Author

Fengxia Su

BGI ResearchORCID 0000-0003-0724-6284Unclaimed 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 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Assay:DNA methylation· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Huanming YangiD· 2 shared jian Zi WangiD· 2 shared Linxuan LiiD· 2 shared Xianmei LaniD· 2 shared Xun XuiD· 2 shared Ya Ming GaoiD· 2 shared Aifen ZhouiD· 1 shared Canqing YuiD· 1 shared

Activity by Year

2018-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Huanming YangORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineCell GenomicsPeer-reviewedOct 1, 2024

Multi-trait genome-wide association study in 34,394 Chinese women reveals the genetic architecture of plasma metabolites during pregnancy

SiYang Maggie Liu, Jilong Yao, Liang Lin…·Siqi Liu

This study identifies 30 novel metabolite-gene associations in 34,394 Chinese pregnant women and finds pleiotropy and causal relationships between metabolites and diseases.

12 citations

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicineCell GenomicsPeer-reviewedOct 1, 2024

Genetic analysis of 104 pregnancy phenotypes in 39,194 Chinese women

Xiao Han, Linxuan Li, Meng Yang…·Xin Jin

This study performs a large-scale genetic analysis of 104 pregnancy phenotypes in 39,194 Chinese women, identifying 407 trait-locus associations and uncovering novel genetic insights into pregnancy-related traits.

18 citationstop 4%

humanGWAS summary statistics

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GeneticsbioRxivPreprintNov 7, 2018

Noninvasive prenatal detection of fetal trisomy and single gene disease by shotgun sequencing of placenta originated exosome DNA: a proof-of-concept validation

Weiting Zhang, Sen Lu, Jia Zhao…·Ya Ming Gao

This study validates the use of exosomal DNA from maternal plasma for noninvasive prenatal detection of fetal trisomy and single gene disease.

DOI 10.1101/464503

humanDNA methylation

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