Francesco Calì

Medicine & Life Sciences

1. Mutation 100%
2. Sicily 94%
3. Genes 92%
4. Phenylketonurias 55%
5. Phenylalanine Hydroxylase 47%
6. Population 37%
7. Alleles 36%
8. Y Chromosome 34%
9. Mitochondrial DNA 33%
10. Autistic Disorder 30%
11. Juvenile Myoclonic Epilepsy 30%
12. Haplotypes 28%
13. Epilepsy 28%
14. Italy 27%
15. Exons 27%
16. Microsatellite Repeats 25%
17. Phenotype 25%
18. Autism Spectrum Disorder 24%
19. Intellectual Disability 21%
20. Gene Dosage 21%
21. Chromosomes 19%
22. SARS Virus 19%
23. Missense Mutation 19%
24. Minisatellite Repeats 19%
25. Spinocerebellar Ataxias 18%
26. Multiplex Polymerase Chain Reaction 17%
27. DNA Fingerprinting 16%
28. High-Throughput Nucleotide Sequencing 16%
29. Siblings 15%
30. Restriction Fragment Length Polymorphisms 14%
31. Brain 14%
32. Genetic Heterogeneity 14%
33. Atrophy 14%
34. Lactate Dehydrogenase Deficiency 13%
35. Exome 13%
36. Spinal Muscular Atrophy 13%
37. Brain Diseases 12%
38. Keratoderma, Palmoplantar, Epidermolytic 12%
39. Netherton Syndrome 11%
40. Seizures 11%
41. Epidermolytic Hyperkeratosis 11%
42. Rubinstein-Taybi Syndrome 11%
43. Stroke 11%
44. Molecular Biology 10%
45. PHD Zinc Fingers 10%
46. DiGeorge Syndrome 10%
47. Gene Flow 10%
48. Neurodevelopmental Disorders 10%
49. Introns 10%
50. Dental Anxiety 10%