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Annals of the Rheumatic Diseases|July 9, 2026
Phenotype-specific associations of mosaic chromosomal alterations in systemic sclerosisYuki Nishio, Yuki Ishikawa, Shunsuke Uchiyama, et al.
The New England Journal of Medicine|March 29, 2023
Helicobacter pylori, Homologous-Recombination Genes, and Gastric CancerYoshiaki Usui, Yukari Taniyama, Mikiko Endo, et al.
NPJ Genomic Medicine|December 6, 2025
Clinical characteristics of EYS-associated retinal dystrophy in 291 Japanese patientsYoshito Koyanagi, Yusuke Murakami, Taro Kominami, et al.
Biorxiv : the Preprint Server for Biology|June 9, 2023
Association of genetic variation inHao Yu, Anas M Khanshour, Aki Ushiki, et al.
Elife|January 26, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosisHao Yu, Anas M Khanshour, Aki Ushiki, et al.
American Journal of Human Genetics|August 4, 2016
Contribution of a Non-classical HLA Gene, HLA-DOA, to the Risk of Rheumatoid ArthritisYukinori Okada, Akari Suzuki, Katsunori Ikari, et al.
NPJ Genomic Medicine|October 5, 2022
Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosisMartin Kerick, Marialbert Acosta-Herrera, Carmen Pilar Simeón-Aznar, et al.
American Journal of Medical Genetics. Part A|February 24, 2021
Whole genome sequencing of 45 Japanese patients with intellectual disabilityChihiro Abe-Hatano, Aritoshi Iida, Shunichi Kosugi, et al.
Nature Communications|June 30, 2019
A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathyKonstantinos Nikopoulos, Katarina Cisarova, Mathieu Quinodoz, et al.
Communications Biology|May 20, 2024
A genome-wide association study identifies a locus associated with knee extension strength in older Japanese individualsShuji Ito, Hiroshi Takuwa, Saori Kakehi, et al.
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