Roberta Bordoni

The information published in this page are entirely managed by ROBERTA BORDONI who is completely responsible for it.
Interest areas:

Genomics and Trascriptomics (in bulk and at single-cell level analysis) applied to the study of rare genetic and neurodegenerative diseases.


Contacts

Phone: 02-26422740
Fax: 02-26422770
Address: Via F.lli Cervi 93 Segrate (MI)

International Ids


H-indexes

Google Scholar H-Index: 24
Scopus H-Index: 21
ISI-WoS H-Index: 18

Research products

Spreafico M.; Mangano E.; Mazzola M.; Consolandi C.; Bordoni R.; Battaglia C.; Bicciato S.; Marozzi A.; Pistocchi A.

The Genome-wide impact of Nipblb loss-of-function on Zebrafish gene expression

(2020) in International journal of molecular sciences (Print)
Ferrari, Luca; Mangano, Eleonora; Bonati, Maria Teresa; Monterosso, Ilaria; Capitanio, Daniele; Chiappori, Federica; Brambilla, Ilaria; Gelfi, Cecilia; Battaglia, Cristina; Bordoni, Roberta; Riva, Paola

Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?

(2020) in European journal of human genetics
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 novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia

(2020) in Heart rhythm
Verrillo, Lucia and Mangano, Eleonora and Drongitis, Denise and Merelli, Ivan and Pischedda, Francesca and Piccoli, Giovanni and Consolandi, Clarissa and Bordoni, Roberta and Miano, Maria Giuseppina

A reliable strategy for single-cell RNA sequencing analysis using cryoconserved primary cortical cells.

(2020) in Journal of neuroscience methods
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'

Disease associated tandem repeat genotyping from NGS target sequencing data

(2019) 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), 16-19/06/2018
Ferrari, L.; Mangano, E.; Bonati, M.; Monterosso, I.; Brambilla, I.; Chiapparoni, F.; Battaglia, C.; Bordoni, R.; Riva, P.

Genetic heterogeneity & di/oligogenic inheritance involvement in variable expressivity of Noonan syndrome

(2019) 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, ITALY, 16-19/06/2018
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.

Systematic analysis of the involvement of DNA tandem repeats in Amyotrophic lateral sclerosis from Whole Genome Sequencing data

(2019) 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, ITALY, 16-19/06/2018
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 cortical gene expression variability in a mouse model of X-linked Infantile spsms syndrome

(2019) in Translational medicine @ UniSa
Rossi D1, Gigli L2, Gamberucci A1, Bordoni R3, Pietrelli A3, Lorenzini S1, Pierantozzi E1, Peretto G2, De Bellis G3, Della Bella P2, Ferrari M4, Sorrentino V1, Benedetti S5, Sala S2, Di Resta C6.

A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia

(2019) in Heart rhythm
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 DNA tandem repeats in ALS from Whole Genome Sequencing: Role of FRA10Ac1 gene repeat expansion in ALS

(2019) 52nd European Society of Human Genetics (ESHG) Conference, Gothenburg, 2019
Visualize all the publications (since 2016)