Center for Research in Genetics and Genomics (CIGGUR)

Medicine & Life Sciences

1. Primary Ovarian Insufficiency 100%
2. Mutation 89%
3. Genes 73%
4. Exome 42%
5. Colombia 38%
6. Whole Exome Sequencing 38%
7. High-Throughput Nucleotide Sequencing 37%
8. Phenotype 35%
9. Vitamin B Complex 32%
10. Pharmacogenetics 29%
11. Attention Deficit Disorder with Hyperactivity 29%
12. Genome-Wide Association Study 23%
13. Population 23%
14. Drug-Related Side Effects and Adverse Reactions 21%
15. Missense Mutation 20%
16. Computational Biology 20%
17. Quantitative Trait Loci 19%
18. Vitamin B 12 19%
19. Habitual Abortion 18%
20. Pre-Eclampsia 18%
21. Thiamine 18%
22. Genomics 17%
23. Pharmaceutical Preparations 16%
24. Pregnancy 15%
25. Exons 15%
26. Warfarin 15%
27. Pyridoxine 15%
28. Meta-Analysis 15%
29. Peripheral Nervous System Diseases 15%
30. Genetic Association Studies 14%
31. Fabry Disease 14%
32. Ebstein Anomaly 14%
33. Alleles 13%
34. Transcription Factors 13%
35. Therapeutics 13%
36. X Chromosome 13%
37. cyanocobalamin, pyridoxine, thiamine drug combination 13%
38. Proteins 13%
39. Apraxias 13%
40. Stevens-Johnson Syndrome 12%
41. Duchenne Muscular Dystrophy 12%
42. Single Nucleotide Polymorphism 12%
43. Gene Frequency 12%
44. Dystrophin 11%
45. Long QT Syndrome 11%
46. Neurobiology 11%
47. SARS Virus 11%
48. Spontaneous Abortion 11%
49. Electrocardiography 11%
50. Ataxia 10%
51. Forkhead Transcription Factors 10%
52. Nervous System 10%
53. Pharmacogenomic Testing 10%
54. Cardiomegaly 10%
55. Cytochrome P-450 CYP2C9 10%
56. Clopidogrel 10%
57. Familial premature ovarian failure 10%
58. Vitamin B 6 10%
59. Pain 9%
60. Medical Students 9%
61. Genome 9%
62. Lupus Coagulation Inhibitor 9%
63. Point Mutation 9%
64. Pathology 9%
65. Ceroid Lipofuscinosis, Neuronal, 6 9%
66. Names 9%
67. Ichthyosis 9%
68. Sequence Analysis 9%
69. Eye 9%
70. Infertility 8%
71. origen 8%
72. Kounis Syndrome 8%
73. Channelopathies 8%
74. Immunotherapy 8%
75. Fucosidosis 8%
76. Congenital Pain Insensitivity 8%
77. Self Medication 8%
78. LEOPARD Syndrome 8%
79. RNA Splice Sites 8%
80. Primary Hypertrophic Osteoarthropathy 8%
81. Pandemics 8%
82. Non-Receptor Type 11 Protein Tyrosine Phosphatase 8%
83. Costs and Cost Analysis 8%
84. Biomarkers 8%
85. MutS Proteins 7%
86. Mammalian Chromosomes 7%
87. Colorectal Neoplasms 7%
88. Pharmacogenomic Variants 7%
89. Molecular Biology 7%
90. Genetic Profile 7%
91. Chromosomes, Human, X 7%
92. Genetic Counseling 7%
93. 46,XY Disorders of Sex Development 7%
94. Acute Coronary Syndrome 7%
95. placental alkaline phosphatase 7%
96. Steroid 21-Hydroxylase 7%
97. Nonsense Codon 7%
98. HELLP Syndrome 7%
99. Child 7%
100. Hemophilia A 7%