Publications

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Obesity susceptible novel DNA methylation marker on regulatory region of inflammation gene: results from the Korea Epigenome Study (KES).

Koh IU, Choi NH, Lee K, Yu HY, Yun JH, Kong JH, Kim HJ, Lee S, Kim SC, Kim BJ, Moon S.

BMJ Open Diabetes Res Care. 2020 Aug;8(1):e001338. doi: 10.1136/bmjdrc-2020-001338.

Identification of type 2 diabetes loci in 433,540 East Asian individuals.

Spracklen CN, Horikoshi M, Kim YJ, Lin K, Bragg F, Moon S, Suzuki K, Tam CHT, Tabara Y, Kwak SH, Takeuchi F, Long J, Lim VJY, Chai JF, Chen CH, Nakatochi M, Yao J, Choi HS, Iyengar AK, Perrin HJ, Brotman SM, van de Bunt M, Gloyn AL, Below JE, Boehnke M, Bowden DW, Chambers JC, Mahajan A, McCarthy MI, Ng MCY, Petty LE, Zhang W, Morris AP, Adair LS, Akiyama M, Bian Z, Chan JCN, Chang LC, Chee ML, Chen YDI, Chen YT, Chen Z, Chuang LM, Du S, Gordon-Larsen P, Gross M, Guo X, Guo Y, Han S, Howard AG, Huang W, Hung YJ, Hwang MY, Hwu CM, Ichihara S, Isono M, Jang HM, Jiang G, Jonas JB, Kamatani Y, Katsuya T, Kawaguchi T, Khor CC, Kohara K, Lee MS, Lee NR, Li L, Liu J, Luk AO, Lv J, Okada Y, Pereira MA, Sabanayagam C, Shi J, Shin DM, So WY, Takahashi A, Tomlinson B, Tsai FJ, van Dam RM, Xiang YB, Yamamoto K, Yamauchi T, Yoon K, Yu C, Yuan JM, Zhang L, Zheng W, Igase M, Cho YS, Rotter JI, Wang YX, Sheu WHH, Yokota M, Wu JY, Cheng CY, Wong TY, Shu XO, Kato N, Park KS, Tai ES, Matsuda F, Koh WP, Ma RCW, Maeda S, Millwood IY, Lee J, Kadowaki T, Walters RG, Kim BJ, Mohlke KL, Sim X.

Nature. 2020 Jun;582(7811):240-245. doi: 10.1038/s41586-020-2263-3. Epub 2020 May 6.

Integrated Analysis of Tissue-Specific Promoter Methylation and Gene Expression Profile in Complex Diseases.

Lee K, Moon S, Park MJ, Koh IU, Choi NH, Yu HY, Kim YJ, Kong J, Kang HG, Kim SC, Kim BJ.

Int J Mol Sci. 2020 Jul 17;21(14):5056. doi: 10.3390/ijms21145056.

Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups.

Han S, Hwang MY, Yoon K, Kim YK, Kim YJ, Kim BJ, Moon S.

Genet Epidemiol. 2019 Sep;43(6):617-628. doi: 10.1002/gepi.22208. Epub 2019 May 13.

Programmable Nuclease-Based Integration into Novel Extragenic Genomic Safe Harbor Identified from Korean Population-Based CNV Analysis.

Lee ES, Moon S, Abu-Bonsrah KD, Kim YK, Hwang MY, Kim YJ, Kim S, Hwang NS, Kim HH, Kim BJ.

Mol Ther Oncolytics. 2019 Jul 23;14:253-265. doi: 10.1016/j.omto.2019.07.001. eCollection 2019 Sep 27.

The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits.

Moon S, Kim YJ, Han S, Hwang MY, Shin DM, Park MY, Lu Y, Yoon K, Jang HM, Kim YK, Park TJ, Song DS, Park JL, Lee JE, Kim BJ.

Sci Rep. 2019 Feb 4;9(1):1382. doi: 10.1038/s41598-018-37832-9.

Possible Role of Single Stranded DNA Binding Protein 3 on Skin Hydration by Regulating Epidermal DifferentiationPossible Role of Single Stranded DNA Binding Protein 3 on Skin Hydration by Regulating Epidermal Differentiation

Choi MR, Shin JM, Shin YA, Chang YH, Chang MY, Lim CA, Sohn KC, Seo YJ, Kim CD, Lee JH, Lee Y.

Ann Dermatol. 2018 Aug;30(4):432-440. doi: 10.5021/ad.2018.30.4.432. Epub 2018 Jun 28.

Multiple genotype-phenotype association study reveals intronic variant pair on SIDT2 associated with metabolic syndrome in a Korean population.

Moon S, Lee Y, Won S, Lee J.

Hum Genomics. 2018 Nov 1;12(1):48. doi: 10.1186/s40246-018-0180-4.

Interethnic analyses of blood pressure loci in populations of East Asian and European descent.

Takeuchi F, Akiyama M, Matoba N, Katsuya T, Nakatochi M, Tabara Y, Narita A, Saw WY, Moon S, Spracklen CN, Chai JF, Kim YJ, Zhang L, Wang C, Li H, Li H, Wu JY, Dorajoo R, Nierenberg JN, Wang YX, He J, Bennett DA, Takahashi A, Momozawa Y, Hirata M, Matsuda K, Rakugi H, Nakashima E, Isono M, Shirota M, Hozawa A, Ichihara S, Matsubara T, Yamamoto K, Kohara K, Igase M, Han S, Gordon-Larsen P, Huang W, Lee NR, Adair LS, Hwang MY, Lee J, Chee ML, Sabanayagam C, Zhao W, Liu J, Reilly DF, Sun L, Huo S, Edwards TL, Long J, Chang LC, Chen CH, Yuan JM, Koh WP, Friedlander Y, Kelly TN, Wei WB, Xu L, Cai H, Xiang YB, Lin K, Clarke R, Walters RG, Millwood IY, Li L, Chambers JC, Kooner JS, Elliott P, van der Harst P, International Genomics of Blood Pressure (iGEN-BP) Consortium; Chen Z, Sasaki M, Shu XO, Jonas JB, He J, Heng CK, Chen YT, Zheng W, Lin X, Teo YY, Tai ES, Cheng CY, Wong TY, Sim X, Mohlke KL, Yamamoto M, Kim BJ, Miki T, Nabika T, Yokota M, Kamatani Y, Kubo M, Kato N.

Nat Commun. 2018 Nov 28;9(1):5052. doi: 10.1038/s41467-018-07345-0.

Nonsynonymous Variants in PAX4 and GLP1R Are Associated With Type 2 Diabetes in an East Asian Population.

Kwak SH, Chae J, Lee S, Choi S, Koo BK, Yoon JW, Park JH, Cho B, Moon MK, Lim S, Cho YM, Moon S, Kim YJ, Han S, Hwang MY, Cho YS, Lee MS, Jang HC, Kang HM, Park T, Cho NH, Kim K, Kim JI, Park KS.

Diabetes. 2018 Sep;67(9):1892-1902. doi: 10.2337/db18-0361. Epub 2018 Jun 25.

Use of whole-exome sequencing to determine the genetic basis of signs of skin youthfulness in Korean women.

Chang YH, Shin YA, Kim JH, Kim HM, Lee DW, Chung HK, Kim SJ, Kim CD, Lee JH, Seo YJ, Im M, Lee Y.

J Eur Acad Dermatol Venereol. 2017 Mar;31(3):e138-e141. doi: 10.1111/jdv.13904. Epub 2016 Aug 30.

Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.

Wheeler E, Leong A, Liu CT, Hivert MF, Strawbridge RJ, Podmore C, Li M, Yao J, Sim X, Hong J, Chu AY, Zhang W, Wang X, Chen P, Maruthur NM, Porneala BC, Sharp SJ, Jia Y, Kabagambe EK, Chang LC, Chen WM, Elks CE, Evans DS, Fan Q, Giulianini F, Go MJ, Hottenga JJ, Hu Y, Jackson AU, Kanoni S, Kim YJ, Kleber ME, Ladenvall C, Lecoeur C, Lim SH, Lu Y, Mahajan A, Marzi C, Nalls MA, Navarro P, Nolte IM, Rose LM, Rybin DV, Sanna S, Shi Y, Stram DO, Takeuchi F, Tan SP, van der Most PJ, Vliet-Ostaptchouk JVV, Wong A, Yengo L, Zhao W, Goel A, Larrad MTM, Radke D, Salo P, Tanaka T, van Iperen EPA, Abecasis G, Afaq S, Alizadeh BZ, Bertoni AG, Bonnefond A, B?ttcher Y, Bottinger EP, Campbell H, Carlson OD, Chen CH, Cho YS, Garvey WT, Gieger C, Goodarzi MO, Grallert H, Hamsten A, Hartman CA, Herder C, Hsiung CA, Huang J, Igase M, Isono M, Katsuya T, Khor CC, Kiess W, Kohara K, Kovacs P, Lee J, Lee WJ, Lehne B, Li H, Liu J, Lobbens S, Luan J, Lyssenko V, Meitinger T, Miki T, Miljkovic I, Moon S, Mulas A, M?ller G, M?ller-Nurasyid M, Nagaraja R, Nauck M, Pankow JS, Polasek O, Prokopenko I, Ramos PS, Rasmussen-Torvik L, Rathmann W, Rich SS, Robertson NR, Roden M, Roussel R, Rudan I, Scott RA, Scott WR, Sennblad B, Siscovick DS, Strauch K, Sun L, Swertz M, Tajuddin SM, Taylor KD, Teo YY, Tham YC, T?njes A, Wareham NJ, Willemsen G, Wilsgaard T, Hingorani AD, EPIC-CVD Consortium; EPIC-InterAct Consortium; Lifelines Cohort Study; Egan J, Ferrucci L, Hovingh GK, Jula A, Kivimaki M, Kumari M, Njølstad I, Palmer CNA, R?os MS, Stumvoll M, Watkins H, Aung T, Bl?her M, Boehnke M, Boomsma DI, Bornstein SR, Chambers JC, Chasman DI, Chen YDI, Chen YT, Cheng CY, Cucca F, de Geus EJC, Deloukas P, Evans MK, Fornage M, Friedlander Y, Froguel P, Groop L, Gross MD, Harris TB, Hayward C, Heng CK, Ingelsson E, Kato N, Kim BJ, Koh WP, Kooner JS, K?rner A, Kuh D, Kuusisto J, Laakso M, Lin X, Liu Y, Loos RJF, Magnusson PKE, M?rz W, McCarthy MI, Oldehinkel AJ, Ong KK, Pedersen NL, Pereira MA, Peters A, Ridker PM, Sabanayagam C, Sale M, Saleheen D, Saltevo J, Schwarz PE, Sheu WHH, Snieder H, Spector TD, Tabara Y, Tuomilehto J, van Dam RM, Wilson JG, Wilson JF, Wolffenbuttel BHR, Wong TY, Wu JY, Yuan JM, Zonderman AB, Soranzo N, Guo X, Roberts DJ, Florez JC, Sladek R, Dupuis J, Morris AP, Tai ES, Selvin E, Rotter JI, Langenberg C, Barroso I, Meigs JB.

PLoS Med. 2017 Sep 12;14(9):e1002383. doi: 10.1371/journal.pmed.1002383. eCollection 2017 Sep.

Genome-based exome sequencing analysis identifies GYG1, DIS3L and DDRGK1 are associated with myocardial infarction in Koreans.

Lee JY, Moon S, Kim YK, Lee SH, Lee BS, Park MY, Park JE, Jang Y, Han BG.

J Genet. 2017 Dec;96(6):1041-1046. doi: 10.1007/s12041-017-0854-z.

On the association analysis of CNV data: a fast and robust family-based association method.

Liu M, Moon S, Wang L, Kim S, Kim YJ, Hwang MY, Kim YJ, Elston RC, Kim BJ, Won S.

BMC Bioinformatics. 2017 Apr 18;18(1):217. doi: 10.1186/s12859-017-1622-z.

Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.

Spracklen CN, Chen P, Kim YJ, Wang X, Cai H, Li S, Long J, Wu Y, Wang YX, Takeuchi F, Wu JY, Jung KJ, Hu C, Akiyama K, Zhang Y, Moon S, Johnson TA, Li H, Dorajoo R, He M, Cannon ME, Roman TS, Salfati E, Lin KH, Guo X, Sheu WHH, Absher D, Adair LS, Assimes TL, Aung T, Cai Q, Chang LC, Chen CH, Chien LH, Chuang LM, Chuang SC, Du S, Fan Q, Fann CSJ, Feranil AB, Friedlander Y, Gordon-Larsen P, Gu D, Gui L, Guo Z, Heng CK, Hixson J, Hou X, Hsiung CA, Hu Y, Hwang MY, Hwu CM, Isono M, Juang JMJ, Khor CC, Kim YK, Koh WP, Kubo M, Lee IT, Lee SJ, Lee WJ, Liang KW, Lim B, Lim SH, Liu J, Nabika T, Pan WH, Peng H, Quertermous T, Sabanayagam C, Sandow K, Shi J, Sun L, Tan PC, Tan SP, Taylor KD, Teo YY, Toh SA, Tsunoda T, van Dam RM, Wang A, Wang F, Wang J, Wei WB, Xiang YB, Yao J, Yuan JM, Zhang R, Zhao W, Chen YDI, Rich SS, Rotter JI, Wang TD, Wu T, Lin X, Han BG, Tanaka T, Cho YS, Katsuya T, Jia W, Jee SH, Chen YT, Kato N, Jonas JB, Cheng CY, Shu XO, He J, Zheng W, Wong TY, Huang W, Kim BJ, Tai ES, Mohlke KL, Sim X.

Hum Mol Genet. 2017 May 1;26(9):1770-1784. doi: 10.1093/hmg/ddx062.

Whole-exome sequencing study reveals common copy number variants in protocadherin genes associated with childhood obesity in Koreans.

Moon S, Hwang MY, Jang HB, Han S, Kim YJ, Hwang JY, Lee HJ, Park SI, Song J, Kim BJ.

Int J Obes (Lond). 2017 Apr;41(4):660-663. doi: 10.1038/ijo.2017.12. Epub 2017 Jan 19.

Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.

Li C, Kim YK, Dorajoo R, Li H, Lee IT, Cheng CY, He M, Sheu WHH, Guo X, Ganesh SK, He J, Lee J, Liu J, Hu Y, Rao DC, Tsai FJ, Koh JY, Hu H, Liang KW, Palmas W, Hixson JE, Han S, Teo YY, Wang Y, Chen J, Lu CH, Zheng Y, Gui L, Lee WJ, Yao J, Gu D, Han BG, Sim X, Sun L, Zhao J, Chen CH, Kumari N, He Y, Taylor KD, Raffel LJ, Moon S, Rotter JI, Chen YI, Wu T, Wong TY, Wu JY, Lin X, Tai ES, Kim BJ, Kelly TN.

Circ Cardiovasc Genet. 2017 Apr;10(2):e001527. doi: 10.1161/CIRCGENETICS.116.001527.

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.

Ehret GB, Ferreira T, Chasman DI, … Shin YA, Sim X, Smit JH, …Hamsten A, Wichmann HE, Palmer CNA, Stefansson K, Ridker PM, Loos RJF, Chakravarti A, Deloukas P, Morris AP, Newton-Cheh C, Munroe PB.

Nat Genet. 2016 Oct;48(10):1171-1184. doi: 10.1038/ng.3667. Epub 2016 Sep 12.

Identification of a Copy Number Variation on Chromosome 20q13.12 Associated with Osteoporotic Fractures in the Korean Population.

Park TJ, Hwang MY, Moon S, Hwang JY, Go MJ, Kim BJ.

Genomics Inform. 2016 Dec;14(4):216-221. doi: 10.5808/GI.2016.14.4.216. Epub 2016 Dec 31.

Evaluation of pleiotropic effects among common genetic loci identified for cardio-metabolic traits in a Korean population.

Kim YK, Hwang MY, Kim YJ, Moon S, Han S, Kim BJ.

Cardiovasc Diabetol. 2016 Feb 1;15:20. doi: 10.1186/s12933-016-0337-1.

Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference.

Wen W, Kato N, Hwang JY, Guo X, Tabara Y, Li H, Dorajoo R, Yang X, Tsai FJ, Li S, Wu Y, Wu T, Kim S, Guo X, Liang J, Shungin D, Adair LS, Akiyama K, Allison M, Cai Q, Chang LC, Chen CH, Chen YT, Cho YS, Choi BY, Gao Y, Go MJ, Gu D, Han BG, He M, Hixson JE, Hu Y, Huang T, Isono M, Jung KJ, Kang D, Kim YJ, Kita Y, Lee J, Lee NR, Lee J, Wang Y, Liu JJ, Long J, Moon S, Nakamura Y, Nakatochi M, Ohnaka K, Rao D, Shi J, Sull W, Tan A, Ueshima H, Wu C, Xiang YB, Yamamoto K, Yao J, Ye X, Yokota M, Zhang X, Zheng Y, Qi L, Rotter JI, Jee SH, Lin D, Mohlke KL, He J, Mo Z, Wu JY, Tai ES, Lin X, Miki T, Kim BJ, Takeuchi F, Zheng W, Shu XO.

Sci Rep. 2016 Jan 20;6:17958. doi: 10.1038/srep17958.

Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes.

Imamura M, Takahashi A, Yamauchi T, Hara K, Yasuda K, Grarup N, Zhao W, Wang X, Huerta-Chagoya A, Hu C, Moon S, Long J, Kwak SH, Rasheed A, Saxena R, Ma RCW, Okada Y, Iwata M, Hosoe J, Shojima N, Iwasaki M, Fujita H, Suzuki K, Danesh J, Jørgensen T, Jørgensen ME, Witte DR, Brandslund I, Christensen C, Hansen T, Mercader JM, Flannick J, Moreno-Mac?as H, Burtt NP, Zhang R, Kim YJ, Zheng W, Singh JR, Tam CHT, Hirose H, Maegawa H, Ito C, Kaku K, Watada H, Tanaka Y, Tobe K, Kawamori R, Kubo M, Cho YS, Chan JCN, Sanghera D, Frossard P, Park KS, Shu XO, Kim BJ, Florez JC, Tusi?-Luna T, Jia W, Tai ES, Pedersen O, Saleheen D, Maeda S, Kadowaki T.

Nat Commun. 2016 Jan 28;7:10531. doi: 10.1038/ncomms10531.

Genome-wide association study of serum lipids confirms previously reported associations as well as new associations of common SNPs within PCSK7 gene with triglyceride.

Kurano M, Tsukamoto K, Kamitsuji S, Kamatani N, Hara M, Ishikawa T, Kim BJ, Moon S, Kim YJ, Teramoto T.

J Hum Genet. 2016 May;61(5):427-33. doi: 10.1038/jhg.2015.170. Epub 2016 Jan 14.

Identification of a possible susceptibility locus for UVB-induced skin tanning phenotype in Korean females using genome wide association study.

Kwak TJ, Chang YH, Shin YA, Shin JM, Kim JH, Lim SK, Lee SH, Lee MG, Yoon TJ, Kim CD, Lee JH, Koh JS, Seo YK, Chang MY, Lee Y.

Exp Dermatol. 2015 Dec;24(12):942-6. doi: 10.1111/exd.12809. Epub 2015 Sep 15.

Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan.

Ilyas M, Kim JS, Cooper J, Shin YA, Kim HM, Cho YS, Hwang S, Kim H, Moon J, Chung O, Jun J, Rastogi A, Song S, Ko J, Manica A, Rahman Z, Husnain T, Bhak J.

BMC Genomics. 2015 Mar 12;16:172. doi: 10.1186/s12864-015-1290-1. PMID: 25887915

Practical Calling Approach for Exome Array-Based Genome-Wide Association Studies in Korean Population.

Park TJ, Heo L, Moon S, Kim YJ, Oh JH, Han S, Kim BJ.

Int J Genomics. 2015;2015:421715. doi: 10.1155/2015/421715. Epub 2015 Dec 27.

MicroRNA-650 in a copy number-variable region regulates the production of interleukin 6 in human osteosarcoma cells.

Yun JH, Moon S, Lee HS, Hwang MY, Kim YJ, Yu HY, Kim Y, Han BG, Kim BJ, Kim JM.

Oncol Lett. 2015 Oct;10(4):2603-2609. doi: 10.3892/ol.2015.3581. Epub 2015 Aug 7.

Influence of Genetic Variants in EGF and Other Genes on Hematological Traits in Korean Populations by a Genome-Wide Approach.

Kim YK, Oh JH, Kim YJ, Hwang MY, Moon S, Low SK, Takahashi A, Matsuda K, Kubo M, Lee J, Kim BJ.

Biomed Res Int. 2015;2015:914965. doi: 10.1155/2015/914965. Epub 2015 Apr 30.

A genome-wide association study of copy-number variation identifies putative loci associated with osteoarthritis in Koreans.

Moon S, Keam B, Hwang MY, Lee Y, Park S, Oh JH, Kim YJ, Lee HS, Kim NH, Kim YJ, Kim DH, Han BG, Kim BJ, Lee J.

BMC Musculoskelet Disord. 2015 Apr 4;16:76. doi: 10.1186/s12891-015-0531-4.

Combinatorial approach to estimate copy number genotype using whole-exome sequencing data.

Hwang MY, Moon S, Heo L, Kim YJ, Oh JH, Kim YJ, Kim YK, Lee J, Han BG, Kim BJ.

Genomics. 2015 Mar;105(3):145-9. doi: 10.1016/j.ygeno.2014.12.003. Epub 2014 Dec 20.

Variation block-based genomics method for crop plants.

Kim YH, Park HM, Hwang TY, Lee SK, Choi MS, Jho S, Hwang S, Kim HM, Lee D, Kim BC, Hong CP, Cho YS, Kim H, Jeong KH, Seo MJ, Yun HT, Kim SL, Kwon YU, Kim WH, Chun HK, Lim SJ, Shin YA, Choi IY, Kim YS, Yoon HS, Lee SH, Lee S.

BMC Genomics. 2014 Jun 15;15:477. doi: 10.1186/1471-2164-15-477.

Minke whale genome and aquatic adaptation in cetaceans.

Yim HS, Cho YS, Guang X, Kang SG, Jeong JY, Cha SS, Oh HM, Lee JH, Yang EC, Kwon KK, Kim YJ, Kim TW, Kim W, Jeon JH, Kim SJ, Choi DH, Jho S, Kim HM, Ko J, Kim H, Shin YA, Jung HJ, Zheng Y, Wang Z, Chen Y, Chen M, Jiang A, Li E, Zhang S, Hou H, Kim TH, Yu L, Liu S, Ahn K, Cooper J, Park SG, Hong CP, Jin W, Kim HS, Park C, Lee K, Chun S, Morin PA, O'Brien SJ, Lee H, Kimura J, Moon DY, Manica A, Edwards J, Kim BC, Kim S, Wang J, Bhak J, Lee HS, Lee JH.

Nature Genetics 2014 Jan;46(1):88-92. doi: 10.1038/ng.2835. PMID: 24270359

Genome-wide association study identifies candidate Loci associated with platelet count in koreans.

Oh JH, Kim YK, Moon S, Kim YJ, Kim BJ.

Genomics Inform. 2014 Dec;12(4):225-30. doi: 10.5808/GI.2014.12.4.225. Epub 2014 Dec 31.

On the analysis of a repeated measure design in genome-wide association analysis.

Lee Y, Park S, Moon S, Lee J, Elston RC, Lee W, Won S.

Int J Environ Res Public Health. 2014 Nov 28;11(12):12283-303. doi: 10.3390/ijerph111212283.

Genome-wide copy number variation study reveals KCNIP1 as a modulator of insulin secretion.

Lee HS, Moon S, Yun JH, Lee MH, Hwang MY, Kim YJ, Han BG, Kim JM, Kim BJ.

Genomics. 2014 Aug;104(2):113-20. doi: 10.1016/j.ygeno.2014.05.004. Epub 2014 Jun 2.

The tiger genome and comparative analysis with lion and snow leopard genomes.

Cho YS, Hu L, Hou H, Lee H, Xu J, Kwon S, Oh S, Kim HM, Jho S, Kim S, Shin YA, Kim BC, Kim H, Kim CU, Luo SJ, Johnson WE, Koepfli KP, Schmidt-Küntzel A, Turner JA, Marker L, Harper C, Miller SM, Jacobs W, Bertola LD, Kim TH, Lee S, Zhou Q, Jung HJ, Xu X, Gadhvi P, Xu P, Xiong Y, Luo Y, Pan S, Gou C, Chu X, Zhang J, Liu S, He J, Chen Y, Yang L, Yang Y, He J, Liu S, Wang J, Kim CH, Kwak H, Kim JS, Hwang S, Ko J, Kim CB, Kim S, Bayarlkhagva D, Paek WK, Kim SJ, O'Brien SJ, Wang J, Bhak J.

Nat Commun. 2013;4:2433. doi: 10.1038/ncomms3433.

A genome-wide association study in Koreans identifies susceptibility loci for allergic nickel dermatitis.

Kim DS, Kim DH, Lee HM, Jee HJ, Lee Y, Chang MY, Kwak TJ, Kim CH, Shin YA, Lee JH, Yoon TJ, Lee MG.

Int Arch Allergy Immunol. 2013;162(2):184-6. doi: 10.1159/000353235. Epub 2013 Jul 31.

A genome-wide association study of a coronary artery disease risk variant.

Lee JY, Lee BS, Shin DJ, Woo Park K, Shin YA, Joong Kim K, Heo L, Young Lee J, Kyoung Kim Y, Jin Kim Y, Bum Hong C, Lee SH, Yoon D, Jung Ku H, Oh IY, Kim BJ, Lee J, Park SJ, Kim J, Kawk HK, Lee JE, Park HK, Lee JE, Nam HY, Park HY, Shin C, Yokota M, Asano H, Nakatochi M, Matsubara T, Kitajima H, Yamamoto K, Kim HL, Han BG, Cho MC, Jang Y, Kim HS, Euy Park J, Lee JY.

J Hum Genet. 2013 Mar;58(3):120-6. doi: 10.1038/jhg.2012.124. Epub 2013 Jan 31. PMID: 23364394.

Characterization of functional variants in 33 blood pressure loci using 1000 genomes project data

Lim, Ji Eun Shin, Young-Ah Hong, Kyung-Won Jin, Hyun-Seok et al.

Genes & genomics 2013 ISSN : 1976-9571

KGVDB: a population-based genomic map of CNVs tagged by SNPs in Koreans.

Moon S, Jung KS, Kim YJ, Hwang MY, Han K, Lee JY, Park K, Kim BJ.

Bioinformatics. 2013 Jun 1;29(11):1481-3. doi: 10.1093/bioinformatics/btt173. Epub 2013 Apr 26.

Gene-based copy number variation study reveals a microdeletion at 12q24 that influences height in the Korean population.

Kim YK, Moon S, Hwang MY, Kim DJ, Oh JH, Kim YJ, Han BG, Lee JY, Kim BJ

Genomics. 2013 Feb;101(2):134-8. doi: 10.1016/j.ygeno.2012.11.002. Epub 2012 Nov 10.

Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture.

Hwang JY, Lee SH, Go MJ, Kim BJ, Kou I, Ikegawa S, Guo Y, Deng HW, Raychaudhuri S, Kim YJ, Oh JH, Kim Y, Moon S, Kim DJ, Koo H, Cha MJ, Lee MH, Yun JY, Yoo HS, Kang YA, Cho EH, Kim SW, Oh KW, Kang MI, Son HY, Kim SY, Kim GS, Han BG, Cho YS, Cho MC, Lee JY, Koh JM.

J Med Genet. 2013 Apr;50(4):212-9. doi: 10.1136/jmedgenet-2012-101156. Epub 2013 Jan 24.

Genotype instability during long-term subculture of lymphoblastoid cell lines.

Oh JH, Kim YJ, Moon S, Nam HY, Jeon JP, Lee JH, Lee JY, Cho YS.

J Hum Genet. 2013 Jan;58(1):16-20. doi: 10.1038/jhg.2012.123. Epub 2012 Nov 22.

KAREBrowser: SNP database of Korea Association REsource Project.

Hong CB, Kim YJ, Moon SH, Shin YA, Cho YS, Lee JY.

BMB Rep. 2012 Jan;45(1):47-50.

BioSMACK: a linux live CD for genome-wide association analyses.

Hong CB, Kim YJ, Moon S, Shin YA, Go MJ, Kim DJ, Lee JY, Cho YS.

BMB Rep. 2012 Jan;45(1):44-6.

Association between the ABO locus and hematological traits in Korean.

Hong KW, Moon S, Kim YJ, Kim YK, Kim DJ, Kim CS, Kim SS, Kim BJ.

BMC Genet. 2012 Sep 10;13:78. doi: 10.1186/1471-2156-13-78.

Genovar: a detection and visualization tool for genomic variants.

Jung KS, Moon S, Kim YJ, Kim BJ, Park K.

BMC Bioinformatics. 2012 May 8;13 Suppl 7(Suppl 7):S12. doi: 10.1186/1471-2105-13-S7-S12.

Clinical validation of colorectal cancer biomarkers identified from bioinformatics analysis of public expression data.

Jung YJ, Lee SH, Choi HS, Kim SN, Lee EY,Shin YA, Seo JH, Kim BJ, Jung YH, Kim WK, Chun HK, Lee WY, Kim JS.

Clin Cancer Res. 2011 Feb 15;17(4):700-9. doi: 10.1158/1078-0432.CCR-10-1300. Epub 2011 Feb 8.

Genome-wide Survey of Copy Number Variants Associated with Blood Pressure and Body Mass Index in a Korean Population.

Moon SH, Kim YJ, Kim YK, Kim DJ, Lee JY, Go MJ, Shin YA, Hong CB, Kim BJ

Genomics Inform. 2011 Dec;9(4):152-160

Data-driven approach to detect common copy-number variations and frequency profiles in a population-based Korean cohort.

Moon S, Kim YJ, Hong CB, Kim DJ, Lee JY, Kim BJ.

Eur J Hum Genet. 2011 Nov;19(11):1167-72. doi: 10.1038/ejhg.2011.103. Epub 2011 Jul 6.

Clinical validity of the lung cancer biomarkers identified by bioinformatics analysis of public expression data.

Kim BJ, Lee HJ, Choi HY, Shin YA, Nam SY, Seo GJ, Son DS, Jo JS, Kim JS, Lee JS, Kim JO, Kim KM, Lee SH.

Cancer Res. 2007 Aug 1;67(15):7431-8.

ECgene: an alternative splicing database update.

Lee YS, Lee YH, Kim BJ, Shin YA, Nam SY, Kim PR, Kim NS, Chung WH, Kim JS, Lee SH.

Nucleic Acids Res. 2007 Jan;35(Database issue):D99-103. Epub 2006 Nov 28.

FSDB: a frameshift signal database.

Moon S, Byun Y, Han K.

Comput Biol Chem. 2007 Aug;31(4):298-302. doi: 10.1016/j.compbiolchem.2007.05.004. Epub 2007 May 17.

A general computational model for predicting ribosomal frameshifts in genome sequences.

Byun Y, Moon S, Han K.

Comput Biol Med. 2007 Dec;37(12):1796-801. doi: 10.1016/j.compbiomed.2007.06.001. Epub 2007 Aug 2.

Prediction of Ribosomal -1 Frameshifts in the Escherichia coli K12 Genome.

Moon S, Byun Y, Han K.

Lect Notes Bioinformatics. 2006; 4115: 612-621. doi: https://doi.org/10.1007/11816102_65.

Prediction of Readthroughs Based on the Statistical Analysis of Nucleotides Around Stop Codons.

Moon S, Byun Y, Han K.

Lect Notes Comput Sci. 2006; 3991: 276-283. doi: https://doi.org/10.1007/11758501_40.

Web Service for Finding Ribosomal Frameshifts.

Byun Y, Moon S, Han K.

Lect Notes Comput Sci. 2006; 3991: 284-291. doi: https://doi.org/10.1007/11758501_41.

ECgene: genome annotation for alternative splicing.

Kim P, Kim N, Lee Y, Kim B, Shin YA, Lee S.

Nucleic Acids Res. 2005 Jan 1;33(Database issue):D75-9. PMID: 15608289

Prediction of Ribosomal Frameshift Signals of User-Defined Models.

Byun Y, Moon S, Han K.

Lect Notes Comput Sci. 2005; 3514: 948-955. doi: https://doi.org/10.1007/11428831_118.

Predicting genes expressed via -1 and +1 frameshifts.

Moon S, Byun Y, Kim HJ, Jeong S, Han K.

Nucleic Acids Res. 2004 Sep 15;32(16):4884-92. doi: 10.1093/nar/gkh829. Print 2004.

Computational Identification of -1 Frameshift Signals.

Moon S, Byun Y, Han K.

Lect Notes Comput Sci. 2004; 3036: 334-341. doi: https://doi.org/10.1007/978-3-540-24685-5_42.