Author

Yajuan J. Liu

University of WashingtonORCID 0000-0001-6040-3109Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:whole-genome sequencing· 3 Approach:experimental assay· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

He FangiD· 3 shared Stephen M. EackeriD· 2 shared Whitney Neufeld‐Kaiser· 2 shared Alexander Muratov· 1 shared Angela M. Zou· 1 shared Asha Pathak· 1 shared Brad NelsoniD· 1 shared Cate Randall PaschaliD· 1 shared

Activity by Year

2020-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 26 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

He FangORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineJournal of Molecular DiagnosticsPeer-reviewedAug 21, 2025

Evaluation of Genomic Proximity Mapping (GPM) for Detecting Genomic and Chromosomal Structural Variants in Constitutional Disorders

He Fang, Stephen M. Eacker, Yu Wu…·Yajuan J. Liu

This study evaluates Genomic Proximity Mapping (GPM) for detecting structural variants in constitutional disorders, showing high concordance and resolution compared to standard methods.

4 citations

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicineGenetics in Medicine OpenPeer-reviewedJan 1, 2025

Genetic and functional characterization of inherited complex chromosomal rearrangements in a family with multisystem anomalies

He Fang, Stephen M. Eacker, Yu Wu…·Yajuan J. Liu

The paper characterizes an inherited complex chromosomal rearrangement in a family with multisystem anomalies using multiple genomic and functional analyses.

3 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsFrontiers in GeneticsPeer-reviewedSep 22, 2020

Deletion of FUNDC2 and CMC4 on chromosome Xq28 is sufficient to cause hypergonadotropic hypogonadism in men

Xinxian Deng, He Fang, Asha Pathak…·Yajuan J. Liu

This study identifies a deletion of FUNDC2 and CMC4 on Xq28 as sufficient to cause hypergonadotropic hypogonadism in men by disrupting apoptosis, inflammation, and FSH regulation.

11 citations

humanwhole-genome sequencing

𝕏 PostBluesky