宮 冬樹

Medicine & Life Sciences

1. Mutation 100%
2. Genes 60%
3. Intellectual Disability 41%
4. Whole Exome Sequencing 38%
5. Periventricular Nodular Heterotopia 34%
6. Polymicrogyria 33%
7. Missense Mutation 33%
8. Microcephaly 30%
9. Megalencephaly 29%
10. Gene Expression Profiling 28%
11. Raine syndrome 27%
12. Neurodevelopmental Disorders 27%
13. Exome 26%
14. Phenotype 26%
15. Genome-Wide Association Study 25%
16. Retinitis Pigmentosa 24%
17. Capillary Malformations, Congenital, 1 22%
18. Genome 21%
19. Cochlea 21%
20. Exons 21%
21. Hearing Loss 21%
22. Neoplasms 19%
23. Renal Cell Carcinoma 19%
24. Cleft Palate 18%
25. Seizures 18%
26. zebrafish dpysl2b protein 17%
27. Inbred DBA Mouse 17%
28. Hepatocytes 17%
29. Autosomal Recessive Microcephaly with Chorioretinopathy 16%
30. Macaca fascicularis 16%
31. Pedigree 16%
32. Gene Expression 15%
33. Drug Resistant Epilepsy 15%
34. Insulin Receptor 15%
35. Brain 15%
36. Proteins 15%
37. Siblings 14%
38. Retinal Degeneration 13%
39. Absent corpus callosum cataract immunodeficiency 13%
40. Fibronectin Type III Domain 13%
41. Hemorrhagic shock and encephalopathy syndrome 13%
42. Nanopores 13%
43. Interferons 12%
44. Motor Neurons 12%
45. Insulin Resistance 12%
46. Pontocerebellar Hypoplasia 12%
47. Autism Spectrum Disorder 11%
48. Donohue Syndrome 11%
49. Quantitative Trait Loci 11%
50. Orofaciodigital Syndromes 11%