Department of Genetics & Genomics

Medicine & Life Sciences

1. 2-methylbutyrylglycine 10%
2. Amino Acid Substitution 21%
3. Arginine 16%
4. Biomarkers 14%
5. Brain Diseases 11%
6. Cardiomyopathies 17%
7. Cardiovascular Diseases 13%
8. Child 19%
9. China 14%
10. Cholestasis 23%
11. Chromosomes, Human, Pair 2 24%
12. Citric Acid 19%
13. Citrulline 23%
14. Comorbidity 14%
15. Computer Simulation 18%
16. Corpus Callosum 20%
17. Databases 11%
18. Drug Repositioning 25%
19. Early Diagnosis 14%
20. Electron Transport 13%
21. Electron Transport Complex IV 21%
22. Electron-Transferring Flavoproteins 9%
23. electron-transferring-flavoprotein dehydrogenase 25%
24. Enzyme Replacement Therapy 11%
25. Enzymes 33%
26. Ethylmalonic encephalopathy 36%
27. Etoricoxib 29%
28. Exome 25%
29. Failure to Thrive 27%
30. Fatty Acids 15%
31. Fibroblasts 17%
32. Galactosidases 27%
33. Gaucher Disease 24%
34. Gaucher-like disease 40%
35. Genes 64%
36. Genetic Databases 23%
37. Genetic Heterogeneity 21%
38. Genetic Variation 19%
39. Genome-Wide Association Study 38%
40. Glucosylceramidase 19%
41. Glycerol 9%
42. Glycogen Storage Disease Type II 26%
43. GM1 Gangliosidosis 28%
44. Haplotypes 17%
45. Hearing Loss 24%
46. Hepatocellular Carcinoma 14%
47. Hydrogen Sulfide 11%
48. Hypoglycemia 13%
49. Inborn Errors Metabolism 30%
50. Inborn Genetic Diseases 19%
51. Intellectual Disability 17%
52. Jaundice 21%
53. Leigh Disease 27%
54. Liquid Chromatography 21%
55. Liver Diseases 17%
56. Liver Transplantation 23%
57. Lupus Nephritis 22%
58. Lysosomes 20%
59. Machine Learning 20%
60. Matrix Metalloproteinase 15 32%
61. Metabolomics 20%
62. Microcephaly 27%
63. Microcephaly with spastic quadriplegia 15%
64. Missense Mutation 11%
65. Mitochondrial Diseases 28%
66. Mitochondrial Genome 22%
67. Molecular Biology 17%
68. Mothers 11%
69. Mucopolysaccharidosis VI 29%
70. Multiple Acyl Coenzyme A Dehydrogenase Deficiency 44%
71. Mutation 37%
72. Neutral Amino Acid Transport Systems 10%
73. Nitric Oxide 14%
74. Nonsense Codon 12%
75. Obstetrics 16%
76. Opioid Analgesics 16%
77. Pharmaceutical Databases 25%
78. Pharmacology 12%
79. Phenotype 43%
80. Phosphoenolpyruvate carboxykinase deficiency 42%
81. Population 18%
82. Primary Hypertrophic Osteoarthropathy 30%
83. Propionates 23%
84. Propionic Acidemia 13%
85. propionyl-coenzyme A 10%
86. Quadriplegia 22%
87. Saposins 30%
88. SARS Virus 26%
89. Scoliosis 19%
90. Seizures 23%
91. Serine 23%
92. Siblings 20%
93. sulfur dioxygenase 19%
94. Tandem Mass Spectrometry 22%
95. Therapeutics 11%
96. Transaldolase 32%
97. Type I Schindler Disease 36%
98. United Arab Emirates 100%
99. Virulence 18%
100. Whole Exome Sequencing 18%