Southwestern Graduate School of Biomedical Sciences

Medicine & Life Sciences

1. Turner Syndrome 100%
2. X Chromosome 50%
3. Phenotype 50%
4. Primary Ovarian Insufficiency 44%
5. Leri-Weil syndrome 42%
6. Genes 40%
7. Klinefelter Syndrome 34%
8. Germ Cells 31%
9. Haploinsufficiency 30%
10. Cyclin A1 29%
11. Langer mesomelic dysplasia 25%
12. Sex Chromosomes 25%
13. Mutation 21%
14. Obesity 20%
15. T-Lymphocytes 20%
16. Receptor, Melanocortin, Type 4 19%
17. Meiosis 18%
18. Homeobox Genes 18%
19. Introns 17%
20. X Chromosome Inactivation 17%
21. Yeasts 17%
22. Sperm Capacitation 17%
23. ribosomal protein S4 16%
24. Cryptococcosis 16%
25. 21S rRNA 16%
26. Y Chromosome 16%
27. Cytokines 16%
28. Gametogenesis 16%
29. XYY syndrome 47 15%
30. Cyclin A 15%
31. Cyclin A2 14%
32. Melanocortins 14%
33. Gene Dosage 14%
34. Paraventricular Hypothalamic Nucleus 13%
35. Oxytocin 13%
36. Cryptococcus neoformans 13%
37. Th2 Cells 13%
38. Helper-Inducer T-Lymphocytes 12%
39. lipid transfer protein 12%
40. Cell Cycle Checkpoints 12%
41. Spermatogenesis 12%
42. B-Lymphocytes 12%
43. Cell Cycle 11%
44. Interleukin-4 Receptors 11%
45. Interleukin-4 11%
46. Lung 11%
47. Testis 11%
48. Follicular Fluid 10%
49. Th1 Cells 10%
50. Neurons 10%
51. Flagellin 10%
52. Haploidy 10%
53. Antigens 10%
54. Pigmentary Disorder, Reticulate, with Systemic Manifestations 10%
55. Turner Syndrome-Associated Neurocognitive Phenotype 9%
56. Clone Cells 9%
57. B-Cell Lymphoma 9%
58. Anti-Idiotypic Antibodies 9%
59. Y-Linked Genes 9%
60. Karyotype 9%
61. T-Lymphocyte Epitopes 9%
62. DNA 9%
63. Hypospadias 9%
64. Chromosomes, Human, Pair 13 8%
65. Sex Chromosome Disorders 8%
66. Proteins 8%
67. Inbred C57BL Mouse 8%
68. Interferons 8%
69. X-Linked Genes 8%
70. Anorexia 8%
71. Arrest of spermatogenesis 8%
72. Cognition 8%
73. Oocytes 8%
74. Gene Silencing 8%
75. Autistic Disorder 8%
76. Salmonella 8%
77. Hyperphagia 8%
78. SCID Mice 8%
79. Growth 7%
80. Interleukin-5 7%
81. Congresses 7%
82. Ovary 7%
83. monoclonal antibody GK1.5 7%
84. Pseudoautosomal Regions 7%
85. Transgenes 7%
86. human PLTP protein 7%
87. Messenger RNA 7%
88. Psychological Imprinting 7%
89. Child 7%
90. Cleavage Stimulation Factor 7%
91. VACTERL association 7%
92. Mothers 7%
93. Penoscrotal transposition 7%
94. Natural Killer Cells 7%
95. Hypothalamus 7%
96. Chromosome Aberrations 7%
97. Cyclin H 6%
98. rRNA Genes 6%
99. Protein Isoforms 6%
100. Heterozygote 6%