Ferdinand Dhombres
Molecular Biology · 2012–2023
A researcher in the Science corpus: 2 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 10 citations into it
Whom Ferdinand Dhombres trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Ferdinand Dhombres's perspective
Ordered by how strongly the researchers Ferdinand Dhombres trusts endorse each paper. Same corpus, a different order for every researcher.
- Linking Human Diseases to Animal Models Using Ontology-Based Phenotype Annotation (PLoS Biology)
- The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease. (American Journal of Human Genetics)
- Validation of a common data model for active safety surveillance research (J. Am. Medical Informatics Assoc.)
- The National COVID Cohort Collaborative (N3C): Rationale, design, infrastructure, and deployment (J. Am. Medical Informatics Assoc.)
- Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources (Nucleic Acids Res.)
- Unifying the definitions of sudden unexpected death in epilepsy (Epilepsia)
- International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: A Task Force report from the ILAE Commission on Diagnostic Methods (Epilepsia)
- The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data (Nucleic Acids Res.)
- The Matchmaker Exchange: A Platform for Rare Disease Gene Discovery (Human Mutation)
- Basic local alignment search tool.
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 2024: phenotypes around the world (2023) — 333 citations