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shiro Ikegawa
shiro Ikegawa
Unknown affiliation
Verified email at ims.u-tokyo.ac.jp
Title
Cited by
Cited by
Year
Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction
N Ishii, K Ozaki, H Sato, H Mizuno, S Saito, A Takahashi, Y Miyamoto, ...
Journal of human genetics 51 (12), 1087-1099, 2006
7132006
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases
M Kanai, M Akiyama, A Takahashi, N Matoba, Y Momozawa, M Ikeda, ...
Nature genetics 50 (3), 390-400, 2018
6742018
A functional polymorphism in the 5′ UTR of GDF5 is associated with susceptibility to osteoarthritis
Y Miyamoto, A Mabuchi, D Shi, T Kubo, Y Takatori, S Saito, M Fujioka, ...
Nature genetics 39 (4), 529-533, 2007
6112007
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
5352005
Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine
A Okawa, I Nakamura, S Goto, H Moriya, Y Nakamura, S Ikegawa
Nature genetics 19 (3), 271-273, 1998
4661998
The combination of SOX5, SOX6, and SOX9 (the SOX trio) provides signals sufficient for induction of permanent cartilage
T Ikeda, S Kamekura, A Mabuchi, I Kou, S Seki, T Takato, K Nakamura, ...
Arthritis & Rheumatism 50 (11), 3561-3573, 2004
4392004
Genome-wide association study identifies 112 new loci for body mass index in the Japanese population
M Akiyama, Y Okada, M Kanai, A Takahashi, Y Momozawa, M Ikeda, ...
Nature genetics 49 (10), 1458-1467, 2017
4342017
Signalling mediated by the endoplasmic reticulum stress transducer OASIS is involved in bone formation
T Murakami, A Saito, S Hino, S Kondo, S Kanemoto, K Chihara, H Sekiya, ...
Nature cell biology 11 (10), 1205-1211, 2009
3512009
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
K Ishigaki, M Akiyama, M Kanai, A Takahashi, E Kawakami, H Sugishita, ...
Nature genetics 52 (7), 669-679, 2020
3472020
A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility
Y Kochi, Y Okada, A Suzuki, K Ikari, C Terao, A Takahashi, K Yamazaki, ...
Nature genetics 42 (6), 515-519, 2010
3432010
The zinc transporter SLC39A13/ZIP13 is required for connective tissue development; its involvement in BMP/TGF-β signaling pathways
T Fukada, N Civic, T Furuichi, S Shimoda, K Mishima, H Higashiyama, ...
PloS one 3 (11), e3642, 2008
3262008
A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease
S Seki, Y Kawaguchi, K Chiba, Y Mikami, H Kizawa, T Oya, F Mio, M Mori, ...
Nature genetics 37 (6), 607-612, 2005
3262005
A single recurrent mutation in the 5′-UTR of IFITM5 causes osteogenesis imperfecta type V
TJ Cho, KE Lee, SK Lee, SJ Song, KJ Kim, D Jeon, G Lee, HN Kim, ...
The American Journal of Human Genetics 91 (2), 343-348, 2012
2872012
Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis
I Kou, Y Takahashi, TA Johnson, A Takahashi, L Guo, J Dai, X Qiu, ...
Nature genetics 45 (6), 676-679, 2013
2852013
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
CG Boer, K Hatzikotoulas, L Southam, L Stefánsdóttir, Y Zhang, ...
Cell 184 (18), 4784-4818. e17, 2021
2812021
A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis
Y Takahashi, I Kou, A Takahashi, TA Johnson, K Kono, N Kawakami, ...
Nature genetics 43 (12), 1237-1240, 2011
2792011
Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease
A Kinoshita, T Saito, H Tomita, Y Makita, K Yoshida, M Ghadami, ...
Nature genetics 26 (1), 19-20, 2000
2752000
Identification of DIO2 as a new susceptibility locus for symptomatic osteoarthritis
I Meulenbelt, JL Min, S Bos, N Riyazi, JJ Houwing-Duistermaat, ...
Human molecular genetics 17 (12), 1867-1875, 2008
2582008
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia
MJ Rock, J Prenen, VA Funari, TL Funari, B Merriman, SF Nelson, ...
Nature genetics 40 (8), 999-1003, 2008
2552008
PLAP-1/asporin, a novel negative regulator of periodontal ligament mineralization
S Yamada, M Tomoeda, Y Ozawa, S Yoneda, Y Terashima, K Ikezawa, ...
Journal of Biological Chemistry 282 (32), 23070-23080, 2007
2482007
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