Stefan Mundlos
Molecular Biology · 2003–2019
A researcher in the Science corpus: 8 papers; trusts 18 researchers and is trusted by 8 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 92 citations into it; #5,659 of 17,773 by trust here, #3,866 by citations
- Genetics — 21 citations into it; #1,882 of 6,854 by trust here, #1,232 by citations
Whom Stefan Mundlos trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Stephan C. Schuster
- Sebastian Bauer
- Cynthia L. Smith
- Sebastian Köhler
- Peter N. Robinson
- Seung Yon Rhee
- Joanna S. Amberger
Who trusts Stefan Mundlos overall
Papers from Stefan Mundlos's perspective
Ordered by how strongly the researchers Stefan Mundlos 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: a tool for annotating and analyzing human hereditary disease. (American Journal of Human Genetics)
- The OBO Foundry: coordinated evolution of ontologies to support biomedical data integration (Nature Biotechnology)
- Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
- A reference ontology for biomedical informatics: the Foundational Model of Anatomy (Journal of Biomedical Informatics)
- McKusick's Online Mendelian Inheritance in Man (OMIM®) (Nucleic Acids Res.)
- Cytoscape: a software environment for integrated models of biomolecular interaction networks.
- A human phenome-interactome network of protein complexes implicated in genetic disorders (Nature Biotechnology)
- Metrics for GO based protein semantic similarity: a systematic evaluation (BMC Bioinformatics)
- An ontology for cell types (Genome Biology)
Their papers
- Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions (2015) — 1,963 citations
- The single cell transcriptional landscape of mammalian organogenesis (2019) — 3,661 citations
- The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease. (2008) — 1,006 citations
- Clinical diagnostics in human genetics with semantic similarity searches in ontologies. (2009) — 542 citations
- The receptor tyrosine kinase Ror2 is involved in non‐canonical Wnt5a/JNK signalling pathway (2003) — 789 citations
- The Human Phenotype Ontology (2010) — 438 citations
- Formation of new chromatin domains determines pathogenicity of genomic duplications (2016) — 614 citations
- Nosology and Classification of Genetic Skeletal Disorders: 2010 Revision (2011) — 680 citations