Author

Weixin Wang

University of PennsylvaniaORCID 0000-0002-2765-2629Unclaimed ORCID profile · follow to get notified of new preprints

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Weixin Wang1 paper

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Congcong ZhuiD· 1 shared David Alan BennettiD· 1 shared Gaoyuan MengiD· 1 shared Gerard D. SchellenbergiD· 1 shared Gyungah JuniD· 1 shared Jaeyoon ChungiD· 1 shared Jonathan L. HainesiD· 1 shared Junming HuiD· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Congcong ZhuORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineAlzheimer s & DementiaPeer-reviewedFeb 9, 2022

Protein phosphatase 2A, complement component 4, and APOE genotype linked to Alzheimer disease using a systems biology approach

Gyungah Jun, Yang You, Congcong Zhu…·Lindsay A. Farrer

This paper identifies PPP2CB and C4B as key genes linked to Alzheimer's disease through a systems biology approach, showing their association with tau pathology and complement pathway activation.

38 citationstop 4%

humanbulk RNA-seq

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BioinformaticsBioinformaticsPeer-reviewedFeb 22, 2018

Integrative DNA copy number detection and genotyping from sequencing and array-based platforms

Zilu Zhou, Weixin Wang, Li‐San Wang, Nancy Ruonan Zhang

The paper introduces iCNV, a statistical framework for detecting and genotyping DNA copy number variations from sequencing and array data, improving sensitivity and accuracy.

12 citations

whole-exome sequencingwhole-genome sequencing

𝕏 PostBluesky