Li CH - Search Results

1

Nucleotide polymorphism in ARDS outcome: a whole exome sequencing association study.

Xu JY, Liu AR, Wu ZS, Xie JF, Qu XX, Li CH, Meng SS, Liu SQ, Yang CS, Liu L, Huang YZ, Guo FM, Yang Y, Qiu HB. Xu JY, et al. Among authors: li ch. Ann Transl Med. 2021 May;9(9):780. doi: 10.21037/atm-20-5728. Ann Transl Med. 2021. PMID: 34268393 Free PMC article.

2

Targeted exome sequencing identifies five novel loci at genome-wide significance for modulating antidepressant response in patients with major depressive disorder.

Xu Z, Xie C, Xia L, Yuan Y, Zhu H, Huang X, Li C, Tao Y, Qu X, Zhang F, Zhang Z. Xu Z, et al. Transl Psychiatry. 2020 Jan 23;10(1):30. doi: 10.1038/s41398-020-0689-x. Transl Psychiatry. 2020. PMID: 32066657 Free PMC article.

3

Whole-Genome Sequencing Reveals Large ATP8B1 Deletion/Duplications as Second Mutations Missed by Exome-Based Sequencing.

Yang Y, Zhang J, Li LT, Qiu YL, Gong JY, Zhang MH, Li CH, Wang JS. Yang Y, et al. Among authors: li lt, li ch. J Mol Diagn. 2021 Nov;23(11):1491-1499. doi: 10.1016/j.jmoldx.2021.07.028. Epub 2021 Sep 17. J Mol Diagn. 2021. PMID: 34543749 Free article.

4

Molecular defects identified by whole exome sequencing in a child with Fanconi anemia.

Zheng Z, Geng J, Yao RE, Li C, Ying D, Shen Y, Ying L, Yu Y, Fu Q. Zheng Z, et al. Gene. 2013 Nov 10;530(2):295-300. doi: 10.1016/j.gene.2013.08.031. Epub 2013 Aug 22. Gene. 2013. PMID: 23973728

5

Mutations in epigenetic regulators are involved in acute lymphoblastic leukemia relapse following allogeneic hematopoietic stem cell transplantation.

Xiao H, Wang LM, Luo Y, Lai X, Li C, Shi J, Tan Y, Fu S, Wang Y, Zhu N, He J, Zheng W, Yu X, Cai Z, Huang H. Xiao H, et al. Oncotarget. 2016 Jan 19;7(3):2696-708. doi: 10.18632/oncotarget.6259. Oncotarget. 2016. PMID: 26527318 Free PMC article.

6

High-throughput sequencing-based microsatellite genotyping for polyploids to resolve allele dosage uncertainty and improve analyses of genetic diversity, structure and differentiation: A case study of the hexaploid Camellia oleifera.

Cui X, Li C, Qin S, Huang Z, Gan B, Jiang Z, Huang X, Yang X, Li Q, Xiang X, Chen J, Zhao Y, Rong J. Cui X, et al. Mol Ecol Resour. 2022 Jan;22(1):199-211. doi: 10.1111/1755-0998.13469. Epub 2021 Jul 26. Mol Ecol Resour. 2022. PMID: 34260828

7

Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1.

Cen Z, Jiang Z, Chen Y, Zheng X, Xie F, Yang X, Lu X, Ouyang Z, Wu H, Chen S, Yin H, Qiu X, Wang S, Ding M, Tang Y, Yu F, Li C, Wang T, Ishiura H, Tsuji S, Jiao C, Liu C, Xiao J, Luo W. Cen Z, et al. Brain. 2018 Aug 1;141(8):2280-2288. doi: 10.1093/brain/awy160. Brain. 2018. PMID: 29939203

8

Epigenome-Wide Association Analysis Identified Nine Skin DNA Methylation Loci for Psoriasis.

Zhou F, Wang W, Shen C, Li H, Zuo X, Zheng X, Yue M, Zhang C, Yu L, Chen M, Zhu C, Yin X, Tang M, Li Y, Chen G, Wang Z, Liu S, Zhou Y, Zhang F, Zhang W, Li C, Yang S, Sun L, Zhang X. Zhou F, et al. J Invest Dermatol. 2016 Apr;136(4):779-787. doi: 10.1016/j.jid.2015.12.029. Epub 2015 Dec 29. J Invest Dermatol. 2016. PMID: 26743604 Free article.

9

A novel 4.25 kb heterozygous deletion in PAX6 in a Chinese Han family with congenital aniridia combined with cataract and nystagmus.

Qian T, Chen C, Li C, Gong Q, Liu K, Wang G, Schrauwen I, Xu X. Qian T, et al. BMC Ophthalmol. 2021 Oct 5;21(1):353. doi: 10.1186/s12886-021-02120-0. BMC Ophthalmol. 2021. PMID: 34610801 Free PMC article.

10

Distinct non-clock-like signatures of the basal cell carcinomas from three sisters with a lethal Gorlin-Goltz syndrome.

Ye L, Wang L, Peng K, Fang O, Tian Z, Li C, Fu X, Chen Q, Chen J, Luan J, Zhang Z, Zhang Q. Ye L, et al. BMC Med Genomics. 2022 Aug 5;15(1):172. doi: 10.1186/s12920-022-01324-7. BMC Med Genomics. 2022. PMID: 35932013 Free PMC article.

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