Research Topics
Genomes and Genes
Species | Carl A AndersonSummaryAffiliation: University of Oxford Country: UK Publications
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Detail Information
Publications
Evaluating the effects of imputation on the power, coverage, and cost efficiency of genome-wide SNP platformsCarl A Anderson
The Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, OX3 7BN Oxford, UK
Am J Hum Genet 83:112-9. 2008..Platforms consisting of around 1 million SNPs offer poor cost efficiency for SNP association in European populations...
Estimation of variance components for age at menarche in twin familiesCarl A Anderson
Genetic Epidemiology Group, Queensland Institute of Medical Research, Brisbane 4029, Australia
Behav Genet 37:668-77. 2007..50 and 0.54, and common environmental effects to be 0.31 and 0.29, respectively. We conclude that variation in AAM can be explained by additive genetic and common environmental components...
Genome-wide association meta-analysis identifies new endometriosis risk lociDale R Nyholt
Queensland Institute of Medical Research, Brisbane, Queensland, Australia
Nat Genet 44:1355-9. 2012..8 × 10(-11)), indicating that many weakly associated SNPs represent true endometriosis risk loci and that risk prediction and future targeted disease therapy may be transferred across these populations...
Basic statistical analysis in genetic case-control studiesGeraldine M Clarke
Genetic and Genomic Epidemiology Unit, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK
Nat Protoc 6:121-33. 2011..Study design, marker selection and quality control of case-control studies have also been discussed in earlier protocols. The protocol should take ~1 h to complete...
Marker selection for genetic case-control association studiesFredrik H Pettersson
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK
Nat Protoc 4:743-52. 2009..Publicly available web-based resources are utilized to browse and retrieve data, and software, such as Haploview and Goldsurfer2, is applied to investigate LD and to select tagSNPs...
Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationshipCarl A Anderson
Genetic and Genomic Epidemiology Unit, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, UK
Gastroenterology 136:523-9.e3. 2009..Furthermore, the recently identified UC locus at ECM1 requires formal testing for association with CD...
A genome-wide linkage scan for age at menarche in three populations of European descentCarl A Anderson
Queensland Institute of Medical Research, Royal Brisbane Hospital, Queensland 4029, Australia
J Clin Endocrinol Metab 93:3965-70. 2008..Age at menarche (AAM) is an important trait both biologically and socially, a clearly defined event in female pubertal development, and has been associated with many clinically significant phenotypes...
Meta-analysis and imputation refines the association of 15q25 with smoking quantityJason Z Liu
Department of Statistics, University of Oxford, Oxford, UK
Nat Genet 42:436-40. 2010..Our fine-mapping approach identified a SNP showing the highest significance, rs55853698, located within the promoter region of CHRNA5. Conditional analysis also identified a secondary locus (rs6495308) in CHRNA3...
Data quality control in genetic case-control association studiesCarl A Anderson
Genetic and Genomic Epidemiology Unit, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK
Nat Protoc 5:1564-73. 2010..Issues concerning study design and marker selection in case-control studies have been discussed in our earlier protocols. This protocol, which is routinely used in our labs, should take approximately 8 h to complete...
Genome-wide association study identifies a locus at 7p15.2 associated with endometriosisJodie N Painter
Molecular Epidemiology, Queensland Institute of Medical Research, Herston, Queensland, Australia
Nat Genet 43:51-4. 2011..4 × 10⁻⁹ (OR = 1.20, 95% CI 1.13-1.27) for 'all' endometriosis in our combined datasets of 5,586 cases and 9,331 controls. rs12700667 is located in an intergenic region upstream of the plausible candidate genes NFE2L3 and HOXA10...
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseJeffrey C Barrett
Bioinformatics and Statistical Genetics, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK
Nat Genet 40:955-62. 2008..The expanded molecular understanding of the basis of this disease offers promise for informed therapeutic development...
Confirmation of the role of ATG16L1 as a Crohn's disease susceptibility geneJ R Fraser Cummings
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK
Inflamm Bowel Dis 13:941-6. 2007..The aims of the study were to replicate the association with CD, examine subphenotype associations and statistical interactions with CARD15, IL23R, and the IBD5 risk haplotype, as well as explore the association with UC...
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibilityMiles Parkes
Inflammatory Bowel Disease Research Group, Addenbrooke s Hospital, University of Cambridge, Cambridge CB2 2QQ, UK
Nat Genet 39:830-2. 2007..We obtained replication for the autophagy-inducing IRGM gene on chromosome 5q33.1 (replication P = 6.6 x 10(-4), combined P = 2.1 x 10(-10)) and for nine other loci, including NKX2-3, PTPN2 and gene deserts on chromosomes 1q and 5p13...
Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's diseaseSheila A Fisher
Department of Medical and Molecular Genetics, King s College London School of Medicine, 8th Floor Guy s Tower, Guy s Hospital, London SE1 9RT, UK
Nat Genet 40:710-2. 2008..These data provide the first detailed illustration of the genetic relationship between these common inflammatory bowel diseases...
Process characterization of powder blending by near-infrared spectroscopy: blend end-points and beyondZhenqi Shi
Graduate School of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA 15282, USA
J Pharm Biomed Anal 47:738-45. 2008....
A genome-wide linkage study in families with major depression and co-morbid unexplained swellingCarl A Anderson
Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK
Am J Med Genet B Neuropsychiatr Genet 147:356-62. 2008....
A simple linear regression method for quantitative trait loci linkage analysis with censored observationsCarl A Anderson
Institute of Evolutionary Biology, University of Edinburgh, Scotland
Genetics 173:1735-45. 2006..On the basis of linear regression methodology, the grouped linear regression model is computationally simple and fast and can be implemented readily in freely available statistical software...
