Matthew E. Mort

Molecular Biology · 2003–2020

A researcher in the Science corpus: 16 papers; trusts 9 researchers and is trusted by 6 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 222 citations into it; #8,647 of 17,773 by trust here, #3,165 by citations
• Genetics — 174 citations into it; #2,186 of 6,854 by trust here, #478 by citations
• Computational Biology & Bioinformatics — 35 citations into it
• Artificial Intelligence — 22 citations into it
• Statistical Learning Theory — 6 citations into it

Whom Matthew E. Mort trusts overall

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

1. Pauline Crystal Ng
2. Hashem A. Shihab
3. J. Platt
4. Steven Henikoff
5. David N. Cooper
6. Peter D. Stenson
7. Sean R. Eddy
8. Ngak-Leng Sim
9. Huaiyu Zhu
10. Yuhai Wu

Who trusts Matthew E. Mort overall

1. Emidio Capriotti
2. Peter D. Stenson
3. Hashem A. Shihab
4. Xiaoming Liu
5. David N. Cooper
6. Christopher Douville
7. Hannah Carter
8. Ngak-Leng Sim
9. Russ B. Altman
10. Xueqiu Jian

Papers from Matthew E. Mort's perspective

Ordered by how strongly the researchers Matthew E. Mort 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. Performance of mutation pathogenicity prediction methods on missense variants (Human Mutation)
5. PANTHER: a library of protein families and subfamilies indexed by function. (Genome Research)
6. Exome sequencing as a tool for Mendelian disease gene discovery
7. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Proceedings of the National Academy of Sciences of the United States of America)
8. Gene Ontology: tool for the unification of biology
9. A general framework for estimating the relative pathogenicity of human genetic variants
10. Predicting the functional impact of protein mutations: application to cancer genomics

Their papers

• The Human Gene Mutation Database: 2008 update (2009) — 907 citations
• Biological and Functional Relevance of CASP Predictions (2017) — 7 citations
• FATHMM-XF: accurate prediction of pathogenic point mutations via extended features (2017) — 417 citations
• Automated inference of molecular mechanisms of disease from amino acid substitutions (2009) — 811 citations
• Human Gene Mutation Database (HGMD®): 2003 update (2003) — 1,857 citations
• Inferring the molecular and phenotypic impact of amino acid variants with MutPred2 (2020) — 618 citations
• An integrative approach to predicting the functional effects of non-coding and coding sequence variation (2015) — 631 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
• Ranking non-synonymous single nucleotide polymorphisms based on disease concepts (2014) — 207 citations
• The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting (2020) — 670 citations
• Gene expression across mammalian organ development (2019) — 676 citations
• IMHOTEP-a composite score integrating popular tools for predicting the functional consequences of non-synonymous sequence variants. (2016) — 14 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
• The Human Gene Mutation Database (HGMD) and Its Exploitation in the Fields of Personalized Genomics and Molecular Evolution (2012) — 218 citations