Katrine Johannesen

Medicine & Life Sciences

1. Epilepsy 100%
2. Brain Diseases 95%
3. Seizures 63%
4. Intellectual Disability 45%
5. Generalized Epilepsy 39%
6. Phenotype 39%
7. Neurodevelopmental Disorders 31%
8. Genetic Association Studies 28%
9. Electroencephalography 28%
10. Mutation 27%
11. Lemierre Syndrome 22%
12. Genetic Testing 20%
13. Epileptic Syndromes 18%
14. Myoclonic Epilepsy 16%
15. Febrile Seizures 14%
16. Genes 14%
17. Partial Epilepsy 13%
18. Glut1 Deficiency Syndrome 12%
19. Aicardi Syndrome 12%
20. Voltage-Gated Sodium Channels 12%
21. Status Epilepticus 11%
22. Congenital Disorders of Glycosylation 10%
23. Genetic Heterogeneity 10%
24. Sodium Channel Blockers 10%
25. Movement Disorders 10%
26. Absence Epilepsy 9%
27. Therapeutics 9%
28. Sodium Channels 9%
29. Age of Onset 9%
30. Empyema 8%
31. Cognitive Dysfunction 8%
32. Premature Mortality 8%
33. Brain 8%
34. GABA-A Receptors 7%
35. Cognition 7%
36. High-Throughput Nucleotide Sequencing 7%
37. Calcium Channels 7%
38. Muscle Hypotonia 7%
39. Sudden Unexpected Death in Epilepsy 7%
40. Basal Ganglia 7%
41. Sleep 7%
42. Fever 7%
43. Serine 6%
44. GABA Plasma Membrane Transport Proteins 6%
45. Decision Making 6%
46. Jugular Veins 6%
47. N-Methyl-D-Aspartate Receptors 6%
48. Mortality 6%
49. Glutamic Acid 6%
50. Neuroimaging 5%