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3. Estimation of the Required Lipoprotein(a)-Lowering Therapeutic Effect Size for Reduction in Coronary Heart Disease Outcomes: A Mendelian Randomization Analysis

4. Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

5. Associations of autozygosity with a broad range of human phenotypes

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

7. Evaluating the causal relation of ApoA-IV with disease-related traits - A bidirectional two-sample mendelian randomization study

8. A genome-wide association meta-analysis on apolipoprotein A-IV concentrations

9. A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms

10. Association between telomere length and risk of cancer and non-neoplastic diseases a mendelian randomization study

11. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

13. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

14. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

19. New genetic loci link adipose and insulin biology to body fat distribution.

20. Directional dominance on stature and cognition in diverse human populations.

21. New genetic loci link adipose and insulin biology to body fat distribution

22. Directional dominance on stature and cognition in diverse human populations

23. Defining the role of common variation in the genomic and biological architecture of adult human height.

24. Directional dominance on stature and cognition in diverse human populations

26. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.

27. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

29. W48 GENETIC VARIATION WITHIN ADIPONUTRIN IS ASSOCIATED WITH LIPOPROTEIN METABOLISM AND LIVER FUNCTION

34. Evidence of Linkage of Familial Hypoalphalipoproteinemia to a Novel Locus on Chromosome 11q23

36. Genotype-by-sex interaction in the aetiology of type 2 diabetes mellitus: support for sex-specific quantitative trait loci in Hypertension Genetic Epidemiology Network participants.

37. Genome-Wide Meta-Analyses of Smoking Behaviors in African Americans

40. Defining the role of common variation in the genomic and biological architecture of adult human height

41. Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease

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