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The need to develop a patient-centered precision medicine model for adults with chronic disability.
Expert Rev Mol Diagn. 2017 May;17(5):415-418. doi: 10.1080/14737159.2017.1309976. Epub 2017 Apr 3.
2
Toward clinical genomics in everyday medicine: perspectives and recommendations.
Expert Rev Mol Diagn. 2016;16(5):521-32. doi: 10.1586/14737159.2016.1146593. Epub 2016 Feb 24.
3
Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience.
Health Aff (Millwood). 2018 May;37(5):757-764. doi: 10.1377/hlthaff.2017.1557.
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Are we ready for precision health?
Nurs Manage. 2018 Jul;49(7):9-11. doi: 10.1097/01.NUMA.0000538923.68406.3c.
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Finding the right balance between precision medicine and personalized care.
CMAJ. 2017 Aug 21;189(33):E1065-E1068. doi: 10.1503/cmaj.170107.
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Deep Digital Phenotyping and Digital Twins for Precision Health: Time to Dig Deeper.
J Med Internet Res. 2020 Mar 3;22(3):e16770. doi: 10.2196/16770.
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Next generation sequencing: implications in personalized medicine and pharmacogenomics.
Mol Biosyst. 2016 May 24;12(6):1818-30. doi: 10.1039/c6mb00115g.
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Precision Medicine and the Changing Landscape of Research Ethics.
Oncol Nurs Forum. 2016 Mar;43(2):149-50. doi: 10.1188/16.ONF.149-150.
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Exome sequencing a review of new strategies for rare genomic disease research.
Genomics. 2016 Oct;108(3-4):109-114. doi: 10.1016/j.ygeno.2016.06.003. Epub 2016 Jul 4.

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From Diagnosis to Treatment: Exploring the Latest Management Trends in Cervical Intraepithelial Neoplasia.
Cureus. 2023 Dec 10;15(12):e50291. doi: 10.7759/cureus.50291. eCollection 2023 Dec.
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Haemochromatosis patients' research priorities: Towards an improved quality of life.
Health Expect. 2023 Dec;26(6):2293-2301. doi: 10.1111/hex.13830. Epub 2023 Jul 28.
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Clinical application of next-generation sequencing to the practice of neurology.
Lancet Neurol. 2019 May;18(5):492-503. doi: 10.1016/S1474-4422(19)30033-X.
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Collaborative science unites researchers and a novel spastic ataxia gene.
Ann Neurol. 2018 Jun;83(6):1072-1074. doi: 10.1002/ana.25262.

本文引用的文献

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Opportunities and challenges of whole-genome and -exome sequencing.
BMC Genet. 2017 Feb 14;18(1):14. doi: 10.1186/s12863-017-0479-5.
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Embracing Integrative Multiomics Approaches.
Int J Genomics. 2016;2016:1715985. doi: 10.1155/2016/1715985. Epub 2016 Sep 4.
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Analysis of protein-coding genetic variation in 60,706 humans.
Nature. 2016 Aug 18;536(7616):285-91. doi: 10.1038/nature19057.
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Genetic Misdiagnoses and the Potential for Health Disparities.
N Engl J Med. 2016 Aug 18;375(7):655-65. doi: 10.1056/NEJMsa1507092.
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Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias.
Hum Mutat. 2016 Dec;37(12):1340-1353. doi: 10.1002/humu.23063. Epub 2016 Sep 2.
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Clinical exome sequencing in neurologic disease.
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The genetic background of Parkinson's disease: current progress and future prospects.
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Generating and evaluating evidence of the clinical utility of molecular diagnostic tests in oncology.
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