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1. Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

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

3. Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts

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

5. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

6. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

7. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

8. GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

9. Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function

10. Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels

11. Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

12. Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis

13. Genetic variation at 16q24.2 is associated with small vessel stroke

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

15. Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

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

17. Association of Forced Vital Capacity with the Developmental Gene NCOR2

18. Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

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

20. Gene × dietary pattern interactions in obesity: Analysis of up to 68 317 adults of European ancestry

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

22. Genome-wide association analysis identifies six new loci associated with forced vital capacity

23. Genome-wide association analysis identifies six new loci associated with forced vital capacity

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

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

26. Best Practices and Joint Calling of the HumanExome BeadChip: The CHARGE Consortium

27. Genome-Wide Joint Meta-Analysis of SNP and SNP-by-Smoking Interaction Identifies Novel Loci for Pulmonary Function

28. Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction

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