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2. Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

3. The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects

4. The association between lower educational attainment and depression owing to shared genetic effects? Results in ~ 25 000 subjects

5. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

7. Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.

8. Phantom epistasis between unlinked loci.

9. Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color

10. Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

11. Meta-analyses identify DNA methylation associated with kidney function and damage

12. Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability (Nature Genetics, (2018), 50, 5, (652-656), 10.1038/s41588-018-0100-5)

13. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

14. Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses

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

16. Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances

17. Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

18. Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

19. Appraising the causal relevance of DNA methylation for risk of lung cancer

20. Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

21. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

22. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

23. Biological interpretation of genome-wide association studies using predicted gene functions

24. Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes

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

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

27. Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes

28. Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

29. Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

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

31. Biological interpretation of genome-wide association studies using predicted gene functions

32. Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study

33. Association between telomere length and risk of cancer and non-neoplastic diseases: A Mendelian randomization study

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

36. Appraising the causal relevance of DNA methylation for risk of lung cancer

37. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study

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

39. Genetic Relationship between Schizophrenia and Nicotine Dependence

40. Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysis

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

43. The association between lower educational attainment and depression owing to shared genetic effects? Results in ∼25 000 subjects: Results in ~25,000 subjects

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

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

47. The association between lower educational attainment and depression owing to shared genetic effects? Results in ∼25 000 subjects

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

49. Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index

50. Extensive QTL and association analyses of the QTLMAS2009 Data

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