Edward V. Ball
Genetics · 2000–2020
A researcher in the Science corpus: 12 papers; trusts 1 researcher and is trusted by 5 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 138 citations into it; #3,046 of 6,854 by trust here, #109 by citations
Whom Edward V. Ball trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Edward V. Ball overall
Papers from Edward V. Ball's perspective
Ordered by how strongly the researchers Edward V. Ball trusts endorse each paper. Same corpus, a different order for every researcher.
- The Human Gene Mutation Database: 2008 update
- Exome sequencing as a tool for Mendelian disease gene discovery
- Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models (Human Mutation)
- Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
- Mapping copy number variation by population scale genome sequencing (Nature)
- Genome sequence of the Brown Norway rat yields insights into mammalian evolution (Nature)
- A Draft Sequence of the Neandertal Genome (Science)
- RefSeq: an update on mammalian reference sequences
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- Cloud-Coffee: implementation of a parallel consistency-based multiple alignment algorithm in the T-Coffee package and its benchmarking on the Amazon Elastic-Cloud (Bioinform.)
Their papers
- The Human Gene Mutation Database: 2008 update (2009) — 907 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- Evolutionary and Biomedical Insights from the Rhesus Macaque Genome (2007) — 1,385 citations
- Human Gene Mutation Database (HGMD®): 2003 update (2003) — 1,857 citations
- The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies (2017) — 1,216 citations
- Insights into hominid evolution from the gorilla genome sequence (2012) — 719 citations
- The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting (2020) — 670 citations
- The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine (2013) — 1,335 citations
- Deleterious- and disease-allele prevalence in healthy individuals: insights from current predictions, mutation databases, and population-scale resequencing. (2012) — 279 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
- The Human Gene Mutation Database (HGMD) and Its Exploitation in the Fields of Personalized Genomics and Molecular Evolution (2012) — 218 citations
- Human Gene Mutation Database—A biomedical information and research resource (2000) — 295 citations