Meng Wang
Affiliations: | 2012-2017 | Center for Bioinformatics | Peking University, Beijing, Beijing Shi, China |
Google:
"Meng Wang"Parents
Sign in to add mentor| Liping Wei | grad student | 2012-2017 | Peking University |
| Yi Zhang | post-doc | 2019- | Harvard Medical School (Neurotree) |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Ding F, Wang Q, Xie C, et al. (2023) The impact of mulberry leaf extract at three different levels on reducing the glycemic index of white bread. Plos One. 18: e0288911 |
| Wang Y, Wang M, Djekidel MN, et al. (2021) eccDNAs are apoptotic products with high innate immunostimulatory activity. Nature. 599: 308-314 |
| Yang X, Yang C, Zheng X, et al. (2020) MosaicBase: A Knowledgebase of Postzygotic Mosaic Variants in Noncancer Disease-related and Healthy Human Individuals. Genomics, Proteomics & Bioinformatics |
| Shah AA, Zhang G, Li K, et al. (2020) Excess of RALGAPB de novo variants in neurodevelopmental disorders. European Journal of Medical Genetics. 104041 |
| Clark WT, Kasak L, Bakolitsa C, et al. (2019) Assessment of predicted enzymatic activity of alpha-N-acetylglucosaminidase (NAGLU) variants of unknown significance for CAGI 2016. Human Mutation |
| Zhou WZ, Zhang J, Li Z, et al. (2019) Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. Human Mutation |
| Yang C, Li J, Wu Q, et al. (2018) AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder. Database : the Journal of Biological Databases and Curation. 2018 |
| Wang M, Tai C, E W, et al. (2018) DeFine: deep convolutional neural networks accurately quantify intensities of transcription factor-DNA binding and facilitate evaluation of functional non-coding variants. Nucleic Acids Research |
| Wang M, Wei L. (2016) iFish: predicting the pathogenicity of human nonsynonymous variants using gene-specific/family-specific attributes and classifiers. Scientific Reports. 6: 31321 |
| Xu X, Yang X, Wu Q, et al. (2015) Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome. Human Mutation |