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[국외]
1. Kwon MJ, Roh KH, Park H, Woo HY. Comparison of the Anyplex II HPV28 assay with the Hybrid Capture 2 assay for the detection of HPV infection. J Clin Virol. 2014 Jan 30.
2. Shin SY, Kwon MJ, Park H, Woo HY. Comparison of Chronic Kidney Disease Prevalence Examined by the Chronic Kidney Disease Epidemiology Collaboration Equation With That by the Modification of Diet in Renal Disease Equation in Korean Adult Population. J Clin Lab Anal. 2014 Feb 27.
3. Shin SY, Kwon MJ, Song J, Park H, Woo HY. Measurement of serum total vitamin D (25-OH) using automated immunoassay in comparison with liquid chromatography tandem-mass spectrometry. J Clin Lab Anal. 2013 Jul;27(4):284-9.
4. Chang Y, Yun KE, Jung HS, Kim CW, Kwon MJ, Sung E, Ryu S. A1C and coronary artery calcification in nondiabetic men and women. Arterioscler Thromb Vasc Biol. 2013 Aug;33(8):2026-31.
5. Chang Y, Sung E, Yun KE, Jung HS, Kim CW, Kwon MJ, Cho SI, Ryu S. Weight change as a predictor of incidence and remission of insulin resistance. PLoS One. 2013 May 22;8(5):e63690.
6. Yun KE, Chang Y, Jung HS, Kim CW, Kwon MJ, Park SK, Sung E, Shin H, Park HS, Ryu S. Impact of body mass index on the risk of colorectal adenoma in a metabolically healthy population. Cancer Res. 2013 Jul 1;73(13):4020-7.
7. Kim CW, Yun KE, Jung HS, Chang Y, Choi ES, Kwon MJ, Lee EH, Woo EJ, Kim NH, Shin H, Ryu S. Sleep duration and quality in relation to non-alcoholic fatty liver disease in middle-aged workers and their spouses. J Hepatol. 2013 Aug;59(2):351-7.
8. Kim YJ, Kwon MJ, Woo HY, Paik SY. Prevalence of human papillomavirus infection and genotype distribution determined by the cyclic-catcher melting temperature analysis in Korean medical checkup population. J Microbiol. 2013 Oct;51(5):665-70.
9. Woo HY, Park H, Kwon MJ, Chang Y, Ryu S. Association of prostate specific antigen concentration with lifestyle characteristics in Korean men. Asian Pac J Cancer Prev. 2012;13(11):5695-9.
10. Huh JY, Kwon MJ, Seo KY, Kim MK, Chae KY, Kim SH, Ki CS, Yoon MS, Kim DH. Novel nonsense GNAS mutation in a 14-month-old boy with plate-like osteoma cutis and medulloblastoma. J Dermatol. 2014 Feb 11.
11. Oh SI, Park A, Kim HJ, Oh KW, Choi H, Kwon MJ, Ki CS, Kim HT, Kim SH. Spectrum of Cognitive Impairment in Korean ALS Patients without Known Genetic Mutations. PLoS One. 2014 Feb 3;9(2):e87163.
12. Kwon MJ, Yi C, Ki CS, Lee NY, Joo EJ, Yeom JS, Woo HY, Park H. Necrotizing pneumonia and empyema in an immunocompetent patient caused by Nocardia cyriacigeorgica and identified by 16S rRNA and secA1 sequencing. Ann Lab Med. 2014 Jan;34(1):71-5.
13. Huh HJ, Cho KH, Lee JE, Kwon MJ, Ki CS, Lee PH. Identification of ATM mutations in Korean siblings with ataxia-telangiectasia. Ann Lab Med. 2013 May;33(3):217-20.
14. Kwon MJ, Jeon GW, Lee SJ, Sin JB, Ki CS. Clinical and genetic analysis of a Korean patient with X-linked chondrodysplasia punctata: identification of a novel splicing mutation in the ARSE gene. Ann Clin Lab Sci. 2013 Winter;43(1):70-5.
15. Jang JH, Kwon MJ, Choi WJ, Oh KW, Koh SH, Ki CS, Kim SH. Analysis of the C9orf72 hexanucleotide repeat expansion in Korean patients with familial and sporadic amyotrophic lateral sclerosis. Neurobiol Aging. 2013 Apr;34(4):1311.e7-9.
16. Sohn YB, Ki CS, Park SW, Cho SY, Ko AR, Kwon MJ, Kim JY, Park HD, Kim OH, Jin DK. Clinical, biochemical, and genetic analysis of two korean patients with trichorhinophalangeal syndrome type I and growth hormone deficiency. Ann Clin Lab Sci. 2012 Summer;42(3):307-12.
17. Kim D, Cho SY, Yeau SH, Park SW, Sohn YB, Kwon MJ, Kim JY, Ki CS, Jin DK. Two novel insulin receptor gene mutations in a patient with rabson-mendenhall syndrome: the first korean case confirmed by biochemical, and molecular evidence. J Korean Med Sci. 2012 May;27(5):565-8.
18. Kwon MJ, Lee CG, Yu HJ, Nam SH, Lee J, Ki CS, Lee M. Clinical Features and Genetic Analysis of Children with Hyperekplexia in Korea. J Child Neurol. 2011 Apr 24.
19. Kwon MJ, Nam SH, Lee J, Lee CG, Yu HJ, Ki CS, Lee M. Clinical and genetic analysis of three korean children with pyridoxine-dependent epilepsy. Ann Clin Lab Sci. 2012 Winter;42(1):65-72.
20. Baek W, Koh SH, Kim YS, Kim HY, Kwon MJ, Ki CS, Kim SH. A novel exon 3 mutation (P66S) in the SOD1 gene in familial ALS. Can J Neurol Sci. 2012 Mar;39(2):245-6.
21. Kwon MJ, Baek W, Ki CS, Kim HY, Koh SH, Kim JW, Kim SH. Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS. Neurobiol Aging. 2012 May;33(5):1017.e17-23. Epub 2012 Jan 15.
22. Kwon MJ, Jang JH, Lee JE, Ki CS, Kim JW, Nam SJ, Yang JH. Spectra of BRCA1 and BRCA2 mutations in Korean patients with breast cancer: the importance of whole-gene sequencing. J Hum Genet. 2012 Mar;57(3):212-5.
23. Kwon MJ, Ki CS, Kim JY, Lee ST, Kim JW, Kang SY. Multiplex Ligation-Dependent Probe Amplification (MLPA) Assay for the Detection of Mitochondrial DNA Deletion in Chronic Progressive External Ophthalmoplegia (CPEO). Ann Clin Lab Sci. 2011 Fall;41(4):385-9.
24. Lee ST, Lee DH, Kim JY, Kwon MJ, Kim JW, Hong YH, Lee YW, Ki CS. Molecular screening of the TSH receptor (TSHR) and thyroid peroxidase (TPO) genes in Korean patients with nonsyndromic congenital hypothyroidism. Clin Endocrinol (Oxf). 2011 Nov;75(5):715-21.
25. Baek W, Koh SH, Park JS, Kim YS, Kim HY, Kwon MJ, Ki CS, Kim SH. A novel codon4 mutation (A4F) in the SOD1gene in familial amyotrophic lateral sclerosis. J Neurol Sci. 2011 Jul 15;306(1-2):157-9.
26. Yoon J, Kim SH, Ki CS, Kwon MJ, Lim MJ, Kwon SR, Joo K, Moon CG, Park W. Carrier woman of Duchenne muscular dystrophy mimicking inflammatory myositis. J Korean Med Sci. 2011 Apr;26(4):587-91.
27. Kwon MJ, On YK, Huh W, Ko JW, Kim DK, Kim JS, Lee SY. Low dose requirement for warfarin treatment in a patient with CYP2C9*3/*13 genotype. Clin Chim Acta. 2011 Nov 20;412(23-24):2343-5.
28. Kwon MJ, Lee GH, Lee MK, Kim JY, Yoo HS, Ki CS, Chang YS, Kim JW, Park WS. PHOX2B mutations in patients with Ondine-Hirschsprung disease and a review of the literature. Eur J Pediatr. 2011 Oct;170(10):1267-71.
29. Kwon MJ, Yoo KY, Lee KO, Kim SH, Kim HJ. Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea. Blood Coagul Fibrinolysis. 2011 Mar;22(2):102-5.
30. Kwon MJ, Lee ST, Kim JW, Sung DH, Ki CS. Clinical and genetic analysis of a Korean family with hereditary spastic paraplegia type 3. Ann Clin Lab Sci. 2010 Fall;40(4):375-9.
31. Kwon MJ, Lee ST, Kim BJ, Sung DH, Kim JW, Ki CS. Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in the Korean population. Ann Clin Lab Sci. 2010 Spring;40(2):156-62.
32. Kwon MJ, Kim HJ, Lee KO, Jung CW, Kim SH. Molecular genetic analysis of Korean patients with coagulation factor XII deficiency. Blood Coagul Fibrinolysis. 2010 Jun;21(4):308-12.
33. Kwon MJ, Kim HJ, Kim JW, Lee KH, Sohn KH, Cho HJ, On YK, Kim JS, Lee SY. Determination of plasma warfarin concentrations in Korean patients and its potential for clinical application. Korean J Lab Med. 2009 Dec;29(6):515-23.
34. Kwon MJ, Kim HJ, Bang SH, Kim SH. Severe factor XI deficiency in a Korean woman with a novel missense mutation (Val498Met) and duplication G mutation in exon 13 of the F11 gene. Blood Coagul Fibrinolysis. 2008 Oct;19(7):679-83.
35. Kwon MJ, Boo SH, Kim HJ, Cho YS, Chung WH, Hong SH. A novel splice site mutation in the EYA1 gene in a Korean family with branchio-oto (BO) syndrome. Acta Otolaryngol. 2009 Jun;129(6):688-93.
36. Kwon MJ, Yoo KY, Kim HJ, Kim SH. Identification of mutations in the F9 gene including exon deletion by multiplex ligation-dependent probe amplification in 33 unrelated Korean patients with haemophilia B. Haemophilia. 2008 Sep;14(5):1069-75.
37. Kwon MJ, Lee SY. [Evaluation of GLUCOCARD X-METER glucose monitoring system]. Korean J Lab Med. 2008 Feb;28(1):8-15.
38.Kim SR, Kwon MJ, Lee JH, Lee NY. Chronic meningitis caused by Erysipelothrix rhusiopathiae. J Med Microbiol. 2007 Oct;56(Pt 10):1405-6.

[국내]
1. 박사학위, Molecular Genetic Analysis in Korean Patients with Amyotrophic Lateral Sclerosis. 2011.08 성균관대학교
2. 석사학위, 한국인 제1형 근긴장성 이영양증 환자의 분자유전학적 특성. 2008.06 충북대학교
3. Lee G, Kwon MJ, Sung SI, Choi YB, Kim JK, Yoo HS, Kim ES, Ki CS, Chang YS, Park WS. AEC Syndrome Confirmed by Genetic Study in Neonate: A Case Report. Korean J Perinatol. 2011 Dec;22(4):367-371. Korean.
4. Yi C, Shin SY, Kim KH, Woo HY, Kwon MJ, Park HS. Evaluation of Changes in Appropriateness of Blood Transfusion in a Tertiary Care Hospital after Advertising the Transfusion Guideline Proposed in 2009. Lab Med Online. Vol. 3, No. 2: 97-103, April 2013.
5. Shin SY, Lim HJ, Yi C, Yu S, Kwon MJ, Park H, Kim YJ, Jung CL, Woo HY. Comparison of Two Automated Immunoassays for the Detection of Anti-Hepatitis A Virus Total Immunoglobulin and IgM. J Lab Med Qual Assur. 2011 Dec;33(2):103-109. Korean.
6. Shin SY, Kwon MJ, Woo HY, Park H, Kim YJ. Preliminary Evaluation of the URiSCAN SUPER and Usefulness of a New Urine Reagent Strip to Detect Ascorbic Acid. J Lab Med Qual Assur. 2011 Dec;33(2):63-69. Korean.
7. Kim SH, Ki CS, Kim S, Kwon MJ, Kim JW, Park SS, Kim JS, Lee YK, Kong SY, Ki SJ, Han SH, Seo EJ, CHo HC, Kim EJ, Kim PW. Annual Report on External Quality Assessment in Diagnostic Genetics in Korea (2009). J Lab Med Qual Assur. 2010 Jun;32(1):147-170. Korean.