Jordi Deu-Pons
Database J. Biol. Databases Curation · 2013–2020
A researcher in the Science corpus: 7 papers; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Papers from Jordi Deu-Pons's perspective
Ordered by how strongly the researchers Jordi Deu-Pons trusts endorse each paper. Same corpus, a different order for every researcher.
- Analysis of protein-coding genetic variation in 60,706 humans
- Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database (Human Mutation)
- Mutational landscape and significance across 12 major cancer types (Nature)
- Exploring the Genomes of Cancer Cells: Progress and Promise (Science)
- Landscape of somatic mutations in 560 breast cancer whole genome sequences (Nature)
- dbSNP: the NCBI database of genetic variation
- A CENSUS OF HUMAN CANCER GENES (Nature Reviews. Cancer)
- ClinVar: public archive of interpretations of clinically relevant variants
- HTSeq—a Python framework to work with high-throughput sequencing data (bioRxiv)
- The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data (Nucleic Acids Res.)
Their papers
- DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes (2015) — 1,063 citations
- Cancer Genome Interpreter annotates the biological and clinical relevance of tumor alterations (2017) — 501 citations
- DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants (2016) — 2,488 citations
- OncodriveFML: a general framework to identify coding and non-coding regions with cancer driver mutations (2016) — 309 citations
- IntOGen-mutations identifies cancer drivers across tumor types (2013) — 559 citations
- A compendium of mutational cancer driver genes (2020) — 1,056 citations
- Analyses of non-coding somatic drivers in 2,658 cancer whole genomes (2020) — 508 citations