 in recovered individuals 163
Bioinformatics for Next Generation Sequencing Data 161
TRPA1 mediates damage of the retina induced by ischemia and reperfusion in mice 160
High-resolution Nanopore methylome-maps reveal random hyper-methylation at CpG-poor regions as driver of chemoresistance in leukemias 157
3Precision systems medicine in urological Tumors – Molecular profiling and functional testing 157
Benzo[a]pyrene impairs the migratory ability of human GnRH neuroblasts through the inhibition of RhoA/ROCK pathway 155
Polyploid tubular cells initiate a TGF-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury 154
TRiCoLOR: tandem repeat profiling using whole-genome long-read sequencing data 154
Discovering chimeric transcripts in paired-end RNA-seq data by using EricScript. 154
From multitude to singularity: An up-to-date overview of scRNA-seq data generation and analysis 154
PyPore: a python toolbox for nanopore sequencing data handling 151
GASOLINE: detecting germline and somatic structural variants from long-reads data 144
NANOR: A user-friendly R package to analyze and compare nanopore sequencing data 139
Digital droplet PCR versus quantitative PCR for lipoprotein (a) kringle IV type 2 repeat polymorphism genetic characterization 136
Precision Trial Drawer, a Computational Tool to Assist Planning of Genomics-Driven Trials in Oncology 136
VISOR: a versatile haplotype-aware structural variant simulator for short and long read sequencing 133
Versatile Quality Control Methods for Nanopore Sequencing 130
Detection of runs of homozygosity from whole exome sequencing data: state of the art and perspectives for clinical, population and epidemiological studies. 117
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients 115
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization. 91
PHGDH drives 5-FU chemoresistance in colorectal cancer through the Hedgehog signaling 68
Benchmarking DNA Foundation Models for zero-shot variant effect prediction: the role of context, training, and architecture 60
PoreMeth2 for decoding the evolution of methylome alterations with nanopore sequencing 49
Totale 21.084
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Categoria #
all - tutte 54.635
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 54.635
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2024/20255.041 152 496 297 769 1.419 657 87 339 213 162 219 231
2025/20266.096 601 758 436 483 764 255 737 277 404 443 223 715
2026/2027131 131 0 0 0 0 0 0 0 0 0 0 0
Totale 21.170