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26 results on '"Stringham, Heather M."'

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

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

3. SMIM1absence is associated with reduced energy expenditure and excess weight

4. The trans-ancestral genomic architecture of glycemic traits

5. Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

6. Exome sequencing of Finnish isolates enhances rare-variant association power

7. Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

8. A catalog of genetic loci associated with kidney function from analyses of a million individuals

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

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

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

12. Exome-wide association study of plasma lipids in >300,000 individuals

13. Novel association of TM6SF2rs58542926 genotype with increased serum tyrosine levels and decreased apoB-100 particles in Finns

14. Rare and low-frequency coding variants alter human adult height

15. Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

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

17. The genetic architecture of type 2 diabetes

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

19. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

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

21. Cosegregation of Open-angle Glaucoma and the Nail-Patella Syndrome

22. Clinical Phenotype of Juvenile-onset Primary Open-angle Glaucoma Linked to Chromosome 1q

23. Fine Localization of the Nijmegen Breakage Syndrome Gene to 8q21: Evidence for a Common Founder Haplotype

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

26. Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power

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