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Zilin Li
Zilin Li
School of Mathematics and Statistics, Northeast Normal University
Verified email at nenu.edu.cn - Homepage
Title
Cited by
Cited by
Year
Control for population structure and relatedness for binary traits in genetic association studies via logistic mixed models
H Chen, C Wang, MP Conomos, AM Stilp, Z Li, T Sofer, AA Szpiro, ...
The American Journal of Human Genetics 98 (4), 653-666, 2016
3992016
ACAT: a fast and powerful p value combination method for rare-variant analysis in sequencing studies
Y Liu, S Chen, Z Li, AC Morrison, E Boerwinkle, X Lin
The American Journal of Human Genetics 104 (3), 410-421, 2019
2342019
Genome sequencing analysis identifies Epstein–Barr virus subtypes associated with high risk of nasopharyngeal carcinoma
M Xu, Y Yao, H Chen, S Zhang, SM Cao, Z Zhang, B Luo, Z Liu, Z Li, ...
Nature genetics 51 (7), 1131-1136, 2019
1552019
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
X Li, Z Li, H Zhou, SM Gaynor, Y Liu, H Chen, R Sun, R Dey, DK Arnett, ...
Nature genetics 52 (9), 969-983, 2020
1542020
Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole-genome sequencing studies
H Chen, JE Huffman, JA Brody, C Wang, S Lee, Z Li, SM Gogarten, ...
The American Journal of Human Genetics 104 (2), 260-274, 2019
1222019
Test for rare variants by environment interactions in sequencing association studies
X Lin, S Lee, MC Wu, C Wang, H Chen, Z Li, X Lin
Biometrics 72 (1), 156-164, 2016
892016
Dynamic scan procedure for detecting rare-variant association regions in whole-genome sequencing studies
Z Li, X Li, Y Liu, J Shen, H Chen, H Zhou, AC Morrison, E Boerwinkle, ...
The American Journal of Human Genetics 104 (5), 802-814, 2019
502019
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
Z Li, X Li, H Zhou, SM Gaynor, MS Selvaraj, T Arapoglou, C Quick, Y Liu, ...
Nature Methods, 1-13, 2022
422022
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome
H Zhou, T Arapoglou, X Li, Z Li, X Zheng, J Moore, A Asok, S Kumar, ...
Nucleic Acids Research 51 (D1), D1300-D1311, 2023
402023
Whole genome sequence analysis of blood lipid levels in> 66,000 individuals
MS Selvaraj, X Li, Z Li, A Pampana, DY Zhang, J Park, S Aslibekyan, ...
Nature communications 13 (1), 1-18, 2022
322022
Variable selection and estimation in generalized linear models with the seamless \itL_\rm0 penalty
Z Li, S Wang, X Lin
Canadian Journal of Statistics 40 (4), 745-769, 2012
242012
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
X Li, C Quick, H Zhou, SM Gaynor, Y Liu, H Chen, MS Selvaraj, R Sun, ...
Nature genetics 55 (1), 154-164, 2023
192023
A multi-dimensional integrative scoring framework for predicting functional variants in the human genome
X Li, G Yung, H Zhou, R Sun, Z Li, K Hou, MJ Zhang, Y Liu, T Arapoglou, ...
The American Journal of Human Genetics 109 (3), 446-456, 2022
162022
STAAR Workflow: A cloud-based workflow for scalable and reproducible rare variant analysis
SM Gaynor, KE Westerman, LL Ackovic, X Li, Z Li, AK Manning, ...
Bioinformatics 38 (11), 3116-3117, 2022
112022
Integration of multiomic annotation data to prioritize and characterize inflammation and immune‐related risk variants in squamous cell lung cancer
R Sun, M Xu, X Li, S Gaynor, H Zhou, Z Li, Y Bossé, S Lam, MS Tsao, ...
Genetic epidemiology 45 (1), 99-114, 2021
82021
Simultaneous detection of signal regions using quadratic scan statistics with applications to whole genome association studies
Z Li, Y Liu, X Lin
Journal of the American Statistical Association 117 (538), 823-834, 2022
72022
Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations
EV Feofanova, MR Brown, T Alkis, AM Manuel, X Li, UA Tahir, Z Li, ...
Nature Communications 14 (1), 3111, 2023
52023
A versatile toolkit for molecular QTL mapping and meta-analysis at scale
C Quick, L Guan, Z Li, X Li, R Dey, Y Liu, L Scott, X Lin
bioRxiv, 2020.12. 18.423490, 2020
52020
A minimax optimal ridge-type set test for global hypothesis with applications in whole genome sequencing association studies
Y Liu, Z Li, X Lin
Journal of the American Statistical Association 117 (538), 897-908, 2022
42022
Genome-wide cross-trait analysis and Mendelian randomization reveal a shared genetic etiology and causality between COVID-19 and venous thromboembolism
X Huang, M Yao, P Tian, JYY Wong, Z Li, Z Liu, JV Zhao
Communications Biology 6 (1), 441, 2023
32023
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