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