| Emergence, Retention and Selection: A Trilogy of Origination for Functional De Novo Proteins from Ancestral LncRNAs in Primates JY Chen, QS Shen, WZ Zhou, J Peng, BZ He, Y Li, CJ Liu, X Luan, W Ding, ... PLoS genetics 11 (7), e1005391, 2015 | 58 | 2015 |
| AutoPVS1: An automatic classification tool for PVS1 interpretation of null variants J Xiang, J Peng, Z Peng Human Mutation 41 (9), 1488-1498, 2020 | 41 | 2020 |
| Concurrent hearing and genetic screening in a general newborn population L Guo, J Xiang, L Sun, X Yan, J Yang, H Wu, K Guo, J Peng, X Xie, Y Yin, ... Human genetics 139, 521-530, 2020 | 39 | 2020 |
| Evolutionary interrogation of human biology in well-annotated genomic framework of rhesus macaque SJ Zhang, CJ Liu, P Yu, X Zhong, JY Chen, X Yang, J Peng, S Yan, ... Molecular biology and evolution 31 (5), 1309-1324, 2014 | 39 | 2014 |
| Increased diagnostic yield by reanalysis of data from a hearing loss gene panel Y Sun, J Xiang, Y Liu, S Chen, J Yu, J Peng, Z Liu, L Chen, J Sun, Y Yang, ... BMC Medical Genomics 12, 1-8, 2019 | 32 | 2019 |
| Characterizing sensitivity and coverage of clinical WGS as a diagnostic test for genetic disorders Y Sun, F Liu, C Fan, Y Wang, L Song, Z Fang, R Han, Z Wang, X Wang, ... BMC medical genomics 14, 1-13, 2021 | 26 | 2021 |
| Selectively constrained RNA editing regulation crosstalks with piRNA biogenesis in primates XZ Yang, JY Chen, CJ Liu, J Peng, YR Wee, X Han, C Wang, X Zhong, ... Molecular Biology and Evolution 32 (12), 3143-3157, 2015 | 24 | 2015 |
| RhesusBase PopGateway: genome-wide population genetics atlas in rhesus macaque X Zhong, J Peng, QS Shen, JY Chen, H Gao, X Luan, S Yan, X Huang, ... Molecular Biology and Evolution 33 (5), 1370-1375, 2016 | 23 | 2016 |
| Evolutionarily significant A-to-I RNA editing events originated through G-to-A mutations in primates NA An, W Ding, XZ Yang, J Peng, BZ He, QS Shen, F Lu, A He, YE Zhang, ... Genome biology 20, 1-12, 2019 | 18 | 2019 |
| VIP‐HL: Semi‐automated ACMG/AMP variant interpretation platform for genetic hearing loss J Peng, J Xiang, X Jin, J Meng, N Song, L Chen, A Abou Tayoun, Z Peng Human Mutation 42 (12), 1567-1575, 2021 | 11 | 2021 |
| Clinical impacts of genome-wide noninvasive prenatal testing for rare autosomal trisomy J Xiang, R Li, J He, X Wang, L Yao, N Song, F Fu, S Zhou, J Wang, X Gao, ... American Journal of Obstetrics & Gynecology MFM 5 (1), 100790, 2023 | 10 | 2023 |
| Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach J Wang, J Xiang, L Chen, H Luo, X Xu, N Li, C Cui, J Xu, N Song, J Peng, ... Scientific Reports 11 (1), 4036, 2021 | 8 | 2021 |
| 在恒河猴基因组学框架下研究人类演化与调控 钟晓明， 申晴， 彭继光， 李玉梅， 李川昀 生命科学 29 (3), 230-236, 2017 | 1 | 2017 |
| The Next Generation of Population-Based DFNB16 Carrier Screening and Diagnosis: STRC Copy-Number Variant Analysis from Genome Sequencing Data J Xiang, J Peng, X Sun, Z Lin, D Li, H Ye, S Wang, Y Bai, X Wang, P Du, ... Clinical Chemistry 69 (7), 763-770, 2023 | | 2023 |
| Cover, Volume 42, Issue 12 J Peng, J Xiang, X Jin, J Meng, N Song, L Chen, A Abou Tayoun, Z Peng Human Mutation 42 (12), i-i, 2021 | | 2021 |
| Cover, Volume 41, Issue 9 J Xiang, J Peng, S Baxter, Z Peng Human Mutation 41 (9), i-i, 2020 | | 2020 |
Chuan-Yun liProfessor of Genomic Medicine, Peking Universitypku.edu.cn의 이메일 확인됨
