MAGI, ALBERTO
MAGI, ALBERTO
Ingegneria dell'Informazione
372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment.
2012 Marseglia G; Scordo MR; Pescucci C; Nannetti G; Biagini E; Scandurra V; Gerundino F; Magi A; Benelli M; Torricelli F.
3Precision systems medicine in urological Tumors – Molecular profiling and functional testing
2017 L. Mazzarella, R. D’aurizio, G. Frige, A. Guida, E. Belloni, E. Marino, L. Bernard1,P. Pelicci, A. Magi
5Genome-wide identification of actionable copy number alterations from targeted sequencing panels with Excavator2
2017 Mazzarella, L; D'aurizio, R; Frige, G; Guida, A; Belloni, E; Marino, E; Bernard, L; Pelicci, P; Magi, A
6Precision Trial Designer: A computational tool to assist in the design of genomics-driven trials in oncology
2017 Mazzarella, L; Melloni, G; Guida, A; Curigliano, G; Botteri, E; Esposito, A; Kamal, M; Le Tourneau, C; Magi, A; Riva, L; Pelicci, P
A microRNA profile of pediatric glioblastoma: The role of NUCKS1 upregulation
2019 Giunti, Laura; Da Ros, Martina; De Gregorio, Veronica; Magi, Alberto; Landini, Samuela; Mazzinghi, Benedetta; Buccoliero, Anna Maria; Genitori, Lorenzo; Giglio, Sabrina; Sardi, Iacopo
A model of anti-angiogenesis: differential transcriptosome profiling of microvascular endothelial cells from diffuse systemic sclerosis patients.
2006 Giusti B;Fibbi G;Margheri F;Serratì S;Rossi L;Poggi F;Lapini I;Magi A;Del Rosso A;Cinelli M;Guiducci S;Kahaleh B;Bazzichi L;Bombardieri S;Matucci Cerinic M;Gensini GF;Del Rosso M;Abbate R
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)
2018 Fuselli S.; Baptista R.P.; Panziera A.; Magi A.; Guglielmi S.; Tonin R.; Benazzo A.; Bauzer L.G.; Mazzoni C.J.; Bertorelle G.
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman
2016 Palombo, Flavia; Al-Wardy, Nadia; Ruscone, Guido Alberto Gnecchi; Oppo, Manuela; Kindi, Mohammed Nasser Al; Angius, Andrea; Al Lamki, Khalsa; Girotto, Giorgia; Giangregorio, Tania; Benelli, Matteo; Magi, Alberto; Seri, Marco; Gasparini, Paolo; Cucca, Francesco; Sazzini, Marco; Al Khabori, Mazin; Pippucci, Tommaso; Romeo, Giovanni
A shifting level model algorithm that identifies aberrations in array-CGH data
2010 A. Magi;M. Benelli;G. Marseglia;G. Nannetti;M. R. Scordo;F. Torricelli
A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria.
2013 Mannelli F; Bencini S; Peruzzi B; Cutini I; Sanna A; Benelli M; Magi A; Gianfaldoni G; Rotunno G; Carrai V; Gelli AM; Valle V; Santini V; Notaro R; Luzzatto L; Bosi A.
A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria.
2012 Mannelli F;Bencini S;Peruzzi B;Cutini I;Sanna A;Benelli M;Magi A;Gianfaldoni G;Rotunno G;Carrai V;Gelli AM;Valle V;Santini V;Notaro R;Luzzatto L;Bosi A
A transcriptomic profile predicts clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy
2016 Mini, E; D’Aurizio, R; Perrone, G; Magi, A; Lapucci, A; Tassi, R; Napoli, C; Picariello, L; Landini, I; Brugia, M; Mazzei, T; Tonelli, F; Nobili, S
A very fast and accurate method for calling aberrations in array-CGH data.
2010 M. Benelli;G. Marseglia;G. Nannetti;R. Paravidino;F. Zara;F. D. Bricarelli;F. Torricelli;A. Magi
Abstract 2471: Pan-cancer catalog of Differentially Methylated Regions by Rocker-meth, a new computational method
2019 Benelli, Matteo; Magi, Alberto; Romagnoli, Dario; Franceschini, Gian Marco; Biagioni, Chiara; Migliaccio, Ilenia; Malorni, Luca; Leo, Angelo Di; Demichelis, Francesca
Acute kidney injury promotes development of papillary renal cell adenoma and carcinoma from renal progenitor cells.
2020 Peired AJ, Antonelli G, Angelotti ML, Allinovi M, Guzzi F, Sisti A, Semeraro R, Conte C, Mazzinghi B, Nardi S, Melica ME, De Chiara L, Lazzeri E, Lasagni L, Lottini T, Landini S, Giglio S, Mari A, Di Maida F, Antonelli A, Porpiglia F, Schiavina R, Ficarra V, Facchiano D, Gacci M, Serni S, Carini M, Netto GJ, Roperto RM, Magi A, Christiansen CF, Rotondi M, Liapis H, Anders HJ, Minervini A, Raspollini MR, Romagnani P.
Apolipoprotein(a) kringle-IV type 2 copy number variation is associated with venous thromboembolism
2016 Sticchi, Elena; Magi, Alberto; Kamstrup, Pia R.; Marcucci, Rossella; Prisco, Domenico; Martinelli, Ida; Mannucci, Pier Mannuccio; Abbate, Rosanna; Giusti, Betti
Assessment of fibrinolytic activity by measuring the lysis time of a tissue-factor-induced clot: a feasibility evaluation.
2010 A.P. Cellai; D. Lami; A. Magi; A.A. Liotta; A. Rogolino; E. Antonucci ; B. Bandinelli; R. Abbate; D. Prisco
AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics
2020 Magi, Alberto; Giangregorio, Tania; Semeraro, Roberto; Carangelo, Giulia; Palombo, Flavia; Romeo, Giovanni; Seri, Marco; Pippucci, Tommaso
Bicuspid Aortic Valve: Role of Multiple Gene Variants in Influencing the Clinical Phenotype
2018 Sticchi, Elena; De Cario, Rosina; Magi, Alberto; Giglio, Sabrina; Provenzano, Aldesia; Nistri, Stefano; Pepe, Guglielmina; Giusti, Betti
Bioinformatics for Next Generation Sequencing Data
2010 Magi A.; Benelli M.; Gozzini A.; Girolami F.; Torricelli F.; Brandi M.L.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment. | 2012 | Marseglia G; Scordo MR; Pescucci C; Nannetti G; Biagini E; Scandurra V; Gerundino F; Magi A; Benelli M; Torricelli F. | |
| 3Precision systems medicine in urological Tumors – Molecular profiling and functional testing | 2017 | L. Mazzarella, R. D’aurizio, G. Frige, A. Guida, E. Belloni, E. Marino, L. Bernard1,P. Pelicci, A. Magi | |
| 5Genome-wide identification of actionable copy number alterations from targeted sequencing panels with Excavator2 | 2017 | Mazzarella, L; D'aurizio, R; Frige, G; Guida, A; Belloni, E; Marino, E; Bernard, L; Pelicci, P; Magi, A | |
| 6Precision Trial Designer: A computational tool to assist in the design of genomics-driven trials in oncology | 2017 | Mazzarella, L; Melloni, G; Guida, A; Curigliano, G; Botteri, E; Esposito, A; Kamal, M; Le Tourneau, C; Magi, A; Riva, L; Pelicci, P | |
| A microRNA profile of pediatric glioblastoma: The role of NUCKS1 upregulation | 2019 | Giunti, Laura; Da Ros, Martina; De Gregorio, Veronica; Magi, Alberto; Landini, Samuela; Mazzinghi, Benedetta; Buccoliero, Anna Maria; Genitori, Lorenzo; Giglio, Sabrina; Sardi, Iacopo | |
| A model of anti-angiogenesis: differential transcriptosome profiling of microvascular endothelial cells from diffuse systemic sclerosis patients. | 2006 | Giusti B;Fibbi G;Margheri F;Serratì S;Rossi L;Poggi F;Lapini I;Magi A;Del Rosso A;Cinelli M;Guiducci S;Kahaleh B;Bazzichi L;Bombardieri S;Matucci Cerinic M;Gensini GF;Del Rosso M;Abbate R | |
| 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) | 2018 | Fuselli S.; Baptista R.P.; Panziera A.; Magi A.; Guglielmi S.; Tonin R.; Benazzo A.; Bauzer L.G.; Mazzoni C.J.; Bertorelle G. | |
| A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman | 2016 | Palombo, Flavia; Al-Wardy, Nadia; Ruscone, Guido Alberto Gnecchi; Oppo, Manuela; Kindi, Mohammed Nasser Al; Angius, Andrea; Al Lamki, Khalsa; Girotto, Giorgia; Giangregorio, Tania; Benelli, Matteo; Magi, Alberto; Seri, Marco; Gasparini, Paolo; Cucca, Francesco; Sazzini, Marco; Al Khabori, Mazin; Pippucci, Tommaso; Romeo, Giovanni | |
| A shifting level model algorithm that identifies aberrations in array-CGH data | 2010 | A. Magi;M. Benelli;G. Marseglia;G. Nannetti;M. R. Scordo;F. Torricelli | |
| A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria. | 2013 | Mannelli F; Bencini S; Peruzzi B; Cutini I; Sanna A; Benelli M; Magi A; Gianfaldoni G; Rotunno G; Carrai V; Gelli AM; Valle V; Santini V; Notaro R; Luzzatto L; Bosi A. | |
| A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria. | 2012 | Mannelli F;Bencini S;Peruzzi B;Cutini I;Sanna A;Benelli M;Magi A;Gianfaldoni G;Rotunno G;Carrai V;Gelli AM;Valle V;Santini V;Notaro R;Luzzatto L;Bosi A | |
| A transcriptomic profile predicts clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy | 2016 | Mini, E; D’Aurizio, R; Perrone, G; Magi, A; Lapucci, A; Tassi, R; Napoli, C; Picariello, L; Landini, I; Brugia, M; Mazzei, T; Tonelli, F; Nobili, S | |
| A very fast and accurate method for calling aberrations in array-CGH data. | 2010 | M. Benelli;G. Marseglia;G. Nannetti;R. Paravidino;F. Zara;F. D. Bricarelli;F. Torricelli;A. Magi | |
| Abstract 2471: Pan-cancer catalog of Differentially Methylated Regions by Rocker-meth, a new computational method | 2019 | Benelli, Matteo; Magi, Alberto; Romagnoli, Dario; Franceschini, Gian Marco; Biagioni, Chiara; Migliaccio, Ilenia; Malorni, Luca; Leo, Angelo Di; Demichelis, Francesca | |
| Acute kidney injury promotes development of papillary renal cell adenoma and carcinoma from renal progenitor cells. | 2020 | Peired AJ, Antonelli G, Angelotti ML, Allinovi M, Guzzi F, Sisti A, Semeraro R, Conte C, Mazzinghi B, Nardi S, Melica ME, De Chiara L, Lazzeri E, Lasagni L, Lottini T, Landini S, Giglio S, Mari A, Di Maida F, Antonelli A, Porpiglia F, Schiavina R, Ficarra V, Facchiano D, Gacci M, Serni S, Carini M, Netto GJ, Roperto RM, Magi A, Christiansen CF, Rotondi M, Liapis H, Anders HJ, Minervini A, Raspollini MR, Romagnani P. | |
| Apolipoprotein(a) kringle-IV type 2 copy number variation is associated with venous thromboembolism | 2016 | Sticchi, Elena; Magi, Alberto; Kamstrup, Pia R.; Marcucci, Rossella; Prisco, Domenico; Martinelli, Ida; Mannucci, Pier Mannuccio; Abbate, Rosanna; Giusti, Betti | |
| Assessment of fibrinolytic activity by measuring the lysis time of a tissue-factor-induced clot: a feasibility evaluation. | 2010 | A.P. Cellai; D. Lami; A. Magi; A.A. Liotta; A. Rogolino; E. Antonucci ; B. Bandinelli; R. Abbate; D. Prisco | |
| AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics | 2020 | Magi, Alberto; Giangregorio, Tania; Semeraro, Roberto; Carangelo, Giulia; Palombo, Flavia; Romeo, Giovanni; Seri, Marco; Pippucci, Tommaso | |
| Bicuspid Aortic Valve: Role of Multiple Gene Variants in Influencing the Clinical Phenotype | 2018 | Sticchi, Elena; De Cario, Rosina; Magi, Alberto; Giglio, Sabrina; Provenzano, Aldesia; Nistri, Stefano; Pepe, Guglielmina; Giusti, Betti | |
| Bioinformatics for Next Generation Sequencing Data | 2010 | Magi A.; Benelli M.; Gozzini A.; Girolami F.; Torricelli F.; Brandi M.L. |