David G Clayton

发表

Control of confounding of genetic associations in stratified populations.

Mark D Shriver, C. Hoggart, D. Clayton, 2003, American journal of human genetics.

Shared and distinct genetic variants in type 1 diabetes and celiac disease.

Cisca Wijmenga, Ross McManus, Vincent Plagnol, 2008, The New England journal of medicine.

SNP allele frequency estimation in DNA pools and variance components analysis.

Panos Deloukas, Pelin Akan, Kate Downes, 2004, BioTechniques.

Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene‐gene and gene‐environment interactions, and parent‐of‐origin effects

Heather J Cordell, D. Clayton, H. Cordell, 2004, Genetic epidemiology.

Remapping the insulin gene/IDDM2 locus in type 1 diabetes.

Mark I McCarthy, Heather J Cordell, Jaakko Tuomilehto, 2004, Diabetes.

Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus.

Adrian Vella, Cristian Guja, Susan M Ring, 2004, Diabetes.

Localization of a type 1 diabetes locus in the IL2RA/CD25 region by use of tag single-nucleotide polymorphisms.

Adrian Vella, Wendy McArdle, Susan M Ring, 2005, American journal of human genetics.

Betting odds and genetic associations.

D. Clayton, David G Clayton, Duncan C. Thomas, 2004, Journal of the National Cancer Institute.

Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene.

Sergey Nejentsev, Constantin Ionescu-Tirgoviste, Jaakko Tuomilehto, 2004, Human molecular genetics.

Sex chromosomes and genetic association studies

D. Clayton, David G Clayton, 2009, Genome Medicine.

Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes

Mark Atkinson, Vincent Plagnol, Neil M Walker, 2007, Nature Genetics.

Complement factor H variant Y402H is a major risk determinant for geographic atrophy and choroidal neovascularization in smokers and nonsmokers.

D. Clayton, A. Bird, A. Moore, 2006, Investigative ophthalmology & visual science.