Wang J - Search Results

1

Correction: The novel TP53 3'-end methylation pattern associated with its expression would be a potential biomarker for breast cancer detection.

Zeng F, Heng J, Guo X, Wang Y, Wu W, Tang L, Chen M, Wang S, Deng H, Wang J. Zeng F, et al. Among authors: wang j, wang y, wang s. Breast Cancer Res Treat. 2024 Nov;208(2):469. doi: 10.1007/s10549-024-07424-5. Breast Cancer Res Treat. 2024. PMID: 39115724 No abstract available.

2

The novel TP53 3'-end methylation pattern associated with its expression would be a potential biomarker for breast cancer detection.

Zeng F, Heng J, Guo X, Wang Y, Wu W, Tang L, Chen M, Wang S, Deng H, Wang J. Zeng F, et al. Among authors: wang j, wang y, wang s. Breast Cancer Res Treat. 2020 Feb;180(1):237-245. doi: 10.1007/s10549-020-05536-2. Epub 2020 Jan 25. Breast Cancer Res Treat. 2020. PMID: 31983017

3

Analysis of BRCA1/2 mutation spectrum and prevalence in unselected Chinese breast cancer patients by next-generation sequencing.

Li G, Guo X, Tang L, Chen M, Luo X, Peng L, Xu X, Wang S, Xiao Z, Yi W, Dai L, Wang J. Li G, et al. Among authors: wang j, wang s. J Cancer Res Clin Oncol. 2017 Oct;143(10):2011-2024. doi: 10.1007/s00432-017-2465-8. Epub 2017 Jun 29. J Cancer Res Clin Oncol. 2017. PMID: 28664449

4

Prevalence and spectrum of AKT1, PIK3CA, PTEN and TP53 somatic mutations in Chinese breast cancer patients.

Li G, Guo X, Chen M, Tang L, Jiang H, Day JX, Xie Y, Peng L, Xu X, Li J, Wang S, Xiao Z, Dai L, Wang J. Li G, et al. Among authors: wang j, wang s. PLoS One. 2018 Sep 13;13(9):e0203495. doi: 10.1371/journal.pone.0203495. eCollection 2018. PLoS One. 2018. PMID: 30212483 Free PMC article. Clinical Trial.

5

Mutation screening of 10 cancer susceptibility genes in unselected breast cancer patients.

Xie Y, Li G, Chen M, Guo X, Tang L, Luo X, Wang S, Yi W, Dai L, Wang J. Xie Y, et al. Among authors: wang j, wang s. Clin Genet. 2018 Jan;93(1):41-51. doi: 10.1111/cge.13063. Epub 2017 Sep 25. Clin Genet. 2018. PMID: 28580595

6

Comprehensive analysis of serum tumor markers and BRCA1/2 germline mutations in Chinese ovarian cancer patients.

Deng H, Chen M, Guo X, Heng J, Xu X, Peng L, Jiang H, Li G, Day JX, Li J, Shan D, Li Y, Zhou Y, Liu B, Dai L, Wang X, Wang J. Deng H, et al. Among authors: wang x, wang j. Mol Genet Genomic Med. 2019 Jun;7(6):e672. doi: 10.1002/mgg3.672. Epub 2019 Apr 10. Mol Genet Genomic Med. 2019. PMID: 30972954 Free PMC article.

7

ALMS1 null mutations: a common cause of Leber congenital amaurosis and early-onset severe cone-rod dystrophy.

Xu Y, Guan L, Xiao X, Zhang J, Li S, Jiang H, Jia X, Yin Y, Guo X, Wang J, Zhang Q. Xu Y, et al. Among authors: wang j. Clin Genet. 2016 Apr;89(4):442-447. doi: 10.1111/cge.12617. Epub 2015 Jun 22. Clin Genet. 2016. PMID: 26010121

8

Using a combination of whole-exome sequencing and homozygosity mapping to identify a novel mutation of SCARB2.

He M, Tang BS, Li N, Mao X, Li J, Zhang JG, Xiao JJ, Wang J, Jiang H, Shen L, Guo JF, Xia K, Wang JL. He M, et al. Among authors: wang j, wang jl. Clin Genet. 2014 Dec;86(6):598-600. doi: 10.1111/cge.12338. Epub 2014 Mar 13. Clin Genet. 2014. PMID: 24620919 No abstract available.

9

SPG35 contributes to the second common subtype of AR-HSP in China: frequency analysis and functional characterization of FA2H gene mutations.

Liao X, Luo Y, Zhan Z, Du J, Hu Z, Wang J, Guo J, Hu Z, Yan X, Pan Q, Xia K, Tang B, Shen L. Liao X, et al. Among authors: wang j. Clin Genet. 2015;87(1):85-9. doi: 10.1111/cge.12336. Epub 2014 Jan 26. Clin Genet. 2015. PMID: 24359114

10

PLA2G6 gene mutation in autosomal recessive early-onset parkinsonism in a Chinese cohort.

Shi CH, Tang BS, Wang L, Lv ZY, Wang J, Luo LZ, Shen L, Jiang H, Yan XX, Pan Q, Xia K, Guo JF. Shi CH, et al. Among authors: wang l, wang j. Neurology. 2011 Jul 5;77(1):75-81. doi: 10.1212/WNL.0b013e318221acd3. Epub 2011 Jun 22. Neurology. 2011. PMID: 21700586

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