ANGIUS, Andrea
ANGIUS, Andrea
Universita' degli Studi di SASSARI
A large-scale screening identified in USH2A gene the P3272L founder pathogenic variant explaining familial Usher syndrome in Sardinia, Italy
2024-01-01 Serra, Rita; Rallo, Vincenzo; Steri, Maristella; Olla, Stefania; Piras, Maria Grazia; Marongiu, Michele; Gorospe, Myriam; Schlessinger, David; Pinna, Antonio; Fiorillo, Edoardo; Cucca, Francesco; Angius, Andrea
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman
2017-01-01 Palombo, F; Al Wardy, N; Ruscone, G. A. G; Oppo, Manuela; Kindi, M. N. A; Angius, Andrea; Al Lamki, K; Girotto, G; Giangregorio, T; Benelli, M; Magi, A; Seri, M; Gasparini, P; Cucca, Francesco; Sazzini, M; Al Khabori, M; Pippucci, T; Romeo, G.
A Novel null homozygous mutation confirmsCACNA2D2as a gene mutated in epileptic encephalopathy
2013-01-01 Cucca, Francesco; Pippucci, Tommaso; Palombo, Flavia; Maresca, Alessandra; Angius, Andrea; Liguori, Rocco; Seri, Marco; Carelli, Valerio; Parmeggiani, Antonia; Crisponi, Laura; Valentino, Maria Lucia
A Portrait of Intratumoral Genomic and Transcriptomic Heterogeneity at Single-Cell Level in Colorectal Cancer
2021-01-01 Angius, Andrea; Scanu, Antonio Mario; Arru, Caterina; Muroni, Maria Rosaria; Carru, Ciriaco; Porcu, Alberto; Cossu-Rocca, Paolo; De Miglio, Maria Rosaria
Assessing the Predictive Power of the Hemoglobin/Red Cell Distribution Width Ratio in Cancer: A Systematic Review and Future Directions
2023-01-01 Coradduzza, D; Medici, S; Chessa, C; Zinellu, A; Madonia, M; Angius, A; Carru, C; DE MIGLIO, Maria Rosaria
BAT2 and BAT3 polymorphisms as novel genetic risk factors for rejection after HLA-related SCT
2014-01-01 Piras, Is; Angius, Andrea; Andreani, M; Testi, M; Lucarelli, G; Floris, Matteo; Marktel, S; Ciceri, F; La Nasa, G; Fleischhauer, K; Roncarolo, Mg; Bulfone, A; Gregori, S; Bacchetta, R.
BAT2 AND BAT3 POLYMORPHISMS AS NOVEL GENETIC RISK FACTORS FOR REJECTION AFTER HLA-RELATED STEM CELL TRANSPLANTATION
2014-01-01 Piras, Is; Angius, A; Andreani, M; Testi, M; Floris, M; Marktel, S; Ciceri, F; La Nasa, G; Fleischhauer, K; Roncarolo, Mg; Bulfone, A; Bacchetta, R; Gregori, S
Biomarker dynamics affecting neoadjuvant therapy response and outcome of HER2-positive breast cancer subtype
2023-01-01 Orrù, S; Pascariello, E; Pes, B; Rallo, V; Barbara, R; Muntoni, M; Notari, F; Fancello, G; Mocci, C; Muroni, Mr; Cossu Rocca, P; Angius, A; DE MIGLIO, Maria Rosaria
Deciphering clinical significance of BCL11A isoforms and protein expression roles in triple-negative breast cancer subtype
2022-01-01 Angius, A.; Pira, G.; Cossu-Rocca, P.; Sotgiu, G.; Saderi, L.; Muroni, M. R.; Virdis, P.; Piras, D.; Vincenzo, R.; Carru, C.; Coradduzza, D.; Uras, M. G.; Cottu, P.; Fancellu, A.; Orru, S.; Uva, P.; De Miglio, M. R.
Epigenetics, stem cells, and autophagy: Exploring a path involving miRNA
2019-01-01 Balzano, F.; Campesi, I.; Cruciani, S.; Garroni, G.; Bellu, E.; Giudici, S. D.; Angius, A.; Oggiano, A.; Rallo, Vincenzo; Capobianco, G.; Dessole, S.; Ventura, C.; Montella, A.; Maioli, M.
Genomic history of the Sardinian population
2018-01-01 Chiang, C. W. K.; Marcus, J. H.; Sidore, C.; Biddanda, A.; Al-Asadi, H.; Zoledziewska, M.; Pitzalis, M.; Busonero, F.; Maschio, A.; Pistis, G.; Steri, M.; Angius, A.; Lohmueller, K. E.; Abecasis, G. R.; Schlessinger, D.; Cucca, F.; Novembre, J.
Harnessing Minimal Residual Disease as a Predictor for Colorectal Cancer: Promising Horizons Amidst Challenges
2023-01-01 Wen, Xiaofen; Coradduzza, Donatella; Shen, Jiaxin; Scanu, Antonio Mario; Muroni, Maria Rosaria; Massidda, Matteo; Rallo, Vincenzo; Carru, Ciriaco; Angius, Andrea; De Miglio, Maria Rosaria
High differentiation among eight villages in a secluded area of Sardinia revealed by genome-wide high density SNPs analysis
2009-01-01 Pistis, Giorgio; Persico, Ivana; Sassu, Alessandro; Picciau, Andrea; Fraumene, Cristina; Mocci, Evelina; Atzeni, Rossano; Cosso, Massimiliano; Angius, Andrea; Piras, Ignazio; Prodi, Dionigio A.; Manias, Maria Teresa; Pirastu, Mario
Integrated Analysis of miRNA and mRNA Endorses a Twenty miRNAs Signature for Colorectal Carcinoma
2019-01-01 Angius, Andrea; Uva, Paolo; Pira, Giovanna; Muroni, Maria Rosaria; Sotgiu, Giovanni; Saderi, Laura; Uleri, Elena; Caocci, Maurizio; Ibba, Gabriele; Cesaraccio, Maria Rosaria; Serra, Caterina; Carru, Ciriaco; Manca, Alessandra; Sanges, Francesca; Porcu, Alberto; Dolei, Antonia; Scanu, Antonio Mario; Rocca, Paolo Cossu; De Miglio, Maria Rosaria
Landscape of transcriptome variations uncovering known and novel driver events in colorectal carcinoma
2020-01-01 Pira, Giovanna; Uva, Paolo; Scanu, Antonio Mario; Rocca, Paolo Cossu; Murgia, Luciano; Uleri, Elena; Piu, Claudia; Porcu, Alberto; Carru, Ciriaco; Manca, Alessandra; Persico, Ivana; Muroni, Maria Rosaria; Sanges, Francesca; Serra, Caterina; Dolei, Antonia; Angius, Andrea; De Miglio, Maria Rosaria
Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations
2009-01-01 Mocci, Evelina; Fanciulli, Manuela; Pirastu, Nicola; Cabras, Valentina; Fraumene, Cristina; Sassu, Alessandro; Picciau, Andrea; Serra, Donatella; Biino, Ginevra; Pirastu, Mario; Concas, Maria P.; Adamo, Mauro; Persico, Ivana; Prodi, Dionigio A.; Angius, Andrea
miRNA-135b Contributes to Triple Negative Breast Cancer Molecular Heterogeneity: Different Expression Profile in Basal-like Versus non-Basal-like Phenotypes
2018-01-01 Uva, Paolo; Cossu-Rocca, Paolo; Loi, Federica; Pira, Giovanna; Murgia, Luciano; Orrù, Sandra; Floris, Matteo; Muroni, Maria Rosaria; Sanges, Francesca; Carru, Ciriaco; Angius, Andrea; De Miglio, Maria Rosaria
Multiple bilateral retinal astrocytic hamartomas in Usher syndrome
2022-01-01 Serra, R.; Coscas, F.; Angius, A.; Pinna, A.
Novel mutations in c2orf71 causing an early onset form of cone-rod dystrophy: A molecular diagnosis after 20 years of clinical follow-up
2019-01-01 Serra, Rita; Floris, Matteo; Pinna, Antonio; Boscia, Francesco; Cucca, Francesco; Angius, Andrea
Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome
2018-01-01 Angius, A.; Cossu, S.; Uva, P.; Oppo, M.; Onano, Stefano; Persico, I.; Fotia, G.; Atzeni, R.; Cuccuru, G.; Asunis, M.; Cucca, F.; Pruna, D.; Crisponi, L.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A large-scale screening identified in USH2A gene the P3272L founder pathogenic variant explaining familial Usher syndrome in Sardinia, Italy | 1-gen-2024 | Serra, Rita; Rallo, Vincenzo; Steri, Maristella; Olla, Stefania; Piras, Maria Grazia; Marongiu, Michele; Gorospe, Myriam; Schlessinger, David; Pinna, Antonio; Fiorillo, Edoardo; Cucca, Francesco; Angius, Andrea | |
| A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman | 1-gen-2017 | Palombo, F; Al Wardy, N; Ruscone, G. A. G; Oppo, Manuela; Kindi, M. N. A; Angius, Andrea; Al Lamki, K; Girotto, G; Giangregorio, T; Benelli, M; Magi, A; Seri, M; Gasparini, P; Cucca, Francesco; Sazzini, M; Al Khabori, M; Pippucci, T; Romeo, G. | |
| A Novel null homozygous mutation confirmsCACNA2D2as a gene mutated in epileptic encephalopathy | 1-gen-2013 | Cucca, Francesco; Pippucci, Tommaso; Palombo, Flavia; Maresca, Alessandra; Angius, Andrea; Liguori, Rocco; Seri, Marco; Carelli, Valerio; Parmeggiani, Antonia; Crisponi, Laura; Valentino, Maria Lucia | |
| A Portrait of Intratumoral Genomic and Transcriptomic Heterogeneity at Single-Cell Level in Colorectal Cancer | 1-gen-2021 | Angius, Andrea; Scanu, Antonio Mario; Arru, Caterina; Muroni, Maria Rosaria; Carru, Ciriaco; Porcu, Alberto; Cossu-Rocca, Paolo; De Miglio, Maria Rosaria | |
| Assessing the Predictive Power of the Hemoglobin/Red Cell Distribution Width Ratio in Cancer: A Systematic Review and Future Directions | 1-gen-2023 | Coradduzza, D; Medici, S; Chessa, C; Zinellu, A; Madonia, M; Angius, A; Carru, C; DE MIGLIO, Maria Rosaria | |
| BAT2 and BAT3 polymorphisms as novel genetic risk factors for rejection after HLA-related SCT | 1-gen-2014 | Piras, Is; Angius, Andrea; Andreani, M; Testi, M; Lucarelli, G; Floris, Matteo; Marktel, S; Ciceri, F; La Nasa, G; Fleischhauer, K; Roncarolo, Mg; Bulfone, A; Gregori, S; Bacchetta, R. | |
| BAT2 AND BAT3 POLYMORPHISMS AS NOVEL GENETIC RISK FACTORS FOR REJECTION AFTER HLA-RELATED STEM CELL TRANSPLANTATION | 1-gen-2014 | Piras, Is; Angius, A; Andreani, M; Testi, M; Floris, M; Marktel, S; Ciceri, F; La Nasa, G; Fleischhauer, K; Roncarolo, Mg; Bulfone, A; Bacchetta, R; Gregori, S | |
| Biomarker dynamics affecting neoadjuvant therapy response and outcome of HER2-positive breast cancer subtype | 1-gen-2023 | Orrù, S; Pascariello, E; Pes, B; Rallo, V; Barbara, R; Muntoni, M; Notari, F; Fancello, G; Mocci, C; Muroni, Mr; Cossu Rocca, P; Angius, A; DE MIGLIO, Maria Rosaria | |
| Deciphering clinical significance of BCL11A isoforms and protein expression roles in triple-negative breast cancer subtype | 1-gen-2022 | Angius, A.; Pira, G.; Cossu-Rocca, P.; Sotgiu, G.; Saderi, L.; Muroni, M. R.; Virdis, P.; Piras, D.; Vincenzo, R.; Carru, C.; Coradduzza, D.; Uras, M. G.; Cottu, P.; Fancellu, A.; Orru, S.; Uva, P.; De Miglio, M. R. | |
| Epigenetics, stem cells, and autophagy: Exploring a path involving miRNA | 1-gen-2019 | Balzano, F.; Campesi, I.; Cruciani, S.; Garroni, G.; Bellu, E.; Giudici, S. D.; Angius, A.; Oggiano, A.; Rallo, Vincenzo; Capobianco, G.; Dessole, S.; Ventura, C.; Montella, A.; Maioli, M. | |
| Genomic history of the Sardinian population | 1-gen-2018 | Chiang, C. W. K.; Marcus, J. H.; Sidore, C.; Biddanda, A.; Al-Asadi, H.; Zoledziewska, M.; Pitzalis, M.; Busonero, F.; Maschio, A.; Pistis, G.; Steri, M.; Angius, A.; Lohmueller, K. E.; Abecasis, G. R.; Schlessinger, D.; Cucca, F.; Novembre, J. | |
| Harnessing Minimal Residual Disease as a Predictor for Colorectal Cancer: Promising Horizons Amidst Challenges | 1-gen-2023 | Wen, Xiaofen; Coradduzza, Donatella; Shen, Jiaxin; Scanu, Antonio Mario; Muroni, Maria Rosaria; Massidda, Matteo; Rallo, Vincenzo; Carru, Ciriaco; Angius, Andrea; De Miglio, Maria Rosaria | |
| High differentiation among eight villages in a secluded area of Sardinia revealed by genome-wide high density SNPs analysis | 1-gen-2009 | Pistis, Giorgio; Persico, Ivana; Sassu, Alessandro; Picciau, Andrea; Fraumene, Cristina; Mocci, Evelina; Atzeni, Rossano; Cosso, Massimiliano; Angius, Andrea; Piras, Ignazio; Prodi, Dionigio A.; Manias, Maria Teresa; Pirastu, Mario | |
| Integrated Analysis of miRNA and mRNA Endorses a Twenty miRNAs Signature for Colorectal Carcinoma | 1-gen-2019 | Angius, Andrea; Uva, Paolo; Pira, Giovanna; Muroni, Maria Rosaria; Sotgiu, Giovanni; Saderi, Laura; Uleri, Elena; Caocci, Maurizio; Ibba, Gabriele; Cesaraccio, Maria Rosaria; Serra, Caterina; Carru, Ciriaco; Manca, Alessandra; Sanges, Francesca; Porcu, Alberto; Dolei, Antonia; Scanu, Antonio Mario; Rocca, Paolo Cossu; De Miglio, Maria Rosaria | |
| Landscape of transcriptome variations uncovering known and novel driver events in colorectal carcinoma | 1-gen-2020 | Pira, Giovanna; Uva, Paolo; Scanu, Antonio Mario; Rocca, Paolo Cossu; Murgia, Luciano; Uleri, Elena; Piu, Claudia; Porcu, Alberto; Carru, Ciriaco; Manca, Alessandra; Persico, Ivana; Muroni, Maria Rosaria; Sanges, Francesca; Serra, Caterina; Dolei, Antonia; Angius, Andrea; De Miglio, Maria Rosaria | |
| Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations | 1-gen-2009 | Mocci, Evelina; Fanciulli, Manuela; Pirastu, Nicola; Cabras, Valentina; Fraumene, Cristina; Sassu, Alessandro; Picciau, Andrea; Serra, Donatella; Biino, Ginevra; Pirastu, Mario; Concas, Maria P.; Adamo, Mauro; Persico, Ivana; Prodi, Dionigio A.; Angius, Andrea | |
| miRNA-135b Contributes to Triple Negative Breast Cancer Molecular Heterogeneity: Different Expression Profile in Basal-like Versus non-Basal-like Phenotypes | 1-gen-2018 | Uva, Paolo; Cossu-Rocca, Paolo; Loi, Federica; Pira, Giovanna; Murgia, Luciano; Orrù, Sandra; Floris, Matteo; Muroni, Maria Rosaria; Sanges, Francesca; Carru, Ciriaco; Angius, Andrea; De Miglio, Maria Rosaria | |
| Multiple bilateral retinal astrocytic hamartomas in Usher syndrome | 1-gen-2022 | Serra, R.; Coscas, F.; Angius, A.; Pinna, A. | |
| Novel mutations in c2orf71 causing an early onset form of cone-rod dystrophy: A molecular diagnosis after 20 years of clinical follow-up | 1-gen-2019 | Serra, Rita; Floris, Matteo; Pinna, Antonio; Boscia, Francesco; Cucca, Francesco; Angius, Andrea | |
| Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome | 1-gen-2018 | Angius, A.; Cossu, S.; Uva, P.; Oppo, M.; Onano, Stefano; Persico, I.; Fotia, G.; Atzeni, R.; Cuccuru, G.; Asunis, M.; Cucca, F.; Pruna, D.; Crisponi, L. |