Elsebet Østergaard

Medicine & Life Sciences

1. Mutation 100%
2. Succinate-CoA Ligases 75%
3. Phenotype 58%
4. Mitochondrial DNA 49%
5. Genetic Association Studies 40%
6. Mitochondrial Diseases 36%
7. Genes 36%
8. Genetic Counseling 32%
9. Cytochrome-c Oxidase Deficiency 30%
10. Riboflavin Deficiency 30%
11. Electron Transport 30%
12. Molecular Biology 29%
13. Methylmalonic acidemia 29%
14. Acyl-CoA Dehydrogenase 28%
15. Labor Presentation 28%
16. RNA, Transfer, Met 27%
17. Usher Syndromes 27%
18. Albinism 27%
19. Myoglobinuria 27%
20. Brain Diseases 27%
21. Leigh Disease 26%
22. Missense Mutation 26%
23. Cell Nucleus Division 26%
24. Hearing Loss 25%
25. Cataract 25%
26. Leukoencephalopathies 23%
27. Dental Plaque 23%
28. Maternal Inheritance 22%
29. Pelizaeus-Merzbacher Disease 22%
30. Seizures 20%
31. Gene Deletion 20%
32. Autosomal Recessive 48 Deafness 20%
33. Melanocytes 20%
34. Capsicum 19%
35. Age of Onset 19%
36. Nuclear Proteins 18%
37. Autism Spectrum Disorder 18%
38. Muscles 18%
39. Mitochondrial Proteins 17%
40. Intellectual Disability 16%
41. 3-Methylglutaconic Aciduria 16%
42. Oxidoreductases 16%
43. Methylation 16%
44. Muscle Hypotonia 16%
45. Transgenic Mice 16%
46. Heterozygote 16%
47. Renal Insufficiency 15%
48. Fibroblasts 15%
49. Multicenter Studies 15%
50. human NDUFAF2 protein 15%