Search Results - "Frayling, T M"
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Estimating sleep parameters using an accelerometer without sleep diary
Published in Scientific reports (28-08-2018)“…Wrist worn raw-data accelerometers are used increasingly in large-scale population research. We examined whether sleep parameters can be estimated from these…”
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C-reactive protein levels and body mass index: elucidating direction of causation through reciprocal Mendelian randomization
Published in International Journal of Obesity (01-02-2011)“…Context: The assignment of direction and causality within networks of observational associations is problematic outside randomized control trials, and the…”
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Genome-wide association studies: the good, the bad and the ugly
Published in Clinical medicine (London, England) (01-08-2014)Get full text
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Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population
Published in Diabetologia (01-01-2007)“…India has the greatest number of diabetic subjects in any one country, but the genetic basis of type 2 diabetes mellitus in India is poorly understood. Common…”
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Is the thrifty genotype hypothesis supported by evidence based on confirmed type 2 diabetes- and obesity-susceptibility variants
Published in Diabetologia (01-09-2009)“…Aims/hypothesis According to the thrifty genotype hypothesis, the high prevalence of type 2 diabetes and obesity is a consequence of genetic variants that have…”
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genetic link between type 2 diabetes and prostate cancer
Published in Diabetologia (01-10-2008)“…Epidemiological studies suggest that men with type 2 diabetes are less likely than non-diabetic men to develop prostate cancer. The cause of this association…”
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FTO gene variants are strongly associated with type 2 diabetes in South Asian Indians
Published in Diabetologia (01-02-2009)“…Aims and hypothesis Variants of the FTO (fat mass and obesity associated) gene are associated with obesity and type 2 diabetes in white Europeans, but these…”
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Common genetic variation in the melatonin receptor 1B gene (MTNR1B) is associated with decreased early-phase insulin response
Published in Diabetologia (01-08-2009)“…Aims/hypothesis We investigated whether variation in MTNR1B, which was recently identified as a common genetic determinant of fasting glucose levels in…”
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An FTO variant is associated with Type 2 diabetes in South Asian populations after accounting for body mass index and waist circumference
Published in Diabetic medicine (01-06-2011)“…Diabet. Med. 28, 673–680 (2011) Aims A common variant, rs9939609, in the FTO (fat mass and obesity) gene is associated with adiposity in Europeans, explaining…”
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A common variant of the interleukin 6 receptor ( ) gene increases IL-6r and IL-6 levels, without other inflammatory effects
Published in Genes and immunity (01-10-2007)“…Interleukin-6 (IL-6) is a key inflammatory cytokine, signalling to most tissues by binding to a soluble IL-6 receptor (sIL-6r), making a complex with gp130. We…”
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Beta cell glucose sensitivity is decreased by 39% in non-diabetic individuals carrying multiple diabetes-risk alleles compared with those with no risk alleles
Published in Diabetologia (01-11-2008)“…Aims/hypothesis Novel type 2 diabetes-susceptibility loci have been identified with evidence that individually they mediate the increased diabetes risk through…”
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Genetic studies of diabetes following the advent of the genome-wide association study: where do we go from here
Published in Diabetologia (01-11-2007)Get full text
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Multiple genetic variants explain measurable variance in type 2 diabetes-related traits in Pakistanis
Published in Diabetologia (01-08-2012)“…Aims/hypothesis Multiple genetic variants are associated with type 2 diabetes-related traits in Europeans, but their role in South Asian populations needs…”
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Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes
Published in Diabetologia (01-12-2008)“…Aims/hypothesis There are strong associations between measures of inflammation and type 2 diabetes, but the causal directions of these associations are not…”
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Large-scale studies of the association between variation at the TNF/LTA locus and susceptibility to type 2 diabetes
Published in Diabetologia (01-10-2005)“…The proinflammatory cytokine TNF-alpha has been implicated in the pathogenesis of insulin resistance and type 2 diabetes, and variation in the gene encoding…”
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Assessing association of common variation in the C1Q gene cluster with systemic lupus erythematosus
Published in Clinical and experimental immunology (01-08-2010)“…Recent studies have tested genetic variation at the C1QA, C1QB and C1QC (complement component 1, q subcomponent, A chain, complement component 1, q…”
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role for coding functional variants in HNF4A in type 2 diabetes susceptibility
Published in Diabetologia (01-01-2011)“…Aims/hypothesis Rare mutations in the gene HNF4A, encoding the transcription factor hepatocyte nuclear factor 4α (HNF-4A), account for ~5% of cases of MODY and…”
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association of common genetic variants in the APOA5, LPL and GCK genes with longitudinal changes in metabolic and cardiovascular traits
Published in Diabetologia (2009)“…Aims/hypothesis Common genetic variants influence plasma triacylglycerol, HDL-cholesterol (HDL-C) and glucose levels in cross-sectional studies. However, the…”
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Sequencing PDX1 (insulin promoter factor 1) in 1788 UK individuals found 5% had a low frequency coding variant, but these variants are not associated with Type 2 diabetes
Published in Diabetic medicine (01-06-2011)“…Diabet. Med. 28, 681–684 (2011) Aim Genome‐wide association studies have identified > 30 common variants associated with Type 2 diabetes (> 5% minor allele…”
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Mutations in the human Delta homologue, DLL3 , cause axial skeletal defects in spondylocostal dysostosis
Published in Nature genetics (01-04-2000)“…Spondylocostal dysostosis (SD, MIM 277300) is a group of vertebral malsegmentation syndromes with reduced stature resulting from axial skeletal defects. SD is…”
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