Tom R. Gaunt
Genetics · 2012–2020
A researcher in the Science corpus: 15 papers; trusts 10 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Genetics — 205 citations into it; #6,378 of 6,854 by trust here, #519 by citations
- Molecular Biology — 157 citations into it; #16,713 of 17,773 by trust here, #3,737 by citations
- Statistical Learning Theory — 6 citations into it
Whom Tom R. Gaunt trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Tom R. Gaunt overall
Papers from Tom R. Gaunt's perspective
Ordered by how strongly the researchers Tom R. Gaunt trusts endorse each paper. Same corpus, a different order for every researcher.
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.
- Predicting deleterious amino acid substitutions.
- Human non-synonymous SNPs: server and survey. (Nucleic Acids Research)
- Basic local alignment search tool.
- PANTHER: a library of protein families and subfamilies indexed by function. (Genome Research)
- The Human Gene Mutation Database: 2008 update
- Hidden Markov models in computational biology. Applications to protein modeling.
- Predicting the effects of amino acid substitutions on protein function.
- Performance of mutation pathogenicity prediction methods on missense variants (Human Mutation)
- Automated inference of molecular mechanisms of disease from amino acid substitutions
Their papers
- FATHMM-XF: accurate prediction of pathogenic point mutations via extended features (2017) — 417 citations
- Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models (2012) — 1,269 citations
- The UK10K project identifies rare variants in health and disease (2015) — 1,063 citations
- An integrative approach to predicting the functional effects of non-coding and coding sequence variation (2015) — 631 citations
- Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity (2016) — 815 citations
- DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis. (2016) — 799 citations
- Ranking non-synonymous single nucleotide polymorphisms based on disease concepts (2014) — 207 citations
- HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials (2015) — 671 citations
- The MRC IEU OpenGWAS data infrastructure (2020) — 798 citations
- Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases (2019) — 633 citations
- The Avon Longitudinal Study of Parents and Children (ALSPAC): an update on the enrolled sample of index children in 2019 (2019) — 734 citations
- The MR-Base platform supports systematic causal inference across the human phenome (2018) — 6,483 citations
- LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis (2016) — 890 citations
- Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) — 384 citations
- Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data (2014) — 637 citations