Xihong Lin

发表

Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium

M. Fornage, A. Reiner, J. Rotter, 2023, bioRxiv.

Testing a Large Number of Composite Null Hypotheses Using Conditionally Symmetric Multidimensional Gaussian Mixtures in Genome-Wide Studies

Ryan Sun, Z. McCaw, Xihong Lin, 2023, 2309.12584.

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale

Ivana V. Yang, Andrew D. Johnson, Ryan D. Hernandez, 2020, Nature Genetics.

A framework for detecting noncoding rare variant associations of large-scale whole-genome sequencing studies

May E. Montasser, Nicholette D. Palmer, A. Reiner, 2021, bioRxiv.

Ensemble methods for testing a global null

Zhonghua Liu, Xihong Lin, Yaowu Liu, 2023, Journal of the Royal Statistical Society Series B: Statistical Methodology.

Group testing via hypergraph factorization applied to COVID-19

B. Cleary, Rounak Dey, D. Hong, 2022, Nature Communications.

Whole genome association testing in 333,100 individuals across three biobanks identifies rare non-coding single variant and genomic aggregate associations with height

Nicholette D. Palmer, J. Murabito, S. Redline, 2023, bioRxiv.

Rare-variant association testing for sequencing data with the sequence kernel association test.

Xihong Lin, M. Boehnke, T. Cai, 2011, American journal of human genetics.

Accurate and efficient estimation of local heritability using summary statistics and the linkage disequilibrium matrix

Hui Li, Xihong Lin, Rahul Mazumder, 2023, Nature communications.

Single-cell RNA sequencing reveals placental response under environmental stress

J. Rangel-Moreno, M. Garcia-Hernandez, Eric Van Buren, 2024, Nature communications.

Semi-supervised machine learning method for predicting homogeneous ancestry groups to assess Hardy-Weinberg equilibrium in diverse whole-genome sequencing studies.

C. Reeves, N. Stitziel, Xihao Li, 2024, American journal of human genetics.