Federico Tessadori

Medicine & Life Sciences

1. Zebrafish 100%
2. Heart 46%
3. Intellectual Disability 30%
4. Cardiac Myocytes 24%
5. Genes 23%
6. Mutation 22%
7. Embryonic Structures 20%
8. Histones 20%
9. Blepharo-cheilo-dontic syndrome 18%
10. Barber Say syndrome 18%
11. Ablepharon macrostomia syndrome 18%
12. Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 18%
13. Phytochrome B 17%
14. Lactate Dehydrogenase Deficiency 17%
15. Morphogenesis 17%
16. Myocardium 16%
17. Genome 16%
18. Macrostomia 15%
19. Clustered Regularly Interspaced Short Palindromic Repeats 14%
20. Cardiac Arrhythmias 14%
21. Zebrafish Proteins 14%
22. Transcription Factors 12%
23. Microtubule-Organizing Center 12%
24. Proprotein Convertases 12%
25. Glutaminase 12%
26. cohesins 12%
27. KATP Channels 12%
28. Microcephaly 12%
29. Channelopathies 12%
30. Chromatin 12%
31. Loss of Function Mutation 11%
32. Protein Isoforms 11%
33. Single-Cell Analysis 11%
34. Pyridoxal Phosphate 11%
35. Glutamic Acid 11%
36. Voltage-Gated Potassium Channels 11%
37. Phenotype 11%
38. Arabidopsis 11%
39. Long QT Syndrome 11%
40. Forensic Anthropology 11%
41. Transposition of Great Vessels 11%
42. Catenins 10%
43. Connexins 10%
44. Heterochromatin 10%
45. Inborn Genetic Diseases 10%
46. Muscular Diseases 10%
47. Human Genetics 10%
48. Connexin 43 10%
49. Muscle Hypotonia 10%
50. Myofibrils 10%