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30 results on '"Nolte, IM"'

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1. Genetic architecture reconciles linkage and association studies of complex traits.

2. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

3. Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

4. Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries.

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

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

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

8. Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.

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

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

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

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

13. Genotype-covariate interaction effects and the heritability of adult body mass index.

14. Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.

15. Genome-wide analysis identifies 12 loci influencing human reproductive behavior.

16. Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.

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

18. Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.

19. Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.

20. Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index.

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

22. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.

23. Discovery and refinement of loci associated with lipid levels.

24. Common variants associated with plasma triglycerides and risk for coronary artery disease.

25. Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.

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

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

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

29. A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).

30. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.

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