Biochemistry, Genetics and Molecular Biology

1. Genetics 100%
2. Genome-Wide Association Study 80%
3. Whole Genome Sequencing 58%
4. Rare Variant 57%
5. Birth Weight 57%
6. Allele 50%
7. Genetic Divergence 46%
8. Single Nucleotide Polymorphism 37%
9. Body Mass 33%
10. Offspring 31%
11. Genetic Variation 29%
12. Blood Pressure 28%
13. Genetic Determinism 27%
14. Haplotype 23%
15. Low Birth Weight 23%
16. Single-Nucleotide Polymorphism 22%
17. Minor Allele Frequency 20%
18. Mendelian Randomization 18%
19. DOT1L 18%
20. Genotyping 18%
21. Genome Wide Association Study 15%
22. Metabolite 13%
23. BTNL2 13%
24. ALDH1A2 13%
25. Intraflagellar Transport 13%
26. Matrix Gla Protein 13%
27. Methylation 13%
28. PIK3R1 13%
29. Fibroblast Growth Factor Receptor 3 13%
30. Insulin Resistance 13%
31. Human Leukocyte Antigen 13%
32. Thyroid Function 13%
33. Thyroid-Stimulating Hormone 13%
34. Fat Mass 13%
35. Hemoglobin Blood Level 13%
36. Amplicon 13%
37. Guanosine Diphosphate Mannose 13%
38. Metabolomics 13%
39. Triacylglycerol Blood Level 13%
40. Oxidative Stress 13%
41. Bisulfite Sequencing 13%
42. Synaptic Transmission 13%
43. Dystroglycan 13%
44. Mannose 13%
45. Gene Linkage Disequilibrium 12%
46. Gene Locus 12%
47. Glycosylation 10%
48. Fetus Growth 10%
49. Chromosome 12 9%
50. Structural Equation Modeling 9%