Martin Jakob Larsen

Medicine & Life Sciences

1. Autistic Disorder 17%
2. Biopsy 19%
3. Breast Neoplasms 78%
4. choline transporter 18%
5. Cognition 23%
6. Cognitive Aging 26%
7. Datasets 17%
8. Deleted in Azoospermia 1 Protein 23%
9. DNA Methylation 24%
10. Epigenomics 17%
11. Estrogen Receptors 16%
12. Exome 22%
13. Fetal Death 25%
14. Floating-harbor syndrome 21%
15. Gene Expression 25%
16. Gene Expression Profiling 22%
17. Genes 56%
18. Genotype 39%
19. Germ-Line Mutation 19%
20. Hereditary Hemorrhagic Telangiectasia 30%
21. High-Throughput Nucleotide Sequencing 100%
22. Hydrops Fetalis 29%
23. Hyper-IgM Immunodeficiency Syndrome 18%
24. I-kappa B Kinase 16%
25. Intellectual Disability 48%
26. Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia 22%
27. Large Granular Lymphocytic Leukemia 16%
28. Long Noncoding RNA 70%
29. Lymph Nodes 20%
30. Mediator Complex 16%
31. Methyl-CpG-Binding Protein 2 16%
32. Monozygotic Twins 61%
33. Mutation 84%
34. Neoplasm Metastasis 54%
35. Neoplasms 48%
36. Nervous System Malformations 17%
37. Neurodevelopmental Disorders 47%
38. NF-kappa B kinase 19%
39. Noonan Syndrome 31%
40. Phenotype 46%
41. phosphatidylinositol glycan-class A protein 23%
42. Proteins 22%
43. Regulatory Factor X Transcription Factors 21%
44. RNA 26%
45. Squamous Cell Carcinoma 41%
46. Squamous Cell Carcinoma of Head and Neck 18%
47. Synaptotagmin I 17%
48. Twins 34%
49. Type 1 Microcephalic osteodysplastic primordial dwarfism 22%
50. Whole Exome Sequencing 50%