Monica Rosa Miozzo

Medicine & Life Sciences

1. Methylation 100%
2. Chromosomes 88%
3. Genes 78%
4. Neoplasms 67%
5. Cytogenetics 63%
6. Epigenomics 63%
7. Papillary Thyroid Cancer 56%
8. Mutation 52%
9. X Chromosome Inactivation 51%
10. Karyotype 47%
11. Beckwith-Wiedemann Syndrome 43%
12. Mosaicism 42%
13. X Chromosome 42%
14. Monosomy 40%
15. Biliary Liver Cirrhosis 40%
16. Fetal Growth Retardation 38%
17. Chromosome Aberrations 38%
18. Pregnancy 35%
19. Gene Expression 34%
20. Breast Neoplasms 33%
21. Fluorescence In Situ Hybridization 32%
22. Placenta 31%
23. Cytogenetic Analysis 31%
24. Chromosomes, Human, Pair 10 30%
25. Phenotype 30%
26. Lung Neoplasms 29%
27. DNA Methylation 28%
28. Glioblastoma 27%
29. Alleles 27%
30. Intellectual Disability 27%
31. Chromosomes, Human, Pair 7 26%
32. Chordoma 25%
33. Coronavirus 25%
34. Glioma 24%
35. Fetus 24%
36. Growth 23%
37. Cell Line 23%
38. High-Throughput Nucleotide Sequencing 23%
39. Y Chromosome 22%
40. Turner Syndrome 22%
41. Umbilical Hernia 22%
42. Brachydactyly 22%
43. Loss of Heterozygosity 21%
44. Ring Chromosomes 21%
45. Genomic Imprinting 21%
46. Proto-Oncogenes 20%
47. Dermatofibrosarcoma 20%
48. Silver-Russell Syndrome 20%
49. Mothers 20%
50. Monozygotic Twins 20%