Sebastian Köhler

Molecular Biology · 2008–2023

A researcher in the Science corpus: 13 papers; trusts 8 researchers and is trusted by 16 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 167 citations into it; #3,374 of 17,773 by trust here, #2,434 by citations
• Genetics — 101 citations into it; #1,130 of 6,854 by trust here, #492 by citations

Whom Sebastian Köhler trusts overall

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

1. Peter N. Robinson
2. Joanna S. Amberger
3. Ada Hamosh
4. Cynthia L. Smith
5. Risi Kondor
6. C. Mungall
7. Carol A. Bocchini
8. Barry Smith
9. Alan F. Scott
10. Cornelius Rosse

Who trusts Sebastian Köhler overall

1. Peter N. Robinson
2. J. Chen
3. Yves Moreau
4. Oded Magger
5. Saket Navlakha
6. Yaling Nie
7. Xiujuan Wang
8. C. Mungall
9. Peter Csermely
10. Stefan Mundlos

Papers from Sebastian Köhler's perspective

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

1. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
2. The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information (Genome Biology)
3. Uberon, an integrative multi-species anatomy ontology
4. McKusick's Online Mendelian Inheritance in Man (OMIM®) (Nucleic Acids Res.)
5. The Human Phenotype Ontology in 2017 (Nucleic Acids Res.)
6. dbSNP: the NCBI database of genetic variation
7. Basic local alignment search tool.
8. OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
9. Representation of rare diseases in health information systems: The orphanet approach to serve a wide range of end users (Human Mutation)
10. Cytoscape: a software environment for integrated models of biomolecular interaction networks.

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
• 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
• 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 Human Phenotype Ontology in 2024: phenotypes around the world (2023) — 333 citations
• The Human Phenotype Ontology in 2021 (2020) — 1,031 citations