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22 results on '"Bottinger, E.P. (Erwin)"'

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1. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

2. The Polygenic and Monogenic Basis of Blood Traits and Diseases

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

4. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

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

6. Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations

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

8. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits

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

10. 1000 Genomes-based metaanalysis identifies 10 novel loci for kidney function

11. CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

12. Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

13. Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

14. An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group

15. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

16. Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

17. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

18. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

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

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

21. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

22. Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

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