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1. Genetic risk factors underlying white matter hyperintensities and cortical atrophy

2. Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration

3. Cerebral white matter hyperintensities indicate severity and progression of coronary artery calcification

4. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

5. Arterial stiffness and its influence on cerebral morphology and cognitive function

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

7. Evidence of polygenic regulation of the physiological presence of neurofilament light chain in human serum

8. Spatial distributions of white matter hyperintensities on brain MRI: A pooled analysis of individual participant data from 11 memory clinic cohorts

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

10. Incidental findings of typical iNPH imaging signs in asymptomatic subjects with subclinical cognitive decline

11. Free water diffusion MRI and executive function with a speed component in healthy aging

12. The Cost of Understanding—XAI Algorithms towards Sustainable ML in the View of Computational Cost

13. Cerebral small vessel disease genomics and its implications across the lifespan

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

15. Serum neurofilament light levels in normal aging and their association with morphologic brain changes

16. Determining the OPTIMAL DTI analysis method for application in cerebral small vessel disease

17. Associations of autozygosity with a broad range of human phenotypes

18. Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

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

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

21. Serum NfL in Alzheimer Dementia: Results of the Prospective Dementia Registry Austria

22. Minor Structural Differences in the Cervical Spine Between Patients With Cervical Dystonia and Age-Matched Healthy Controls

23. Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume

24. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

25. Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

26. Novel genetic loci associated with hippocampal volume

27. Circle of Willis variants are not associated with thrombectomy outcomes

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

29. New insights into the genetic etiology of Alzheimer's disease and related dementias

30. Kidney function, brain morphology and cognition in the elderly: sex differences in the Austrian Stroke Prevention Study

31. Inclusivity insights: two urban development projects in Johannesburg

32. Factors influencing serum neurofilament light chain levels in normal aging

33. Genome-wide Association Study Meta-analysis of Neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration

34. Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

35. Free water imaging in healthy brain aging and first signs of brain pathology

36. The relationship between plasma free fatty acids, cognitive function and structural integrity of the brain in middle-aged healthy humans

37. Prediction of dementia using diffusion tensor MRI measures: the OPTIMAL collaboration

38. Association of vitamin D metabolites with cognitive function and brain atrophy in elderly individuals - the Austrian stroke prevention study

39. Microstructural Tissue Changes in Alzheimer Disease Brains: Insights from Magnetization Transfer Imaging

40. Genetic architecture of orbital telorism

41. Heritability of R2* iron in the basal ganglia and cortex

42. Genome-wide analysis in over 1 million individuals reveals over 2,000 independent genetic signals for blood pressure

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

44. Intracranial Pulsatility in Relation to Severity and Progression of Cerebral White Matter Hyperintensities

45. Simple MRI score aids prediction of dementia in cerebral small vessel disease

46. Strategic white matter hyperintensity locations for cognitive impairment:A multicenter lesion-symptom mapping study in 3525 memory clinic patients

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

48. Investigating the genetic and environmental basis of head micromovements during MRI

49. Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

50. Predicting atrial fibrillation after cryptogenic stroke via a clinical risk score-a prospective observational study

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