Lee S - Search Results

1

Knowledge-driven binning approach for rare variant association analysis: application to neuroimaging biomarkers in Alzheimer's disease.

Kim D, Basile AO, Bang L, Horgusluoglu E, Lee S, Ritchie MD, Saykin AJ, Nho K. Kim D, et al. Among authors: lee s. BMC Med Inform Decis Mak. 2017 May 18;17(Suppl 1):61. doi: 10.1186/s12911-017-0454-0. BMC Med Inform Decis Mak. 2017. PMID: 28539126 Free PMC article.

2

Evaluating the Calibration and Power of Three Gene-Based Association Tests of Rare Variants for the X Chromosome.

Ma C, Boehnke M, Lee S; GoT2D Investigators. Ma C, et al. Among authors: lee s. Genet Epidemiol. 2015 Nov;39(7):499-508. doi: 10.1002/gepi.21935. Epub 2015 Oct 10. Genet Epidemiol. 2015. PMID: 26454253 Free PMC article.

3

Association analysis of rare variants near the APOE region with CSF and neuroimaging biomarkers of Alzheimer's disease.

Nho K, Kim S, Horgusluoglu E, Risacher SL, Shen L, Kim D, Lee S, Foroud T, Shaw LM, Trojanowski JQ, Aisen PS, Petersen RC, Jack CR Jr, Weiner MW, Green RC, Toga AW, Saykin AJ; Alzheimer’s Disease Neuroimaging Initiative (ADNI). Nho K, et al. Among authors: lee s. BMC Med Genomics. 2017 May 24;10(Suppl 1):29. doi: 10.1186/s12920-017-0267-0. BMC Med Genomics. 2017. PMID: 28589856 Free PMC article.

4

A Fast and Accurate Algorithm to Test for Binary Phenotypes and Its Application to PheWAS.

Dey R, Schmidt EM, Abecasis GR, Lee S. Dey R, et al. Among authors: lee s. Am J Hum Genet. 2017 Jul 6;101(1):37-49. doi: 10.1016/j.ajhg.2017.05.014. Epub 2017 Jun 8. Am J Hum Genet. 2017. PMID: 28602423 Free PMC article.

5

Unified Sequence-Based Association Tests Allowing for Multiple Functional Annotations and Meta-analysis of Noncoding Variation in Metabochip Data.

He Z, Xu B, Lee S, Ionita-Laza I. He Z, et al. Among authors: lee s. Am J Hum Genet. 2017 Sep 7;101(3):340-352. doi: 10.1016/j.ajhg.2017.07.011. Epub 2017 Aug 24. Am J Hum Genet. 2017. PMID: 28844485 Free PMC article.

6

Rare-variant association tests in longitudinal studies, with an application to the Multi-Ethnic Study of Atherosclerosis (MESA).

He Z, Lee S, Zhang M, Smith JA, Guo X, Palmas W, Kardia SLR, Ionita-Laza I, Mukherjee B. He Z, et al. Among authors: lee s. Genet Epidemiol. 2017 Dec;41(8):801-810. doi: 10.1002/gepi.22081. Epub 2017 Oct 27. Genet Epidemiol. 2017. PMID: 29076270 Free PMC article.

7

Codon bias among synonymous rare variants is associated with Alzheimer's disease imaging biomarker.

Miller JE, Shivakumar MK, Risacher SL, Saykin AJ, Lee S, Nho K, Kim D. Miller JE, et al. Among authors: lee s. Pac Symp Biocomput. 2018;23:365-376. Pac Symp Biocomput. 2018. PMID: 29218897 Free PMC article.

8

Multi-SKAT: General framework to test for rare-variant association with multiple phenotypes.

Dutta D, Scott L, Boehnke M, Lee S. Dutta D, et al. Among authors: lee s. Genet Epidemiol. 2019 Feb;43(1):4-23. doi: 10.1002/gepi.22156. Epub 2018 Oct 8. Genet Epidemiol. 2019. PMID: 30298564 Free PMC article.

9

UK Biobank Whole-Exome Sequence Binary Phenome Analysis with Robust Region-Based Rare-Variant Test.

Zhao Z, Bi W, Zhou W, VandeHaar P, Fritsche LG, Lee S. Zhao Z, et al. Among authors: lee s. Am J Hum Genet. 2020 Jan 2;106(1):3-12. doi: 10.1016/j.ajhg.2019.11.012. Epub 2019 Dec 19. Am J Hum Genet. 2020. PMID: 31866045 Free PMC article.

10

Trans-ethnic meta-analysis of rare variants in sequencing association studies.

Shi J, Boehnke M, Lee S. Shi J, et al. Among authors: lee s. Biostatistics. 2021 Oct 13;22(4):706-722. doi: 10.1093/biostatistics/kxz061. Biostatistics. 2021. PMID: 31883325 Free PMC article.

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