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1. A Catalogue of Structural Variation across Ancestrally Diverse Asian Genomes

2. Author Correction: Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

3. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

4. Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

5. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

6. Genetic insights into resting heart rate and its role in cardiovascular disease.

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

8. Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk

9. General and abdominal adiposity and hypertension in eight world regions: a pooled analysis of 837 population-based studies with 7·5 million participants

12. Worldwide trends in underweight and obesity from 1990 to 2022: a pooled analysis of 3663 population-representative studies with 222 million children, adolescents, and adults

14. An atlas of genetic scores to predict multi-omic traits

15. Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.

16. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.

17. Risk prediction models for type 2 diabetes using either fasting plasma glucose or HbA1c in Chinese, Malay, and Indians: Results from three multi-ethnic Singapore cohorts

18. The Singapore National Precision Medicine Strategy

19. A five-safes approach to a secure and scalable genomics data repository

20. The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits

21. Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

22. Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk

23. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

24. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.

25. Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

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

27. Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

28. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

29. Overlap of high-risk individuals predicted by family history, and genetic and non-genetic breast cancer risk prediction models: implications for risk stratification

30. Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations

31. Breast cancer risks associated with missense variants in breast cancer susceptibility genes

32. Analysis of clinically relevant variants from ancestrally diverse Asian genomes

33. Identification of genetic effects underlying type 2 diabetes in South Asian and European populations

34. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

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

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

38. A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes

39. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

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

41. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

42. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

44. Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood

45. A Low-Frequency Inactivating Akt2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.

46. Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians

47. Genome-Wide Interaction Analysis with DASH Diet Score Identified Novel Loci for Systolic Blood Pressure

48. Characterizing the Relationship between Expression Quantitative Trait Loci (eQTLs), DNA Methylation Quantitative Trait Loci (mQTLs), and Breast Cancer Risk Variants.

49. Novel Genetic Loci Associated With Retinal Microvascular Diameter

50. APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups

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