Iben Bache

Medicine & Life Sciences

1. Haploinsufficiency 100%
2. Genes 70%
3. Intellectual Disability 66%
4. Dyslexia 47%
5. Congenital Heart Defects 43%
6. Phenotype 39%
7. Autistic Disorder 39%
8. Epilepsy 38%
9. Language Development Disorders 31%
10. Mobius Syndrome 30%
11. Plagiocephaly 30%
12. plexin 29%
13. Myopia 27%
14. Semaphorins 26%
15. Adolescent Development 25%
16. Generalized Epilepsy 25%
17. Eye Manifestations 24%
18. Cytogenetics 24%
19. X-Linked Genes 23%
20. Denmark 23%
21. Turner Syndrome 23%
22. Multifactorial Inheritance 23%
23. Obesity 22%
24. Autism Spectrum Disorder 22%
25. Hepatomegaly 22%
26. von Hippel-Lindau Disease 22%
27. Amenorrhea 21%
28. Retinoids 21%
29. Corpus Callosum 20%
30. Acetylation 19%
31. Child Development 19%
32. Cytoplasmic and Nuclear Receptors 19%
33. Mutation 18%
34. Lysine 18%
35. Chromosome Deletion 18%
36. Mood Disorders 18%
37. Bipolar Disorder 18%
38. Histones 17%
39. Psychotic Disorders 17%
40. Fluorescence In Situ Hybridization 17%
41. Chromosomes 17%
42. Siblings 17%
43. Chromosome 21 monosomy 16%
44. Genetic Association Studies 16%
45. Autoimmune Diseases 16%
46. Myocardium 15%
47. Human Development 15%
48. Hemangioblastoma 15%