Eric Boerwinkle
Genetics · 2000–2019
A researcher in the Science corpus: 63 papers; trusts 41 researchers and is trusted by 39 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 852 citations into it; #499 of 6,854 by trust here, #34 by citations
- Molecular Biology — 588 citations into it; #1,388 of 17,773 by trust here, #421 by citations
- Computational Biology & Bioinformatics — 89 citations into it
- Cancer Research — 84 citations into it; #946 of 1,780 by trust here, #392 by citations
- Evaluation & Benchmarks — 15 citations into it
- Medical & Health AI — 11 citations into it
Whom Eric Boerwinkle trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Kai Wang
- Xiaoming Liu
- Pauline Crystal Ng
- Xueqiu Jian
- Steven Henikoff
- B. Reva
- Prateek Kumar
- Peter D. Stenson
- Mingyao Li
- Yoav Freund
Who trusts Eric Boerwinkle overall
- Xiaoming Liu
- Xiaoming Liu
- B. Feng
- Abhishek Niroula
- Chunlei Wu
- J. Goldstein
- Rajarshi Ghosh
- Konrad J. Karczewski
- Chang Li
- Xiao-Xia Chang
Papers from Eric Boerwinkle's perspective
Ordered by how strongly the researchers Eric Boerwinkle trusts endorse each paper. Same corpus, a different order for every researcher.
- The Human Gene Mutation Database: 2008 update
- dbSNP: the NCBI database of genetic variation
- Predicting the effects of amino acid substitutions on protein function.
- Predicting deleterious amino acid substitutions.
- Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes.
- 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)
- dbNSFP: A Lightweight Database of Human Non-synonymous SNPs and Their Functional Predictions (Human Mutation)
- Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor
- Performance of mutation pathogenicity prediction methods on missense variants (Human Mutation)
- RefSeq: an update on mammalian reference sequences
Their papers
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes (2012) — 1,698 citations
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- dbNSFP: A Lightweight Database of Human Non-synonymous SNPs and Their Functional Predictions (2011) — 817 citations
- A framework for the interpretation of de novo mutation in human disease (2014) — 1,035 citations
- Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies. (2015) — 1,063 citations
- A Common Allele on Chromosome 9 Associated with Coronary Heart Disease (2007) — 1,486 citations
- Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer’s disease (2013) — 4,257 citations
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
- dbNSFP v2.0: A Database of Human Non-synonymous SNVs and Their Functional Predictions and Annotations (2013) — 625 citations
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) — 1,860 citations
- Replicating genotype–phenotype associations (2007) — 1,394 citations
- Multiple Novel Loci are Associated with Indices of Renal Function and Chronic Kidney Disease (2009) — 639 citations
- dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Non-synonymous and Splice Site SNVs (2016) — 928 citations
- In silico prediction of splice-altering single nucleotide variants in the human genome (2014) — 481 citations
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) — 1,642 citations
- Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus (2000) — 1,471 citations
- Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study (2008) — 702 citations
- A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) — 2,034 citations
- Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) — 2,422 citations
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) — 1,140 citations