Annie Olry
Molecular Biology · 2012–2019
A researcher in the Science corpus: 4 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 29 citations into it
- Artificial Intelligence — 5 citations into it
Whom Annie Olry trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Annie Olry's perspective
Ordered by how strongly the researchers Annie Olry 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)
- The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data (Nucleic Acids Res.)
- The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species (bioRxiv)
- Biomedical Ontologies in Action: Role in Knowledge Management, Data Integration and Decision Support (Yearbook of Medical Informatics)
- Executive control function: a review of its promise and challenges for clinical research. A report from the Committee on Research of the American Neuropsychiatric Association. (The Journal of Neuropsychiatry and Clinical Neurosciences)
- Studies in Health Technology and Informatics
- OWL: Web Ontology Language (Encyclopedia of Database Systems)
- Online Mendelian Inheritance in Man 'OMIM'. (Indian Journal of Dermatology, Venereology and Leprology)
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
- Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database (2019) — 1,322 citations