Lyndal Henden

Medicine & Life Sciences

1. Amyotrophic Lateral Sclerosis 100%
2. Amyotrophic lateral sclerosis 1 91%
3. Frontotemporal Dementia With Motor Neuron Disease 42%
4. Microsatellite Repeats 31%
5. Mutation 30%
6. Frontotemporal Dementia 27%
7. MEHMO syndrome 24%
8. Charcot-Marie-Tooth disease, X-linked recessive, 3 23%
9. Genes 22%
10. mouse TDP-43 protein 22%
11. MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome 19%
12. Intellectual Disability 19%
13. Neurodegenerative Diseases 18%
14. Whole Genome Sequencing 17%
15. Age of Onset 15%
16. Neural Cell Adhesion Molecule L1 15%
17. RNA Sequence Analysis 15%
18. X Chromosome 14%
19. Myoclonic Epilepsy 14%
20. Single Nucleotide Polymorphism 13%
21. Kynurenine 13%
22. RNA Splicing Factors 13%
23. Genome 13%
24. Superoxide Dismutase-1 12%
25. Catalogs 12%
26. Datasets 12%
27. Population Dynamics 12%
28. Haplotypes 12%
29. RNA 11%
30. Nerve Tissue 11%
31. Molecular Dynamics Simulation 11%
32. Central Nervous System 11%
33. Genetic Variation 11%
34. Sclerosis 10%
35. Proline 10%
36. Glutamine 10%
37. DNA 9%
38. Exome 9%
39. Introns 9%
40. High-Throughput Nucleotide Sequencing 9%
41. Motor Neurons 9%
42. Dipeptides 8%
43. Motor Cortex 8%
44. Proteins 8%
45. Software 7%
46. 1-(2'-tetrahydrothienyl) 5-fluorouracil 7%
47. Spinal Cord 7%
48. Alleles 7%
49. Epilepsy, Myoclonic, Benign Adult Familial, Type 2 7%