Federico Tessadori

Medicine & Life Sciences

1. Zebrafish 100%
2. Heart 47%
3. Intellectual Disability 31%
4. Mutation 23%
5. Genes 22%
6. Embryonic Structures 21%
7. Histones 20%
8. Blepharo-cheilo-dontic syndrome 19%
9. Barber Say syndrome 19%
10. Ablepharon macrostomia syndrome 18%
11. Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 18%
12. Phytochrome B 18%
13. Lactate Dehydrogenase Deficiency 18%
14. Cardiac Myocytes 16%
15. Macrostomia 16%
16. Genome 15%
17. Myocardium 15%
18. Cardiac Arrhythmias 15%
19. Zebrafish Proteins 15%
20. Morphogenesis 13%
21. Transcription Factors 13%
22. Microtubule-Organizing Center 13%
23. Proprotein Convertases 13%
24. Glutaminase 12%
25. cohesins 12%
26. KATP Channels 12%
27. Microcephaly 12%
28. Channelopathies 12%
29. Clustered Regularly Interspaced Short Palindromic Repeats 12%
30. Chromatin 12%
31. Loss of Function Mutation 12%
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 11%
43. Connexins 11%
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. Desmin 10%