Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis A Suzuki, R Yamada, X Chang, S Tokuhiro, T Sawada, M Suzuki, ... Nature genetics 34 (4), 395-402, 2003 | 1441 | 2003 |
Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction K Ozaki, Y Ohnishi, A Iida, A Sekine, R Yamada, T Tsunoda, H Sato, ... Nature genetics 32 (4), 650-654, 2002 | 1299 | 2002 |
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease K Yamazaki, D McGovern, J Ragoussis, M Paolucci, H Butler, D Jewell, ... Human molecular genetics 14 (22), 3499-3506, 2005 | 605 | 2005 |
An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis H Kizawa, I Kou, A Iida, A Sudo, Y Miyamoto, A Fukuda, A Mabuchi, ... Nature genetics 37 (2), 138-144, 2005 | 547 | 2005 |
Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-α secretion in vitro K Ozaki, K Inoue, H Sato, A Iida, Y Ohnishi, A Sekine, H Sato, K Odashiro, ... Nature 429 (6987), 72-75, 2004 | 311 | 2004 |
Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease K Yamazaki, M Takazoe, T Tanaka, T Ichimori, S Saito, A Iida, Y Onouchi, ... Journal of human genetics 49 (12), 664-668, 2004 | 160 | 2004 |
Catalog of 605 single-nucleotide polymorphisms (snps) among 13 genes encoding human atp-binding cassette transporters: abca4, abca7, abca8, abcd1, abcd3, abcd4, abce1, abcf1 … A Iida, S Saito, A Sekine, C Mishima, Y Kitamura, K Kondo, S Harigae, ... Journal of human genetics 47 (6), 285-310, 2002 | 159 | 2002 |
A functional single nucleotide polymorphism in the core promoter region of CALM1 is associated with hip osteoarthritis in Japanese H Mototani, A Mabuchi, S Saito, M Fujioka, A Iida, Y Takatori, A Kotani, ... Human molecular genetics 14 (8), 1009-1017, 2005 | 155 | 2005 |
Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR) S Saito, A Iida, A Sekine, Y Miura, C Ogawa, S Kawauchi, S Higuchi, ... Journal of human genetics 47 (4), 147-171, 2002 | 147 | 2002 |
A functional SNP in BNC2 is associated with adolescent idiopathic scoliosis Y Ogura, I Kou, S Miura, A Takahashi, L Xu, K Takeda, Y Takahashi, ... The American Journal of Human Genetics 97 (2), 337-342, 2015 | 144 | 2015 |
Mutations in B3GALT6, which encodes a glycosaminoglycan linker region enzyme, cause a spectrum of skeletal and connective tissue disorders M Nakajima, S Mizumoto, N Miyake, R Kogawa, A Iida, H Ito, H Kitoh, ... The American Journal of Human Genetics 92 (6), 927-934, 2013 | 144 | 2013 |
A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population K Ozaki, H Sato, A Iida, H Mizuno, T Nakamura, Y Miyamoto, A Takahashi, ... Nature genetics 38 (8), 921-925, 2006 | 131 | 2006 |
Expansion of GGC repeat in GIPC1 is associated with oculopharyngodistal myopathy J Deng, J Yu, P Li, X Luan, L Cao, J Zhao, M Yu, W Zhang, H Lv, Z Xie, ... The American Journal of Human Genetics 106 (6), 793-804, 2020 | 129 | 2020 |
Citrullination of RGG motifs in FET proteins by PAD4 regulates protein aggregation and ALS susceptibility C Tanikawa, K Ueda, A Suzuki, A Iida, R Nakamura, N Atsuta, G Tohnai, ... Cell reports 22 (6), 1473-1483, 2018 | 126* | 2018 |
Molecular Strategy for Detecting Metastatic Cancers with Use of Multiple Tumor-specific MAGE-A Genes I Miyashiro, C Kuo, K Huynh, A Iida, D Morton, A Bilchik, A Giuliano, ... Clinical Chemistry 47 (3), 505-512, 2001 | 126 | 2001 |
Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association … N Kamatani, A Sekine, T Kitamoto, A Iida, S Saito, A Kogame, E Inoue, ... The American Journal of Human Genetics 75 (2), 190-203, 2004 | 110 | 2004 |
Single nucleotide polymorphisms in the gene encoding Krüppel-like factor 7 are associated with type 2 diabetes A Kanazawa, Y Kawamura, A Sekine, A Iida, T Tsunoda, A Kashiwagi, ... Diabetologia 48, 1315-1322, 2005 | 108 | 2005 |
Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes A Iida, A Sekine, S Saito, Y Kitamura, T Kitamoto, S Osawa, C Mishima, ... Journal of human genetics 46 (4), 225-240, 2001 | 105 | 2001 |
Three hundred twenty-six genetic variations in genes encoding nine members of ATP-binding cassette, subfamily B (ABCB/MDR/TAP), in the Japanese population S Saito, A Iida, A Sekine, Y Miura, C Ogawa, S Kawauchi, S Higuchi, ... Journal of human genetics 47 (1), 38-50, 2002 | 104 | 2002 |
CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations M Ogasawara, A Iida, T Kumutpongpanich, A Ozaki, Y Oya, H Konishi, ... Acta Neuropathologica Communications 8, 1-8, 2020 | 100 | 2020 |