Gervais O, Ueno K, Kawai Y, Hitomi Y, Misawa K, Teraguchi S, Wang Y-Y, Tokunaga K, and Nagasaki M. Genomic heritabilities and correlations of 17 traits related to obesity and associated conditions in the Japanese population. G3 2020 Apr, Epub ahead of print.
Wichukchinda N, Pakdee J, Kunhapan P, Imunchot W, Toyo-Oka L, Tokunaga K, and Mahasirimongkol S. Haplotype-specific PCR for NAT2 Diplotyping. Hum Genome Var. 7: e13, 2020.
Tantivitayakul P, Ruangchai W, Juthayothin T, Smittipat N, Disratthakit A, Mahasirimongkol S, Viratyosin W, Tokunaga K, and Palittapongarnpim P. Homoplastic Single Nucleotide Polymorphisms Contributed to Phenotypic Diversity in Mycobacterium Tuberculosis. Sci. Rep. 10(1): e8024, 2020.
Shimada M, Miyagawa T, Kodama T, Toyoda H, Tokunaga K, and Honda M. Metabolome analysis using cerebrospinal fluid from narcolepsy type 1 patients. Sleep 2020 May, Epub ahead of print.
Yoshihara H, Sugiura-Ogasawara M, Ozawa F, Kitaori T, Ozaki Y, Aoki K, Shibata Y, Ugawa S, Nishiyama T, Omae Y, and Tokunaga K. Polo-like kinase 4 and Stromal antigen 3 are not associated with recurrent pregnancy loss caused by embryonic aneuploidy. Hum. Genome Var. 7: e18. 2020
Kakuta Y, Ichikawa R, Fuyuno Y, Hirano A, Umeno J, Torisu T, Watanabe K, Asakura A, Nakano T, Izumiyama Y, Okamoto D, Naito T, Moroi R, Kuroha M, Kanazawa Y, Kimura T, Shiga H, Naito T, Esaki M, Kawai Y, Tokunaga K, Nakamura M, Matsumoto T, Nagasaki M, Kinouchi Y, Unno M, and Masamune A. An Integrated Genomic and Transcriptomic Analysis Reveals Candidates of Susceptibility Genes for Crohn’s Disease in Japanese Populations. Sci. Rep. 10(1): e10236, 2020.
Shimada M, Miyagawa T, Kodama T, Toyoda H, Tokunaga K, and Honda M. Metabolome analysis using cerebrospinal fluid from narcolepsy type 1 patients. Sleep 2020 May, Epub ahead of print.
Jia X, Yamamura T, Gbadegesin R, McNulty M, Song K, Nagano C, Hitomi Y, Lee D, Aiba Y, Khor S-S, Ueno K, Kawai Y, Nagasaki M, Noiri E, Horinouchi T, Kaito H, Hamada R, Okamoto T, Kamei K, Kaku Y, Fujimaru R, Tanaka R, Shima Y, RCGCINSJ, Baek J, Kang HG, Ha IS, Han KH, Yang EM, KCHRDC, Abeyagunawardena A, Lane B, Chryst-Stangl M, Esezobor C, Solarin A, MPNC, Dossier C, Deschenes G, NEPHROVIR, Vivarelli M, Debiec H, Ishikura K, Matsuo M, Nozu K, Ronco P, Cheong HI, Sampson MG, Tokunaga K, and Iijima K. Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome. Kidney Int. 2020 June, Epub ahead of print.
Huang YH, Liao SF, Khor SS, Lin YJ, Chen HY, Chang YH, Huang YH, Lu SN, Lee HW, Ko WY, Huang C, Liu PC, Chen YJ, Wu PF, Chu HW, Wu PE, Tokunaga K, Shen CY, Lee MH. Large-scale Genome-Wide Association Study Identifies HLA Class II Variants Associated With Chronic HBV Infection: A Study From Taiwan Biobank. Aliment Pharmacol. Ther. 2020 June, Epub ahead of print.
Yoshida K, Yokota K, Kutswada Y, Nakayama K, Watanabe K, Matsumoto A, Miyashita H, Khor S-S, Tokunaga K, and Nagasaki M. Genome-wide association study of lean non-alcoholic fatty liver disease suggests HLA as a novel candidate locus. Hepatoogy Communications (in press)