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Initiatives & Research
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population
Chikashi Terao, Ryo Yamada, Koichiro Ohmura, et al.
Genome-wide association study identifies a susceptibility locus for HCV-induced hepatocellular carcinoma
Vinod Kumar, Naoya Kato, Yuji Urabe, et al.
Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility
Vinod Kumar, Keitaro Matsuo, Atsushi Takahashi, et al.
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids
Pei-Chieng Cha, Atsushi Takahashi, Naoya Hosono, et al.
Common variation in GPC5 is associated with acquired nephrotic syndrome
Koji Okamoto, Katsushi Tokunaga, Kent Doi, et al.
Association between single nucleotide polymorphisms within genes encoding sirtuin families and diabetic nephropathy in Japanese subjects with type 2 diabetes
Shiro Maeda, Daisuke Koya, Shin-Ichi Araki, et al.
Replication analysis of SNPs on 9p21.2 and 19p13.3 with amyotrophic lateral sclerosis in East Asians
Aritoshi Iida, Atsushi Takahashi, Min Deng, et al.
Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population
R. Cui, Y. Okada, S. G. Jang, et al.
Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population
Siew-Kee Low, Hitoshi Zembutsu, Atsushi Takahashi, et al.
Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus
Yukinori Okada, Atsushi Takahashi, Hiroko Ohmiya, et al.
Genome-wide association study identifies HLA-A*3101 allele as a genetic risk factor for carbamazepine-induced cutaneous adverse drug reactions in Japanese population
Takeshi Ozeki, Taisei Mushiroda, Amara Yowang, et al.
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population
Asako Aoki, Kouichi Ozaki, Hiroshi Sato, et al.
PADI4 polymorphism predisposes male smokers to rheumatoid arthritis
Yuta Kochi, Mohamed M. Thabet, Akari Suzuki, et al.
Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility
Suyoun Chung, Hidewaki Nakagawa, Motohide Uemura, et al.
Association study of TRAF1-C5 polymorphisms with susceptibility to rheumatoid arthritis and systemic lupus erythematosus in Japanese
K. Nishimoto, Y. Kochi, K. Ikari, et al.
HLA-DRB1*0901 lowers anti-cyclic citrullinated peptide antibody levels in Japanese patients with rheumatoid arthritis
Yukinori Okada, Akari Suzuki, Ryo Yamada, et al.
Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations
Daiki Miki, Michiaki Kubo, Atsushi Takahashi, et al.
Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese
Pei-Chieng Cha, Taisei Mushiroda, Atsushi Takahashi, et al.
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B
Toshimasa Yamauchi, Kazuo Hara, Shiro Maeda, et al.
A functional variant in NKX3.1 associated with prostate cancer susceptibility down-regulates NKX3.1 expression
Shusuke Akamatsu, Ryo Takata, Kyota Ashikawa, et al.
A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population
Mitsuko Nakashima, Suyoun Chung, Atsushi Takahashi, et al.
Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population
Ryo Takata, Shusuke Akamatsu, Michiaki Kubo, et al.
A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese
Satoko Uno, Hitoshi Zembutsu, Akira Hirasawa, et al.
Establishment of a standardized system to perform population structure analyses with limited sample size or with different sets of SNP genotypes
Natsuhiko Kumasaka, Yumi Yamaguchi-Kabata, Atsushi Takahashi, et al.
Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population
Hiroshi Koriyama, Hironori Nakagami, Tomohiro Katsuya, et al.
Genome-wide association study of pancreatic cancer in Japanese population
Siew-Kee Low, Aya Kuchiba, Hitoshi Zembutsu, et al.
Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population
Tomonaga Matsushita, Junji Umeno, Yoichiro Hirakawa, et al.
A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility
Yuta Kochi, Yukinori Okada, Akari Suzuki, et al.
A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci
Yukinori Okada, Yoichiro Kamatani, Atsushi Takahashi, et al.
Genome-wide association study of intracranial aneurysm identifies three new risk loci
Katsuhito Yasuno, Kaya Bilguvar, Philippe Bijlenga, et al.
Making a haplotype catalog with estimated frequencies based on SNP homozygotes
Yumi Yamaguchi-Kabata, Tatsuhiko Tsunoda, Atsushi Takahashi, et al.
Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count
The textile plot: a new linkage disequilibrium display of multiple-single nucleotide polymorphism genotype data
Natsuhiko Kumasaka, Yusuke Nakamura and Naoyuki Kamatani.
A single nucleotide polymorphism in KCNQ1 is associated with susceptibility to diabetic nephropathy in japanese subjects with type 2 diabetes
Toshihiko Ohshige, Yasushi Tanaka, Shin-ichi Araki, et al.
Genome-wide association study of hematological and biochemical traits in a Japanese population
Yoichiro Kamatani, Koichi Matsuda, Yukinori Okada, et al.
Functional SNP of ARHGEF10 confers risk of atherothrombotic stroke
Tomonaga Matsushita, Kyota Ashikawa, Koji Yonemoto, et al.
COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer
I. P. M. Tomlinson, M. Dunlop, H. Campbell, et al.
Effects of structural variations of APOBEC3A and APOBEC3B genes in chronic hepatitis B virus infection
Hiromi Abe, Hidenori Ochi, Toshiro Maekawa, et al.
Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression
Pei-Chieng Cha, Taisei Mushiroda, Hitoshi Zembutsu, et al.
Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation
Ching-Lung Cheung, Benjamin Y. Y. Chan, Vivian Chan, et al.
Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk
Ri Cui, Yoichiro Kamatani, Atsushi Takahashi, et al.
CYP2D6 genotyping for functional-gene dosage analysis by allele copy number detection
Naoya Hosono, Mamoru Kato, Kazuma Kiyotani, et al.
Estimation of the warfarin dose with clinical and pharmacogenetic data
T. E. Klein, R. B. Altman, N. Eriksson, et al.
A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians
Yoichiro Kamatani, Sukanya Wattanapokayakit, Hidenori Ochi, et al.
Association study of genetic polymorphism in ABCC4 with cyclophosphamide-induced adverse drug reactions in breast cancer patients
Siew-Kee Low, Kazuma Kiyotani, Taisei Mushiroda, et al.
Lack of association between variations of PDE4D and ischemic stroke in the Japanese population
Tomonaga Matsushita, Michiaki Kubo, Koji Yonemoto, et al.
Nucleotide variations in genes encoding carbonic anhydrase 8 and 10 associated with femoral bone mineral density in Japanese female with osteoporosis
Seijiro Mori, Ikuyo Kou, Hidenori Sato, et al.
Contribution of a haplotype in the HLA region to anti-cyclic citrullinated peptide antibody positivity in rheumatoid arthritis, independently of HLA-DRB1
Yukinori Okada, Ryo Yamada, Akari Suzuki, et al.
Replication study for the association of new meta-analysis-derived risk loci with susceptibility to type 2 diabetes in 6,244 Japanese individuals
S. Omori, Y. Tanaka, M. Horikoshi, et al.
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson’s disease
Wataru Satake, Yuko Nakabayashi, Ikuko Mizuta, et al.
