Author
Uppsala UniversityORCID 0000-0002-1150-1586Unclaimed ORCID profile · follow to get notified of new preprints
5 papers
Recent·Most cited
Alex Handler Wagner, Brian Walsh, Georgia Mayfield…·Adam A. Margolin
The paper harmonizes clinical interpretations of cancer genomic variants across six knowledgebases, improving overlap and matching with patient cohorts.
Joana Carlevaro-Fita, Andrés Lanzós, Lars Feuerbach…·S. Cenk Şahinalp
The paper introduces the Cancer LncRNA Census (CLC), a curated resource of lncRNAs with causative roles in cancer, and shows their genomic and evolutionary features.
Marta Paczkowska, Jonathan Barenboim, Nardnisa Sintupisut…·Leonidas Salichos
ActivePathways integrates multivariate omics data to identify enriched pathways, revealing cancer driver genes and prognostic pathways in breast cancer.
Radhakrishnan Sabarinathan, Oriol Pich, Iñigo Martincorena…·on behalf of the PCAWG Drivers and Functional Interpretation Group and the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Network
This paper identifies driver mutations across 2,500 tumors from 37 cancer types, revealing a whole-genome panorama of genomic events that underlie tumor development.
Radhakrishnan Sabarinathan, Loris Mularoni, Jordi Deu-Pons…·Nuria Lopez-Bigas
The paper shows that DNA-binding proteins reduce nucleotide excision repair activity, leading to higher mutation rates at their binding sites in melanoma.