Kosuke Taniguchi

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 12

Top Venues

Human genome variation

Molecular genetics & genomic medicine

Journal of medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Layla Masuda, Akihiro Hasegawa, Hiromi Kamura, Fuyuki Hasegawa, Michihiro Yamamura, Kosuke Taniguchi, Yuki Ito, Kenichiro Hata, Osamu Samura, Aikou Okamoto
Missense BICD2 variants in fetuses with congenital arthrogryposis and pterygia. Human genome variation 11 (1) (2024)
Layla Masuda, Akihiro Hasegawa, Hiromi Kamura, Fuyuki Hasegawa, Michihiro Yamamura, Kosuke Taniguchi, Yuki Ito, Kenichiro Hata, Osamu Samura, Aikou Okamoto
Missense BICD2 variants in fetuses with congenital arthrogryposis and pterygia. Human genome variation 11 (1) (2024)
Layla Masuda, Akihiro Hasegawa, Hiromi Kamura, Fuyuki Hasegawa, Michihiro Yamamura, Kosuke Taniguchi, Yuki Ito, Kenichiro Hata, Osamu Samura, Aikou Okamoto
Missense BICD2 variants in fetuses with congenital arthrogryposis and pterygia. Human genome variation 11 (1) (2024)
Ichiro Takeuchi, Kanako Tanase-Nakao, Ayame Ogawa, Tohru Sugawara, Osuke Migita, Makoto Kashima, Touko Yamazaki, Akihiro Iguchi, Yasuhiro Naiki, Toru Uchiyama, Junya Tamaoki, Hiroki Maeda, Hirotaka Shimizu, Toshinao Kawai, Kosuke Taniguchi, Hiromi Hirata, Makoto Kobayashi, Kimikazu Matsumoto, Kiyoshi Naruse, Kenichiro Hata, Hidenori Akutsu, Takashi Kato, Satoshi Narumi, Katsuhiro Arai, Akira Ishiguro
Congenital anaemia associated with loss-of-function variants in DNA polymerase epsilon 1. Journal of medical genetics (2023)
Kyoko Oshina, Yoshimasa Kamei, Asuka Hori, Fuyuki Hasegawa, Kosuke Taniguchi, Ohsuke Migita, Atsuo Itakura, Kenichiro Hata
A novel FLNA variant in a fetus with skeletal dysplasia. Human genome variation 9 (1) (2022)
Kyoko Oshina, Yoshimasa Kamei, Asuka Hori, Fuyuki Hasegawa, Kosuke Taniguchi, Ohsuke Migita, Atsuo Itakura, Kenichiro Hata
A novel FLNA variant in a fetus with skeletal dysplasia. Human genome variation 9 (1) (2022)
Kyoko Oshina, Yoshimasa Kamei, Asuka Hori, Fuyuki Hasegawa, Kosuke Taniguchi, Ohsuke Migita, Atsuo Itakura, Kenichiro Hata
A novel FLNA variant in a fetus with skeletal dysplasia. Human genome variation 9 (1) (2022)
Kyoko Oshina, Yoshimasa Kamei, Asuka Hori, Fuyuki Hasegawa, Kosuke Taniguchi, Ohsuke Migita, Atsuo Itakura, Kenichiro Hata
A novel FLNA variant in a fetus with skeletal dysplasia. Human genome variation 9 (1) (2022)
Kyoko Oshina, Yoshimasa Kamei, Asuka Hori, Fuyuki Hasegawa, Kosuke Taniguchi, Ohsuke Migita, Atsuo Itakura, Kenichiro Hata
A novel FLNA variant in a fetus with skeletal dysplasia. Human genome variation 9 (1) (2022)
Yukari Kobayashi, Yuki Ito, Kosuke Taniguchi, Kana Harada, Michihiro Yamamura, Taisuke Sato, Ken Takahashi, Hiroshi Kawame, Kenichiro Hata, Osamu Samura, Aikou Okamoto
Novel missense COL2A1 variant in a fetus with achondrogenesis type II. Human genome variation 9 (1) (2022)
Kosuke Taniguchi, Mikihiro Inoue, Katsuhiro Arai, Keiichi Uchida, Osuke Migita, Yui Akemoto, Junya Hirayama, Ichiro Takeuchi, Hirotaka Shimizu, Kenichiro Hata
Novel TNFAIP3 microdeletion in a girl with infantile-onset inflammatory bowel disease complicated by a severe perianal lesion. Human genome variation 8 (1) (2021)
Ken Takahashi, Taisuke Sato, Miyuki Nishiyama, Aiko Sasaki, Kosuke Taniguchi, Ohsuke Migita, Seiji Wada, Kenichiro Hata, Haruhiko Sago
Monochorionic diamniotic twins of discordant external genitalia with 45,X/46,XY mosaicism. Molecular genetics & genomic medicine 8 (9) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Kosuke Taniguchi