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1. The Predictive Utility of Omic Scores for COPD-related Traits

2. Proteomics of CT Emphysema Subtypes. The Subpopulations and Intermediate Outcome Measures in COPD Study (SPIROMICS)

3. Association of CT-Assessed Dysanapsis With Interstitial Lung Abnormalities in Older Adults

5. A Genome-wide Association Study of Dysanapsis Among Adults and Children

6. Proteomics of COPD-Related Phenotypes in the General Population. The Multi-Ethnic Study of Atherosclerosis (MESA) Lung Study

7. Race/ethnic, Ancestral, Social, and Environmental Correlates of Lung Function Decline: The Multi-Ethnic Study of Atherosclerosis (MESA) Lung Study

8. Cross-ancestry investigation of venousc genomic predictors

9. Stroke genetics informs drug discovery and risk prediction across ancestries

10. The Genetic Landscape of Renal Complications in Type 1 Diabetes

11. Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.

12. Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts

13. 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

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

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

16. Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis

17. Identification of non-HLA genes associated with development of islet autoimmunity and type 1 diabetes in the prospective TEDDY cohort

19. Systemic Biomarkers of Lung Function and FEV1 Decline Across Multiple Cohorts

20. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

21. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

22. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting.

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

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

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

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

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

29. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article

30. Novel Association Between Immune-Mediated Susceptibility Loci and Persistent Autoantibody Positivity in Type 1 Diabetes

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

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

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

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

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

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

37. Confirmation of novel type 1 diabetes risk loci in families

38. Contrasting the Genetic Background of Type 1 Diabetes and Celiac Disease Autoimmunity

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

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

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

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

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

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

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