Laura Murphy

Medicine & Life Sciences

1. Genome-Wide Association Study 100%
2. Single Nucleotide Polymorphism 80%
3. Autistic Disorder 79%
4. Asperger Syndrome 67%
5. Cilia 55%
6. Capsid Proteins 54%
7. Protein Transport 52%
8. N-Methyl-D-Aspartate Receptors 47%
9. Cyclic AMP 47%
10. Endoplasmic Reticulum 45%
11. Intellectual Disability 45%
12. Neurons 40%
13. Mitochondria 39%
14. Chromosomes 37%
15. Learning 35%
16. Mutation 33%
17. Synapses 32%
18. Aptitude 32%
19. Membranes 31%
20. Dyneins 31%
21. Kinesin 30%
22. Psychological Power 22%
23. Synaptic Transmission 22%
24. Mental Disorders 19%
25. Coat Protein Complex I 15%
26. Genome 14%
27. Schizophrenia 14%
28. Neurodevelopmental Disorders 14%
29. Whole Genome Sequencing 13%
30. X Chromosome 13%
31. Genes 13%
32. Academic Success 12%
33. Zebrafish 12%
34. Health 11%
35. Neuronal Plasticity 11%
36. Stereotyped Behavior 11%
37. Nucleic Acid Regulatory Sequences 10%
38. Information Storage and Retrieval 10%
39. Sequence Homology 10%
40. Psychiatry 10%
41. Quality Control 10%
42. Language Development 10%
43. Color 9%
44. DNA 9%
45. Gene Frequency 9%
46. Genetic Promoter Regions 9%
47. Alleles 8%
48. Interpersonal Relations 8%
49. Carrier Proteins 8%
50. Genomics 8%