Seunggeun (Shawn) Lee
Seunggeun (Shawn) Lee
Associate Professor of Data Science, Seoul National University
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Citeret af
Rare-variant association testing for sequencing data with the sequence kernel association test
MC Wu, S Lee, T Cai, Y Li, M Boehnke, X Lin
The American Journal of Human Genetics 89 (1), 82-93, 2011
Rare-variant association analysis: study designs and statistical tests
S Lee, GR Abecasis, M Boehnke, X Lin
The American Journal of Human Genetics 95 (1), 5-23, 2014
Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies
S Lee, MJ Emond, MJ Bamshad, KC Barnes, MJ Rieder, DA Nickerson, ...
The American Journal of Human Genetics 91 (2), 224-237, 2012
Optimal tests for rare variant effects in sequencing association studies
S Lee, MC Wu, X Lin
Biostatistics 13 (4), 762-775, 2012
Genomewide association for schizophrenia in the CATIE study: results of stage 1
PF Sullivan, D Lin, JY Tzeng, E van den Oord, D Perkins, TS Stroup, ...
Molecular psychiatry 13 (6), 570-584, 2008
Sequence kernel association tests for the combined effect of rare and common variants
I Ionita-Laza, S Lee, V Makarov, JD Buxbaum, X Lin
The American Journal of Human Genetics 92 (6), 841-853, 2013
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies
W Zhou, JB Nielsen, LG Fritsche, R Dey, MB Elvestad, BN Wolford, ...
Nature Genetics 50, 1335–1341, 2018
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13. 2
FA Wright, LJ Strug, VK Doshi, CW Commander, SM Blackman, L Sun, ...
Nature genetics 43 (6), 539-546, 2011
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
JB Nielsen, RB Thorolfsdottir, LG Fritsche, W Zhou, MW Skov, SE Graham, ...
Nature genetics 50 (9), 1234-1239, 2018
General framework for meta-analysis of rare variants in sequencing association studies
S Lee, TM Teslovich, M Boehnke, X Lin
The American Journal of Human Genetics 93 (1), 42-53, 2013
Chronic gastrointestinal symptoms and quality of life in the Korean population
JJ Jeong, MG Choi, YS Cho, SG Lee, JH Oh, JM Park, YK Cho, IS Lee, ...
World journal of gastroenterology: WJG 14 (41), 6388, 2008
Detecting rare variant effects using extreme phenotype sampling in sequencing association studies
IJ Barnett, S Lee, X Lin
Genetic epidemiology 37 (2), 142-151, 2013
Test for interactions between a genetic marker set and environment in generalized linear models
X Lin, S Lee, DC Christiani, X Lin
Biostatistics 14 (4), 667-681, 2013
Convergence and prediction of principal component scores in high-dimensional settings
S Lee, F Zou, FA Wright
Annals of statistics 38 (6), 3605, 2010
Family-based association tests for sequence data, and comparisons with population-based association tests
I Ionita-Laza, S Lee, V Makarov, JD Buxbaum, X Lin
European Journal of Human Genetics 21 (10), 1158-1162, 2013
Kernel machine SNP‐set testing under multiple candidate kernels
MC Wu, A Maity, S Lee, EM Simmons, QE Harmon, X Lin, SM Engel, ...
Genetic epidemiology 37 (3), 267-275, 2013
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
A fast and accurate algorithm to test for binary phenotypes and its application to PheWAS
R Dey, EM Schmidt, GR Abecasis, S Lee
The American Journal of Human Genetics 101 (1), 37-49, 2017
GEE‐based SNP set association test for continuous and discrete traits in family‐based association studies
X Wang, S Lee, X Zhu, S Redline, X Lin
Genetic epidemiology 37 (8), 778-786, 2013
Quantification of population structure using correlated SNPs by shrinkage principal components
F Zou, S Lee, MR Knowles, FA Wright
Human heredity 70 (1), 9-22, 2010
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Artikler 1–20