Kong SW - Search Results

1

Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort.

Lee IH, Smith MR, Yazdani A, Sandhu S, Walker DI, Mandl KD, Jones DP, Kong SW. Lee IH, et al. Among authors: kong sw. Hum Genomics. 2022 Dec 8;16(1):67. doi: 10.1186/s40246-022-00440-w. Hum Genomics. 2022. PMID: 36482414 Free PMC article.

2

Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders.

Kong SW, Collins CD, Shimizu-Motohashi Y, Holm IA, Campbell MG, Lee IH, Brewster SJ, Hanson E, Harris HK, Lowe KR, Saada A, Mora A, Madison K, Hundley R, Egan J, McCarthy J, Eran A, Galdzicki M, Rappaport L, Kunkel LM, Kohane IS. Kong SW, et al. PLoS One. 2012;7(12):e49475. doi: 10.1371/journal.pone.0049475. Epub 2012 Dec 5. PLoS One. 2012. PMID: 23227143 Free PMC article.

3

Pathway-based outlier method reveals heterogeneous genomic structure of autism in blood transcriptome.

Campbell MG, Kohane IS, Kong SW. Campbell MG, et al. Among authors: kong sw. BMC Med Genomics. 2013 Sep 24;6:34. doi: 10.1186/1755-8794-6-34. BMC Med Genomics. 2013. PMID: 24063311 Free PMC article.

4

Prioritizing disease-linked variants, genes, and pathways with an interactive whole-genome analysis pipeline.

Lee IH, Lee K, Hsing M, Choe Y, Park JH, Kim SH, Bohn JM, Neu MB, Hwang KB, Green RC, Kohane IS, Kong SW. Lee IH, et al. Among authors: kong sw. Hum Mutat. 2014 May;35(5):537-47. doi: 10.1002/humu.22520. Epub 2014 Mar 6. Hum Mutat. 2014. PMID: 24478219 Free PMC article.

5

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.

Vassy JL, Lautenbach DM, McLaughlin HM, Kong SW, Christensen KD, Krier J, Kohane IS, Feuerman LZ, Blumenthal-Barby J, Roberts JS, Lehmann LS, Ho CY, Ubel PA, MacRae CA, Seidman CE, Murray MF, McGuire AL, Rehm HL, Green RC; MedSeq Project. Vassy JL, et al. Among authors: kong sw. Trials. 2014 Mar 20;15:85. doi: 10.1186/1745-6215-15-85. Trials. 2014. PMID: 24645908 Free PMC article. Clinical Trial.

6

Reducing false-positive incidental findings with ensemble genotyping and logistic regression based variant filtering methods.

Hwang KB, Lee IH, Park JH, Hambuch T, Choe Y, Kim M, Lee K, Song T, Neu MB, Gupta N, Kohane IS, Green RC, Kong SW. Hwang KB, et al. Among authors: kong sw. Hum Mutat. 2014 Aug;35(8):936-44. doi: 10.1002/humu.22587. Epub 2014 Jun 24. Hum Mutat. 2014. PMID: 24829188 Free PMC article.

7

Summarizing polygenic risks for complex diseases in a clinical whole-genome report.

Kong SW, Lee IH, Leshchiner I, Krier J, Kraft P, Rehm HL, Green RC, Kohane IS, MacRae CA; MedSeq Project. Kong SW, et al. Genet Med. 2015 Jul;17(7):536-44. doi: 10.1038/gim.2014.143. Epub 2014 Oct 23. Genet Med. 2015. PMID: 25341114 Free PMC article.

8

I148M variant in PNPLA3 reduces central adiposity and metabolic disease risks while increasing nonalcoholic fatty liver disease.

Park JH, Cho B, Kwon H, Prilutsky D, Yun JM, Choi HC, Hwang KB, Lee IH, Kim JI, Kong SW. Park JH, et al. Among authors: kong sw. Liver Int. 2015 Dec;35(12):2537-46. doi: 10.1111/liv.12909. Epub 2015 Jul 23. Liver Int. 2015. PMID: 26148225

9

Learning a Comorbidity-Driven Taxonomy of Pediatric Pulmonary Hypertension.

Ong MS, Mullen MP, Austin ED, Szolovits P, Natter MD, Geva A, Cai T, Kong SW, Mandl KD. Ong MS, et al. Among authors: kong sw. Circ Res. 2017 Aug 4;121(4):341-353. doi: 10.1161/CIRCRESAHA.117.310804. Epub 2017 Jun 13. Circ Res. 2017. PMID: 28611076 Free PMC article.

10

Comprehensive Analysis of Tissue-wide Gene Expression and Phenotype Data Reveals Tissues Affected in Rare Genetic Disorders.

Feiglin A, Allen BK, Kohane IS, Kong SW. Feiglin A, et al. Among authors: kong sw. Cell Syst. 2017 Aug 23;5(2):140-148.e2. doi: 10.1016/j.cels.2017.06.016. Epub 2017 Aug 16. Cell Syst. 2017. PMID: 28822752 Free PMC article.

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