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Your search keyword '"Watkins, H."' showing total 37 results

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37 results on '"Watkins, H."'

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

2. Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

3. Erratum to: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

4. Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations

5. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

6. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

7. Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116))

8. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (vol 42, pg 105, 2010)

9. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

10. Large-scale association analysis identifies new risk loci for coronary artery disease

11. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits.

12. GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification.

13. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.

14. The trans-ancestral genomic architecture of glycemic traits.

15. Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.

16. Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.

17. Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.

18. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.

19. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.

20. Association analyses based on false discovery rate implicate new loci for coronary artery disease.

21. Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.

22. Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.

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

24. Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

25. A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.

26. Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.

27. Meta-analysis of gene-level tests for rare variant association.

28. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.

29. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.

30. Large-scale association analysis identifies new risk loci for coronary artery disease.

31. Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.

32. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.

33. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.

34. Genome-wide association study identifies eight loci associated with blood pressure.

35. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.

37. A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

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