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1. Higher plasma CXCL12 levels predict incident myocardial infarction and death in chronic kidney disease: findings from the Chronic Renal Insufficiency Cohort study

2. Angioid streaks associated with abetalipoproteinemia.

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

4. A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

5. Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease-Brief Report

6. MitoScape: A big-data, machine-learning platform for obtaining mitochondrial DNA from next-generation sequencing data

7. Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals

8. Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

9. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

10. Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes

11. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

12. Lipoprotein(a) and Risk of Myocardial Infarction and Death in Chronic Kidney Disease Findings From the CRIC Study (Chronic Renal Insufficiency Cohort)

13. Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms

14. Large-scale gene-centric analysis identifies novel variants for coronary artery disease

15. Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels

16. Genetically Determined Height and Coronary Artery Disease

17. Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction

18. Neuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathy

19. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.

20. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

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

22. Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis

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

24. Genetically determined height and coronary artery disease

25. Loci influencing blood pressure identified using a cardiovascular gene-centric array (vol 22, pg 1663, 2013)

26. Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia

27. Erratum: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height ((The American Journal of Human Genetics (2010) 88 (6-18))

28. Erratum: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci (American Journal of Human Genetics (2012) 90 (410-425))

29. Homocysteine and coronary heart disease: Meta-analysis of MTHFR case-control studies, avoiding publication bias

30. Association between C reactive protein and coronary heart disease: mendelian randomisation analysis based on individual participant data

31. Prospective study of insulin-like growth factor-I, insulin-like growth factor binding protein 3, genetic variants in the IGF-1 and IGFBP-3 genes and risk of coronary artery disease

32. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

33. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

34. Common Variants at 10 Genomic Loci Influence Hemoglobin A(1C) Levels via Glycemic and Nonglycemic Pathways

35. Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

36. Defining the role of common variation in the genomic and biological architecture of adult human height.

37. Genome-Wide Association Study Identifies a Novel Locus Contributing to Type 2 Diabetes Susceptibility in Sikhs of Punjabi Origin From India

38. Large-scale association analysis identifies new risk loci for coronary artery disease

39. Genome-Wide association study of coronary heart disease and its risk factors in 8,090 african americans: The nhlbi CARe project

40. Biological, clinical and population relevance of 95 loci for blood lipids

41. A Genome-Wide Association Study Reveals Variants in ARL15 that Influence Adiponectin Levels

42. N-Glycosylation regulates endothelial lipase-mediated phospholipid hydrolysis in apoE- and apoA-I-containing high density lipoproteins

50. A Gaussian copula approach for the analysis of secondary phenotypes in case-control genetic association studies.

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