Medicine & Life Sciences

1. Parkinsonian Disorders 75%
2. Mutation 60%
3. Frontotemporal Dementia 57%
4. Progressive Supranuclear Palsy 31%
5. Genes 29%
6. Synucleins 28%
7. Dementia 25%
8. Frontotemporal Lobar Degeneration 24%
9. Chromosomes, Human, Pair 17 19%
10. Pathology 19%
11. Perry Syndrome 19%
12. Neurodegenerative Diseases 18%
13. Microtubule-Associated Proteins 18%
14. Leucine 18%
15. Alzheimer Disease 18%
16. Multiple System Atrophy 18%
17. Substantia Nigra 17%
18. Leukoencephalopathies 17%
19. Essential Tremor 17%
20. Colony-Stimulating Factor Receptors 16%
21. Lewy Bodies 16%
22. Phosphotransferases 15%
23. Tremor 15%
24. Brain 15%
25. Age of Onset 14%
26. Macrophage Colony-Stimulating Factor 13%
27. Tauopathies 12%
28. Levodopa 12%
29. Atrophy 12%
30. Progranulins 11%
31. Autopsy 11%
32. Phenotype 11%
33. Genome-Wide Association Study 10%
34. Haplotypes 10%
35. Amyotrophic Lateral Sclerosis 10%
36. Neuroglia 10%
37. Dystonia 9%
38. Exons 9%
39. Single Nucleotide Polymorphism 9%
40. Inborn Genetic Diseases 8%
41. White Matter 8%
42. Parkinson Disease, Familial, Type 1 8%
43. Alleles 8%
44. Frontotemporal Dementia With Motor Neuron Disease 8%
45. Pallidopontonigral Degeneration 7%
46. Dystonic Disorders 7%
47. Ubiquitin 7%