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2. Genetic links between ovarian ageing, cancer risk and de novo mutation rates

3. Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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