Medicine & Life Sciences

1. Mutation 100%
2. Frontotemporal Dementia 80%
3. Frontotemporal Lobar Degeneration 77%
4. Genes 46%
5. Dementia 40%
6. Phenotype 37%
7. Whole Exome Sequencing 36%
8. Microtubule-Associated Proteins 33%
9. Brain Diseases 30%
10. Neurodevelopmental Disorders 30%
11. Intellectual Disability 29%
12. Atrophy 27%
13. Epilepsy 26%
14. Exome 26%
15. Brain 26%
16. Seizures 25%
17. Chromosomes, Human, Pair 9 23%
18. MELAS Syndrome 22%
19. Angelman Syndrome 22%
20. Age of Onset 22%
21. Alexander Disease 22%
22. Magnetic Resonance Imaging 19%
23. Loss of Function Mutation 18%
24. Mitochondrial Diseases 18%
25. Friedreich Ataxia 18%
26. Genetic Association Studies 18%
27. Muscle Hypotonia 18%
28. Late Onset Disorders 17%
29. Multiple Sclerosis 17%
30. Progranulins 16%
31. White Matter 16%
32. Kennerknecht Sorgo Oberhoffer syndrome 15%
33. Genetic Testing 14%
34. Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 14%
35. Failure to Thrive 14%
36. Woodhouse Sakati syndrome 14%
37. Neuroimaging 13%
38. Mitochondrial Complex III Deficiency 13%
39. Cerebroretinal Microangiopathy with Calcifications and Cysts 13%
40. Open Reading Frames 13%
41. Population Biological Variation 13%
42. Missense Mutation 13%
43. Kleefstra Syndrome 12%
44. Gene Components 12%
45. Biomarkers 11%
46. Uridine Diphosphate Glucose Dehydrogenase 11%
47. Anesthetics 11%
48. Congenital Pain Insensitivity 11%
49. Granulins 11%