Ana Rath
Molecular Biology · 2012–2020
A researcher in the Science corpus: 5 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 36 citations into it
- Artificial Intelligence — 5 citations into it
Whom Ana Rath trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Ana Rath overall
Papers from Ana Rath's perspective
Ordered by how strongly the researchers Ana Rath trusts endorse each paper. Same corpus, a different order for every researcher.
- The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information (Genome Biology)
- The Human Phenotype Ontology in 2017 (Nucleic Acids Res.)
- Improved exome prioritization of disease genes through cross-species phenotype comparison (Genome Research)
- Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources (Nucleic Acids Res.)
- Feasibility and utility of applications of the common data model to multiple, disparate observational health databases (J. Am. Medical Informatics Assoc.)
- The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data (Nucleic Acids Res.)
- Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology (Epilepsia)
- OMIM.org: leveraging knowledge across phenotype–gene relationships (Nucleic Acids Res.)
- The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species (bioRxiv)
- Serving the enterprise and beyond with informatics for integrating biology and the bedside (i2b2)
Their papers
- Representation of rare diseases in health information systems: The orphanet approach to serve a wide range of end users (2012) — 351 citations
- The Human Phenotype Ontology in 2017 (2016) — 742 citations
- Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources (2018) — 616 citations
- The Human Phenotype Ontology in 2021 (2020) — 1,031 citations
- Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database (2019) — 1,322 citations