Sfoglia per Autore
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.
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
WNP: A Novel Algorithm for Gene Products Annotation from Weighted Functional Networks.
2012 Magi A, Tattini L, Benelli M, Giusti B, Abbate R, Ruffo S
Desmoglein-2-integrin Beta-8 interaction regulates actin assembly in endothelial cells: deregulation in systemic sclerosis
2013 Giusti, B; Margheri, F; Rossi, L; Lapini, I; Magi, A; Serratì, S; Chillà, A; Laurenzana, A; Magnelli, L; Calorini, L; Bianchini, F; Fibbi, G; Abbate, R; Del Rosso, M
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)
2013 Giusti, Betti; Margheri, Francesca; Rossi, Luciana; Lapini, Ilaria; Magi, Alberto; Serratã¬, Simona; Chillã , Anastasia; Laurenzana, Anna; Magnelli, Lucia; Calorini, Lido; Bianchini, Francesca; Fibbi, Gabriella; Abbate, Rosanna; Mario Del, Rosso
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.
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
2013 A. Magi; L. Tattini; I. Cifola; R. D'Aurizio; M. Benelli; E. Mangano; C. Battaglia; E. Bonora; A. Kurg; M. Seri; P. Magini; B. Giusti; G. Romeo; T. Pippucci; G. De Bellis; R. Abbate; G.F. Gensini
Moment estimation in discrete shifting level model applied to fast array-CGH segmentation
2013 A. Gandolfi; M. Benelli; A. Magi; S. Chiti
Detection of runs of homozygosity from whole exome sequencing data: state of the art and perspectives for clinical, population and epidemiological studies.
2014 Pippucci T; Magi A; Gialluisi A; Romeo G.
Genome-wide copy number analysis in pediatric glioblastoma multiforme.
2014 Giunti L;Pantaleo M;Sardi I;Provenzano A;Magi A;Cardellicchio S;Castiglione F;Tattini L;Novara F;Buccoliero AM;de Martino M;Genitori L;Zuffardi O;Giglio S
H3M2: detection of runs of homozygosity from whole-exome sequencing data.
2014 Magi A;Tattini L;Palombo F;Benelli M;Gialluisi A;Giusti B;Abbate R;Seri M;Gensini GF;Romeo G;Pippucci T
H3M2: Detection of runs of homozygosity from whole-exome sequencing data
2014 Magi, Alberto
Characterization and identification of hidden rare variants in the human genome
2015 Magi, Alberto; D'Aurizio, Romina; Palombo, Flavia; Cifola, Ingrid; Tattini, Lorenzo; Semeraro, Roberto; Pippucci, Tommaso; Giusti, Betti; Romeo, Giovanni; Abbate, Rosanna; Gensini, Gian Franco
Epilepsy with auditory features: A heterogeneous clinico-molecular disease
2015 Pippucci, Tommaso; Licchetta, Laura; Baldassari, Sara; Palombo, Flavia; Menghi, Veronica; D'Aurizio, Romina; Leta, Chiara; Stipa, Carlotta; Boero, Giovanni; D'Orsi, Giuseppe; Magi, Alberto; Scheffer, Ingrid; Seri, Marco; Tinuper, Paolo; Bisulli, Francesca
Detection of Genomic Structural Variants from Next-Generation Sequencing Data
2015 Tattini, Lorenzo; D'Aurizio, Romina; Magi, Alberto
Characterization of MinION nanopore data for resequencing analyses
2016 Magi, Alberto; Giusti, Betti; Tattini, Lorenzo
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
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
RNA sequencing reveals a distinct transcriptomic profile predictive of 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.; Nobili, S.
D13Global gene expression profile reveals a distinct transcriptomic profile predictive of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy
2016 Tassi, R.; Mini, E.; D'Aurizio, R.; Perrone, G.; Magi, A.; Lapucci, A.; Napoli, C.; Picariello, L.; Brugia, M.; Landini, I.; Mazzei, T.; Tonelli, F.; Nobili, S.
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. | |
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 | |
WNP: A Novel Algorithm for Gene Products Annotation from Weighted Functional Networks. | 2012 | Magi A, Tattini L, Benelli M, Giusti B, Abbate R, Ruffo S | |
Desmoglein-2-integrin Beta-8 interaction regulates actin assembly in endothelial cells: deregulation in systemic sclerosis | 2013 | Giusti, B; Margheri, F; Rossi, L; Lapini, I; Magi, A; Serratì, S; Chillà, A; Laurenzana, A; Magnelli, L; Calorini, L; Bianchini, F; Fibbi, G; Abbate, R; Del Rosso, M | |
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) | 2013 | Giusti, Betti; Margheri, Francesca; Rossi, Luciana; Lapini, Ilaria; Magi, Alberto; Serratã¬, Simona; Chillã , Anastasia; Laurenzana, Anna; Magnelli, Lucia; Calorini, Lido; Bianchini, Francesca; Fibbi, Gabriella; Abbate, Rosanna; Mario Del, Rosso | |
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. | |
EXCAVATOR: detecting copy number variants from whole-exome sequencing data | 2013 | A. Magi; L. Tattini; I. Cifola; R. D'Aurizio; M. Benelli; E. Mangano; C. Battaglia; E. Bonora; A. Kurg; M. Seri; P. Magini; B. Giusti; G. Romeo; T. Pippucci; G. De Bellis; R. Abbate; G.F. Gensini | |
Moment estimation in discrete shifting level model applied to fast array-CGH segmentation | 2013 | A. Gandolfi; M. Benelli; A. Magi; S. Chiti | |
Detection of runs of homozygosity from whole exome sequencing data: state of the art and perspectives for clinical, population and epidemiological studies. | 2014 | Pippucci T; Magi A; Gialluisi A; Romeo G. | |
Genome-wide copy number analysis in pediatric glioblastoma multiforme. | 2014 | Giunti L;Pantaleo M;Sardi I;Provenzano A;Magi A;Cardellicchio S;Castiglione F;Tattini L;Novara F;Buccoliero AM;de Martino M;Genitori L;Zuffardi O;Giglio S | |
H3M2: detection of runs of homozygosity from whole-exome sequencing data. | 2014 | Magi A;Tattini L;Palombo F;Benelli M;Gialluisi A;Giusti B;Abbate R;Seri M;Gensini GF;Romeo G;Pippucci T | |
H3M2: Detection of runs of homozygosity from whole-exome sequencing data | 2014 | Magi, Alberto | |
Characterization and identification of hidden rare variants in the human genome | 2015 | Magi, Alberto; D'Aurizio, Romina; Palombo, Flavia; Cifola, Ingrid; Tattini, Lorenzo; Semeraro, Roberto; Pippucci, Tommaso; Giusti, Betti; Romeo, Giovanni; Abbate, Rosanna; Gensini, Gian Franco | |
Epilepsy with auditory features: A heterogeneous clinico-molecular disease | 2015 | Pippucci, Tommaso; Licchetta, Laura; Baldassari, Sara; Palombo, Flavia; Menghi, Veronica; D'Aurizio, Romina; Leta, Chiara; Stipa, Carlotta; Boero, Giovanni; D'Orsi, Giuseppe; Magi, Alberto; Scheffer, Ingrid; Seri, Marco; Tinuper, Paolo; Bisulli, Francesca | |
Detection of Genomic Structural Variants from Next-Generation Sequencing Data | 2015 | Tattini, Lorenzo; D'Aurizio, Romina; Magi, Alberto | |
Characterization of MinION nanopore data for resequencing analyses | 2016 | Magi, Alberto; Giusti, Betti; Tattini, Lorenzo | |
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 | |
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 | |
RNA sequencing reveals a distinct transcriptomic profile predictive of 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.; Nobili, S. | |
D13Global gene expression profile reveals a distinct transcriptomic profile predictive of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy | 2016 | Tassi, R.; Mini, E.; D'Aurizio, R.; Perrone, G.; Magi, A.; Lapucci, A.; Napoli, C.; Picariello, L.; Brugia, M.; Landini, I.; Mazzei, T.; Tonelli, F.; Nobili, S. |
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