Rikke Steensbjerre Møller

Medicin og biovidenskab

1. Epilepsy 100%
2. Brain Diseases 64%
3. Seizures 48%
4. Neurodevelopmental Disorders 38%
5. Phenotype 34%
6. Mutation 34%
7. Intellectual Disability 32%
8. Genes 27%
9. Generalized Epilepsy 24%
10. Myoclonic Epilepsy 19%
11. Idiopathic Generalized Epilepsy 13%
12. Genetic Association Studies 12%
13. Epileptic Syndromes 12%
14. Electroencephalography 12%
15. Partial Epilepsy 11%
16. Mowat-Wilson syndrome 10%
17. Infantile Spasms 10%
18. Brain 9%
19. Genetic Testing 9%
20. Movement Disorders 9%
21. Exome 8%
22. Rolandic Epilepsy 7%
23. Episodic Ataxia 7%
24. Status Epilepticus 7%
25. Muscle Hypotonia 7%
26. Microcephaly 7%
27. Malformations of Cortical Development 7%
28. Sodium Channels 6%
29. Sleep 6%
30. Autism Spectrum Disorder 6%
31. Febrile Seizures 6%
32. High-Throughput Nucleotide Sequencing 5%
33. Infantile Epileptic-Dyskinetic Encephalopathy 5%
34. Congenital Disorders of Glycosylation 5%
35. Aicardi Syndrome 5%
36. Absence Epilepsy 5%
37. Proteins 5%
38. Autistic Disorder 5%
39. Precision Medicine 5%
40. Therapeutics 5%
41. Whole Exome Sequencing 5%
42. GABA-A Receptors 5%
43. Progressive Myoclonic Epilepsy 5%