Lee IH - Search Results

1

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. Among authors: lee ih. PLoS One. 2012;7(12):e49475. doi: 10.1371/journal.pone.0049475. Epub 2012 Dec 5. PLoS One. 2012. PMID: 23227143 Free PMC article.

2

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: lee k. 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.

3

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: lee k, lee ih. 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.

4

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. Among authors: lee ih. 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.

5

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: lee ih. Liver Int. 2015 Dec;35(12):2537-46. doi: 10.1111/liv.12909. Epub 2015 Jul 23. Liver Int. 2015. PMID: 26148225

6

Measuring coverage and accuracy of whole-exome sequencing in clinical context.

Kong SW, Lee IH, Liu X, Hirschhorn JN, Mandl KD. Kong SW, et al. Among authors: lee ih. Genet Med. 2018 Dec;20(12):1617-1626. doi: 10.1038/gim.2018.51. Epub 2018 Apr 12. Genet Med. 2018. PMID: 29789557 Free PMC article.

7

Comparative analysis of whole-genome sequencing pipelines to minimize false negative findings.

Hwang KB, Lee IH, Li H, Won DG, Hernandez-Ferrer C, Negron JA, Kong SW. Hwang KB, et al. Among authors: lee ih. Sci Rep. 2019 Mar 1;9(1):3219. doi: 10.1038/s41598-019-39108-2. Sci Rep. 2019. PMID: 30824715 Free PMC article.

8

The Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry composition.

Lee IH, Negron JA, Hernandez-Ferrer C, Alvarez WJ, Mandl KD, Kong SW. Lee IH, et al. Hum Mutat. 2020 Feb;41(2):387-396. doi: 10.1002/humu.23942. Epub 2019 Nov 15. Hum Mutat. 2020. PMID: 31691385 Free PMC article.

9

Human autologous iPSC-derived dopaminergic progenitors restore motor function in Parkinson's disease models.

Song B, Cha Y, Ko S, Jeon J, Lee N, Seo H, Park KJ, Lee IH, Lopes C, Feitosa M, Luna MJ, Jung JH, Kim J, Hwang D, Cohen BM, Teicher MH, Leblanc P, Carter BS, Kordower JH, Bolshakov VY, Kong SW, Schweitzer JS, Kim KS. Song B, et al. Among authors: lee ih, lee n. J Clin Invest. 2020 Feb 3;130(2):904-920. doi: 10.1172/JCI130767. J Clin Invest. 2020. PMID: 31714896 Free PMC article.

10

A survey of genetic variants in SARS-CoV-2 interacting domains of ACE2, TMPRSS2 and TLR3/7/8 across populations.

Lee IH, Lee JW, Kong SW. Lee IH, et al. Among authors: lee jw. Infect Genet Evol. 2020 Nov;85:104507. doi: 10.1016/j.meegid.2020.104507. Epub 2020 Aug 26. Infect Genet Evol. 2020. PMID: 32858233 Free PMC article.

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