Hans Rudolf Lytchoff Eiberg

Medicine & Life Sciences

1. Mutation 100%
2. Genes 86%
3. Glucose Tolerance Test 47%
4. Obesity 42%
5. Type 2 Diabetes Mellitus 40%
6. Glucose 40%
7. Population 39%
8. Alleles 38%
9. Receptors, Serotonin, 5-HT4 37%
10. Hereditary Spastic Paraplegia 37%
11. Phenotype 36%
12. Cataract 29%
13. Insulin Secretion 29%
14. Oculocutaneous albinism type 2 28%
15. Migraine Disorders 28%
16. Hepatocyte Nuclear Factor 1 28%
17. Greenland 27%
18. Denmark 26%
19. Eye Color 25%
20. Breast Neoplasms 24%
21. Single Nucleotide Polymorphism 24%
22. Insulin 24%
23. Exons 23%
24. Genome 22%
25. Chromosomes 22%
26. Epigenomics 22%
27. Myotonic Dystrophy 21%
28. Serotonin 21%
29. C-Peptide 21%
30. Microcephaly 20%
31. Serum 19%
32. Environmental Pollutants 19%
33. Congenital primary aphakia 19%
34. Nucleotides 19%
35. Positron-Emission Tomography 19%
36. Inuits 18%
37. Trichilemmal Cyst 1 18%
38. Laurin-Sandrow syndrome 17%
39. polyalanine 17%
40. Haplotypes 17%
41. Hair Color 17%
42. Huntington Disease-Like Syndrome 17%
43. Checkpoint Kinase 2 16%
44. Patterson Stevenson syndrome 16%
45. European Continental Ancestry Group 16%
46. Fasting 16%
47. Introns 15%
48. Loss of Heterozygosity 15%
49. Adipose Tissue 15%
50. Genetic Variation 15%