| Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database J Li, T Cai, Y Jiang, H Chen, X He, C Chen, X Li, Q Shao, X Ran, Z Li, ... Molecular psychiatry 21 (2), 290-297, 2016 | 227 | 2016 |
| VarCards: an integrated genetic and clinical database for coding variants in the human genome J Li, L Shi, K Zhang, Y Zhang, S Hu, T Zhao, H Teng, X Li, Y Jiang, L Ji, ... Nucleic Acids Research 46 (D1), D1039-D1048, 2018 | 161 | 2018 |
| A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis D Zhou, Y Jiang, X Zhong, NJ Cox, C Liu, ER Gamazon Nature genetics 52 (11), 1239-1246, 2020 | 146 | 2020 |
| Genetic landscape of papillary thyroid carcinoma in the Chinese population J Liang, W Cai, D Feng, H Teng, F Mao, Y Jiang, S Hu, X Li, Y Zhang, ... The Journal of pathology 244 (2), 215-226, 2018 | 112 | 2018 |
| swDMR: a sliding window approach to identify differentially methylated regions based on whole genome bisulfite sequencing Z Wang, X Li, Y Jiang, Q Shao, Q Liu, BY Chen, D Huang PloS one 10 (7), e0132866, 2015 | 61 | 2015 |
| Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing J Wu, P Yu, X Jin, X Xu, J Li, Z Li, M Wang, T Wang, X Wu, Y Jiang, W Cai, ... Journal of genetics and genomics 45 (10), 527-538, 2018 | 41 | 2018 |
| Identification of de novo germline mutations and causal genes for sporadic diseases using trio‐based whole‐exome/genome sequencing ZB Jin, Z Li, Z Liu, Y Jiang, XB Cai, J Wu Biological Reviews 93 (2), 1014-1031, 2018 | 39 | 2018 |
| Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism Y Du, Z Li, Z Liu, N Zhang, R Wang, F Li, T Zhang, Y Jiang, X Zhi, Z Wang, ... Genetics in Medicine 22 (1), 170-180, 2020 | 33 | 2020 |
| A statistical framework for mapping risk genes from de novo mutations in whole-genome-sequencing studies Y Liu, Y Liang, AE Cicek, Z Li, J Li, RA Muhle, M Krenzer, Y Mei, Y Wang, ... The American Journal of Human Genetics 102 (6), 1031-1047, 2018 | 30 | 2018 |
| mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing J Li, Y Jiang, T Wang, H Chen, Q Xie, Q Shao, X Ran, K Xia, ZS Sun, J Wu Journal of medical genetics 52 (4), 275-281, 2015 | 29 | 2015 |
| mirDNMR: a gene-centered database of background de novo mutation rates in human Y Jiang, Z Li, Z Liu, D Chen, W Wu, Y Du, L Ji, ZB Jin, W Li, J Wu Nucleic Acids Research, gkw1044, 2016 | 18 | 2016 |
| Skeleton Genetics: a comprehensive database for genes and mutations related to genetic skeletal disorders C Chen, Y Jiang, C Xu, X Liu, L Hu, Y Xiang, Q Chen, D Chen, H Li, X Xu, ... Database 2016, baw127, 2016 | 18 | 2016 |
| Transcription factor POU3F2 regulates TRIM8 expression contributing to cellular functions implicated in schizophrenia C Ding, C Zhang, R Kopp, L Kuney, Q Meng, L Wang, Y Xia, Y Jiang, ... Molecular psychiatry 26 (7), 3444-3460, 2021 | 16 | 2021 |
| BrainEXP: a database featuring with spatiotemporal expression variations and co-expression organizations in human brains C Jiao, P Yan, C Xia, Z Shen, Z Tan, Y Tan, K Wang, Y Jiang, L Huang, ... Bioinformatics 35 (1), 172-174, 2019 | 11 | 2019 |
| 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 |
| mirVAFC: A web server for prioritizations of pathogenic sequence variants from exome sequencing data via classifications Z Li, Z Liu, Y Jiang, D Chen, X Ran, ZS Sun, J Wu Human Mutation 38 (1), 25-33, 2017 | 5 | 2017 |
| Whole-genome sequencing and its application in the research and diagnoses of genetic diseases Q Shao, Y Jiang, J Wu Yi Chuan= Hereditas 36 (11), 1087-1098, 2014 | 4 | 2014 |
Jinchen LiCentral South UniversityVerified email at csu.edu.cn
