Fredrik Mertens

Medicin och livsvetenskap

1. Gene Fusion 100%
2. Neoplasms 97%
3. Cytogenetics 74%
4. Chromosome Aberrations 70%
5. Sarcoma 70%
6. Fluorescence In Situ Hybridization 63%
7. Chromosomes 52%
8. Genes 51%
9. Lipoma 42%
10. Ring Chromosomes 40%
11. Neurofibrosarcoma 34%
12. Liposarcoma 33%
13. Karyotype 31%
14. Bone and Bones 24%
15. Fibrosarcoma 23%
16. Chromosomes, Human, Pair 12 23%
17. Exons 23%
18. Cytogenetic Analysis 22%
19. Comparative Genomic Hybridization 20%
20. Chromosome Banding 19%
21. Myxoid Liposarcoma 19%
22. Osteosarcoma 18%
23. Synovial Sarcoma 18%
24. Single Nucleotide Polymorphism 17%
25. Giant Cell Tumor of Bone 16%
26. Squamous Cell Carcinoma of Head and Neck 16%
27. Gene Expression 15%
28. Synovial Fluid 15%
29. Mutation 14%
30. Dermatofibrosarcoma 14%
31. Trisomy 14%
32. DNA 14%
33. Molecular Biology 14%
34. Genetic Markers 14%
35. Polymerase Chain Reaction 14%
36. Gene Rearrangement 13%
37. Chondrosarcoma 13%
38. Neurofibromatosis 1 12%
39. Fine Needle Biopsy 12%
40. Proteins 12%
41. Angiomatoid Fibrous Histiocytoma 12%
42. Breast Neoplasms 11%
43. Chromosomes, Human, Pair 22 11%
44. Telomere 11%
45. Clear Cell Sarcoma 10%
46. Proto-Oncogene Proteins c-sis 10%
47. Metaphase 10%
48. Chromosome Breakpoints 10%
49. Osteoarthritis 10%
50. Extraskeletal Myxoid Chondrosarcoma 10%