dr. Hennie Brüggenwirth

Medicine & Life Sciences

1. Exome 100%
2. Angelman Syndrome 86%
3. Prader-Willi Syndrome 79%
4. Marfan Syndrome 75%
5. Aortic Diseases 73%
6. Whole Exome Sequencing 69%
7. Neurodevelopmental Disorders 69%
8. Uniparental Disomy 69%
9. Cohort Studies 60%
10. Genomics 59%
11. Uncertainty 54%
12. Induced Pluripotent Stem Cells 44%
13. Meta-Analysis 43%
14. Systematic Reviews 43%
15. Muscle Hypotonia 39%
16. Genes 38%
17. Guidelines 37%
18. Mothers 37%
19. Pregnancy 35%
20. Fetus 35%
21. Scoliosis 34%
22. Health 32%
23. snRNP Core Proteins 32%
24. Intellectual Disability 30%
25. Cell Respiration 27%
26. Transcriptome 27%
27. Genetic Counseling 26%
28. Phenotype 25%
29. Inborn Genetic Diseases 24%
30. Neurons 24%
31. Uniparental disomy of chromosome 2 23%
32. Information Dissemination 23%
33. Psychology 22%
34. Endosomes 21%
35. Occipital Lobe 21%
36. Tremor 20%
37. Retrospective Studies 19%
38. Brain 19%
39. Parietal Lobe 19%
40. Synapses 17%
41. Aneurysm 17%
42. Reverse Transcription 17%
43. Genotype 16%
44. Hyperphagia 16%
45. Pituitary Hormones 16%
46. Lower Extremity 15%
47. Medical Laboratory Personnel 15%
48. Prenatal Diagnosis 14%
49. Physical Examination 14%
50. Thoracic Aortic Aneurysm 12%