Mads Bak

Medicin og biovidenskab

1. Genome 100%
2. MicroRNAs 99%
3. Genes 96%
4. Chromothripsis 93%
5. Phenotype 62%
6. Intellectual Disability 57%
7. Haploinsufficiency 54%
8. Mutation 52%
9. High-Throughput Nucleotide Sequencing 47%
10. Chromosomes 37%
11. Whole Genome Sequencing 37%
12. Human Embryonic Stem Cells 34%
13. Brain 32%
14. Single Nucleotide Polymorphism 32%
15. Mouse Mirn122 microRNA 30%
16. Cytogenetics 30%
17. human MIRN204 microRNA 28%
18. Ring Chromosomes 28%
19. Transcription Factors 27%
20. Polycomb-Group Proteins 26%
21. Proteins 26%
22. Paternal Inheritance 26%
23. Histone Demethylases 25%
24. Human Genome 24%
25. Ring Chromosome 14 Syndrome 24%
26. Mobius Syndrome 23%
27. Ectrodactyly 23%
28. CpG Islands 22%
29. Lung Neoplasms 22%
30. Actinobacillus pleuropneumoniae 22%
31. plexin 22%
32. X-Linked Mental Retardation 22%
33. histone H3 trimethyl Lys4 22%
34. DNA 22%
35. locked nucleic acid 21%
36. Usher Syndromes 21%
37. Polycomb Repressive Complex 2 21%
38. Exome 21%
39. Inuits 21%
40. Chromosomes, Human, Pair 20 21%
41. Spinocerebellar Degenerations 20%
42. Long Noncoding RNA 20%
43. Semaphorins 20%
44. Embryonic Stem Cells 20%
45. Neurodevelopmental Disorders 19%
46. Polymerase Chain Reaction 19%
47. Gene Expression 18%
48. Untranslated RNA 18%
49. Complementary RNA 18%
50. Comparative Genomic Hybridization 18%