Search

Your search keyword '"Fornage, Myriam"' showing total 2,863 results

Search Constraints

Start Over You searched for: Author "Fornage, Myriam" Remove constraint Author: "Fornage, Myriam"
2,863 results on '"Fornage, Myriam"'

Search Results

1. Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries

2. Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores.

3. Determinants of mosaic chromosomal alteration fitness.

4. Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration

5. Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

6. Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas

7. Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification.

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

9. Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk

10. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.

11. Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

12. Rare variant contribution to the heritability of coronary artery disease

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

15. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

16. Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function

17. The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

18. Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals.

19. Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.

20. Plasma metabolites associated with cognitive function across race/ethnicities affirming the importance of healthy nutrition

21. Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.

22. Alzheimers Disease Genetic Risk, Cognition, and Brain Aging in Midlife.

23. Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI

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

25. A polygenic risk score for Alzheimer’s disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S.

26. Genetic loci of beta-aminoisobutyric acid are associated with aging-related mild cognitive impairment

27. Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups

28. Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study.

29. Genetic associations between sleep traits and cognitive ageing outcomes in the Hispanic Community Health Study/Study of Latinos

30. Interaction analysis of ancestry-enriched variants with APOE-ɛ4 on MCI in the Study of Latinos-Investigation of Neurocognitive Aging

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

32. Correlations between complex human phenotypes vary by genetic background, gender, and environment

33. Rare coding variants in RCN3 are associated with blood pressure

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

35. Rare genetic variants explain missing heritability in smoking.

36. A population‐based meta‐analysis of circulating GFAP for cognition and dementia risk

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

38. Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

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

40. A Mendelian randomization study of genetic liability to post-traumatic stress disorder and risk of ischemic stroke

41. Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

42. Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program

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

44. Clonal Hematopoiesis Is Associated With Higher Risk of Stroke

45. Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

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

47. Clonal hematopoiesis is associated with protection from Alzheimer’s disease

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

49. Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

50. The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.

Catalog

Books, media, physical & digital resources