Núria Queralt-Rosinach
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 Núria Queralt-Rosinach overall
Papers from Núria Queralt-Rosinach's perspective
Ordered by how strongly the researchers Núria Queralt-Rosinach 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 Reactome pathway knowledgebase (Nucleic Acids Res.)
- The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
- The Ensembl Variant Effect Predictor
- Disease Ontology: a backbone for disease semantic integration (Nucleic Acids Res.)
- Representation of rare diseases in health information systems: The orphanet approach to serve a wide range of end users (Human Mutation)
- PANTHER version 10: expanded protein families and functions, and analysis tools
- OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
- ClinVar: public archive of interpretations of clinically relevant variants
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