Search

Your search keyword '"Chasman, Daniel I"' showing total 1,651 results

Search Constraints

Start Over You searched for: Author "Chasman, Daniel I" Remove constraint Author: "Chasman, Daniel I"
1,651 results on '"Chasman, Daniel I"'

Search Results

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

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

3. Broadcasters, receivers, functional groups of metabolites, and the link to heart failure by revealing metabolomic network connectivity

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

5. Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

6. Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance

7. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

8. Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

9. Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

10. Genetic diversity fuels gene discovery for tobacco and alcohol use

11. Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning

12. Clonal hematopoiesis of indeterminate potential, DNA methylation, and risk for coronary artery disease

13. Understanding the complex genetic architecture connecting rheumatoid arthritis, osteoporosis and inflammation: discovering causal pathways

15. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

16. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

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

18. Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

19. The Pharmacogenetics of Statin Therapy on Clinical Events: No Evidence that Genetic Variation Affects Statin Response on Myocardial Infarction

20. Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

22. Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations.

23. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

24. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.

25. Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

26. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

27. Genome-wide association study identifies 48 common genetic variants associated with handedness

28. Evidence in the UK Biobank for the underdiagnosis of erythropoietic protoporphyria

29. Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

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

31. A saturated map of common genetic variants associated with human height

32. Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels

33. Statin-induced LDL cholesterol response and type 2 diabetes: a bidirectional two-sample Mendelian randomization study.

34. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.

35. 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

36. Rare Genetic Variants Associated With Sudden Cardiac Death in Adults

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

38. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

39. Gene-lifestyle interactions in the genomics of human complex traits

40. Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

41. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

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

43. Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease

45. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

46. Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

47. Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

Catalog

Books, media, physical & digital resources