Meral Gunay-Aygun

Medicine & Life Sciences

1. Agenesis of Cerebellar Vermis 100%
2. Ciliopathies 48%
3. Autosomal Recessive Polycystic Kidney 42%
4. Mutation 32%
5. Congenital Hepatic Fibrosis 30%
6. Cilia 26%
7. Kidney Diseases 17%
8. Gray Platelet Syndrome 15%
9. Genes 15%
10. Blood Platelets 15%
11. Chediak-Higashi Syndrome 13%
12. Phenotype 13%
13. Kidney 13%
14. Liver Diseases 13%
15. Portal Hypertension 12%
16. Prader-Willi Syndrome 11%
17. Fibroblasts 9%
18. Cystic Kidney Diseases 9%
19. Whole Exome Sequencing 9%
20. Liver 8%
21. Autosomal Dominant Polycystic Kidney 8%
22. Muscle Hypotonia 8%
23. Intellectual Disability 8%
24. Growth Hormone 8%
25. Molecular Biology 8%
26. Polycystic Kidney Diseases 7%
27. Proteins 7%
28. Jeune syndrome 7%
29. Platelet Storage Pool Deficiency 7%
30. Cardiomyopathies 7%
31. Platelet Alpha-Delta Storage Pool Deficiency 7%
32. Child 6%
33. Retinal Degeneration 6%
34. Joubert Syndrome 10 6%
35. Neuroimaging 6%
36. Organelles 6%
37. COACH syndrome 6%
38. Exons 6%
39. Natural History 6%
40. Brachydactyly type C 6%
41. Oculodigitoesophagoduodenal syndrome 5%
42. Oculocutaneous Albinism 5%
43. Precursor Cell Lymphoblastic Leukemia-Lymphoma 5%
44. Tooth 5%
45. Brain Diseases 5%
46. Orofaciodigital Syndromes 5%
47. Coloboma 5%
48. 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency 5%
49. Obesity 5%
50. Trisomy mosaicism Chromosome 15 5%