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 | 32 | 2021 |
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 | 20 | 2020 |
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 | 7 | 2021 |
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 | 7 | 2020 |
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 | 5 | 2022 |
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 | 3 | 2022 |
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 | 3 | 2021 |
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 | 1 | 2024 |
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 | 1 | 2023 |
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 | 1 | 2023 |
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 | 1 | 2022 |
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 | 1 | 2020 |
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 |