Chris Wallace

Genetics · 2007–2021

A researcher in the Science corpus: 12 papers; trusts 23 researchers and is trusted by 7 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 188 citations into it; #2,136 of 6,854 by trust here, #126 by citations
• Molecular Biology — 105 citations into it
• Epidemiology — 16 citations into it
• Rheumatology — 8 citations into it

Whom Chris Wallace trusts overall

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

1. Tomaz Berisa
2. Joseph K. Pickrell
3. Farhad Hormozdiari
4. Christian Benner
5. Peter M. Visscher
6. Chris C. A. Spencer
7. Naomi R. Wray
8. Eric E. Schadt
9. G. McVean
10. Jimmy Zhenli Liu

Who trusts Chris Wallace overall

1. Christopher N. Foley
2. James R. Staley
3. Philip G. Breen

Papers from Chris Wallace's perspective

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

1. FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
2. 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
3. Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics (PLoS Genetics)
4. Genomewide association studies and assessment of the risk of disease. (New England Journal of Medicine)
5. Detection and interpretation of shared genetic influences on 42 human traits (Nature Genetics)
6. Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets (Nature Genetics)
7. Candidate Causal Regulatory Effects by Integration of Expression QTLs with Complex Trait Genetic Associations (PLoS Genetics)
8. Approximately independent linkage disequilibrium blocks in human populations (bioRxiv)
9. Integrative approaches for large-scale transcriptome-wide association studies (Nature Genetics)
10. Defining the role of common variation in the genomic and biological architecture of adult human height

Their papers

• Genome-wide association analysis identifies 20 loci that influence adult height (2008) — 819 citations
• A more accurate method for colocalisation analysis allowing for multiple causal variants (2021) — 447 citations
• Eliciting priors and relaxing the single causal variant assumption in colocalisation analyses (2019) — 340 citations
• Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers (2015) — 661 citations
• Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics (2013) — 3,608 citations
• Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease (2011) — 835 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
• Faculty Opinions recommendation of Genome-wide association study identifies eight loci associated with blood pressure. (2009) — 1,206 citations
• Common variants near MC4R are associated with fat mass, weight and risk of obesity (2008) — 1,371 citations
• Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2008) — 1,801 citations
• Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes (2007) — 1,532 citations
• Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) — 9,550 citations