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

2. Methylation patterns associated with C-reactive protein in racially and ethnically diverse populations

3. Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

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

5. Determinants of mosaic chromosomal alteration fitness.

6. Genetic variants for head size share genes and pathways with cancer

7. Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

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

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

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

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

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

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

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

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

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

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

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

21. Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

22. Proteome Network Analysis Identifies Potential Biomarkers for Brain Aging

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

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

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

26. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

27. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

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

29. Rare genetic variants explain missing heritability in smoking.

30. Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study

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

32. Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application

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

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

35. Genomic Studies Across the Lifespan Point to Early Mechanisms Determining Subcortical Volumes

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

37. Biomedical consequences of elevated cholesterol-containing lipoproteins and apolipoproteins on cardiovascular and non-cardiovascular outcomes

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

39. Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

40. New insights into the genetic etiology of Alzheimer’s disease and related dementias

41. Clonal Hematopoiesis Is Associated With Higher Risk of Stroke

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

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

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

45. A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment

46. Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease

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

48. Whole genome sequence analysis of blood lipid levels in >66,000 individuals

49. Associations of Pulmonary Function with MRI Brain Volumes: A Coordinated Multi-Study Analysis

50. Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

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