| 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 | 2465 | 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 | 1015 | 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 | 954 | 2012 |
| 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 | 813 | 2018 |
| Optimal tests for rare variant effects in sequencing association studies S Lee, MC Wu, X Lin Biostatistics 13 (4), 762-775, 2012 | 713 | 2012 |
| 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 | 460 | 2018 |
| 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 | 456 | 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 | 454 | 2013 |
| 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 | 272 | 2011 |
| 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 | 234 | 2013 |
| 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 | 156 | 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 14 (41), 6388-6394, 2008 | 141 | 2008 |
| 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 | 132 | 2020 |
| 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 | 130 | 2017 |
| 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 | 122 | 2013 |
| 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 | 113 | 2020 |
| 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 | 95 | 2019 |
| 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 | 94 | 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 | 94 | 2010 |
| 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), 100192, 2022 | 92 | 2022 |
