Yi-Min Sun - Search Results

Year	Number of Results
2004	1
2005	1
2006	1
2008	2
2010	3
2011	2
2012	2
2013	5
2014	6
2015	5
2016	8
2017	8
2018	3
2019	8
2020	7
2021	9
2022	7
2023	10
2024	2

1

Single-cell analysis of peripheral blood from high-altitude pulmonary hypertension patients identifies a distinct monocyte phenotype.

Wu XH, He YY, Chen ZR, He ZY, Yan Y, He Y, Wang GM, Dong Y, Yang Y, Sun YM, Ren YH, Zhao QY, Yang XD, Wang LY, Fu CJ, He M, Zhang SJ, Fu JF, Liu H, Jing ZC. Wu XH, et al. Among authors: sun ym. Nat Commun. 2023 Mar 31;14(1):1820. doi: 10.1038/s41467-023-37527-4. Nat Commun. 2023. PMID: 37002243 Free PMC article.

2

The genetic spectrum of a cohort of patients clinically diagnosed as Parkinson's disease in mainland China.

Sun YM, Zhou XY, Liang XN, Lin JR, Xu YD, Chen C, Wei SD, Chen QS, Liu FT, Zhao J, Tang YL, Shen B, Gan LH, Lu B, Ding ZT, An Y, Wu JJ, Wang J. Sun YM, et al. NPJ Parkinsons Dis. 2023 May 17;9(1):76. doi: 10.1038/s41531-023-00518-9. NPJ Parkinsons Dis. 2023. PMID: 37198191 Free PMC article.

3

Huntington's Disease: Relationship Between Phenotype and Genotype.

Sun YM, Zhang YB, Wu ZY. Sun YM, et al. Mol Neurobiol. 2017 Jan;54(1):342-348. doi: 10.1007/s12035-015-9662-8. Epub 2016 Jan 7. Mol Neurobiol. 2017. PMID: 26742514 Review.

4

Primary rectal teratoma with fistula formation.

Liu BY, Wu MH, Xiong J, Sun YM. Liu BY, et al. Among authors: sun ym. Asian J Surg. 2022 Dec;45(12):2763-2765. doi: 10.1016/j.asjsur.2022.06.017. Epub 2022 Jun 15. Asian J Surg. 2022. PMID: 35717298 Free article. No abstract available.

5

Propagated α-synucleinopathy recapitulates REM sleep behaviour disorder followed by parkinsonian phenotypes in mice.

Shen Y, Yu WB, Shen B, Dong H, Zhao J, Tang YL, Fan Y, Yang YF, Sun YM, Luo SS, Chen C, Liu FT, Wu JJ, Xiao BG, Yu H, Koprich JB, Huang ZL, Wang J. Shen Y, et al. Among authors: sun ym. Brain. 2020 Dec 5;143(11):3374-3392. doi: 10.1093/brain/awaa283. Brain. 2020. PMID: 33170925

6

¹⁸ F-Florzolotau Positron Emission Tomography Imaging of Tau Pathology in the Living Brains of Patients with Corticobasal Syndrome.

Liu FT, Lu JY, Li XY, Jiao FY, Chen MJ, Yao RX, Liang XN, Ju ZZ, Ge JJ, Li G, Shen B, Wu P, Song J, Li J, Sun YM, Wu JJ, Yen TC, Luo JF, Zhao QH, Zuo C, Wang J; Progressive Supranuclear Palsy Neuroimage Initiative. Liu FT, et al. Among authors: sun ym. Mov Disord. 2023 Apr;38(4):579-588. doi: 10.1002/mds.29338. Epub 2023 Feb 7. Mov Disord. 2023. PMID: 36750757

7

Autosomal dominant Parkinson's disease caused by the recently identified LRRK2 N1437D mutation in a Chinese family: Clinical features, imaging findings, and functional impact.

Sun YM, Gan LH, Peng F, Zhou XY, Chen QS, Liu FT, Tang YL, Wu P, Lu JY, Ge JJ, Yen TC, Zuo CT, Song B, Wu JJ, Wang J. Sun YM, et al. Parkinsonism Relat Disord. 2023 Jun;111:105441. doi: 10.1016/j.parkreldis.2023.105441. Epub 2023 May 12. Parkinsonism Relat Disord. 2023. PMID: 37201327

8

Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review.

Peng F, Sun YM, Quan C, Wang J, Wu JJ. Peng F, et al. Among authors: sun ym. Orphanet J Rare Dis. 2019 Apr 25;14(1):83. doi: 10.1186/s13023-019-1053-1. Orphanet J Rare Dis. 2019. PMID: 31023339 Free PMC article. Review.

9

Objective and quantitative assessment of motor function in Parkinson's disease-from the perspective of practical applications.

Yang K, Xiong WX, Liu FT, Sun YM, Luo S, Ding ZT, Wu JJ, Wang J. Yang K, et al. Among authors: sun ym. Ann Transl Med. 2016 Mar;4(5):90. doi: 10.21037/atm.2016.03.09. Ann Transl Med. 2016. PMID: 27047949 Free PMC article. Review.

10

Association of the TBK1 mutation p.Ile334Thr with frontotemporal dementia and literature review.

Yu H, Yu W, Luo SS, Yang YJ, Liu FT, Zhang Y, Chen Y, Sun YM, Wu JJ. Yu H, et al. Among authors: sun ym. Mol Genet Genomic Med. 2019 Mar;7(3):e547. doi: 10.1002/mgg3.547. Epub 2019 Jan 22. Mol Genet Genomic Med. 2019. PMID: 30672142 Free PMC article. Review.

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