Sebastian Köhler
Orcid: 0000-0002-5316-1399Affiliations:
- Charité - University Medicine Berlin, Germany
According to our database1,
Sebastian Köhler
authored at least 25 papers
between 2009 and 2022.
Collaborative distances:
Collaborative distances:
Timeline
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Online presence:
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on scopus.com
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on orcid.org
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on github.com
On csauthors.net:
Bibliography
2022
Database J. Biol. Databases Curation, 2022
2021
2020
The Monarch Initiative in 2019: an integrative data and analytic platform connecting phenotypes to genotypes across species.
Nucleic Acids Res., 2020
2019
Semantic integration of clinical laboratory tests from electronic health records for deep phenotyping and biomarker discovery.
npj Digit. Medicine, 2019
Nucleic Acids Res., 2019
Nucleic Acids Res., 2019
Representing glycophenotypes: semantic unification of glycobiology resources for disease discovery.
Database J. Biol. Databases Curation, 2019
2018
An ontology-based method for assessing batch effect adjustment approaches in heterogeneous datasets.
Bioinform., 2018
Database J. Biol. Databases Curation, 2018
2017
The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species.
Nucleic Acids Res., 2017
Aligning the Human Phenotype and Mammalian Phenotype Ontology using Dead Simple Ontology Design Patterns.
Proceedings of the 8th International Conference on Biomedical Ontology (ICBO 2017), Newcastle-upon-Tyne, United Kingdom, September 13th, 2017
2016
Proceedings of the Joint International Conference on Biological Ontology and BioCreative, 2016
2015
Automatic concept recognition using the Human Phenotype Ontology reference and test suite corpora.
Database J. Biol. Databases Curation, 2015
Proceedings of the Multiple Classifier Systems - 12th International Workshop, 2015
Prediction of Human Gene - Phenotype Associations by Exploiting the Hierarchical Structure of the Human Phenotype Ontology.
Proceedings of the Bioinformatics and Biomedical Engineering, 2015
2014
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.
Nucleic Acids Res., 2014
The influence of disease categories on gene candidate predictions from model organism phenotypes.
J. Biomed. Semant., 2014
Walking the interactome for candidate prioritization in exome sequencing studies of Mendelian diseases.
Bioinform., 2014
2013
Phenotype informatics (Network approaches towards understanding the diseasome) (Phänotyp-Informatik) (Netzwerk-Ansätze zur Analyse genetisch beeinflusster Erkrankungen)
PhD thesis, 2013
PhenoDigm: analyzing curated annotations to associate animal models with human diseases.
Database J. Biol. Databases Curation, 2013
2012
Bioinform., 2012
2011
BMC Bioinform., 2011
BMC Bioinform., 2011
2009
Proceedings of the Algorithms in Bioinformatics, 9th International Workshop, 2009