Janet Piñero González
Molecular Biology · 2015–2019
A researcher in the Science corpus: 3 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 46 citations into it
- Genetics — 30 citations into it
- Artificial Intelligence — 6 citations into it
- Computational Biology & Bioinformatics — 6 citations into it
Whom Janet Piñero González trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Olivier Bodenreider
- Tunca Dogan
- Martina Kutmon
- Allan Peter Davis
- Laurent Gil
- Joanna S. Amberger
- Sebastian Köhler
Who trusts Janet Piñero González overall
- Charlotte A. Nelson
- Jimin Pei
- Atul J. Butte
- Liis Kolberg
- Zhan Tong
- William L. Hamilton
- Guangyan Zhou
- Kexin Huang
- Chen Cao
- Sergio E. Baranzini
Papers from Janet Piñero González's perspective
Ordered by how strongly the researchers Janet Piñero González trusts endorse each paper. Same corpus, a different order for every researcher.
- The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data (Nucleic Acids Res.)
- dbSNP: the NCBI database of genetic variation
- The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
- OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
- Representation of rare diseases in health information systems: The orphanet approach to serve a wide range of end users (Human Mutation)
- The Reactome pathway knowledgebase (Nucleic Acids Res.)
- The Ensembl Variant Effect Predictor
- ClinVar: public archive of interpretations of clinically relevant variants
- Disease Ontology: a backbone for disease semantic integration (Nucleic Acids Res.)
- 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
- The DisGeNET knowledge platform for disease genomics: 2019 update (2019) — 2,560 citations
- DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants (2016) — 2,488 citations