Rene Pierpont

Medicine & Life Sciences

1. Noonan Syndrome 100%
2. Adrenoleukodystrophy 81%
3. Cardiofaciocutaneous syndrome 69%
4. Child 28%
5. Fragile X Syndrome 24%
6. Neurofibromatosis 1 23%
7. Mitogen-Activated Protein Kinases 21%
8. Transplants 20%
9. Language 20%
10. Down Syndrome 19%
11. Mutation 18%
12. UDP-galactose translocator 18%
13. Genotype 18%
14. Short-Term Memory 16%
15. Social Skills 16%
16. Memory 15%
17. Hypophosphatasia 14%
18. Siblings 14%
19. Demyelinating Diseases 14%
20. Congenital Disorders of Glycosylation 14%
21. Fragile X Mental Retardation Protein 14%
22. Nervous System 13%
23. Autistic Disorder 13%
24. Intellectual Disability 13%
25. Mucopolysaccharidosis I 13%
26. Language Development 13%
27. Hematopoietic Stem Cells 12%
28. Therapeutic Human Experimentation 12%
29. Child Language 12%
30. Biomarkers 12%
31. Neurofibromatoses 11%
32. Benchmarking 11%
33. Mosaicism 11%
34. Genes 11%
35. Aptitude 11%
36. Phenotype 11%
37. Social Behavior 10%
38. Psychological Adaptation 10%
39. Seizures 10%
40. Attention Deficit Disorder with Hyperactivity 10%
41. Parenting 10%
42. Vitamin B 12 10%
43. Hematopoietic Stem Cell Transplantation 9%
44. Erythropoietin 9%
45. Psychological Practice 9%
46. Enzyme Replacement Therapy 9%
47. Cell Transplantation 9%