Author

Xue Qiang Zeng

Yale UniversityORCID 0000-0002-6064-5340Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Boyang LiiD· 2 shared Hongyu ZhaoiD· 2 shared Richard P. LiftoniD· 2 shared Sheng Chih JiniD· 2 shared Adam J. KundishoraiD· 1 shared Alejandro BerensteiniD· 1 shared Alfred Pokmeng SeeiD· 1 shared Aman B. PateliD· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Boyang LiORCID

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2 papers

Recent·Most cited

Genetic dysregulation of an endothelial Ras signaling network in vein of Galen malformations

Shujuan Zhao, Kedous Y. Mekbib, Martijn A. van der Ent, Garrett Allington, Andrew E. Prendergast, Jocelyn E. Chau, Hannah Louise Smith, John P. Shohfi, Jack Ocken, Daniel Durán, Charuta Gavankar Furey, Hao Thi Le, Phan Q. Duy, Benjamin C. Reeves, Junhui Zhang, , Kristopher Thomas Kahle

The paper identifies genetic variants in RASA1 and EPHB4 associated with vein of Galen malformations through exome analysis and single-cell transcriptomics.

bioRxiv · Mar 18, 2023 · PreprintGenomics

Quantifying concordant genetic effects of de novo mutations on multiple disorders

Hanmin Guo, Lin Hou, Yu Shi, Sheng Chih Jin, Xue Qiang Zeng, Boyang Li, Richard P. Lifton, Martina K. Brueckner, Hongyu Zhao, Qiongshi Lu

This paper introduces EncoreDNM, a statistical framework to quantify shared genetic effects of de novo mutations between disorders using exome-wide summary data, revealing abundant pairwise enrichment correlations.

eLife · Jun 6, 2022Peer-reviewedGenetics