Biomedicin

Medicin och livsvetenskap

1. Allergic Rhinitis 100%
2. Genetic Variation 82%
3. Type 1 von Willebrand Disease 77%
4. von Willebrand Factor 74%
5. Mutation 73%
6. Hemophilia A 68%
7. Single Nucleotide Polymorphism 57%
8. Genes 52%
9. von Willebrand Diseases 50%
10. Venous Thromboembolism 49%
11. Population 43%
12. Hemophilia B 40%
13. High-Throughput Nucleotide Sequencing 39%
14. Polymerase Chain Reaction 37%
15. Toll-Like Receptors 32%
16. Haplotypes 32%
17. Alleles 25%
18. Exons 23%
19. Protein S Deficiency 22%
20. Qa-SNARE Proteins 21%
21. Gene Frequency 20%
22. C-Type Lectins 20%
23. Kallikreins 19%
24. Asthma 19%
25. Nucleotides 19%
26. Mosaicism 18%
27. Mutation Rate 17%
28. Multigene Family 16%
29. Ions 15%
30. Mothers 13%
31. Case-Control Studies 13%
32. Exome 13%
33. Carrier Proteins 12%
34. DNA 12%
35. Prostatic Neoplasms 11%
36. Genome-Wide Association Study 11%
37. Genotype 11%
38. Age of Onset 11%
39. Data Aggregation 10%
40. Cohort Studies 10%
41. Phenotype 9%
42. Introns 9%
43. Missense Mutation 8%
44. Databases 8%
45. Minisatellite Repeats 8%
46. Linkage Disequilibrium 8%
47. Limit of Detection 8%
48. Weibel-Palade Bodies 7%
49. Genetic Association Studies 7%
50. Thrombophilia 7%
51. Thrombophilia due to Activated Protein C Resistance 7%
52. Prothrombin 6%
53. Blood Group Antigens 6%
54. Sequence Deletion 6%
55. Toll-Like Receptor 10 6%
56. Peptide Hydrolases 6%
57. alpha 1-Antitrypsin Deficiency 6%
58. Odds Ratio 6%
59. Anticoagulants 6%
60. Gene Deletion 5%
61. Antithrombin Proteins 5%
62. Change Management 5%
63. Protein C Deficiency 5%
64. Chromosomes 5%
65. Multiplex Polymerase Chain Reaction 5%
66. Aptitude 5%
67. Sensitivity and Specificity 5%