John Reynolds

Medicine & Life Sciences

1. Genomic Instability 100%
2. DNA Replication 64%
3. Microcephaly 62%
4. DNA Damage 59%
5. Mutation 56%
6. Homologous Recombination 46%
7. DNA Repair 44%
8. Autosomal recessive 1 Spinocerebellar ataxia 41%
9. Methylation 41%
10. Phenotype 38%
11. Neuropathology 31%
12. DNA Helicases 31%
13. Dwarfism 31%
14. Thyroid Epithelial Cells 30%
15. DNA 28%
16. Nucleosomes 26%
17. Polynucleotide 5'-Hydroxyl-Kinase 26%
18. Double-Stranded DNA Breaks 26%
19. Genes 25%
20. Histones 25%
21. Fanconi Anemia 25%
22. RecQ Helicases 23%
23. Chromosomal Instability 23%
24. Zebrafish 23%
25. Thyroid Neoplasms 23%
26. Strudwick syndrome 21%
27. Single-Stranded DNA Breaks 20%
28. Coxa Vara 18%
29. Genome 18%
30. Chromosomes 18%
31. Phosphoric Monoester Hydrolases 17%
32. G-Quadruplexes 16%
33. Chromosome Aberrations 16%
34. Missense Mutation 15%
35. Agammaglobulinemia 15%
36. Nose 15%
37. Chromosome Breakage 15%
38. Camptothecin 14%
39. Recombinational DNA Repair 14%
40. Tooth Root 14%
41. Inheritance Patterns 14%
42. Early-onset ataxia with oculomotor apraxia and hypoalbuminemia 14%
43. Chromatids 14%
44. Cell Line 13%
45. Aptitude 12%
46. Histone-Lysine N-Methyltransferase 12%
47. Scoliosis 12%
48. Histone Chaperones 11%
49. Cell Division 10%
50. Ichthyosis 10%