John Dean

Medicine & Life Sciences

1. Mutation 100%
2. Megalencephaly 88%
3. Solitary Kidney 82%
4. Long QT Syndrome 81%
5. Myotonic Dystrophy 80%
6. Methylenetetrahydrofolate Reductase (NADPH2) 80%
7. Marfan Syndrome 80%
8. Failure to Thrive 79%
9. Hyperlipoproteinemia Type II 77%
10. Whole Exome Sequencing 74%
11. Genetic Testing 71%
12. Vitamin B 12 69%
13. Cleft Palate 68%
14. Sudden Cardiac Death 68%
15. Phenotype 65%
16. Genes 59%
17. Haplotypes 58%
18. Sequence Analysis 58%
19. Sutures 57%
20. Chromatin Assembly and Disassembly 55%
21. Autopsy 52%
22. Epilepsy 52%
23. Language 49%
24. Hypertrophic Cardiomyopathy 47%
25. Child 47%
26. Adenosine Triphosphatases 47%
27. Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 47%
28. Parents 47%
29. Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 46%
30. Dilated Cardiomyopathy 45%
31. Cardiomyopathies 40%
32. Liver 32%
33. Channelopathies 29%
34. Genotype 28%
35. Forensic Medicine 26%
36. Metagenomics 25%
37. Ryanodine Receptor Calcium Release Channel 25%
38. Population 24%
39. Sudden Death 21%
40. Loeys-Dietz Syndrome 21%
41. Speech Disorders 21%
42. Cardiology 20%
43. Ectopia Lentis 20%
44. Fibrillins 19%
45. Neurodevelopmental Disorders 18%
46. Whole Genome Sequencing 18%
47. Virulence 18%
48. Scotland 18%
49. Transforming Growth Factor-beta Type I Receptor 17%
50. Ions 17%