Author

Jing Xian Teo

SingHealthORCID 0000-0002-5083-1852Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Patrick B. O. TaniD· 2 shared Saumya Shekhar JamuariD· 2 shared Sock Hoai ChaniD· 2 shared Weng Khong LimiD· 2 shared Yasmin M. BylstraiD· 2 shared Bin Tean TehiD· 1 shared Cheng Xi YangiD· 1 shared Chengxi Yang· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Patrick B. O. TanORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Implementing Reproductive Carrier Screening to Include Diverse Asian Populations: Insights from Singapore

Yasmin M. Bylstra, Myrabeth Yeo Juann, Jing Xian Teo, Jeannette Goh, Christina Choi, Shermaine Chan, Christine Song, Jasmine Chew Yin Goh, Nellie B S Chai, Jane Andrea Lieviant, Hui Jin Toh, Sock Hoai Chan, Robin D. Blythe, Melody A. Menezes, Chengxi Yang, , Saumya Shekhar Jamuar

The paper describes the implementation of a reproductive carrier screening program in Singapore, focusing on diverse Asian populations and highlighting community engagement and initial outcomes.

BMC Medicine · Oct 7, 2026Peer-reviewedGenetic & Genomic Medicine

Family History Assessment Significantly Enhances Delivery of Precision Medicine in the Genomics Era

Yasmin M. Bylstra, Weng Khong Lim, Sylvia Kam, Koei Wan Tham, Rebekah Ryanne Wu, Jing Xian Teo, Sonia Dávila, Jyn Ling Kuan, Sock Hoai Chan, Nicolas Bertin, Cheng Xi Yang, Steve Rozen, Bin Tean Teh, Khung Keong Yeo, Stuart A. Cook, , Patrick B. O. Tan

This study shows that family history collection improves the detection of pathogenic variants in genomic data, enhancing precision medicine by identifying high-risk individuals.

Genome Medicine · Jan 7, 2021Peer-reviewedGenomics