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
Genome-wide association study to identify genes related to myocardial infarction
Ozaki Kouichi , Ohnishi Yozo , Iida Aritoshi , Yamada Ryo
Circulation journal: official journal of the Japanese Circulation Society 66 315 -315
2002
Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients
Obara Wataru , Iida Aritoshi , Yasushi Suzuki , Toshihiro Tanaka
Journal of Human Genetics 48 ( 6) 293 -299
72
2003
Three Aberrant Splicing Variants of the HMGIC Gene Transcribed in Uterine Leiomyomas
Kurose Keisuke , Mine Nobuya , Iida Aritoshi , Nagai Hisaki
日本医科大学老人病研究所紀要 8 77 -82
2002
Mapping of a New Target Region of Allelic Loss to a 2-cM Interval at 22q 13.1 in Primary Breast Cancer
Iida Aritoshi , Kurose Keisuke , Isobe Rie , Akiyama Futoshi
日本医科大学老人病研究所紀要 4 95 -99
1998
[SNP collection, pharmacogenomics, and the future of drug therapy].
Akihiro Sekine , Aritoshi Iida , Yusuke Nakamura , Susumu Saito
Gan to kagaku ryoho. Cancer & chemotherapy 29 ( 9) 1665
2002
Whole genome sequencing of 45 Japanese patients with intellectual disability
Jun Natsume , Yukihide Momozawa , Yasuo Hachiya , Shunichi Kosugi
American Journal of Medical Genetics Part A 185 ( 5) 1468 -1480
2021
Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling.
Chisa Shukunami , Kalpana Gowrishankar , Katta M. Girisha , Shiro Ikegawa
Nature Communications 12 ( 1) 2046 -2046
2021
Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes.
Theerawat Kumutpongpanich , Masashi Ogasawara , Ayami Ozaki , Hiroyuki Ishiura
JAMA Neurology
2021
Correlation of Allelic Losses and Clinicopathological Factors in Primary Breast Cancers.
Mitsuru Emi , Satoshi Matsumoto , Aritoshi Iida , Kazuhiro Tsukamoto
Breast Cancer 4 ( 4) 243 -246
36
1997
Japanese Efforts in Pharmacogenomics
Aritoshi Iida , Yusuke Nakamura
Current Pharmacogenomics 1 ( 3) 203 -215
3
2003
Optineurin mutations in Japanese amyotrophic lateral sclerosis
Aritoshi Iida , Naoya Hosono , Motoki Sano , Tetsumasa Kamei
Journal of Neurology, Neurosurgery, and Psychiatry 83 ( 2) 233 -235
40
2012
Large-scale screening of TARDBP mutation in amyotrophic lateral sclerosis in Japanese.
Aritoshi Iida , Tetsumasa Kamei , Motoki Sano , Shuichi Oshima
Neurobiology of Aging 33 ( 4) 786 -790
38
2012
Replication analysis of SNPs on 9p21.2 and 19p13.3 with amyotrophic lateral sclerosis in East Asians.
Aritoshi Iida , Atsushi Takahashi , Min Deng , Yun Zhang
Neurobiology of Aging 32 ( 4) 7 -7
32
2011
Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese
Aritoshi Iida , Naoya Hosono , Motoki Sano , Tetsumasa Kamei
Neurobiology of Aging 33 ( 8) 1843.e19 -1843.e24
37
2012
Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-α secretion in vitro
Kouichi Ozaki , Katsumi Inoue , Hiroshi Sato , Aritoshi Iida
Nature 429 ( 6987) 72 -75
219
2004
Functional single-nucleotide polymorphisms in the secretogranin III (SCG3) gene that form secretory granules with appetite-related neuropeptides are associated with obesity.
Takahiro Nakamura , Tatsuhiko Tsunoda , Seika Kamohara , Yoshio Nakata
The Journal of Clinical Endocrinology and Metabolism 92 ( 3) 1145 -1154
30
2007
Novel DDR2 mutation identified by whole exome sequencing in a Moroccan patient with spondylo‐meta‐epiphyseal dysplasia, short limb‐abnormal calcification type
Maria Mansouri , Hülya Kayserili , Siham Chafai Elalaoui , Gen Nishimura
American Journal of Medical Genetics Part A 170 ( 2) 460 -465
4
2016
Molecular Strategy for Detecting Metastatic Cancers with Use of Multiple Tumor-specific MAGE-A Genes
Isao Miyashiro , Christine Kuo , Kelly Huynh , Aritoshi Iida
Clinical Chemistry 47 ( 3) 505 -512
85
2001
Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathy.
Atsuko Nishikawa , Aritoshi Iida , Shinichiro Hayashi , Mariko Okubo
Molecular Genetics & Genomic Medicine 7 ( 5)
1
2019
Ectopic Expression of Ptf1a Induces Spinal Defects, Urogenital Defects, and Anorectal Malformations in Danforth's Short Tail Mice
Kei Semba , Kimi Araki , Ken-ichirou Matsumoto , Hiroko Suda
PLoS Genetics 9 ( 2) e1003204
16
2013