Liang S - Search Results

1

A novel pathogenic large germline deletion in adenomatous polyposis coli gene in a Chinese family with familial adenomatous polyposis.

Zhang Z, Liang S, Huang H, Wang D, Zhang X, Wu J, Chen H, Wang Y, Rong T, Zhou Y, Banerjee S. Zhang Z, et al. Among authors: liang s. Oncotarget. 2016 Aug 2;7(31):50392-50400. doi: 10.18632/oncotarget.10408. Oncotarget. 2016. PMID: 27391059 Free PMC article.

2

Targeted next generation sequencing identifies two novel mutations in SEPN1 in rigid spine muscular dystrophy 1.

Dai Y, Liang S, Huang Y, Chen L, Banerjee S. Dai Y, et al. Among authors: liang s. Oncotarget. 2016 Dec 20;7(51):83843-83849. doi: 10.18632/oncotarget.13337. Oncotarget. 2016. PMID: 27863379 Free PMC article.

3

Novel phenotypes of NF1 patients from unrelated Chinese families with tibial pseudarthrosis and anemia.

Banerjee S, Lei D, Liang S, Yang L, Liu S, Wei Z, Tang JP. Banerjee S, et al. Among authors: liang s. Oncotarget. 2017 Jun 13;8(24):39695-39702. doi: 10.18632/oncotarget.13932. Oncotarget. 2017. PMID: 27980226 Free PMC article.

4

A novel pathogenic splice acceptor site germline mutation in intron 14 of the APC gene in a Chinese family with familial adenomatous polyposis.

Wang D, Liang S, Zhang Z, Zhao G, Hu Y, Liang S, Zhang X, Banerjee S. Wang D, et al. Among authors: liang s. Oncotarget. 2017 Mar 28;8(13):21327-21335. doi: 10.18632/oncotarget.15570. Oncotarget. 2017. PMID: 28423518 Free PMC article.

5

Targeted next generation sequencing identified novel mutations in RPGRIP1 associated with both retinitis pigmentosa and Leber's congenital amaurosis in unrelated Chinese patients.

Huang H, Wang Y, Chen H, Chen Y, Wu J, Chiang PW, Fan N, Su Y, Deng J, Chen D, Li Y, Zhang X, Zhang M, Liang S, Banerjee S, Qi M, Liu X. Huang H, et al. Among authors: liang s. Oncotarget. 2017 May 23;8(21):35176-35183. doi: 10.18632/oncotarget.17052. Oncotarget. 2017. PMID: 28456785 Free PMC article.

6

A novel pathogenic single nucleotide germline deletion in APC gene in a four generation Chinese family with familial adenomatous polyposis.

Zhang Z, Liang S, Wang D, Liang S, Li Y, Wang B, Jiang T, Zhao G, Zhang X, Banerjee S. Zhang Z, et al. Among authors: liang s. Sci Rep. 2017 Sep 27;7(1):12357. doi: 10.1038/s41598-017-10395-x. Sci Rep. 2017. PMID: 28955048 Free PMC article.

7

A novel mutation in NF1 is associated with diverse intra-familial phenotypic variation and astrocytoma in a Chinese family.

Banerjee S, Dai Y, Liang S, Chen H, Wang Y, Tang L, Wu J, Huang H. Banerjee S, et al. Among authors: liang s. J Clin Neurosci. 2016 Sep;31:182-4. doi: 10.1016/j.jocn.2015.12.034. Epub 2016 May 24. J Clin Neurosci. 2016. PMID: 27234610

8

A novel heterozygous germline deletion in MSH2 gene in a five generation Chinese family with Lynch syndrome.

Wu B, Ji W, Liang S, Ling C, You Y, Xu L, Zhong ME, Xiao Y, Qiu HZ, Lu JY, Banerjee S. Wu B, et al. Among authors: liang s. Oncotarget. 2017 Jul 14;8(33):55194-55203. doi: 10.18632/oncotarget.19234. eCollection 2017 Aug 15. Oncotarget. 2017. PMID: 28903413 Free PMC article.

9

Whole exome sequencing identified a novel DAG1 mutation in a patient with rare, mild and late age of onset muscular dystrophy-dystroglycanopathy.

Dai Y, Liang S, Dong X, Zhao Y, Ren H, Guan Y, Yin H, Li C, Chen L, Cui L, Banerjee S. Dai Y, et al. Among authors: liang s. J Cell Mol Med. 2019 Feb;23(2):811-818. doi: 10.1111/jcmm.13979. Epub 2018 Nov 18. J Cell Mol Med. 2019. PMID: 30450679 Free PMC article.

10

An LMNB1 Duplication Caused Adult-Onset Autosomal Dominant Leukodystrophy in Chinese Family: Clinical Manifestations, Neuroradiology and Genetic Diagnosis.

Dai Y, Ma Y, Li S, Banerjee S, Liang S, Liu Q, Yang Y, Peng B, Cui L, Jin L. Dai Y, et al. Among authors: liang s. Front Mol Neurosci. 2017 Jul 18;10:215. doi: 10.3389/fnmol.2017.00215. eCollection 2017. Front Mol Neurosci. 2017. PMID: 28769756 Free PMC article.

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