Elsebet Østergaard

Medicine & Life Sciences

1. Mutation 100%
2. Mitochondrial Diseases 90%
3. Leigh Disease 60%
4. Phenotype 48%
5. Genes 45%
6. Mitochondrial DNA 44%
7. Electron Transport 41%
8. Succinate-CoA Ligases 40%
9. Genetic Association Studies 29%
10. Fibroblasts 28%
11. Mitochondrial Encephalomyopathies 28%
12. Pyruvate Carboxylase Deficiency Disease 26%
13. Exome 25%
14. Denmark 25%
15. Muscle Hypotonia 25%
16. Proteins 24%
17. succinyl-coenzyme A 24%
18. Neurodevelopmental Disorders 24%
19. Multicenter Studies 23%
20. Muscles 21%
21. Fatal Infantile Lactic Acidosis 19%
22. Enzymes 19%
23. Molecular Biology 19%
24. Seizures 19%
25. Threonine-tRNA Ligase 19%
26. Genetic Background 18%
27. Optic Atrophy 17%
28. Isolated 1 Microphthalmia 17%
29. Dystonia 16%
30. Oxidative Phosphorylation 16%
31. Eiken Skeletal Dysplasia 16%
32. Methylmalonic acidemia 16%
33. Missense Mutation 16%
34. Age of Onset 16%
35. Epilepsy 16%
36. Genome 15%
37. Transfer RNA 14%
38. 3-Methylglutaconic Aciduria 14%
39. Intellectual Disability 14%
40. PTH-related peptide-1 PTHrP-1 14%
41. Blomstrand type Chondrodysplasia 14%
42. RNA, Transfer, Met 14%
43. Pyruvate Carboxylase 13%
44. asfotase alfa 13%
45. DNA Methylation 13%
46. Survival 12%
47. Inborn Genetic Diseases 12%
48. Basal Ganglia 12%
49. Hearing Loss 12%
50. Microvillus inclusion disease 12%