Peter D. Stenson

Molecular Biology · 2000–2020

A researcher in the Science corpus: 19 papers; trusts 19 researchers and is trusted by 12 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 281 citations into it; #4,965 of 17,773 by trust here, #713 by citations
• Genetics — 227 citations into it; #1,579 of 6,854 by trust here, #64 by citations
• Computational Biology & Bioinformatics — 44 citations into it
• Cancer Research — 39 citations into it; #1,387 of 1,780 by trust here, #611 by citations
• Artificial Intelligence — 24 citations into it
• Evaluation & Benchmarks — 10 citations into it
• Medical & Health AI — 5 citations into it

Whom Peter D. Stenson trusts overall

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

1. David N. Cooper
2. Pauline Crystal Ng
3. Hashem A. Shihab
4. Ngak-Leng Sim
5. Kim D. Pruitt
6. Gonçalo R. Abecasis
7. Yongwook Choi
8. Steven Henikoff
9. Matthew E. Mort
10. Ada Hamosh

Who trusts Peter D. Stenson overall

1. Xiaoming Liu
2. Hashem A. Shihab
3. Christopher Douville
4. David N. Cooper
5. Xueqiu Jian
6. Abhishek Niroula
7. Yi-Fei Huang
8. Vanessa E. Gray
9. Eric Boerwinkle
10. Hannah Carter

Papers from Peter D. Stenson's perspective

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

1. The Human Gene Mutation Database: 2008 update
2. Predicting deleterious amino acid substitutions.
3. Predicting the effects of amino acid substitutions on protein function.
4. Basic local alignment search tool.
5. Performance of mutation pathogenicity prediction methods on missense variants (Human Mutation)
6. PANTHER: a library of protein families and subfamilies indexed by function. (Genome Research)
7. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.
8. Automated inference of molecular mechanisms of disease from amino acid substitutions
9. The human genome browser at UCSC.
10. Human non-synonymous SNPs: server and survey. (Nucleic Acids Research)

Their papers

• The Human Gene Mutation Database: 2008 update (2009) — 907 citations
• A global reference for human genetic variation (2015) — 16,925 citations
• Genome sequence of the Brown Norway rat yields insights into mammalian evolution (2004) — 2,140 citations
• Evolutionary and Biomedical Insights from the Rhesus Macaque Genome (2007) — 1,385 citations
• The human gene damage index as a gene-level approach to prioritizing exome variants (2015) — 236 citations
• Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models (2012) — 1,269 citations
• Identifying Mendelian disease genes with the Variant Effect Scoring Tool (2013) — 530 citations
• Human Gene Mutation Database (HGMD®): 2003 update (2003) — 1,857 citations
• Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST‐Indel) (2015) — 138 citations
• The Evaluation of Tools Used to Predict the Impact of Missense Variants Is Hindered by Two Types of Circularity (2015) — 342 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
• M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity (2016) — 797 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