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1. Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study

2. Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study

3. Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

4. Exploring the role of genetic confounding in the association between maternal and offspring body mass index: evidence from three birth cohorts

5. Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

6. Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

7. Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

8. Assessment of the genetic and clinical determinants of fracture risk: Genome wide association and mendelian randomisation study

9. Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero

10. Association between telomere length and risk of cancer and non-neoplastic diseases a mendelian randomization study

11. Epigenome-wide Association of DNA Methylation in Whole Blood With Bone Mineral Density

12. Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus

13. Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis

14. Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus

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

16. Genome-wide association study identifies 74 loci associated with educational attainment

17. A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts

18. Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

19. Heritability and genome-wide association analyses of sleep duration in children: The EAGLE consortium

20. Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium

21. Association of Forced Vital Capacity with the Developmental Gene NCOR2

22. Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

23. Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

24. Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

25. Genetic sharing with cardiovascular disease risk factors and diabetes reveals novel bone mineral density loci

26. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

27. Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder

28. Phenotypic Dissection of Bone Mineral Density Reveals Skeletal Site Specificity and Facilitates the Identification of Novel Loci in the Genetic Regulation of Bone Mass Attainment

29. Phenotypic Dissection of Bone Mineral Density Reveals Skeletal Site Specificity and Facilitates the Identification of Novel Loci in the Genetic Regulation of Bone Mass Attainment

30. Genetic variation associated with differential educational attainment in adults has anticipated associations with school performance in children

31. Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

32. Genome Wide Association Identifies Common Variants at the SERPINA6/SERPINA1 Locus Influencing Plasma Cortisol and Corticosteroid Binding Globulin

33. Common variation near ROBO2 is associated with expressive vocabulary in infancy

34. Genome-wide association study of height-adjusted BMI in childhood identifies functional variant in ADCY3

35. Harmonization of neuroticism and extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: An application of item response theory

36. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

37. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

38. GWAS of 126,559 individuals identifies genetic variants associated with educational attainment

39. Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

40. Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants

41. Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates

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. Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus

44. Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

45. Common variants at 12q15 and 12q24 are associated with infant head circumference

46. WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk

47. Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk

48. Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

49. Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: Results of genome-wide association analyses including 4659 European individuals

50. A genome-wide association study reveals variants in ARL15 that influence adiponectin levels

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