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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

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

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

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

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

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

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

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

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

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

19. Rare genetic variants explain missing heritability in smoking

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

45. Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection

48. The Promises and Pitfalls of Genoeconomics

50. Genetic architecture of subcortical brain structures in 38,851 individuals

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