Yufeng Shen

Affiliations: 
Systems Biology Columbia University Medical Center, New York 
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"Yufeng Shen"
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Xu C, Bao S, Wang Y, et al. (2024) Reference-informed prediction of alternative splicing and splicing-altering mutations from sequences. Genome Research
Watkins WS, Hernandez EJ, Miller TA, et al. (2024) Genome Sequencing is Critical for Forecasting Outcomes following Congenital Cardiac Surgery. Medrxiv : the Preprint Server For Health Sciences
Zhong G, Zhao Y, Zhuang D, et al. (2024) PreMode predicts mode-of-action of missense variants by deep graph representation learning of protein sequence and structural context. Biorxiv : the Preprint Server For Biology
Xiao F, Zhang X, Morton SU, et al. (2024) Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease. Nature Genetics
Zhao Y, Zhong G, Hagen J, et al. (2023) A probabilistic graphical model for estimating selection coefficient of missense variants from human population sequence data. Medrxiv : the Preprint Server For Health Sciences
Petit F, Longoni M, Wells J, et al. (2023) PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects. American Journal of Human Genetics
Zhong G, Choi YA, Shen Y. (2023) VBASS enables integration of single cell gene expression data in Bayesian association analysis of rare variants. Communications Biology. 6: 774
Griffin EL, Nees SN, Morton SU, et al. (2023) Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study. Circulation. Genomic and Precision Medicine. e003791
Zhang H, Xu MS, Fan X, et al. (2022) Predicting functional effect of missense variants using graph attention neural networks. Nature Machine Intelligence. 4: 1017-1028
Fan X, Pan H, Tian A, et al. (2022) SHINE: protein language model-based pathogenicity prediction for short inframe insertion and deletion variants. Briefings in Bioinformatics
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