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1. Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk

2. Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease

3. Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

4. Rare variant contribution to the heritability of coronary artery disease

5. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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

7. Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

8. Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

9. Genetic diversity fuels gene discovery for tobacco and alcohol use

10. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

11. Rare coding variants in RCN3 are associated with blood pressure

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

13. Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

14. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

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

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

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

18. Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts

19. A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment

20. Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

21. Epigenome-wide association study of mitochondrial genome copy number.

22. Association of mitochondrial DNA copy number with cardiometabolic diseases

23. A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program

24. Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

25. Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes

26. Population sequencing data reveal a compendium of mutational processes in the human germ line.

27. Allele-specific variation at APOE increases nonalcoholic fatty liver disease and obesity but decreases risk of Alzheimer’s disease and myocardial infarction

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

29. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.

30. Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

31. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

32. Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

33. Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.

34. Inherited causes of clonal haematopoiesis in 97,691 whole genomes

35. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.

36. Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels

37. Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

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

39. Insulin Resistance Exacerbates Genetic Predisposition to Nonalcoholic Fatty Liver Disease in Individuals Without Diabetes

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

41. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

42. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies

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

44. Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease

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

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

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

49. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

50. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.

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