Author

Seiji Wada

National Center For Child Health and DevelopmentORCID 0000-0002-8654-6623Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioengineering· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Organism:rat· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Katsusuke OZAWAiD· 2 shared Asuka HoriiD· 1 shared Eiji KobayashiiD· 1 shared Fuyuki Hasegawa· 1 shared Haruhiko SagoiD· 1 shared Hiroko Ogata‐KawataiD· 1 shared K. OkamuraiD· 1 shared Kana Fukui· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersBioengineering

Katsusuke OZAWAORCID

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2 papers

Recent·Most cited

Fetal Kidney Transplantation for In Utero Fetuses

Keita Morimoto, Shuichiro Yamanaka, Kenji Matsui, Yoshitaka Kinoshita, Yuka Inage, Shutaro Yamamoto, Nagisa Koda, Naoto Matsumoto, Yatsumu Saito, Tsuyoshi Takamura, Toshinari Fujimoto, Shohei Fukunaga, Susumu Tajiri, Kei Matsumoto, Katsusuke OZAWA, , Takashi Yokoo

This paper describes a novel fetal therapy approach using transplanted fetal kidneys from different species to provide a bridge to dialysis in affected fetuses, demonstrating successful urine production and long-term function without immunosuppressants.

Communications Biology · Mar 3, 2025Peer-reviewedBioengineering

Re-evaluation of whole exome sequencing, including intronic region, in combination with genetic intolerance score for foetal structural anomalies, is helpful for diagnosis, especially in X-linked disorders

Kosuke Taniguchi, Fuyuki Hasegawa, Yuka Okazaki, Asuka Hori, Hiroko Ogata‐Kawata, Saki Aoto, Osuke Migita, Tomoko Kawai, Kazuhiko Nakabayashi, K. Okamura, Kana Fukui, Seiji Wada, Katsusuke OZAWA, Yushi Ito, Haruhiko Sago, Kenichiro Hata

This study improves diagnostic yield in fetal structural anomalies using whole exome sequencing by re-evaluating variants, including introns, with LOEUF scores, particularly for X-linked disorders.

medRxiv · Feb 5, 2023 · PreprintGenetic & Genomic Medicine