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1. The genetic landscape of neuro-related proteins in human plasma

3. DNAm scores for serum GDF15 and NT-proBNP levels associate with a range of traits affecting the body and brain

4. Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes

6. Epigenetic scores of blood-based proteins as biomarkers of general cognitive function and brain health

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

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

9. DNA methylation-based predictors of metabolic traits in Scottish and Singaporean cohorts

10. Identification of circulating proteins associated with general cognitive function among middle-aged and older adults

11. DNA methylation GrimAge version 2

12. Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

13. Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate

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

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

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

17. Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

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

20. Refining epigenetic prediction of chronological and biological age

21. Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

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

23. Early Developmental EEG and Seizure Phenotypes in a Full Gene Deletion of Ubiquitin Protein Ligase E3A Rat Model of Angelman Syndrome.

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

26. Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

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

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

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

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

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

33. Longitudinal dynamics of clonal hematopoiesis identifies gene-specific fitness effects

34. Blood-based epigenome-wide association study and prediction of alcohol consumption.

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

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

40. Blood-based epigenome-wide analyses of cognitive abilities

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

43. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

44. An epigenetic predictor of death captures multi-modal measures of brain health

45. Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability

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

47. Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach.

48. Blood- and brain-based genome-wide association studies of smoking

49. Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability

50. Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes

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