Paul Piccinelli

Medicine & Life Sciences

1. Whole Exome Sequencing 100%
2. Desmoplastic Small Round Cell Tumor 55%
3. Embryonal Rhabdomyosarcoma 50%
4. Stroke 47%
5. Large-Core Needle Biopsy 45%
6. Genes 43%
7. Rhabdomyosarcoma 41%
8. Sensorineural Hearing Loss 39%
9. Cluster Analysis 37%
10. Single Nucleotide Polymorphism 32%
11. Neoplasms 30%
12. Child 22%
13. Bone and Bones 20%
14. Chromosomes 20%
15. Gene Amplification 20%
16. DNA 19%
17. Breast Neoplasms 16%
18. Audiology 14%
19. Bilateral Hearing Loss 13%
20. Alveolar Rhabdomyosarcoma 13%
21. Drug Receptors 11%
22. Chimeric Antigen Receptors 11%
23. Pediatrics 11%
24. Mitochondrial DNA 10%
25. Trastuzumab 10%
26. Gene Fusion 9%
27. Receptor Protein-Tyrosine Kinases 9%
28. Hearing 8%
29. Tumor Suppressor Genes 8%
30. Pendred syndrome 8%
31. Rehabilitation 7%
32. Usher Syndromes 7%
33. Parents 7%
34. Audiologists 7%
35. Alleles 7%
36. Young Adult 7%
37. Genetic Phenomena 6%
38. Proteins 6%
39. RNA 6%
40. Cochlear Implants 5%
41. Therapeutics 5%
42. Ophthalmologists 5%
43. Physical Therapists 5%
44. T-Lymphocytes 5%
45. Genetic Background 5%
46. Heterozygote 5%
47. Gene Expression 5%
48. Genome-Wide Association Study 5%
49. Pediatricians 5%
50. Genetic Testing 5%