Author

Yu-Heng Liu

Westlake University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:benchmark study· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Organism:human· 1 Research Focus:imputation· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Beisha TangiD· 1 shared Cheng‐Da YuaniD· 1 shared Chun-Fu YuiD· 1 shared David KarasikiD· 1 shared Fei HuangiD· 1 shared Geng TianiD· 1 shared Hou‐Feng ZhengiD· 1 shared Ji-Jian Yang· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Beisha TangORCID

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1 paper

Recent·Most cited

SEAD: an augmented reference panel with 22,134 haplotypes boosts the rare variants imputation and GWAS analysis in Asian population

Mengyuan Yang, Jia-Dong Zhong, Xin Li, Geng Tian, Wei-Yang Bai, Yi-Hu Fang, Mo-Chang Qiu, Cheng‐Da Yuan, Chun-Fu Yu, Nan Li, Ji-Jian Yang, Yu-Heng Liu, Shihui Yu, Wei-Wei Zhao, Jun-Quan Liu, , Hou‐Feng Zheng

The paper introduces SEAD, an Asian reference panel that improves rare variant imputation and GWAS analysis, identifying a novel association between SNTG1 and hip BMD.

medRxiv · Dec 23, 2023 · PreprintGenetic & Genomic Medicine