关注
Sihan Liu
Sihan Liu
West China Hospital, Sichuan University
在 wchscu.cn 的电子邮件经过验证
标题
引用次数
引用次数
年份
LncRNA-AC006129.1 reactivates a SOCS3-mediated anti-inflammatory response through DNA methylation-mediated CIC downregulation in schizophrenia
C Ni, W Jiang, Z Wang, Z Wang, J Zhang, X Zheng, Z Liu, H Ou, T Jiang, ...
Molecular Psychiatry 26 (8), 4511-4528, 2021
322021
Integrative analyses prioritize GNL3 as a risk gene for bipolar disorder
Q Meng, L Wang, R Dai, J Wang, Z Ren, S Liu, Y Xia, Y Jiang, F Duan, ...
Molecular Psychiatry 25 (11), 2672-2684, 2020
202020
Agonal factors distort gene-expression patterns in human postmortem brains
J Dai, Y Chen, R Dai, Y Jiang, J Tian, S Liu, M Xu, M Li, J Zhou, C Liu, ...
Frontiers in Neuroscience 15, 614142, 2021
72021
DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data
Y Jiang, G Giase, K Grennan, AW Shieh, Y Xia, L Han, Q Wang, Q Wei, ...
PLoS computational biology 16 (4), e1007522, 2020
72020
Whole-genome sequencing combined RNA-sequencing analysis of patients with mutations in SET binding protein 1
L Liu, X Feng, S Liu, Y Zhou, X Dong, H Yao, B Tan
Frontiers in Neuroscience 16, 980000, 2022
52022
Case Report: Exome and RNA Sequencing Identify a Novel de novo Missense Variant in HNRNPK in a Chinese Patient With Au-Kline Syndrome
X Pan, S Liu, L Liu, X Zhang, H Yao, B Tan
Frontiers in Genetics 13, 853028, 2022
32022
Brain transcriptional regulatory architecture and schizophrenia etiology converge between East Asian and European ancestral populations
S Liu, Y Chen, F Wang, Y Jiang, F Duan, Y Xia, Z Ning, M Li, W Qiu, C Ma, ...
bioRxiv, 2021.02. 04.922880, 2021
32021
NCAD v1. 0: a database for non-coding variant annotation and interpretation
X Feng, S Liu, K Li, F Bu, H Yuan
Journal of Genetics and Genomics 51 (2), 230-242, 2024
12024
Whole exome sequencing and transcriptome analysis in two unrelated patients with novel SET mutations
X Pan, S Liu, X Feng, L Liu, X Zhang, G Qian, N Liang, H Yao, X Dong, ...
Journal of Human Genetics 68 (12), 867-874, 2023
12023
Expanding the mutational and clinical spectrum of Chinese intellectual disability patients with two novel CTCF variants
B Tan, S Liu, X Feng, X Pan, G Qian, L Liu, X Zhang, H Yao, X Dong
Frontiers in Pediatrics 11, 1195862, 2023
12023
seGMM: A new tool for gender determination from massively parallel sequencing data
S Liu, Y Zeng, C Wang, Q Zhang, M Chen, X Wang, L Wang, Y Lu, H Guo, ...
Frontiers in Genetics 13, 850804, 2022
12022
Cell group analysis reveals changes in upper-layer neurons associated with schizophrenia
R Dai, L Chen, S Liu, CT Wu, Y Chen, Y Jiang, J Dai, Q Wang, R Kopp, ...
bioRxiv, 2020.10. 22.351213, 2020
12020
Brain eQTLs of European, African American, and Asian ancestry improve interpretation of schizophrenia GWAS
Y Chen, S Liu, Z Ren, F Wang, Y Jiang, R Dai, F Duan, C Han, Z Ning, ...
medRxiv, 2024.02. 13.24301833, 2024
2024
Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss
S Liu, M Zhong, Y Huang, Q Zhang, T Chen, X Xu, W Peng, X Wang, ...
Genome Medicine 15 (1), 116, 2023
2023
系统目前无法执行此操作,请稍后再试。
文章 1–14