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1. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

2. Association of oxidative stress and inflammatory metabolites with Alzheimer’s disease cerebrospinal fluid biomarkers in mild cognitive impairment

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

5. Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.

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

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

8. Understanding the complex genetic architecture connecting rheumatoid arthritis, osteoporosis and inflammation: discovering causal pathways

9. Circulating metabolites modulated by diet are associated with depression

10. GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification

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

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

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

15. Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

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

18. Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome‐wide association study in over 12,000 non‐demented participants

21. Large-scale association analyses identify host factors influencing human gut microbiome composition

22. Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

23. Genome-wide association study identifies 48 common genetic variants associated with handedness

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

25. Association of common genetic variants with brain microbleeds: A Genome-wide Association Study

26. Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

27. Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation

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

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

30. Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

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

32. A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration

33. Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.

34. Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

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

36. Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness

37. Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry

38. Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.

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

40. Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia

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

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

43. A meta-analysis of genome-wide association studies identifies multiple longevity genes.

44. A genome-wide association study identifies genetic loci associated with specific lobar brain volumes

45. Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

46. Altered bile acid profile in mild cognitive impairment and Alzheimer's disease: Relationship to neuroimaging and CSF biomarkers

47. Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

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

49. Altered bile acid profile associates with cognitive impairment in Alzheimer's disease—An emerging role for gut microbiome

50. Association of metformin, sulfonylurea and insulin use with brain structure and function and risk of dementia and Alzheimer's disease: Pooled analysis from 5 cohorts.

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