Wang S - Search Results

1

A model for postzygotic mosaicisms quantifies the allele fraction drift, mutation rate, and contribution to de novo mutations.

Ye AY, Dou Y, Yang X, Wang S, Huang AY, Wei L. Ye AY, et al. Among authors: wang s. Genome Res. 2018 Jul;28(7):943-951. doi: 10.1101/gr.230003.117. Epub 2018 Jun 6. Genome Res. 2018. PMID: 29875290 Free PMC article.

2

Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals.

Huang AY, Xu X, Ye AY, Wu Q, Yan L, Zhao B, Yang X, He Y, Wang S, Zhang Z, Gu B, Zhao HQ, Wang M, Gao H, Gao G, Zhang Z, Yang X, Wu X, Zhang Y, Wei L. Huang AY, et al. Among authors: wang m, wang s. Cell Res. 2014 Nov;24(11):1311-27. doi: 10.1038/cr.2014.131. Epub 2014 Oct 14. Cell Res. 2014. PMID: 25312340 Free PMC article.

3

Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome.

Xu X, Yang X, Wu Q, Liu A, Yang X, Ye AY, Huang AY, Li J, Wang M, Yu Z, Wang S, Zhang Z, Wu X, Wei L, Zhang Y. Xu X, et al. Among authors: wang m, wang s. Hum Mutat. 2015 Sep;36(9):861-72. doi: 10.1002/humu.22819. Epub 2015 Jul 24. Hum Mutat. 2015. PMID: 26096185 Free PMC article.

4

Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations.

Dou Y, Yang X, Li Z, Wang S, Zhang Z, Ye AY, Yan L, Yang C, Wu Q, Li J, Zhao B, Huang AY, Wei L. Dou Y, et al. Among authors: wang s. Hum Mutat. 2017 Aug;38(8):1002-1013. doi: 10.1002/humu.23255. Epub 2017 May 30. Hum Mutat. 2017. PMID: 28503910 Free PMC article.

5

Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort.

Yang X, Liu A, Xu X, Yang X, Zeng Q, Ye AY, Yu Z, Wang S, Huang AY, Wu X, Wu Q, Wei L, Zhang Y. Yang X, et al. Among authors: wang s. Sci Rep. 2017 Nov 15;7(1):15677. doi: 10.1038/s41598-017-15814-7. Sci Rep. 2017. PMID: 29142202 Free PMC article.

6

Distinctive types of postzygotic single-nucleotide mosaicisms in healthy individuals revealed by genome-wide profiling of multiple organs.

Huang AY, Yang X, Wang S, Zheng X, Wu Q, Ye AY, Wei L. Huang AY, et al. Among authors: wang s. PLoS Genet. 2018 May 15;14(5):e1007395. doi: 10.1371/journal.pgen.1007395. eCollection 2018 May. PLoS Genet. 2018. PMID: 29763432 Free PMC article.

7

ATP1A3 mosaicism in families with alternating hemiplegia of childhood.

Yang X, Yang X, Chen J, Li S, Zeng Q, Huang AY, Ye AY, Yu Z, Wang S, Jiang Y, Wu X, Wu Q, Wei L, Zhang Y. Yang X, et al. Among authors: wang s. Clin Genet. 2019 Jul;96(1):43-52. doi: 10.1111/cge.13539. Epub 2019 Apr 3. Clin Genet. 2019. PMID: 30891744 Free PMC article.

8

Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations.

Zhou WZ, Zhang J, Li Z, Lin X, Li J, Wang S, Yang C, Wu Q, Ye AY, Wang M, Wang D, Pu TZ, Wu YY, Wei L. Zhou WZ, et al. Among authors: wang m, wang d, wang s. Hum Mutat. 2019 Jun;40(6):801-815. doi: 10.1002/humu.23724. Epub 2019 Apr 29. Hum Mutat. 2019. PMID: 30763456 Free PMC article.

9

Rtt105 functions as a chaperone for replication protein A to preserve genome stability.

Li S, Xu Z, Xu J, Zuo L, Yu C, Zheng P, Gan H, Wang X, Li L, Sharma S, Chabes A, Li D, Wang S, Zheng S, Li J, Chen X, Sun Y, Xu D, Han J, Chan K, Qi Z, Feng J, Li Q. Li S, et al. Among authors: wang x, wang s. EMBO J. 2018 Sep 3;37(17):e99154. doi: 10.15252/embj.201899154. Epub 2018 Jul 31. EMBO J. 2018. PMID: 30065069 Free PMC article.

10

Live visualization of genomic loci with BiFC-TALE.

Hu H, Zhang H, Wang S, Ding M, An H, Hou Y, Yang X, Wei W, Sun Y, Tang C. Hu H, et al. Among authors: wang s. Sci Rep. 2017 Jan 11;7:40192. doi: 10.1038/srep40192. Sci Rep. 2017. PMID: 28074901 Free PMC article.

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