Harrison Gabel

Medicine & Life Sciences

1. DNA Methylation 100%
2. Rett Syndrome 90%
3. Neurons 83%
4. Caenorhabditis elegans 74%
5. Genes 73%
6. Brain 73%
7. Methyl-CpG-Binding Protein 2 63%
8. Gene Expression 59%
9. Epigenomics 54%
10. RNA Interference 53%
11. Genome 48%
12. Methylation 43%
13. Mutation 36%
14. Epigenome 35%
15. Chromatin 34%
16. Phenotype 34%
17. Haploinsufficiency 31%
18. bis(2,3,3,3-tetrachloropropyl) ether 29%
19. Neurodevelopmental Disorders 26%
20. MicroRNAs 25%
21. Chromatin Assembly and Disassembly 25%
22. Nervous System 24%
23. Proteins 23%
24. CHARGE Syndrome 22%
25. Transcription Factors 22%
26. Phosphorylation 21%
27. 5-hydroxymethylcytosine 21%
28. Anaphase-Promoting Complex-Cyclosome 20%
29. Exonucleases 19%
30. Autistic Disorder 18%
31. Cerebellum 18%
32. Co-Repressor Proteins 18%
33. Heterochromatin 17%
34. Microcephaly 17%
35. Small Interfering RNA 16%
36. Retinoblastoma 16%
37. Purkinje Cells 16%
38. Threonine 15%
39. Fibroblasts 15%
40. Datasets 15%
41. Intellectual Disability 15%
42. Learning 15%
43. RNA 14%
44. DNA 14%
45. Ubiquitin 14%
46. Transcriptional Activation 12%
47. Reading 12%
48. Obesity 12%
49. Transcriptome 11%
50. Schizosaccharomyces 11%