NeuroGenomics and Informatics Center

Medicine & Life Sciences

1. Alzheimer Disease 100%
2. Genome-Wide Association Study 44%
3. Genes 41%
4. Mutation 30%
5. Genome 29%
6. Single Nucleotide Polymorphism 29%
7. Cerebrospinal Fluid 26%
8. Amyloid 25%
9. Brain 18%
10. Frontotemporal Dementia 16%
11. Meta-Analysis 15%
12. Blood Pressure 13%
13. Alleles 12%
14. Pathology 12%
15. Parkinson Disease 11%
16. Stroke 11%
17. Biomarkers 11%
18. Frontotemporal Lobar Degeneration 11%
19. Endophenotypes 9%
20. Exome 9%
21. Age of Onset 9%
22. Phenotype 9%
23. Neurodegenerative Diseases 8%
24. African Americans 8%
25. Genetic Variation 8%
26. Genotype 8%
27. Smoking 8%
28. Cognitive Dysfunction 8%
29. Induced Pluripotent Stem Cells 7%
30. Progressive Supranuclear Palsy 7%
31. Tauopathies 7%
32. Datasets 7%
33. Whole Genome Sequencing 7%
34. Dementia 7%
35. Population 7%
36. Lipids 7%
37. Genomics 7%
38. Neurons 7%
39. Apolipoproteins E 7%
40. Apolipoprotein E4 7%
41. Progranulins 7%
42. Microglia 7%
43. Hydrocephalus 7%
44. Whole Exome Sequencing 6%
45. Amyloid beta-Protein Precursor 6%
46. Cerebral Hemorrhage 6%
47. Gene-Environment Interaction 6%
48. Odds Ratio 6%
49. Gene Expression 5%
50. Proteins 5%
51. Amyotrophic lateral sclerosis 1 5%
52. 2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazole 5%
53. Neuroimaging 5%
54. Amyotrophic Lateral Sclerosis 5%
55. Genetic Loci 5%
56. Haplotypes 5%
57. Astrocytes 5%
58. Multifactorial Inheritance 5%
59. Microtubule-Associated Proteins 5%