Department of Genetics & Genomics

Medicine & Life Sciences

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