Sebastian Bauer
Molecular Biology · 2007–2014
A researcher in the Science corpus: 7 papers; trusts 5 researchers and is trusted by 25 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 72 citations into it; #2,088 of 17,773 by trust here, #3,125 by citations
- Genetics — 32 citations into it; #1,028 of 6,854 by trust here, #675 by citations
Whom Sebastian Bauer trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Sebastian Bauer overall
- Peter N. Robinson
- Fran Supek
- Stuart G. Jantzen
- Stefan Mundlos
- J. Chen
- Sebastian Köhler
- Yves Moreau
- Ben J. G. Sutherland
- Matko Bosnjak
- Oded Magger
Papers from Sebastian Bauer's perspective
Ordered by how strongly the researchers Sebastian Bauer trusts endorse each paper. Same corpus, a different order for every researcher.
- Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
- Cytoscape: a software environment for integrated models of biomolecular interaction networks.
- Uberon, an integrative multi-species anatomy ontology
- McKusick's Online Mendelian Inheritance in Man (OMIM®) (Nucleic Acids Res.)
- The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information (Genome Biology)
- The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease. (American Journal of Human Genetics)
- The Database of Interacting Proteins: 2004 update (Nucleic Acids Res.)
- STRING: a database of predicted functional associations between proteins (Nucleic Acids Res.)
- Entrez Gene: gene-centered information at NCBI (Nucleic Acids Res.)
- Representation of rare diseases in health information systems: The orphanet approach to serve a wide range of end users (Human Mutation)
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
- Improved exome prioritization of disease genes through cross-species phenotype comparison (2014) — 366 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
- Clinical diagnostics in human genetics with semantic similarity searches in ontologies. (2009) — 542 citations