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2. The role of accelerometer-derived sleep traits on glycated haemoglobin and glucose levels: a Mendelian randomization study

5. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

9. The impact of Mendelian sleep and circadian genetic variants in a population setting

10. The power of genetic diversity in genome-wide association studies of lipids

11. A saturated map of common genetic variants associated with human height

12. Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

13. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

14. Higher maternal adiposity reduces offspring birthweight if associated with a metabolically favourable profile

16. Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

17. An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

19. Penetrance of Pathogenic Genetic Variants Associated With Premature Ovarian Insufficiency

21. Rare and low-frequency coding variants alter human adult height

22. Genome-wide associations for birth weight and correlations with adult disease

23. Sleep characteristics across the lifespan in 1.1 million people from the Netherlands, United Kingdom and United States: a systematic review and meta-analysis

24. Prosaposin is a regulator of progranulin levels and oligomerization.

25. Colorectal cancer risk stratification using a polygenic risk score in symptomatic patients presenting to primary care — a UK Biobank retrospective cohort study

27. Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome

28. Using human genetics to understand the disease impacts of testosterone in men and women

30. Directional dominance on stature and cognition in diverse human populations

31. Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes

32. New genetic loci link adipose and insulin biology to body fat distribution

33. Genetic studies of body mass index yield new insights for obesity biology

34. Defining the role of common variation in the genomic and biological architecture of adult human height

35. SMIM1 absence is associated with reduced energy expenditure and excess weight

36. Hyperglycaemia is a causal risk factor for upper limb pathologies.

37. Does physical activity moderate the association between shorter leukocyte telomere length and incident coronary heart disease? Data from 54,180 UK Biobank participants

39. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

40. No Interactions Between Previously Associated 2-Hour Glucose Gene Variants and Physical Activity or BMI on 2-Hour Glucose Levels

41. A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone–Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone Regulation

42. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.

43. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

44. Hundreds of variants clustered in genomic loci and biological pathways affect human height

45. Colorectal cancer risk stratification using a polygenic risk score in symptomatic primary care patients—a UK Biobank retrospective cohort study

46. Using Mendelian Randomisation methods to understand whether diurnal preference is causally related to mental health

48. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

49. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

50. Loci for insulin processing and secretion provide insight into type 2 diabetes risk

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