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1. Deciphering the genetic landscape of obesity: a data-driven approach to identifying plausible causal genes and therapeutic targets.

2. Proteome-wide mendelian randomization identifies causal plasma proteins in venous thromboembolism development.

3. Genome-wide meta-analysis revealed several genetic loci associated with serum uric acid levels in Korean population: an analysis of Korea Biobank data.

4. Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.

5. Rare GATA6 variants associated with risk of congenital heart disease phenotypes in 200,000 UK Biobank exomes.

6. Implications of germline copy-number variations in psychiatric disorders: review of large-scale genetic studies.

7. Polygenic risk score as clinical utility in psychiatry: a clinical viewpoint.

8. Unique roles of rare variants in the genetics of complex diseases in humans.

9. Multi-omics study for interpretation of genome-wide association study.

10. Artificial intelligence powered statistical genetics in biobanks.

11. Genome editing for the reproduction and remedy of human diseases in mice.

12. Long noncoding RNA variations in cardiometabolic diseases.

13. Block-based association tests for rare variants using Kullback-Leibler divergence.

14. Detecting multiple variants associated with disease based on sequencing data of case-parent trios.

15. Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data set.

16. Identification of FAM13A gene associated with the ratio of FEV1 to FVC in Korean population by genome-wide association studies including gene-environment interactions.

17. A genome-wide association study of third molar agenesis in Japanese and Korean populations.

18. Influence of the NRGN gene on intellectual ability in schizophrenia.

19. A genome-wide association study of a coronary artery disease risk variant.

20. Genome-wide association study identifies GYS2 as a novel genetic factor for polycystic ovary syndrome through obesity-related condition.

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