Peter N. Robinson

Molecular Biology · 2007–2020

A researcher in the Science corpus: 18 papers; trusts 24 researchers and is trusted by 34 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 231 citations into it; #1,453 of 17,773 by trust here, #1,857 by citations
• Genetics — 119 citations into it; #587 of 6,854 by trust here, #397 by citations
• Artificial Intelligence — 64 citations into it

Whom Peter N. Robinson trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Cynthia L. Smith
2. Stephan C. Schuster
3. Sebastian Köhler
4. Sebastian Bauer
5. Joanna S. Amberger
6. Ada Hamosh
7. Seung Yon Rhee
8. Heng Li
9. Carol A. Bocchini
10. Janan T. Eppig

Who trusts Peter N. Robinson overall

1. Sebastian Köhler
2. James E. Harrison
3. C. Mungall
4. Assaf Gottlieb
5. Karen Eilbeck
6. Abhishek Niroula
7. Hui Yang
8. Joanna S. Amberger
9. Stefan Mundlos
10. Jing Wang

Papers from Peter N. Robinson's perspective

Ordered by how strongly the researchers Peter N. Robinson trusts endorse each paper. Same corpus, a different order for every researcher.

1. The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information (Genome Biology)
2. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
3. Representation of rare diseases in health information systems: The orphanet approach to serve a wide range of end users (Human Mutation)
4. McKusick's Online Mendelian Inheritance in Man (OMIM®) (Nucleic Acids Res.)
5. The OBO Foundry: coordinated evolution of ontologies to support biomedical data integration (Nature Biotechnology)
6. The Human Phenotype Ontology in 2017 (Nucleic Acids Res.)
7. Uberon, an integrative multi-species anatomy ontology
8. dbSNP: the NCBI database of genetic variation
9. A reference ontology for biomedical informatics: the Foundational Model of Anatomy (Journal of Biomedical Informatics)
10. DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. (American Journal of Human Genetics)

Their papers

• Walking the interactome for prioritization of candidate disease genes. (2008) — 1,242 citations
• The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data (2013) — 826 citations
• The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease. (2008) — 1,006 citations
• The Human Phenotype Ontology in 2017 (2016) — 742 citations
• Improved exome prioritization of disease genes through cross-species phenotype comparison (2014) — 366 citations
• The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species (2016) — 450 citations
• Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources (2018) — 616 citations
• Ontologizer 2.0 - a multifunctional tool for GO term enrichment analysis and data exploration (2008) — 536 citations
• Improved detection of overrepresentation of Gene-Ontology annotations with parent-child analysis (2007) — 360 citations
• Phenolyzer: phenotype-based prioritization of candidate genes for human diseases (2015) — 362 citations
• Next-generation diagnostics and disease-gene discovery with the Exomiser (2015) — 400 citations
• Clinical diagnostics in human genetics with semantic similarity searches in ontologies. (2009) — 542 citations
• The Human Phenotype Ontology (2010) — 438 citations
• The digital revolution in phenotyping (2015) — 59 citations
• Finding Our Way through Phenotypes (2015) — 303 citations
• A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease. (2016) — 252 citations
• The National COVID Cohort Collaborative (N3C): Rationale, design, infrastructure, and deployment (2020) — 477 citations
• The Human Phenotype Ontology in 2021 (2020) — 1,031 citations