Author

Xiaoxi Jing

Changping LaboratoryORCID 0000-0003-0642-8641Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:imaging· 1

Frequent Co-Authors

Hongen KangiD· 2 shared Jiaxiang ZhangiD· 2 shared Jiecong LiniD· 2 shared Junpeng Zhao· 2 shared Kaiyan Ma· 2 shared Yajie ZhaoiD· 2 shared Chen Xie· 1 shared Haitao ZhangiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Hongen KangORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 22, 2026

Large-scale genome- and phenome-wide analyses reveal the genetic architecture, pathophysiology and comorbidity of restless legs syndrome

Xiaoxi Jing, Zi Wang, Jacob Williams…·Yajie Zhao

This study identifies 15 novel RLS-associated loci and links them to neurodevelopmental programs, while revealing over 100 comorbidities and brain structural associations through genome- and phenome-wide analyses.

DOI 10.64898/2026.05.21.26353752

humanbulk RNA-seq

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BioinformaticsbioRxivPreprintMar 25, 2026

Genome-wide maps of transcription factor footprints identify noncoding variants rewiring gene regulatory networks

Jiecong Lin, Wenyang Dong, Jiaxiang Zhang…·Yajie Zhao

The paper identifies noncoding variants that alter gene regulatory networks using a combination of single-molecule deaminase footprinting and variant effect prediction, applied to UK Biobank genomes.

DOI 10.64898/2026.03.03.708783

humanwhole-genome sequencing

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