Author

Shi‐Heng Wang

National Health Research InstitutesORCID 0000-0002-8466-2698Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:GWAS summary statistics· 2 Assay:electronic health records· 1 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Research Focus:polygenic risk· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Mark J. DalyiD· 2 shared Wei J. CheniD· 2 shared An‐Chieh FengiD· 1 shared Ashley Dumont· 1 shared Benjamin M. NealeiD· 1 shared Bi-Zhen Kao· 1 shared Che-Yu ChouiD· 1 shared Cheng-Shin YangiD· 1 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Mark J. DalyORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineNaturePeer-reviewedOct 15, 2025

Population-Specific Polygenic Risk Scores Developed for the Han Chinese

Hung‐Hsin Chen, Chien-Hsiun Chen, Ming‐Chih Hou…·Chih‐Yang Huang

The paper develops population-specific polygenic risk scores for Han Chinese using genomic and electronic health record data, showing strong predictive performance for multiple diseases.

23 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicineCell GenomicsPeer-reviewedNov 16, 2023

Analysis across Taiwan Biobank, Biobank Japan and UK Biobank identifies hundreds of novel loci for 36 quantitative traits

Chia‐Yen Chen, Tzu‐Ting Chen, Yen‐Chen Anne Feng…·Kuang Lin

The paper identifies 979 novel genetic loci for 36 quantitative traits by analyzing data from the Taiwan Biobank, Biobank Japan, and UK Biobank, highlighting the value of diverse populations in GWAS.

82 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsbioRxivPreprintDec 13, 2018

Schizophrenia risk conferred by protein-coding de novo mutations

Daniel P. Howrigan, Samuel A. Rose, Kaitlin E. Samocha…·Benjamin M. Neale

This study examines the contribution of protein-coding de novo mutations to schizophrenia risk using whole-exome sequencing data from parent-offspring trios, finding a modest but polygenic effect.

6 citations

humanwhole-exome sequencing

𝕏 PostBluesky