Robin Ryther

Medicine & Life Sciences

1. Rett Syndrome 100%
2. Type II Isolated Growth Hormone Deficiency 47%
3. Lubs X-linked mental retardation syndrome 46%
4. Epilepsy 37%
5. Methyl-CpG-Binding Protein 2 35%
6. Natural History 32%
7. Mutation 29%
8. Exons 27%
9. Protein Isoforms 26%
10. Small Interfering RNA 24%
11. Pituitary Dwarfism 23%
12. Pediatrics 22%
13. RNA Interference 22%
14. Phenotype 21%
15. Generalized Epilepsy with Febrile Seizures Plus 20%
16. Seizures 19%
17. Atypical Rett Syndrome 17%
18. Somatotrophs 17%
19. Parents 15%
20. X Chromosome Inactivation 15%
21. Partial Epilepsy 13%
22. Drug Resistant Epilepsy 13%
23. TOR Serine-Threonine Kinases 13%
24. Anti-Anxiety Agents 13%
25. Child Behavior 12%
26. Febrile Seizures 11%
27. Alleles 11%
28. Growth Hormone 11%
29. Psychometrics 11%
30. Cause of Death 9%
31. Sleep 9%
32. Clinical Trials 8%
33. Quality of Life 8%
34. Anxiety 8%
35. Genotype 8%
36. Genes 8%
37. RNA 8%
38. Cohort Studies 8%
39. Neurodevelopmental Disorders 7%
40. Health Care Outcome Assessment 7%
41. Therapeutics 7%
42. Child 6%
43. Arm 5%
44. Hormones 5%
45. Nucleotides 5%
46. Introns 5%
47. Genetic Enhancer Elements 5%
48. Constipation 5%
49. Walking 5%