Sung H - Search Results

1

Evaluation of random forests performance for genome-wide association studies in the presence of interaction effects.

Kim Y, Wojciechowski R, Sung H, Mathias RA, Wang L, Klein AP, Lenroot RK, Malley J, Bailey-Wilson JE. Kim Y, et al. Among authors: sung h. BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S64. doi: 10.1186/1753-6561-3-s7-s64. BMC Proc. 2009. PMID: 20018058 Free PMC article.

2

A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease.

Mathias RA, Kim Y, Sung H, Yanek LR, Mantese VJ, Hererra-Galeano JE, Ruczinski I, Wilson AF, Faraday N, Becker LC, Becker DM. Mathias RA, et al. Among authors: sung h. BMC Med Genomics. 2010 Jun 7;3:22. doi: 10.1186/1755-8794-3-22. BMC Med Genomics. 2010. PMID: 20529293 Free PMC article.

3

Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data.

Simpson CL, Justice CM, Krishnan M, Wojciechowski R, Sung H, Cai J, Green T, Lewis D, Behneman D, Wilson AF, Bailey-Wilson JE. Simpson CL, et al. Among authors: sung h. BMC Proc. 2011 Nov 29;5 Suppl 9(Suppl 9):S83. doi: 10.1186/1753-6561-5-S9-S83. BMC Proc. 2011. PMID: 22373393 Free PMC article.

4

Performance of random forests and logic regression methods using mini-exome sequence data.

Kim Y, Li Q, Cropp CD, Sung H, Cai J, Simpson CL, Perry B, Dasgupta A, Malley JD, Wilson AF, Bailey-Wilson JE. Kim Y, et al. Among authors: sung h. BMC Proc. 2011 Nov 29;5 Suppl 9(Suppl 9):S104. doi: 10.1186/1753-6561-5-S9-S104. BMC Proc. 2011. PMID: 22373484 Free PMC article.

5

Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression.

Sung H, Kim Y, Cai J, Cropp CD, Simpson CL, Li Q, Perry BC, Sorant AJ, Bailey-Wilson JE, Wilson AF. Sung H, et al. BMC Proc. 2011 Nov 29;5 Suppl 9(Suppl 9):S15. doi: 10.1186/1753-6561-5-S9-S15. BMC Proc. 2011. PMID: 22373501 Free PMC article.

6

Type I error rates of rare single nucleotide variants are inflated in tests of association with non-normally distributed traits using simple linear regression methods.

Schwantes-An TH, Sung H, Sabourin JA, Justice CM, Sorant AJM, Wilson AF. Schwantes-An TH, et al. Among authors: sung h. BMC Proc. 2016 Oct 18;10(Suppl 7):385-388. doi: 10.1186/s12919-016-0060-7. eCollection 2016. BMC Proc. 2016. PMID: 27980666 Free PMC article.

7

ComPaSS-GWAS: A method to reduce type I error in genome-wide association studies when replication data are not available.

Sabourin JA, Cropp CD, Sung H, Brody LC, Bailey-Wilson JE, Wilson AF. Sabourin JA, et al. Among authors: sung h. Genet Epidemiol. 2019 Feb;43(1):102-111. doi: 10.1002/gepi.22168. Epub 2018 Oct 18. Genet Epidemiol. 2019. PMID: 30334581 Free PMC article.

8

Genome-wide association study of café-au-lait macule number in neurofibromatosis type 1.

Sung H, Hyland PL, Pemov A, Sabourin JA, Baldwin AM, Bass S, Teshome K, Luo W; Frederick National Laboratory for Cancer Research; Widemann BC, Stewart DR, Wilson AF. Sung H, et al. Mol Genet Genomic Med. 2020 Oct;8(10):e1400. doi: 10.1002/mgg3.1400. Epub 2020 Aug 31. Mol Genet Genomic Med. 2020. PMID: 32869517 Free PMC article.

9

Exome-wide association study of treatment-resistant depression suggests novel treatment targets.

Shah SB, Peddada TN, Song C, Mensah M, Sung H, Yavi M, Yuan P, Zarate CA Jr, Mickey BJ, Burmeister M, Akula N, McMahon FJ. Shah SB, et al. Among authors: sung h. Sci Rep. 2023 Aug 1;13(1):12467. doi: 10.1038/s41598-023-38984-z. Sci Rep. 2023. PMID: 37528149 Free PMC article.

10

Intra-familial tests of association between familial idiopathic scoliosis and linked regions on 9q31.3-q34.3 and 16p12.3-q22.2.

Miller NH, Justice CM, Marosy B, Swindle K, Kim Y, Roy-Gagnon MH, Sung H, Behneman D, Doheny KF, Pugh E, Wilson AF. Miller NH, et al. Among authors: sung h. Hum Hered. 2012;74(1):36-44. doi: 10.1159/000343751. Epub 2012 Nov 13. Hum Hered. 2012. PMID: 23154503 Free PMC article.

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