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1. Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (Nature Communications, (2021), 12, 1, (24), 10.1038/s41467-020-19366-9)

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

3. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

4. Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

5. WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene

6. WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene

7. Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium

8. An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis

9. Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals

10. Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation

11. Erratum to: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

12. Skewed X-inactivation is common in the general female population

13. ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

14. GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

15. PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

16. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

17. Genome-wide identification of directed gene networks using large-scale population genomics data

18. A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy

19. Fifteen Genetic Loci Associated with the Electrocardiographic P Wave

20. Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity

21. Discovery of novel heart rate-associated loci using the Exome Chip

22. A systematic SNP selection approach to identify mechanisms underlying disease aetiology: Linking height to post-menopausal breast and colorectal cancer risk

23. Association of the IGF1 gene with fasting insulin levels

24. Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits

25. A combined linkage and exome sequencing analysis for electrocardiogram parameters in the Erasmus Rucphen family study

26. Genetic variants in RBFOX3 are associated with sleep latency

27. Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs

28. A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

29. Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram

30. Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

31. A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

32. Interferon gamma receptor 2 gene variants are associated with liver fibrosis in the general population: the Rotterdam Study

33. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

34. New genetic loci link adipose and insulin biology to body fat distribution

35. The impact of low-frequency and rare variants on lipid levels

36. Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels

37. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

38. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

39. Heritabilities, proportions of heritabilities explained by GWAS findings, and implications of cross-phenotype effects on PR interval

40. Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval

41. Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

42. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

43. Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

44. The challenges of genome-wide interaction studies: Lessons to learn from the analysis of HDL blood levels

45. Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

46. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

47. Automated workflow-based exploitation of pathway databases provides new insights into genetic associations of metabolite profiles

48. The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis

49. Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions

50. Common variants in mendelian kidney disease genes and their association with renal function

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