Javier García-García

with Bravo · 2016

A researcher in the Science corpus: 1 paper; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Papers from Javier García-García's perspective

Ordered by how strongly the researchers Javier García-García trusts endorse each paper. Same corpus, a different order for every researcher.

1. dbSNP: the NCBI database of genetic variation
2. Representation of rare diseases in health information systems: The orphanet approach to serve a wide range of end users (Human Mutation)
3. The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
4. OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
5. The Ensembl Variant Effect Predictor
6. WikiPathways: capturing the full diversity of pathway knowledge (Nucleic Acids Res.)
7. ClinVar: public archive of interpretations of clinically relevant variants
8. PANTHER version 10: expanded protein families and functions, and analysis tools
9. A global reference for human genetic variation
10. The druggable genome (Nature reviews. Drug discovery)

Their papers

• DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants (2016) — 2,488 citations