Author

Nobuo Fuse

Tohoku UniversityORCID 0000-0003-0237-4746Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 5 Approach:statistical model· 5 Assay:whole-genome sequencing· 3 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:imputation· 1

Frequent Co-Authors

Kengo KinoshitaiD· 4 shared Fumiki KatsuokaiD· 3 shared Jun YasudaiD· 3 shared Masayuki P. YamamotoiD· 3 shared Shu TadakaiD· 3 shared Akihito OtsukiiD· 2 shared Atsushi HozawaiD· 2 shared Atsushi ShimizuiD· 2 shared

Activity by Year

2019-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersGenomics

Kengo KinoshitaORCID

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5 papers

Recent·Most cited

Japonica Array NEO with increased genome-wide coverage and abundant disease risk SNPs

Mika Sakurai‐Yageta, Kazuki Kumada, Chinatsu Gocho, Satoshi Makino, Akira Uruno, Shu Tadaka, Ikuko N. Motoike, Masae Kimura, Shin Ito, Akihito Otsuki, Akira Narita, Hisaaki Kudo, Yuichi Aoki, Inaho Danjoh, Jun Yasuda, , Kengo Kinoshita

The paper introduces Japonica Array NEO, a SNP array for the Japanese population with enhanced coverage and disease risk SNPs, showing high imputation quality and utility in genotyping cohorts.

The Journal of Biochemistry · May 12, 2021Peer-reviewedGenomics

Novel candidates of pathogenic variants of the BRCA1 and BRCA2 genes in a 3,552 Japanese whole-genome sequence dataset (3.5KJPNv2)

Hideki Tokunaga, Keita Iida, Atsushi Hozawa, Soichi Ogishima, Yoh Watanabe, Shogo Shigeta, Muneaki Shimada, Yumi Yamaguchi‐Kabata, Shu Tadaka, Fumiki Katsuoka, Shin Ito, Kazuki Kumada, Yohei Hamanaka, Nobuo Fuse, Kengo Kinoshita, , Jun Yasuda

The paper identifies seven new potentially pathogenic BRCA1/BRCA2 variants in a Japanese population using computational scores and cohort analysis.

PLoS ONE · Jan 11, 2021Peer-reviewedGenetics

Genome-wide association meta-analysis identifies novel GP2 gene risk variants for pancreatic cancer in the Japanese population

Yingsong Lin, Masahiro Nakatochi, Yasuyuki Hosono, Hidemi M. Ito, Yoichiro Kamatani, Akihito Inoko, Hiromi Sakamoto, Fumie Kinoshita, Yumiko Kobayashi, Hiroshi Ishii, Masato Ozaka, Takashi Sasaki, Masato Matsuyama, Naoki Sasahira, Manabu Morimoto, , Keitaro Matsuo

Nature Communications · Jun 24, 2020Peer-reviewedGenetics

A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy

Konstantinos Nikopoulos, Katarina Vizar Cisarova, Mathieu Quinodoz, Hanna Koskiniemi-Kuendig, Noriko Miyake, Pietro Farinelli, Atta Ur Rehman, Muhammad Imran Khan, Andrea Prunotto, Masato Akiyama, Yoichiro Kamatani, Chikashi C. Terao, Fuyuki Miya, Yasuhiro Ikeda, Shinji Ueno, , Carlo Rivolta

The paper identifies a common variant in the Japanese population that shows quasi-Mendelian inheritance patterns in rare retinal ciliopathy.

Nature Communications · Jun 28, 2019Peer-reviewedGenomics

3.5KJPNv2, An allele frequency panel of 3,552 Japanese Individuals

Shu Tadaka, Fumiki Katsuoka, Masao Ueki, Kaname Kojima, Satoshi Makino, Sakae Saito, Akihito Otsuki, Chinatsu Gocho, Mika Sakurai‐Yageta, Inaho Danjoh, Ikuko N. Motoike, Yumi Yamaguchi‐Kabata, Matsuyuki Shirota, S. Koshiba, Masao Nagasaki, , Kengo Kinoshita

The paper constructs a population-level allele frequency panel of 3,552 Japanese individuals using a standardized pipeline and makes it publicly available.

bioRxiv · Jan 25, 2019 · PreprintGenomics