DE LILLO, ANTONELLA
DE LILLO, ANTONELLA
Dipartimento di Biologia
Cross-ancestry genome-wide association studies identified heterogeneous loci associated with differences of allele frequency and regulome tagging between participants of European descent and other ancestry groups from the UK Biobank.
2021-01-01 De Lillo, A; D'Antona, S; Pathak, G; Wendt, F; De Angelis, F; Fuciarelli, M; Polimanti, R
Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosis
2020-01-01 De Lillo, A; Pathak, Ga; De Angelis, F; Di Girolamo, M; Luigetti, M; Sabatelli, M; Perfetto, F; Frusconi, S; Manfellotto, D; Fuciarelli, M; Polimanti, R
Epigenomic Profiles of African-American Transthyretin Val122Ile Carriers Reveals Putatively Dysregulated Amyloid Mechanisms
2021-01-01 Pathak, G; Wendt, F; De Lillo, A; Nunez, Y; Goswami, A; De Angelis, F; Fuciarelli, M; Kranzler, H; Gelernter, J; Polimanti, R
Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis
2017-01-01 Iorio, A; De Lillo, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Sabatelli, M; Pradotto, L; Mauro, A; Mazzeo, A; Stancanelli, C; Perfetto, F; Frusconi, S; My, F; Manfellotto, D; Fuciarelli, M; Polimanti, R
Phenome-wide association study of TTR and RBP4 genes in 361,194 individuals reveals novel insights in the genetics of hereditary and wildtype transthyretin amyloidoses
2019-10-29 De Lillo, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Frusconi, S; Manfellotto, D; Fuciarelli, M; Polimanti, R
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2021 | Cross-ancestry genome-wide association studies identified heterogeneous loci associated with differences of allele frequency and regulome tagging between participants of European descent and other ancestry groups from the UK Biobank. | De Lillo, A; D'Antona, S; Pathak, G; Wendt, F; De Angelis, F; Fuciarelli, M; Polimanti, R | Articolo su rivista | |
| 1-gen-2020 | Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosis | De Lillo, A; Pathak, Ga; De Angelis, F; Di Girolamo, M; Luigetti, M; Sabatelli, M; Perfetto, F; Frusconi, S; Manfellotto, D; Fuciarelli, M; Polimanti, R | Articolo su rivista | |
| 1-gen-2021 | Epigenomic Profiles of African-American Transthyretin Val122Ile Carriers Reveals Putatively Dysregulated Amyloid Mechanisms | Pathak, G; Wendt, F; De Lillo, A; Nunez, Y; Goswami, A; De Angelis, F; Fuciarelli, M; Kranzler, H; Gelernter, J; Polimanti, R | Articolo su rivista | |
| 1-gen-2017 | Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis | Iorio, A; De Lillo, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Sabatelli, M; Pradotto, L; Mauro, A; Mazzeo, A; Stancanelli, C; Perfetto, F; Frusconi, S; My, F; Manfellotto, D; Fuciarelli, M; Polimanti, R | Articolo su rivista | |
| 29-ott-2019 | Phenome-wide association study of TTR and RBP4 genes in 361,194 individuals reveals novel insights in the genetics of hereditary and wildtype transthyretin amyloidoses | De Lillo, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Frusconi, S; Manfellotto, D; Fuciarelli, M; Polimanti, R | Articolo su rivista |