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1. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.

2. Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification.

3. Genome-wide characterization of circulating metabolic biomarkers

4. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

5. Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake

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

8. Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk

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

11. Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

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

15. Exome sequencing of Finnish isolates enhances rare-variant association power

16. Integrative analysis of the genome, transcriptome, and proteome identifies causal mechanisms of complex traits.

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

20. Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups

24. Metabolome-wide Mendelian randomization characterizes heterogeneous and shared causal effects of metabolites on human health

25. A multi-ancestry genome-wide meta-analysis, fine-mapping, and gene prioritization approach to characterize the genetic architecture of adiponectin

26. Biomimetic nanoparticles in ischemic stroke therapy

27. Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion

28. Retraction notice to “Bach2 regulates aberrant activation of B cell in systemic lupus erythematosus and can be negatively regulated by BCR-ABL/PI3K” [Exp. Cell Res. 365 (1), 1 April 2018, Pages 138–144]

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

30. Retraction notice to “NFKB1 mediates Th1/Th17 activation in the pathogenesis of psoriasis” [Cell. Immunol. 331 (2018) 16–21]

31. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

35. Additional file 26 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

36. Additional file 34 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

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

38. Author Correction : The power of genetic diversity in genome-wide association studies of lipids

39. Additional file 6 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

40. Additional file 9 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

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

42. Correction: Author Correction: Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis

43. Distinct transcriptome architectures underlying lupus establishment and exacerbation

44. Common susceptibility variants are shared between schizophrenia and psoriasis in the Han Chinese population

45. N6-Methyladenosine-modified lncRNA LINREP promotes Glioblastoma progression by recruiting the PTBP1/HuR complex

48. Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort

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