BREGANT, Elisa
BREGANT, Elisa
DSMB - DIPARTIMENTO DI SCIENZE MEDICHE E BIOLOGICHE (attivo dal 01/01/2011 al 31/12/2016)
A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases
2024-01-01 Zucco, J.; Baldan, F.; Allegri, L.; Bregant, E.; Passon, N.; Franzoni, A.; D'Elia, A. V.; Faletra, F.; Damante, G.; Mio, C.
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype
2020-01-01 Mio, C.; Allegri, L.; Passon, N.; Bregant, E.; Demori, E.; Franzoni, A.; Driul, D.; Riccio, A.; Damante, G.; Baldan, F.
CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers
2020-01-01 Mio, C.; Passon, N.; Baldan, F.; Bregant, E.; Monaco, E.; Mancini, L.; Demori, E.; Damante, G.
Evaluating the SERCA2 and VEGF mRNAs as Potential Molecular Biomarkers of the Onset and Progression in Huntington's Disease
2015-01-01 Bregant, Elisa; Dubsky de Wittenau, Giorgia; Verriello, Lorenzo; Bergonzi, Paolo; Damante, Giuseppe; Curcio, Francesco; Lonigro, Incoronata; Cesca, Federica; Peterlin, Borut; Zadel, Maja; Siciliano, Gabriele; Ceravolo, Roberto; Petrozzi, Lucia; Pauletto, Giada; Barillari, Giovanni; Lucci, Bruno
Somatic amplifications and deletions in genome of papillary thyroid carcinomas
2015-01-01 Passon, Nadia; Bregant, Elisa; Sponziello, Marialuisa; Dima, BIANCA ANA MARIA; Rosignolo, Francesca; Durante, Cosimo; Celano, Marilena; Russo, Diego; Filetti, Sebastiano; Damante, Giuseppe
The impact of the European Society of Cardiology guidelines and whole exome sequencing on genetic testing in hereditary cardiac diseases
2024-01-01 Mio, C.; Zucco, J.; Fabbro, D.; Bregant, E.; Baldan, F.; Allegri, L.; D'Elia, A. V.; Collini, V.; Imazio, M.; Damante, G.; Faletra, F.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases | 1-gen-2024 | Zucco, J.; Baldan, F.; Allegri, L.; Bregant, E.; Passon, N.; Franzoni, A.; D'Elia, A. V.; Faletra, F.; Damante, G.; Mio, C. | |
| A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype | 1-gen-2020 | Mio, C.; Allegri, L.; Passon, N.; Bregant, E.; Demori, E.; Franzoni, A.; Driul, D.; Riccio, A.; Damante, G.; Baldan, F. | |
| CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers | 1-gen-2020 | Mio, C.; Passon, N.; Baldan, F.; Bregant, E.; Monaco, E.; Mancini, L.; Demori, E.; Damante, G. | |
| Evaluating the SERCA2 and VEGF mRNAs as Potential Molecular Biomarkers of the Onset and Progression in Huntington's Disease | 1-gen-2015 | Bregant, Elisa; Dubsky de Wittenau, Giorgia; Verriello, Lorenzo; Bergonzi, Paolo; Damante, Giuseppe; Curcio, Francesco; Lonigro, Incoronata; Cesca, Federica; Peterlin, Borut; Zadel, Maja; Siciliano, Gabriele; Ceravolo, Roberto; Petrozzi, Lucia; Pauletto, Giada; Barillari, Giovanni; Lucci, Bruno | |
| Somatic amplifications and deletions in genome of papillary thyroid carcinomas | 1-gen-2015 | Passon, Nadia; Bregant, Elisa; Sponziello, Marialuisa; Dima, BIANCA ANA MARIA; Rosignolo, Francesca; Durante, Cosimo; Celano, Marilena; Russo, Diego; Filetti, Sebastiano; Damante, Giuseppe | |
| The impact of the European Society of Cardiology guidelines and whole exome sequencing on genetic testing in hereditary cardiac diseases | 1-gen-2024 | Mio, C.; Zucco, J.; Fabbro, D.; Bregant, E.; Baldan, F.; Allegri, L.; D'Elia, A. V.; Collini, V.; Imazio, M.; Damante, G.; Faletra, F. |