Carlos D. Bustamante

Genetics · 2005–2019

A researcher in the Science corpus: 28 papers; trusts 6 researchers and is trusted by 17 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 289 citations into it; #890 of 6,854 by trust here, #77 by citations
• Molecular Biology — 166 citations into it; #15,414 of 17,773 by trust here, #707 by citations
• Statistics and Probability — 9 citations into it

Whom Carlos D. Bustamante trusts overall

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

1. W. James Kent
2. J. K. Pritchard
3. John Wakeley
4. James Franklin
5. Matthew Stephens

Who trusts Carlos D. Bustamante overall

1. Simon Gravel
2. Daniel R. Schrider
3. James R. Brown
4. Laurent Excoffier
5. P. Hedrick
6. H. Hoekstra
7. Rasmus Nielsen
8. Andrew D. Kern

Papers from Carlos D. Bustamante's perspective

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

1. Generating samples under a Wright-Fisher neutral model of genetic variation (Bioinform.)
2. BLAT--the BLAST-like alignment tool. (Genome Research)
3. A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
4. Inaugural Article: Bayesian Markov chain Monte Carlo sequence analysis reveals varying neutral substitution patterns in mammalian evolution
5. Ncbi reference sequence (refseq): a curated non - redundant sequence database of genomes
6. Genotype, haplotype and copy-number variation in worldwide human populations (Nature)
7. Detecting recent positive selection in the human genome from haplotype structure (Nature)
8. Prediction of deleterious human alleles.
9. Human non-synonymous SNPs: server and survey. (Nucleic Acids Research)
10. Principal components analysis corrects for stratification in genome-wide association studies

Their papers

• A global reference for human genetic variation (2015) — 16,925 citations
• Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes (2012) — 1,698 citations
• A Scan for Positively Selected Genes in the Genomes of Humans and Chimpanzees (2005) — 972 citations
• Natural selection on protein-coding genes in the human genome (2005) — 803 citations
• Genomic scans for selective sweeps using SNP data. (2005) — 1,022 citations
• REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants. (2016) — 2,471 citations
• Assessing the Evolutionary Impact of Amino Acid Mutations in the Human Genome (2008) — 675 citations
• ClinGen--the Clinical Genome Resource. (2015) — 1,269 citations
• Natural selection on genes that underlie human disease susceptibility. (2008) — 241 citations
• Comparative and demographic analysis of orangutan genomes (2011) — 595 citations
• Genomewide SNP variation reveals relationships among landraces and modern varieties of rice (2009) — 635 citations
• A Mutation in the Myostatin Gene Increases Muscle Mass and Enhances Racing Performance in Heterozygote Dogs (2007) — 815 citations
• Genetic analyses of diverse populations improves discovery for complex traits (2019) — 901 citations
• Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study (2017) — 115 citations
• Human demographic history impacts genetic risk prediction across diverse populations (2016) — 1,291 citations
• Estimating Mutation Load in Human Genomes (2015) — 256 citations
• RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference. (2013) — 854 citations
• Great ape genetic diversity and population history (2013) — 858 citations
• An Aboriginal Australian Genome Reveals Separate Human Dispersals into Asia (2011) — 746 citations
• High-throughput single nucleotide polymorphism genotyping for breeding applications in rice using the BeadXpress platform (2011) — 161 citations