BORDONI, ROBERTA
BORDONI, ROBERTA
Istituto di Tecnologie Biomediche - ITB
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort
2023 Paterra, Rosina; Bettinaglio, Paola; Borghi, Arianna; Mangano, Eleonora; Tritto, Viviana; Cesaretti, Claudia; Schettino, Carla; Bordoni, Roberta; Santoro, Claudia; Avignone, Sabrina; Moscatelli, Marco; Melone Mariarosa Anna, Beatrice; Saletti, Veronica; Piluso, Giulio; Natacci, Federica; Riva, Paola; Eoli, Marica
Cell type-specific changes identified by single-cell transcriptomics in Arx mouse model of developmental and epileptic encephalopathy
2023 Verrillo L; Mangano E; Drongitis D; Di Palma R; Schiano Visconte M; Barra A; Merelli I; Piccoli G; Flore G; Consolandi C; Bordoni R;Miano MG
New insights into the molecular basis of spinal neurofibromatosis type 1
2023 Bettinaglio, Paola; Mangano, Eleonora; Tritto, Viviana; Bordoni, Roberta; Paterra, Rosina; Borghi, Arianna; Volonte, Marinella; Battaglia, Cristina; Saletti, Veronica; Cesaretti, Claudia; Natacci, Federica; Melone Mariarosa, A B; Eoli, Marica; Riva, Paola
Author Correction: Genome sequencing of Prototheca zopfii genotypes 1 and 2 provides evidence of a severe reduction in organellar genomes (Scientific Reports, (2018), 8, 1, (14637), 10.1038/s41598-018-32992-0)
2022 Severgnini, Marco; Lazzari, Barbara; Capra, Emanuele; Chessa, Stefania; Luini, Mario; Bordoni, Roberta; Castiglioni, Bianca; Ricchi, Matteo; Cremonesi, Paola
Defective corticogenesis in Arx mouse model of developmental and epileptic encephalopathy caused by polyalanine elongations
2022 Verrillo, L; Mangano, E; Drongitis, D; Di Palma, R; Barra, A; Merelli, I; Piccoli, G; Flore, G; Consolandi, C; Bordoni, R; Miano, Mg
Single-cell transcriptomic analysis of neocortex in Arx mouse model of developmental and epileptic encephalopathy caused by polyalanine elongations
2022 Verrillo L; Mangano E; Drongitis D; Romano F; Barra A; Di Palma R; Piccoli G; Flore G; Consolandi C; Bordoni R;Miano MG
Verrillo L, Mangano E, Drongitis D, Merelli I, Pischedda F, Piccoli G, Consolandi C, Bordoni R and Miano MG.
2021 Verrillo, L; Mangano, E; Drongitis, D; Merelli, I; Pischedda, F; Piccoli, G; Consolandi, C; Bordoni, R; Miano, Mg
A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia
2020 Rossi, Daniela; Gigli, Lorenzo; Gamberucci, Alessandra; Bordoni, Roberta; Pietrelli, Alessandro; Lorenzini, Stefania; Pierantozzi, Enrico; Peretto, Giovanni; DE BELLIS, Gianluca; Della Bella, Paolo; Ferrari, Maurizio; Sorrentino, Vincenzo; Benedetti, Sara; Sala, Simone; Di Resta, Chiara
A reliable strategy for single-cell RNA sequencing analysis using cryoconserved primary cortical cells.
2020 Verrillo, Lucia; Verrillo, Lucia; Mangano, Eleonora; Mangano, Eleonora; Drongitis, ; Denise, ; Merelli, Ivan; Merelli, Ivan; Pischedda, ; Francesca, ; Piccoli, ; Giovanni, ; Consolandi, Clarissa; Consolandi, Clarissa; Bordoni, Roberta; Bordoni, Roberta; Miano, MARIA GIUSEPPINA; Giuseppina, Maria
Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?
2020 Ferrari, Luca; Mangano, Eleonora; Bonati, Maria Teresa; Monterosso, Ilaria; Capitanio, Daniele; Chiappori, Federica; Brambilla, Ilaria; Gelfi, Cecilia; Battaglia, Cristina; Bordoni, Roberta; Riva, Paola
The Genome-wide impact of Nipblb loss-of-function on Zebrafish gene expression
2020 Spreafico, M; Mangano, E; Mazzola, M; Consolandi, C; Bordoni, R; Battaglia, C; Bicciato, S; Marozzi, A; Pistocchi, A
A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia
2019 Rossi, D; Gigli, L; Gamberucci, A; Bordoni, R; Pietrelli, A; Lorenzini, S; Pierantozzi, E; Peretto, G; De Bellis, G; Della Bella, P; Ferrari, M; Sorrentino, V; Benedetti, S; Sala, S; Di Resta, C
Analysis of cortical gene expression variability in a mouse model of X-linked Infantile spsms syndrome
2019 Verrillo L; Tuccillo M; Drongitis D; Mangano E; Franco C; Terrone G; Canzoniero MT; Del Giudice E; Bordoni R; Poeta L; Miano MG.
Analysis of DNA tandem repeats in ALS from Whole Genome Sequencing: Role of FRA10Ac1 gene repeat expansion in ALS
2019 Corrado, L; Genovese, L; Mangano, E; Croce, R; Di Pierro, A; Geraci, F; Bordoni, R; D'Aurizio, R; Barizzone, N; De Marchi, F; Mazzini, L; De Bellis, G; Manzini, G; Severgnini, M; Pellegrini, M; D'Alfonso, S
Analysis of transcriptome landscapes in the epileptogenic cortex of the Arx(GCG)7/Y mouse
2019 Tuccillo, M; Verrillo, L; Drongitis, D; Mangano, E; Consolandi, C; Franco, C; Mallardo, M; Cankaya, I; M, T Canzoniero; Poeta, L; Bordoni, R; Miano, Mg
Disease associated tandem repeat genotyping from NGS target sequencing data
2019 Corrado, L.; Geraci, F.; Severgnini, M.; Di Pierro, A.; Frontini, V.; Mangano, E.; Genovese, L. M.; Barizzone, N.; D'Aurizio, R.; Croce, R.; De Marchi, F.; Mazzini, L.; Brusco, A.; De Bellis, G.; Manzini, G.; Bordoni, R.; Pellegrini, M.; Alfonso, S. D'
Genetic heterogeneity & di/oligogenic inheritance involvement in variable expressivity of Noonan syndrome
2019 Ferrari, L; Mangano, E; Bonati, M; Monterosso, I; Brambilla, I; Chiapparoni, F; Battaglia, C; Bordoni, R; Riva, P
Systematic analysis of the involvement of DNA tandem repeats in Amyotrophic lateral sclerosis from Whole Genome Sequencing data
2019 Corrado, L.; Genovese, L. M.; Mangano, E.; Di Pierro, A.; Barizzone, N.; Bordoni, R.; Geraci, F.; D'Aurizio, R.; Croce, R.; De MArchi, F.; Mazzini, L.; Cantello, R.; De Bellis, G.; Manzini, G.; Severgnini, M.; Pellegrini, M.; D'Alfonso, S.
A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies
2018 Genovese, Lm; Geraci, F; Corrado, L; Mangano, E; D'Aurizio, R; Bordoni, R; Severgnini, M; Manzini, G; De Bellis, G; D'Alfonso, S; Pellegrini, M
Exploring transcriptional single-cell signatures in a mouse model of epilepsy caused by a polyalanine expansion mutation in Aristaless-related homeobox gene.
2018 Tuccillo, M; Mangano, E; Verrillo, L; Poeta, L; Consolandi, C; Padula, A; Franco, C; Drongitis, D; Mallardo, M; Cervicato, G; Canzoniero, L M T; Bordoni, R; Miano, Mg
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort | 1-gen-2023 | Paterra, Rosina; Bettinaglio, Paola; Borghi, Arianna; Mangano, Eleonora; Tritto, Viviana; Cesaretti, Claudia; Schettino, Carla; Bordoni, Roberta; Santoro, Claudia; Avignone, Sabrina; Moscatelli, Marco; Melone Mariarosa Anna, Beatrice; Saletti, Veronica; Piluso, Giulio; Natacci, Federica; Riva, Paola; Eoli, Marica | |
| Cell type-specific changes identified by single-cell transcriptomics in Arx mouse model of developmental and epileptic encephalopathy | 1-gen-2023 | Verrillo L; Mangano E; Drongitis D; Di Palma R; Schiano Visconte M; Barra A; Merelli I; Piccoli G; Flore G; Consolandi C; Bordoni R;Miano MG | |
| New insights into the molecular basis of spinal neurofibromatosis type 1 | 1-gen-2023 | Bettinaglio, Paola; Mangano, Eleonora; Tritto, Viviana; Bordoni, Roberta; Paterra, Rosina; Borghi, Arianna; Volonte, Marinella; Battaglia, Cristina; Saletti, Veronica; Cesaretti, Claudia; Natacci, Federica; Melone Mariarosa, A B; Eoli, Marica; Riva, Paola | |
| Author Correction: Genome sequencing of Prototheca zopfii genotypes 1 and 2 provides evidence of a severe reduction in organellar genomes (Scientific Reports, (2018), 8, 1, (14637), 10.1038/s41598-018-32992-0) | 1-gen-2022 | Severgnini, Marco; Lazzari, Barbara; Capra, Emanuele; Chessa, Stefania; Luini, Mario; Bordoni, Roberta; Castiglioni, Bianca; Ricchi, Matteo; Cremonesi, Paola | |
| Defective corticogenesis in Arx mouse model of developmental and epileptic encephalopathy caused by polyalanine elongations | 1-gen-2022 | Verrillo, L; Mangano, E; Drongitis, D; Di Palma, R; Barra, A; Merelli, I; Piccoli, G; Flore, G; Consolandi, C; Bordoni, R; Miano, Mg | |
| Single-cell transcriptomic analysis of neocortex in Arx mouse model of developmental and epileptic encephalopathy caused by polyalanine elongations | 1-gen-2022 | Verrillo L; Mangano E; Drongitis D; Romano F; Barra A; Di Palma R; Piccoli G; Flore G; Consolandi C; Bordoni R;Miano MG | |
| Verrillo L, Mangano E, Drongitis D, Merelli I, Pischedda F, Piccoli G, Consolandi C, Bordoni R and Miano MG. | 1-gen-2021 | Verrillo, L; Mangano, E; Drongitis, D; Merelli, I; Pischedda, F; Piccoli, G; Consolandi, C; Bordoni, R; Miano, Mg | |
| A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia | 1-gen-2020 | Rossi, Daniela; Gigli, Lorenzo; Gamberucci, Alessandra; Bordoni, Roberta; Pietrelli, Alessandro; Lorenzini, Stefania; Pierantozzi, Enrico; Peretto, Giovanni; DE BELLIS, Gianluca; Della Bella, Paolo; Ferrari, Maurizio; Sorrentino, Vincenzo; Benedetti, Sara; Sala, Simone; Di Resta, Chiara | |
| A reliable strategy for single-cell RNA sequencing analysis using cryoconserved primary cortical cells. | 1-gen-2020 | Verrillo, Lucia; Verrillo, Lucia; Mangano, Eleonora; Mangano, Eleonora; Drongitis, ; Denise, ; Merelli, Ivan; Merelli, Ivan; Pischedda, ; Francesca, ; Piccoli, ; Giovanni, ; Consolandi, Clarissa; Consolandi, Clarissa; Bordoni, Roberta; Bordoni, Roberta; Miano, MARIA GIUSEPPINA; Giuseppina, Maria | |
| Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model? | 1-gen-2020 | Ferrari, Luca; Mangano, Eleonora; Bonati, Maria Teresa; Monterosso, Ilaria; Capitanio, Daniele; Chiappori, Federica; Brambilla, Ilaria; Gelfi, Cecilia; Battaglia, Cristina; Bordoni, Roberta; Riva, Paola | |
| The Genome-wide impact of Nipblb loss-of-function on Zebrafish gene expression | 1-gen-2020 | Spreafico, M; Mangano, E; Mazzola, M; Consolandi, C; Bordoni, R; Battaglia, C; Bicciato, S; Marozzi, A; Pistocchi, A | |
| A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia | 1-gen-2019 | Rossi, D; Gigli, L; Gamberucci, A; Bordoni, R; Pietrelli, A; Lorenzini, S; Pierantozzi, E; Peretto, G; De Bellis, G; Della Bella, P; Ferrari, M; Sorrentino, V; Benedetti, S; Sala, S; Di Resta, C | |
| Analysis of cortical gene expression variability in a mouse model of X-linked Infantile spsms syndrome | 1-gen-2019 | Verrillo L; Tuccillo M; Drongitis D; Mangano E; Franco C; Terrone G; Canzoniero MT; Del Giudice E; Bordoni R; Poeta L; Miano MG. | |
| Analysis of DNA tandem repeats in ALS from Whole Genome Sequencing: Role of FRA10Ac1 gene repeat expansion in ALS | 1-gen-2019 | Corrado, L; Genovese, L; Mangano, E; Croce, R; Di Pierro, A; Geraci, F; Bordoni, R; D'Aurizio, R; Barizzone, N; De Marchi, F; Mazzini, L; De Bellis, G; Manzini, G; Severgnini, M; Pellegrini, M; D'Alfonso, S | |
| Analysis of transcriptome landscapes in the epileptogenic cortex of the Arx(GCG)7/Y mouse | 1-gen-2019 | Tuccillo, M; Verrillo, L; Drongitis, D; Mangano, E; Consolandi, C; Franco, C; Mallardo, M; Cankaya, I; M, T Canzoniero; Poeta, L; Bordoni, R; Miano, Mg | |
| Disease associated tandem repeat genotyping from NGS target sequencing data | 1-gen-2019 | Corrado, L.; Geraci, F.; Severgnini, M.; Di Pierro, A.; Frontini, V.; Mangano, E.; Genovese, L. M.; Barizzone, N.; D'Aurizio, R.; Croce, R.; De Marchi, F.; Mazzini, L.; Brusco, A.; De Bellis, G.; Manzini, G.; Bordoni, R.; Pellegrini, M.; Alfonso, S. D' | |
| Genetic heterogeneity & di/oligogenic inheritance involvement in variable expressivity of Noonan syndrome | 1-gen-2019 | Ferrari, L; Mangano, E; Bonati, M; Monterosso, I; Brambilla, I; Chiapparoni, F; Battaglia, C; Bordoni, R; Riva, P | |
| Systematic analysis of the involvement of DNA tandem repeats in Amyotrophic lateral sclerosis from Whole Genome Sequencing data | 1-gen-2019 | Corrado, L.; Genovese, L. M.; Mangano, E.; Di Pierro, A.; Barizzone, N.; Bordoni, R.; Geraci, F.; D'Aurizio, R.; Croce, R.; De MArchi, F.; Mazzini, L.; Cantello, R.; De Bellis, G.; Manzini, G.; Severgnini, M.; Pellegrini, M.; D'Alfonso, S. | |
| A census of tandemly repeated polymorphic loci in genic regions through the comparative integration of human genome assemblies | 1-gen-2018 | Genovese, Lm; Geraci, F; Corrado, L; Mangano, E; D'Aurizio, R; Bordoni, R; Severgnini, M; Manzini, G; De Bellis, G; D'Alfonso, S; Pellegrini, M | |
| Exploring transcriptional single-cell signatures in a mouse model of epilepsy caused by a polyalanine expansion mutation in Aristaless-related homeobox gene. | 1-gen-2018 | Tuccillo, M; Mangano, E; Verrillo, L; Poeta, L; Consolandi, C; Padula, A; Franco, C; Drongitis, D; Mallardo, M; Cervicato, G; Canzoniero, L M T; Bordoni, R; Miano, Mg |