Meng Wang

2012-2017 Center for Bioinformatics Peking University, Beijing, Beijing Shi, China 
"Meng Wang"


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Liping Wei grad student 2012-2017 Peking University
Yi Zhang post-doc 2019- Harvard Medical School (Neurotree)
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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
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