Michele Iacomino

Medicine & Life Sciences

1. Epilepsy 100%
2. Mutation 89%
3. Brain Diseases 72%
4. elastin microfibril interface located protein 70%
5. Genetic Association Studies 63%
6. Genes 52%
7. Seizures 51%
8. Neurodevelopmental Disorders 48%
9. Whole Exome Sequencing 40%
10. Phenotype 38%
11. Intellectual Disability 36%
12. Malformations of Cortical Development 31%
13. Wieacker syndrome 27%
14. AMPA Receptors 27%
15. Neurobiology 27%
16. Generalized Epilepsy 26%
17. Limb-girdle muscular dystrophy type 2H 23%
18. Complementary RNA 22%
19. Partial Epilepsy 21%
20. Zebrafish 20%
21. Synaptic Transmission 20%
22. Motor Neurons 19%
23. Familial paroxysmal dystonia 19%
24. Proteins 19%
25. Isaacs Syndrome 18%
26. Tripartite Motif Proteins 18%
27. Reflex Epilepsy 18%
28. Autism Spectrum Disorder 17%
29. Progressive Myoclonic Epilepsy 17%
30. Juvenile Myoclonic Epilepsy 17%
31. Arthrogryposis 17%
32. Arnold-Chiari Malformation 16%
33. Brain 16%
34. Coloboma 16%
35. Microphthalmos 16%
36. Missense Mutation 15%
37. Organoids 15%
38. Migraine Disorders 14%
39. Biopsy 14%
40. Neurology 14%
41. Neurofibromatosis 1 14%
42. Lissencephaly 13%
43. Inborn Genetic Diseases 12%
44. Sensation Disorders 12%
45. Movement Disorders 12%
46. Genetic Testing 12%
47. Pediatrics 12%
48. Ataxia 12%
49. Exome 11%
50. Muscles 11%