Holger Luthman

Medicin och livsvetenskap

1. Genes 100%
2. Type 2 Diabetes Mellitus 80%
3. Elderly 71%
4. Bone and Bones 71%
5. Type 1 Diabetes Mellitus 70%
6. Quantitative Trait Loci 65%
7. Single Nucleotide Polymorphism 57%
8. Insulin Secretion 53%
9. Bone Density 45%
10. Phenotype 44%
11. Steroid 21-Hydroxylase 42%
12. Type 4 Cyclic Nucleotide Phosphodiesterase 41%
13. Chromosomes 40%
14. Alleles 39%
15. Addison Disease 39%
16. Genome 37%
17. Bone Morphogenetic Protein 2 36%
18. Glucose 34%
19. Insulin 33%
20. Autoantibodies 32%
21. Autoimmune Diseases 31%
22. Chromosomes, Human, Pair 4 30%
23. Stroke 29%
24. human TFB1M protein 29%
25. Haplotypes 27%
26. Albumins 26%
27. Bone Fractures 26%
28. MHC class II transactivator protein 26%
29. Osteoporosis 25%
30. Apolipoproteins D 24%
31. Parathyroid Hormone 24%
32. gastric inhibitory polypeptide receptor 24%
33. Infantile Hypertrophic 1 Pyloric Stenosis 24%
34. Genetic Variation 23%
35. Diaphragm 23%
36. Activating Transcription Factor 3 22%
37. Inbred F344 Rats 22%
38. Hypertrophic Pyloric Stenosis 22%
39. Exocytosis 21%
40. Receptor, Melanocortin, Type 4 21%
41. Chromosomes, Human, Pair 1 20%
42. Cholestyramine Resin 20%
43. Fetal Diseases 20%
44. Pregnancy in Diabetics 19%
45. Fat Body 19%
46. Islets of Langerhans 19%
47. Epigenome 17%
48. Multifactorial Inheritance 17%
49. Genetic Loci 17%
50. Simvastatin 17%