Alan H. Beggs

Nature Genetics · 2000–2019

A researcher in the Science corpus: 8 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.

Whom Alan H. Beggs trusts overall

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

1. David Genesove
2. Heng Li
3. Daniel Kahneman

Who trusts Alan H. Beggs overall

1. Benjamin J. Keys

Papers from Alan H. Beggs's perspective

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

1. The Human Gene Mutation Database: 2008 update
2. A framework for variation discovery and genotyping using next-generation DNA sequencing data
3. A method and server for predicting damaging missense mutations
4. Distribution and intensity of constraint in mammalian genomic sequence. (Genome Research)
5. BFAST: An Alignment Tool for Large Scale Genome Resequencing (PLoS ONE)
6. Loss Aversion and Seller Behavior: Evidence from the Housing Market
7. dbNSFP: A Lightweight Database of Human Non-synonymous SNPs and Their Functional Predictions (Human Mutation)
8. Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
9. The Sequence Alignment/Map format and SAMtools (Bioinform.)
10. EGASP: the human ENCODE Genome Annotation Assessment Project (Genome Biology)

Their papers

• Anchoring Effects: Evidence from Art Auctions (2009) — 273 citations
• Myozenin: An α-actinin- and γ-filamin-binding protein of skeletal muscle Z lines (2001) — 144 citations
• Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis (2000) — 1,153 citations
• Improving genetic diagnosis in Mendelian disease with transcriptome sequencing (2016) — 689 citations
• Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease (2019) — 624 citations
• An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge (2014) — 308 citations
• ACTN3 genotype is associated with human elite athletic performance. (2003) — 886 citations
• Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis. (2000) — 636 citations