Browsing by Author Lehner, Ben
Showing results 1 to 6 of 6
| Issue Date | Title | Author(s) |
| 22-Aug-2024 | Genome-scale quantification and prediction of pathogenic stop codon readthrough by small molecules | Toledano, Ignasi; Supek, Fran; Lehner, Ben |
| 1-Jan-2018 | Loss of G9a preserves mutation patterns but increases chromatin accessibility, genomic instability and aggressiveness in skin tumours | Avgustinova, Alexandra; Symeonidi, Aikaterini; Castellanos, Andrés; Urdiroz Urricelqui, Uxue; Solé Boldo, Llorenç; Martín, Mercè; Pérez Rodríguez, Ivan; Prats, Neus; Lehner, Ben; Supek, Fran; Aznar Benitah, Salvador |
| 8-Jul-2019 | Scales and mechanisms of somatic mutation rate variation across the human genome | Supek, Fran; Lehner, Ben |
| 1-Feb-2021 | The genetic landscape for amyloid beta fibril nucleation accurately discriminates familial Alzheimer's disease mutations | Seuma, Mireia; Faure, André J.; Badia, Marta; Lehner, Ben; Bolognesi, Benedetta |
| 28-Jun-2022 | The impact of rare germline variants on human somatic mutation processes | Vali-Pour, Mischan; Park, Solip; Espinosa-Carrasco, José; Ortiz Martínez, Daniel; Lehner, Ben; Supek, Fran |
| 17-Jan-2025 | Understanding, predicting and preventing the impact of nonsense mutations on gene expression by deep mutational scanning | Toledano Martin, Ignasi |
