A. Phillips

Genetics · Human Genetics · 2003–2020

A researcher in the Science corpus: 9 papers; trusts 1 researcher and is trusted by 4 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 144 citations into it; #3,422 of 6,854 by trust here, #655 by citations

Whom A. Phillips trusts

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

1. David N. Cooper (in Genetics)

Who trusts A. Phillips

1. David N. Cooper (in Genetics)
2. Peter D. Stenson (in Genetics)
3. Eric Boerwinkle (in Genetics)
4. Xiaoming Liu (in Genetics)

Papers from A. Phillips's perspective

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

1. Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models (Human Mutation)
2. Genome sequence of the Brown Norway rat yields insights into mammalian evolution (Nature)
3. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
4. A Draft Sequence of the Neandertal Genome (Science)
5. M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity
6. RefSeq: an update on mammalian reference sequences
7. The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003
8. Three-dimensional reconstruction of protein networks provides insight into human genetic disease (Nature Biotechnology)
9. Human Gene Mutation Database—A biomedical information and research resource (Human Mutation)
10. 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
• 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
• The Human Gene Mutation Database (HGMD) and Its Exploitation in the Fields of Personalized Genomics and Molecular Evolution (2012) — 218 citations
• Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) — 710 citations