Marianne Lodahl

Medicine & Life Sciences

1. Mohr-Tranebjaerg syndrome 100%
2. Orofaciodigital Syndromes 85%
3. Wolfram Syndrome 82%
4. Ectrodactyly 81%
5. Hearing Loss 81%
6. CHARGE Syndrome 80%
7. Frameshift Mutation 73%
8. Population Biological Variation 61%
9. Dystonia 58%
10. Genetic Counseling 54%
11. Optic Nerve 51%
12. Mutation 51%
13. Autosomal Dominant 10 Deafness 45%
14. Leber's Hereditary Optic Atrophy 42%
15. Age of Onset 26%
16. Genes 25%
17. Retina 24%
18. Optic Nerve Diseases 17%
19. Optic Atrophy 17%
20. Myelin Basic Protein 17%
21. Penetrance 16%
22. Dilated Cardiomyopathy 15%
23. Gene Deletion 15%
24. Nose 13%
25. Chromosome Aberrations 13%
26. Terminator Codon 11%
27. Chromatin Assembly and Disassembly 11%
28. Nonsense Codon 11%
29. Loss of Function Mutation 11%
30. DNA-Binding Proteins 11%
31. Nonsyndromic Deafness 10%
32. Eye 10%
33. Psychological Imprinting 10%
34. Counselors 9%
35. Agammaglobulinemia 9%
36. Arginine 9%
37. Haploinsufficiency 9%
38. Ear 8%
39. Nucleic Acid Repetitive Sequences 8%
40. Congresses 8%
41. Nucleic Acid Regulatory Sequences 8%
42. Retinal Ganglion Cells 8%
43. Spain 8%
44. Homologous Recombination 8%
45. Nuclear Family 7%
46. Genetic Association Studies 7%
47. Central Nervous System 7%
48. Animal Models 7%
49. Hematoxylin 7%
50. Eosine Yellowish-(YS) 7%