Medicine & Life Sciences

1. Gaucher Disease 100%
2. Enzyme Replacement Therapy 60%
3. Mucopolysaccharidoses 38%
4. Exome 36%
5. Genes 31%
6. Brazil 28%
7. Congenital Disorders of Glycosylation 27%
8. Phenotype 26%
9. Mucopolysaccharidosis I 25%
10. Mutation 21%
11. Medical Genetics 20%
12. Genetic Testing 20%
13. Fabry Disease 20%
14. Genomics 19%
15. Neurodevelopmental Disorders 18%
16. Inborn Errors Metabolism 18%
17. Enzymes 17%
18. Human Genetics 16%
19. Intellectual Disability 15%
20. Glucosylceramidase 15%
21. Mucopolysaccharidosis VI 15%
22. Glycosaminoglycans 15%
23. Neonatal Screening 14%
24. Megalencephaly 14%
25. Mucopolysaccharidosis II 14%
26. Therapeutics 14%
27. High-Throughput Nucleotide Sequencing 14%
28. Alleles 14%
29. Maple Syrup Urine Disease 13%
30. Genotype 13%
31. Muscle Hypotonia 13%
32. taliglucerase alfa 12%
33. Glycogen Storage Disease 12%
34. Precision Medicine 12%
35. Undiagnosed Diseases 11%
36. Whole Exome Sequencing 11%
37. Phenylketonurias 11%
38. Glycosylation 11%
39. Liver Glycogen 11%
40. Neuroimaging 10%
41. Contracture 10%
42. Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 10%
43. Exons 10%
44. Rare Diseases 10%
45. Salcedo syndrome 10%
46. Latin America 10%
47. Proteins 10%
48. Focal Segmental Glomerulosclerosis 10%
49. Multiplex Polymerase Chain Reaction 9%
50. Translational Medical Research 9%