Aritoshi Iida
机构: Medical Genome Center, NCNP, Tokyo
每年引用次数
引用次数
引用: 9,358
H-指数: 43
I10-指数 : 115
出版物: 187
High-resolution SNP map of ASPN, a susceptibility gene for osteoarthritis
Aritoshi Iida , Hideki Kizawa , Yusuke Nakamura , Shiro Ikegawa
Journal of Human Genetics 51 ( 2) 151 -154
14
2006
A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction.
Yusuke Ebana , Kouichi Ozaki , Katsumi Inoue , Hiroshi Sato
Journal of Human Genetics 52 ( 3) 220 -229
22
2007
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population
Yoichiro Kamatani , Koichi Matsuda , Tetsuya Ohishi , Shigeru Ohtsubo
Journal of Human Genetics 53 ( 1) 64 -73
24
2008
A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population
Tetsuya Oishi , Aritoshi Iida , Shigeru Otsubo , Yoichiro Kamatani
Journal of Human Genetics 53 ( 2) 151 -162
21
2008
FOXC2 Mutations in Familial and Sporadic Spinal Extradural Arachnoid Cyst
Yoji Ogura , Shoji Yabuki , Aritoshi Iida , Ikuyo Kou
PLoS ONE 8 ( 11) e80548
15
2013
Association of single-nucleotide polymorphisms in MTMR9 gene with obesity
Takahiro Yanagiya , Atsushi Tanabe , Aritoshi Iida , Susumu Saito
Human Molecular Genetics 16 ( 24) 3017 -3026
47
2007
A functional single nucleotide polymorphism in the core promoter region of CALM1 is associated with hip osteoarthritis in Japanese
Hideyuki Mototani , Akihiko Mabuchi , Susumu Saito , Mikihiro Fujioka
Human Molecular Genetics 14 ( 8) 1009 -1017
110
2005
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease
Keiko Yamazaki , Dermot McGovern , Jiannis Ragoussis , Marta Paolucci
Human Molecular Genetics 14 ( 22) 3499 -3506
421
2005
Mutations in B3GALT6, which Encodes a Glycosaminoglycan Linker Region Enzyme, Cause a Spectrum of Skeletal and Connective Tissue Disorders
Masahiro Nakajima , Shuji Mizumoto , Noriko Miyake , Ryo Kogawa
American Journal of Human Genetics 92 ( 6) 927 -934
73
2013
Compound Heterozygosity for Null Mutations and a Common Hypomorphic Risk Haplotype in TBX6 Causes Congenital Scoliosis.
Kazuki Takeda , Ikuyo Kou , Noriaki Kawakami , Aritoshi Iida
Human Mutation 38 ( 3) 317 -323
28
2017
Clinical and Radiographic Features of the Autosomal Recessive form of Brachyolmia Caused by PAPSS2 Mutations
Aritoshi Iida , Pelin Özlem Simsek-Kiper , Shuji Mizumoto , Touma Hoshino
Human Mutation 34 ( 10) 1381 -1386
19
2013
Identification and In Vivo Functional Characterization of Novel Compound Heterozygous BMP1 Variants in Osteogenesis Imperfecta
Sung Yoon Cho , P.V. Asharani , Ok-Hwa Kim , Aritoshi Iida
Human Mutation 36 ( 2) 191 -195
20
2015
Association between Single-Nucleotide Polymorphisms in Selectin Genes and Immunoglobulin A Nephropathy
Takashi Takei , Aritoshi Iida , Kosaku Nitta , Toshihiro Tanaka
The American Journal of Human Genetics 70 ( 3) 781 -786
67
2002
A case of functional growth hormone deficiency and early growth retardation in a child with IFT172 mutations.
Angela K. Lucas-Herald , Esther Kinning , Aritoshi Iida , Zheng Wang
The Journal of Clinical Endocrinology and Metabolism 100 ( 4) 1221 -1224
20
2015
CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations.
Masashi Ogasawara , Aritoshi Iida , Theerawat Kumutpongpanich , Ayami Ozaki
Acta neuropathologica communications 8 ( 1) 1 -8
5
2020
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 between uncommon SNPs within haplotype blocks and the haplotypes constructed with haplotype-tagging SNPs
Naoyuki Kamatani , Akihiro Sekine , Takuya Kitamoto , Aritoshi Iida
American Journal of Human Genetics 75 ( 2) 190 -203
82
2004
Cover Image, Volume 38, Issue 3
Kazuki Takeda , Ikuyo Kou , Noriaki Kawakami , Aritoshi Iida
Human Mutation 38 ( 3) i -i
2017
A recurrent homozygous ACTN2 variant associated with core myopathy
Michio Inoue , Satoru Noguchi , Kyuto Sonehara , Keiko Nakamura-Shindo
Acta neuropathologica 142 ( 4) 785 -788
10
2021
Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c. 620A> T, in patients with GNE myopathy
Wakako Yoshioka , Aritoshi Iida , Kyuto Sonehara , Kazuki Yamamoto
Scientific Reports 12 ( 1) 21806 -21806
3
2022
Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction
Kouichi Ozaki , Yozo Ohnishi , Aritoshi Iida , Akihiko Sekine
Nature genetics 32 ( 4) 650 -654
1,257
2002