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

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

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

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

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

7. Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease

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

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

11. Genetic insights into resting heart rate and its role in cardiovascular disease

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

16. Unraveling motion in proteins by combining NMR relaxometry and molecular dynamics simulations: A case study on ubiquitin.

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

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

19. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

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

22. Rare genetic variants explain missing heritability in smoking

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

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

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

26. Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

27. Novel methods of recording flow curves in proton irradiated material

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

32. Correction: Association of low-frequency and rare coding variants with information processing speed

34. Telomere length is not a main factor for the development of islet autoimmunity and type 1 diabetes in the TEDDY study

35. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

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

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

39. GA4GH: International policies and standards for data sharing across genomic research and healthcare

40. A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

42. What makes a habitat a home? Habitat associations of juvenile European sea bass, Dicentrarchus labrax, in estuarine nurseries.

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

46. Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

47. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

48. Association of low-frequency and rare coding variants with information processing speed

49. Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function

50. Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes

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