Yongchen Yang[Author] - Search Results

Year	Number of Results
2001	1
2006	1
2007	1
2008	1
2009	1
2010	1
2011	1
2012	1
2013	1
2014	1
2015	1
2018	1
2019	1
2021	1
2022	1
2023	1
2024	3

1

Compound heterozygous mutations of NDUFV1 identified in a child with mitochondrial complex I deficiency.

Tang X, Xu W, Song X, Ye H, Ren X, Yang Y, Zhang H, Wu S, Lan X. Tang X, et al. Among authors: yang y. Genes Genomics. 2022 Jun;44(6):691-698. doi: 10.1007/s13258-022-01260-x. Epub 2022 Apr 28. Genes Genomics. 2022. PMID: 35482246

2

Origin of the X-chromosome influences the development and treatment outcomes of Turner syndrome.

Zhang Y, Yang Y, Li P, Guo S. Zhang Y, et al. Among authors: yang y. PeerJ. 2021 Dec 9;9:e12354. doi: 10.7717/peerj.12354. eCollection 2021. PeerJ. 2021. PMID: 34966569 Free PMC article.

3

[Mutation analysis of two pedigrees with suspected oculocutaneous albinism].

Ye H, Lan X, Qiao T, Xu W, Tang X, Yang Y, Zhang H. Ye H, et al. Among authors: yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):212-216. doi: 10.3760/cma.j.issn.1003-9406.2019.03.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30835348 Chinese.

4

Application of a Multiplex Ligation-Dependent Probe Amplification-Based Next-Generation Sequencing Approach for the Detection of Pathogenesis of Duchenne Muscular Dystrophy and Spinal Muscular Atrophy Caused by Copy Number Aberrations.

Yang Y, Xia C, Song X, Tang X, Nie X, Xu W, Du C, Zhang H, Luo P. Yang Y, et al. Mol Neurobiol. 2024 Jan;61(1):200-211. doi: 10.1007/s12035-023-03572-9. Epub 2023 Aug 19. Mol Neurobiol. 2024. PMID: 37596438 Free PMC article.

5

Clinical characteristics and identification of novel CNOT1 variants in three unrelated Chinese families with Vissers-Bodmer Syndrome.

Tang X, Lan X, Song X, Xu W, Zhang Y, Wang S, Xiao M, Yang Y, Zhang H, Wu S. Tang X, et al. Among authors: yang y. Heliyon. 2024 Feb 21;10(4):e26743. doi: 10.1016/j.heliyon.2024.e26743. eCollection 2024 Feb 29. Heliyon. 2024. PMID: 38434094 Free PMC article.

6

A rising trend of gastric cardia cancer in Gansu Province of China.

Zhou Y, Zhang Z, Zhang Z, Wu J, Ren D, Yan X, Wang Q, Wang Y, Wang H, Zhang J, Zhu X, Yang Y, Luo C, Guo X, Tang C, Qiao L. Zhou Y, et al. Among authors: yang y. Cancer Lett. 2008 Sep 28;269(1):18-25. doi: 10.1016/j.canlet.2008.04.013. Epub 2008 May 22. Cancer Lett. 2008. PMID: 18501504

7

Adult precursor B lymphoblastic leukemia in Shanghai, China: characterization of phenotype, cytogenetics and outcome for 137 consecutive cases.

Bao L, Gross SA, Ryder J, Wang X, Ji M, Chen Y, Yang Y, Zhu S, Irons RD. Bao L, et al. Among authors: yang y. Int J Hematol. 2009 May;89(4):431-437. doi: 10.1007/s12185-009-0283-8. Epub 2009 Mar 26. Int J Hematol. 2009. PMID: 19322628

8

WT1 mutations and single nucleotide polymorphism rs16754 analysis of patients with pediatric acute myeloid leukemia in a Chinese population.

Chen X, Yang Y, Huang Y, Tan J, Chen Y, Yang J, Dou H, Zou L, Yu J, Bao L. Chen X, et al. Among authors: yang y. Leuk Lymphoma. 2012 Nov;53(11):2195-204. doi: 10.3109/10428194.2012.685732. Epub 2012 May 21. Leuk Lymphoma. 2012. PMID: 22506617

9

The TNF-alpha 238A polymorphism is associated with susceptibility to persistent bone marrow dysplasia following chronic exposure to benzene.

Lv L, Kerzic P, Lin G, Schnatter AR, Bao L, Yang Y, Zou H, Fu H, Ye X, Gross SA, Armstrong TW, Irons RD. Lv L, et al. Among authors: yang y. Leuk Res. 2007 Nov;31(11):1479-85. doi: 10.1016/j.leukres.2007.01.014. Epub 2007 Mar 23. Leuk Res. 2007. PMID: 17367855

10

HLA class II alleles may influence susceptibility to adult dermatomyositis and polymyositis in a Han Chinese population.

Gao X, Han L, Yuan L, Yang Y, Gou G, Sun H, Lu L, Bao L. Gao X, et al. Among authors: yang y. BMC Dermatol. 2014 Jun 4;14:9. doi: 10.1186/1471-5945-14-9. BMC Dermatol. 2014. PMID: 24894810 Free PMC article.

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