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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

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

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

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

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

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

27. Biomimetic nanoparticles in ischemic stroke therapy

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

29. 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]

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

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

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

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

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

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

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

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

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

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

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

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

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

45. Distinct transcriptome architectures underlying lupus establishment and exacerbation

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

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