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1. Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

2. Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores

3. Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

4. Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance

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. Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

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

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

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

11. Deep phenotyping and genomic data from a nationally representative study on dementia in India

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

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

15. Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

17. Bayesian Hierarchical Models for High-Dimensional Mediation Analysis with Coordinated Selection of Correlated Mediators

18. Bayesian Sparse Mediation Analysis with Targeted Penalization of Natural Indirect Effects

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

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

21. Rare genetic variants explain missing heritability in smoking

22. Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning

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

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

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

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

27. Correction: Association of low-frequency and rare coding variants with information processing speed

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

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

30. Whole genome sequence analysis of blood lipid levels in >66,000 individuals

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

33. Association analysis between an epigenetic alcohol risk score and blood pressure.

34. Public comfort with the use of ChatGPT and expectations for healthcare.

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

36. Association analysis between an epigenetic alcohol risk score and blood pressure

38. DNA Methylation at C-Reactive Protein-Associated CpG Sites May Mediate the Pathway Between Educational Attainment and Cognition.

39. Effect of apolipoprotein E ε4 and its modification by sociodemographic characteristics on cognitive measures in South Asians from LASI‐DAD.

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

41. Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program

44. Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

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

46. Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus

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

48. Association of low-frequency and rare coding variants with information processing speed

50. Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes

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