Підписатись
Seunggeun (Shawn) Lee
Seunggeun (Shawn) Lee
Professor of Data Science, Seoul National University
Підтверджена електронна адреса в snu.ac.kr - Домашня сторінка
Назва
Посилання
Посилання
Рік
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
26242011
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
11052014
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
10572012
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
9782018
Optimal tests for rare variant effects in sequencing association studies
S Lee, MC Wu, X Lin
Biostatistics 13 (4), 762-775, 2012
7532012
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
5842018
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
4822013
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
4642008
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
2842011
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
2532013
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
W Zhou, M Kanai, KHH Wu, H Rasheed, K Tsuo, JB Hirbo, Y Wang, ...
Cell Genomics 2 (10), 2022
1752022
Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts
W Zhou, Z Zhao, JB Nielsen, LG Fritsche, J LeFaive, SA Gagliano Taliun, ...
Nature genetics 52 (6), 634-639, 2020
1602020
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
1592013
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
1452017
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
1402008
Exploring and visualizing large-scale genetic associations by using PheWeb
SA Gagliano Taliun, P VandeHaar, AP Boughton, RP Welch, D Taliun, ...
Nature Genetics 52 (6), 550-552, 2020
1362020
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 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
1222013
Convergence and prediction of principal component scores in high-dimensional settings
S Lee, F Zou, FA Wright
Annals of statistics 38 (6), 3605, 2010
992010
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
962013
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