1. |
Møller RS, Hammer TB, Rubboli G, et al. From next-generation sequencing to targeted treatment of non-acquired epilepsies. Expert Rev Mol Diagn, 2019, 19(3): 217-228.
|
2. |
Kim J, Hu C, Moufawad El Achkar C, et al. Patient-customized oligonucleotide therapy for a rare genetic disease. N Engl J Med, 2019, 381(17): 1644-1652.
|
3. |
Denny JC, Collins FS. Precision medicine in 2030-seven ways to transform healthcare. Cell, 2021, 184(6): 1415-1419.
|
4. |
Ramaswami R, Bayer R, Galea S. Precision medicine from a public health perspective. Annu Rev Public Health, 2018, 39: 153-168.
|
5. |
Olson MV. Precision medicine at the crossroads. Hum Genomics, 2017, 11(1): 23.
|
6. |
Matthew DB. Two threats to precision medicine equity. Ethn Dis, 2019, 29(Suppl 3): 629-640.
|
7. |
National Research Council (US) Committee on A Framework for Developing a New Taxonomy of Disease. Toward precision medicine: building a knowledge network for biomedical research and a new taxonomy of disease. Washington D. C. : National Academies Press (US), 2011.
|
8. |
Johnson KB, Wei WQ, Weeraratne D, et al. Precision medicine, AI, and the future of personalized health care. Clin Transl Sci, 2021, 14(1): 86-93.
|
9. |
König IR, Fuchs O, Hansen G, et al. What is precision medicine?. Eur Respir J, 2017, 50(4): 1700391.
|
10. |
Hayden EC. Technology: the $1, 000 genome. Nature, 2014, 507(7492): 294-295.
|
11. |
Nakagawa H, Fujita M. Whole genome sequencing analysis for cancer genomics and precision medicine. Cancer Sci, 2018, 109(3): 513-522.
|
12. |
Paez JG, Jänne PA, Lee JC, et al. EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science, 2004, 304(5676): 1497-1500.
|
13. |
Soda M, Choi YL, Enomoto M, et al. Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer. Nature, 2007, 448(7153): 561-566.
|
14. |
Zhou C, Wu YL, Chen G, et al. Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): a multicentre, open-label, randomised, phase 3 study. Lancet Oncol, 2011, 12(8): 735-742.
|
15. |
Madeddu C, Donisi C, Liscia N, et al. EGFR-mutated non-small cell lung cancer and resistance to immunotherapy: role of the tumor microenvironment. Int J Mol Sci, 2022, 23(12): 6489.
|
16. |
Khera AV, Chaffin M, Aragam KG, et al. Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations. Nat Genet, 2018, 50(9): 1219-1224.
|
17. |
Singh D, Agusti A, Anzueto A, et al. Global strategy for the diagnosis, management, and prevention of chronic obstructive lung disease: the GOLD science committee report 2019. Eur Respir J, 2019, 53(5): 1900164.
|
18. |
McGrath S, Ghersi D. Building towards precision medicine: empowering medical professionals for the next revolution. BMC Med Genomics, 2016, 9(1): 23.
|
19. |
Kalia SS, Adelman K, Bale SJ, et al. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. Genet Med, 2017, 19(2): 249-255.
|
20. |
Freeley M. Current postgraduate training programs and online courses in precision medicine. Expert Rev Mol Diagn, 2020, 20(6): 569-574.
|
21. |
Murphy MJ, Shahriari N, Payette M, et al. Development of a curriculum in molecular diagnostics, genomics and personalized medicine for dermatology trainees. J Cutan Pathol, 2016, 43(10): 858-865.
|