Xihong Lin

52PUBLICATIONS
357CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Epidemiological methodsEnvironmental epidemiologyGene expression (incl. microarray and other genome-wide approaches)Genomics and transcriptomics
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Publications (52)

|Sep 15, 2026
SPLENDID incorporates continuous genetic ancestry in biobank-scale data to improve polygenic risk prediction across diverse populations.

|Jul 01, 2026
Improved heritability partitioning and enrichment analyses using summary statistics with graphREML.

|Apr 15, 2026
EBV strain interacts with host HLA to drive nasopharyngeal carcinoma risk.

|Apr 03, 2026
Rare coding and noncoding variants map 1,342 diseases and biomarkers in 490,549 whole genomes.

Yuxin Yuan, Yuanyuan Guan, Yannuo Feng

|Mar 27, 2026
Comparison of variant callers using 60 532 multi-ancestry whole genome sequences.

Hufeng Zhou, Zilin Li, Derek Shyr

|Feb 27, 2026
Scalable and accurate rare-variant association tests for whole genome sequencing time-to-event analysis in large biobanks.

Shuang Song, Xihao Li, Hufeng Zhou

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Frequent Collaborators

18 joint publications

Xihao Li

13 joint publications

Zilin Li

10 joint publications

Lisa Yanek

8 joint publications

Bruce M Psaty