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1. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

2. Genetic variants associated with longitudinal changes in brain structure across the lifespan

3. Circulating Metabolome and White Matter Hyperintensities in Women and Men

4. Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

6. Association of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

7. DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood

8. Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

9. Improving data availability for brain image biobanking in healthy subjects: Practice-based suggestions from an international multidisciplinary working group

10. Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

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

12. Meta-analyses identify DNA methylation associated with kidney function and damage

13. Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus

14. Human chromosome 7: DNA sequence and biology

16. Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

17. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

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. Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus (vol 13, 1222, 2022)

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