Andrew Findlay

Medicine & Life Sciences

1. Limb-Girdle Muscular Dystrophies 100%
2. Duchenne Muscular Dystrophy 86%
3. Muscular Diseases 60%
4. Exons 47%
5. Dystrophin 43%
6. Mutation 42%
7. Myositis 40%
8. Muscular Dystrophies 39%
9. Muscles 33%
10. Dermatomyositis 30%
11. 6-methylpurine 27%
12. Protein Isoforms 23%
13. Camptocormia 23%
14. Adenine Phosphoribosyltransferase 22%
15. Valosin Containing Protein 21%
16. Missense Mutation 19%
17. Myotonia Congenita 19%
18. Dystroglycans 19%
19. Tetrahymena 19%
20. Internal Ribosome Entry Sites 19%
21. Skeletal Muscle Fibers 18%
22. Exome 18%
23. Lithium Chloride 18%
24. 5'-Nucleotidase 17%
25. Inclusion Body Myositis 17%
26. Antisense Oligonucleotides 15%
27. Therapeutics 15%
28. Antisynthetase syndrome 14%
29. Natural History 13%
30. Ophthalmoplegia 13%
31. Muscle Weakness 13%
32. Vacuoles 13%
33. Proteins 12%
34. Respiratory Insufficiency 12%
35. Phenotype 12%
36. Genetic Therapy 12%
37. Clinical Trials 10%
38. Registries 10%
39. Cell Line 9%
40. Anti-Idiotypic Antibodies 9%
41. Skeletal Muscle 9%
42. Biopsy 9%
43. Reading Frames 8%
44. Sarcopenia 8%
45. Muscular Dystrophy, Limb-Girdle, Type 1D 8%
46. Antibodies 7%
47. Carrier State 7%
48. Autosomal dominant Inclusion body myopathy 7%
49. Genetic Testing 6%
50. Exanthema 6%