À. Bravo
Database J. Biol. Databases Curation · 2015–2016
A researcher in the Science corpus: 2 papers; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Who trusts À. Bravo overall
Papers from À. Bravo's perspective
Ordered by how strongly the researchers À. Bravo trusts endorse each paper. Same corpus, a different order for every researcher.
- dbSNP: the NCBI database of genetic variation
- The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data (Nucleic Acids Res.)
- The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
- The Reactome pathway knowledgebase (Nucleic Acids Res.)
- The Ensembl Variant Effect Predictor
- Representation of rare diseases in health information systems: The orphanet approach to serve a wide range of end users (Human Mutation)
- OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
- Disease Ontology: a backbone for disease semantic integration (Nucleic Acids Res.)
- ClinVar: public archive of interpretations of clinically relevant variants
- WikiPathways: capturing the full diversity of pathway knowledge (Nucleic Acids Res.)
Their papers
- DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes (2015) — 1,063 citations
- DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants (2016) — 2,488 citations