Hilary Vernon

Medicine & Life Sciences

1. Barth Syndrome 100%
2. Cardiolipins 50%
3. Mitochondrial Diseases 37%
4. arginyl-2,'6'-dimethyltyrosyl-lysyl-phenylalaninamide 29%
5. monolysocardiolipin 17%
6. Inborn Errors Metabolism 15%
7. Cardiomyopathies 15%
8. Intellectual Disability 14%
9. Neurodevelopmental Disorders 14%
10. Inborn Genetic Diseases 13%
11. Methylmalonic acidemia 13%
12. Mutation 13%
13. Phenotype 11%
14. Muscle Hypotonia 11%
15. Propionic Acidemia 11%
16. Ornithine Carbamoyltransferase Deficiency Disease 11%
17. Autistic Disorder 11%
18. fibroblast growth factor 21 10%
19. Inborn Urea Cycle Disorder 9%
20. Amino Acids 9%
21. Metabolomics 8%
22. Natural History 8%
23. Leukoencephalopathies 8%
24. Mitochondria 8%
25. Methylmalonic aciduria cblB type 7%
26. Whole Exome Sequencing 7%
27. Kinetics 7%
28. Serine 7%
29. Phenylketonurias 7%
30. Muscular Diseases 7%
31. Mitochondrial Membranes 6%
32. Chronic Renal Insufficiency 6%
33. Therapeutics 6%
34. Neutropenia 6%
35. 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency 6%
36. Exome 6%
37. Lipidomics 6%
38. Inborn Errors Amino Acid Metabolism 6%
39. Genes 6%
40. Ataxia 6%
41. Citrulline 6%
42. Proteins 5%
43. Adenine Phosphoribosyltransferase 5%
44. Medium chain acyl CoA dehydrogenase deficiency 5%
45. Neonatal Screening 5%
46. Brain 5%
47. Neurology 5%
48. Kidney Diseases 5%
49. Lipids 5%
50. Heart Failure 5%