| Year |
Citation |
Score |
| 2025 |
Wang M, Yang X, Wu Q. High-resolution dissection of human cell type-specific enhancers in cis and trans activities. Genomics. 117: 110985. PMID 39755338 DOI: 10.1016/j.ygeno.2025.110985 |
0.517 |
|
| 2023 |
Ding F, Wang Q, Xie C, Wang M, Zhang L, Gao M, Yang Z, Ma J, Shi X, Chen W, Duan S, Yuan P, Li Y, Ma X, Wu Y, et al. The impact of mulberry leaf extract at three different levels on reducing the glycemic index of white bread. Plos One. 18: e0288911. PMID 37561734 DOI: 10.1371/journal.pone.0288911 |
0.362 |
|
| 2021 |
Wang Y, Wang M, Djekidel MN, Chen H, Liu D, Alt FW, Zhang Y. eccDNAs are apoptotic products with high innate immunostimulatory activity. Nature. 599: 308-314. PMID 34671165 DOI: 10.1038/s41586-021-04009-w |
0.668 |
|
| 2020 |
Yang X, Yang C, Zheng X, Xiong L, Tao Y, Wang M, Yongxin Ye A, Wu Q, Dou Y, Luo J, Wei L, Yue Huang A. MosaicBase: A Knowledgebase of Postzygotic Mosaic Variants in Noncancer Disease-related and Healthy Human Individuals. Genomics, Proteomics & Bioinformatics. PMID 32911083 DOI: 10.1016/J.Gpb.2020.05.002 |
0.755 |
|
| 2020 |
Shah AA, Zhang G, Li K, Chenbin L, Kanhar AA, Wang M, Quan Y, Wu H, Shen L, Khan R, Guodong C, Ou J, Hu Z, Xia K, Guo H. Excess of RALGAPB de novo variants in neurodevelopmental disorders. European Journal of Medical Genetics. 104041. PMID 32853829 DOI: 10.1016/j.ejmg.2020.104041 |
0.302 |
|
| 2019 |
Clark WT, Kasak L, Bakolitsa C, Hu Z, Andreoletti G, Babbi G, Bromberg Y, Casadio R, Dunbrack R, Folkman L, Ford CT, Jones D, Katsonis P, Kundu K, Lichtarge O, ... ... Wang M, et al. Assessment of predicted enzymatic activity of alpha-N-acetylglucosaminidase (NAGLU) variants of unknown significance for CAGI 2016. Human Mutation. PMID 31342580 DOI: 10.1002/Humu.23875 |
0.521 |
|
| 2019 |
Zhou WZ, Zhang J, Li Z, Lin X, Li J, Wang S, Yang C, Wu Q, Ye AY, Wang M, Wang D, Pu TZ, Wu YY, Wei L. Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. Human Mutation. PMID 30763456 DOI: 10.1002/Humu.23724 |
0.747 |
|
| 2018 |
Yang C, Li J, Wu Q, Yang X, Huang AY, Zhang J, Ye AY, Dou Y, Yan L, Zhou WZ, Kong L, Wang M, Ai C, Yang D, Wei L. AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder. Database : the Journal of Biological Databases and Curation. 2018. PMID 30339214 DOI: 10.1093/Database/Bay106 |
0.678 |
|
| 2018 |
Wang M, Tai C, E W, Wei L. DeFine: deep convolutional neural networks accurately quantify intensities of transcription factor-DNA binding and facilitate evaluation of functional non-coding variants. Nucleic Acids Research. PMID 29617928 DOI: 10.1093/Nar/Gky215 |
0.495 |
|
| 2016 |
Wang M, Wei L. iFish: predicting the pathogenicity of human nonsynonymous variants using gene-specific/family-specific attributes and classifiers. Scientific Reports. 6: 31321. PMID 27527004 DOI: 10.1038/Srep31321 |
0.503 |
|
| 2015 |
Xu X, Yang X, Wu Q, Liu A, Yang X, Ye AY, Huang AY, Li J, Wang M, Yu Z, Wang S, Zhang Z, Wu X, Wei L, Zhang Y. Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome. Human Mutation. PMID 26096185 DOI: 10.1002/Humu.22819 |
0.702 |
|
| 2014 |
Ding Y, Wang M, He Y, Ye AY, Yang X, Liu F, Meng Y, Gao G, Wei L. "Bioinformatics: introduction and methods," a bilingual Massive Open Online Course (MOOC) as a new example for global bioinformatics education. Plos Computational Biology. 10: e1003955. PMID 25503717 DOI: 10.1371/Journal.Pcbi.1003955 |
0.702 |
|
| 2014 |
Huang AY, Xu X, Ye AY, Wu Q, Yan L, Zhao B, Yang X, He Y, Wang S, Zhang Z, Gu B, Zhao HQ, Wang M, Gao H, Gao G, et al. Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals. Cell Research. 24: 1311-27. PMID 25312340 DOI: 10.1038/Cr.2014.131 |
0.692 |
|
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