河村 理恵

Medicine & Life Sciences

1. Ehlers-Danlos Syndrome 100%
2. Mutation 67%
3. Type 1b Loeys-Dietz Syndrome 61%
4. Joint Instability 48%
5. Intellectual Disability 48%
6. cytokine-like factor-1 48%
7. Crisponi syndrome 48%
8. Contracture 46%
9. High-Throughput Nucleotide Sequencing 46%
10. Pallister-Hall Syndrome 43%
11. Monosomy 43%
12. Perisylvian syndrome 43%
13. carbohydrate sulfotransferases 42%
14. Fluorescence In Situ Hybridization 42%
15. Loss of Function Mutation 40%
16. Loeys-Dietz Syndrome 39%
17. Periventricular Nodular Heterotopia 39%
18. snRNP Core Proteins 39%
19. Muscle Hypotonia 38%
20. Maple Syrup Urine Disease 37%
21. Mosaicism 36%
22. Iliac Aneurysm 35%
23. Arthrogryposis 34%
24. Trisomy 13 Syndrome 33%
25. X Chromosome Inactivation 32%
26. Clubfoot 32%
27. Disorders of Sex Development 31%
28. Chromosomes, Human, Pair 22 31%
29. Peripartum Period 31%
30. Epigenomics 31%
31. Spatial Navigation 30%
32. Haploinsufficiency 30%
33. Alleles 30%
34. Proprioception 30%
35. Turner Syndrome 30%
36. Chimerism 29%
37. Cytokine Receptors 28%
38. Retinoblastoma 28%
39. Phosphopyruvate Hydratase 27%
40. Myelodysplastic Syndromes 26%
41. Genes 26%
42. dermatan-4-sulfotransferase-1 25%
43. Decorin 24%
44. DNA Methylation 23%
45. 2-Oxoglutarate 5-Dioxygenase Procollagen-Lysine 23%
46. Skin 22%
47. Brain Diseases 22%
48. Transforming Growth Factor-beta Type I Receptor 22%
49. Genitalia 21%
50. Telomere 21%