Karen Eilbeck
Molecular Biology · 2001–2017
A researcher in the Science corpus: 9 papers; trusts 11 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Molecular Biology — 126 citations into it; #17,483 of 17,773 by trust here, #901 by citations
- Genetics — 76 citations into it
- Computational Biology & Bioinformatics — 19 citations into it
- Plant Science — 10 citations into it
Whom Karen Eilbeck trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- James Y. Zou
- Peter N. Robinson
- Kai Wang
- Hui Yang
- Katherine S. Pollard
- Ivan A. Adzhubei
- Pablo E. Cingolani
- Johan T. den Dunnen
- Sebastian Köhler
- Stephen F. Altschul
Who trusts Karen Eilbeck overall
Papers from Karen Eilbeck's perspective
Ordered by how strongly the researchers Karen Eilbeck trusts endorse each paper. Same corpus, a different order for every researcher.
- A method and server for predicting damaging missense mutations
- A general framework for estimating the relative pathogenicity of human genetic variants
- Analysis of protein-coding genetic variation in 60,706 humans
- dbNSFP: A Lightweight Database of Human Non-synonymous SNPs and Their Functional Predictions (Human Mutation)
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- ClinGen--the Clinical Genome Resource. (New England Journal of Medicine)
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
- An integrated map of genetic variation from 1,092 human genomes
- A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®) (Human Mutation)
- ClinVar: public archive of interpretations of clinically relevant variants
Their papers
- Gene Ontology Consortium: The Gene Ontology (GO) database and informatics resource (2004) — 4,608 citations
- The Sequence of the Human Genome (2001) — 6,774 citations
- The Sequence Ontology: a tool for the unification of genome annotations (2005) — 868 citations
- The OBO Foundry: coordinated evolution of ontologies to support biomedical data integration (2007) — 2,805 citations
- The Gene Ontology in 2010: extensions and refinements (2009) — 456 citations
- Evolution of the Sequence Ontology terms and relationships (2010) — 110 citations
- The Gene Ontology project in 2008 (2007) — 802 citations
- Settling the score: variant prioritization and Mendelian disease (2017) — 217 citations
- An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge (2014) — 308 citations