John A. Todd

Genetics · 2001–2021

A researcher in the Science corpus: 18 papers; trusts 1 researcher and is trusted by 1 researcher here, as inferred from the citation graph.

Subfields

• Genetics — 221 citations into it; #5,320 of 6,854 by trust here, #115 by citations
• Molecular Biology — 156 citations into it

Whom John A. Todd trusts overall

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

1. J. K. Pritchard

Who trusts John A. Todd overall

1. Elizabeth T. Cirulli
2. J. Wakefield

Papers from John A. Todd's perspective

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

1. High-resolution haplotype structure in the human genome (Nature Genetics)
2. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex (Nature Genetics)
3. Haplotype tagging for the identification of common disease genes (Nature Genetics)
4. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease (Nature Genetics)
5. On the allelic spectrum of human disease. (Trends in Genetics)
6. A Fine-Scale Map of Recombination Rates and Hotspots Across the Human Genome (Science)
7. Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. (American Journal of Human Genetics)
8. Linkage disequilibrium in humans: models and data. (American Journal of Human Genetics)
9. The effects of human population structure on large genetic association studies
10. Genetic analysis of genome-wide variation in human gene expression (Nature)

Their papers

• Haplotype tagging for the identification of common disease genes (2001) — 1,250 citations
• An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci (2021) — 462 citations
• Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics (2020) — 535 citations
• Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England (2021) — 1,098 citations
• SARS-CoV-2 evolution during treatment of chronic infection (2021) — 955 citations
• Genomic atlas of the human plasma proteome (2018) — 1,884 citations
• Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers (2015) — 661 citations
• Bayesian refinement of association signals for 14 loci in 3 common diseases (2012) — 508 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
• Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect against Type 1 Diabetes (2009) — 1,029 citations
• Shared and Distinct Genetic Variants in Type 1 Diabetes and Celiac Disease (2008) — 701 citations
• HLA DR-DQ Haplotypes and Genotypes and Type 1 Diabetes Risk (2008) — 761 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
• A high resolution HLA and SNP haplotype map for disease association studies in the extended human MHC (2006) — 810 citations
• A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region (2006) — 677 citations
• Genome-wide association studies: theoretical and practical concerns (2005) — 1,216 citations
• Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease (2003) — 2,313 citations