Paper Search Results


AuthorId: 2241548119
Limit: 10
Sort by: score
Embedding: s2_recommendations
IP address: 18.116.14.12
Freq flyer: False

authorId(s): 2241548119
Author(s): Xihong Lin
scorecitationCountPaperAuthorsyearMore like thisCompare & ContrastProNE-sSciNCLSpecterGNN
705
Rare-variant association testing for sequencing data with the sequence kernel association test.
Michael C. Wu, Seunggeun Lee, ..., Xihong Lin
2011
165
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale
Xihao Li, Zilin Li, ..., Xihong Lin
2020
8
Group testing via hypergraph factorization applied to COVID-19
D. Hong, Rounak Dey, ..., Edgar Dobriban
2022
6
Deciphering the impact of genomic variation on function.
J. Engreitz, Heather A. Lawson, ..., Meenakshi S. Kagda
2024
6
Accurate and efficient estimation of local heritability using summary statistics and the linkage disequilibrium matrix
Hui Li, Rahul Mazumder, Xihong Lin
2023
6
Whole genome association testing in 333,100 individuals across three biobanks identifies rare non-coding single variant and genomic aggregate associations with height
G. Hawkes, R. Beaumont, ..., M. Weedon
2023
3
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies
Xihao Li, Han Chen, ..., Xihong Lin
2023
3
STAARpipeline: an all-in-one rare-variant tool for biobank-scale whole-genome sequencing data
Xihong Lin, Zilin Li, Harvard T.H. Chan
2022
2
Synthetic surrogates improve power for genome-wide association studies of partially missing phenotypes in population biobanks.
Z. McCaw, Jianhui Gao, ..., Jessica L. Gronsbell
2024
2
Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis
Natalie R. Hasbani, Kenneth E. Westerman, ..., P. D. de Vries
2023

Help Bulk Download
GitHub Final Report (YouTube)
JSALT-2023 Contact us (by email)
BETA Version