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Fumihiko Matsuda

Researcher at Kyoto University

Publications -  454
Citations -  28863

Fumihiko Matsuda is an academic researcher from Kyoto University. The author has contributed to research in topics: Population & Genome-wide association study. The author has an hindex of 69, co-authored 414 publications receiving 24471 citations. Previous affiliations of Fumihiko Matsuda include Massachusetts Institute of Technology & Kanazawa University.

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The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl

TL;DR: The results show that the complex pathway underlying the pathogenesis may be partly shared by the two etiological forms of PTC, but their genetic components do not completely overlap each other, suggesting the presence of other unknown etiology-specific genetic determinants in radiation-related PTC.
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New loci and coding variants confer risk for age-related macular degeneration in East Asians

Ching-Yu Cheng, +103 more
TL;DR: The findings suggest that some of the genetic loci conferring AMD susceptibility in East Asians are shared with Europeans, yet AMD in East Asia may also have a distinct genetic signature.
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Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.

TL;DR: A large-scale genome-wide association study of 168,228 individuals of Japanese ancestry with genotype imputation with genotypes imputation detected eight new susceptibility loci and Japanese-specific rare variants contributing to disease severity and increased cardiovascular mortality, and a trans-ancestry meta-analysis found 35 additional new loci.
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Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis

Jing Cui, +72 more
- 28 Mar 2013 - 
TL;DR: A genome-wide association study of more than 2 million common variants in rheumatoid arthritis patients shows that an allele associated with response to etanercept therapy is also associated with CD84 gene expression, and further that CD84 expression correlates with disease activity.