Kazuhiko Nakabayashi

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 13

Top Venues

Reproductive medicine and biology

Antioxidants (Basel, Switzerland)

Scientific reports

Clinical epigenetics

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

Publications

Toyofumi Hirakawa, Kazuhiko Nakabayashi, Noriko Ito, Kenichiro Hata, Shiori Imi, Mami Shibata, Daichi Urushiyama, Kohei Miyata, Fusanori Yotsumoto, Shin'ichiro Yasunaga, Tsukasa Baba, Shingo Miyamoto
Transwell Culture with Adipose Tissue-Derived Stem Cells and Fertilized Eggs Mimics the In Vivo Development of Fertilized Eggs to Blastocysts in the Fallopian Tube: An Animal Study. Antioxidants (Basel, Switzerland) 13 (6) (2024)
Toyofumi Hirakawa, Kazuhiko Nakabayashi, Noriko Ito, Kenichiro Hata, Shiori Imi, Mami Shibata, Daichi Urushiyama, Kohei Miyata, Fusanori Yotsumoto, Shin'ichiro Yasunaga, Tsukasa Baba, Shingo Miyamoto
Transwell Culture with Adipose Tissue-Derived Stem Cells and Fertilized Eggs Mimics the In Vivo Development of Fertilized Eggs to Blastocysts in the Fallopian Tube: An Animal Study. Antioxidants (Basel, Switzerland) 13 (6) (2024)
Satoshi Tamaoka, Kazuki Saito, Tomoko Yoshida, Kazuhiko Nakabayashi, Kenichi Tatsumi, Toshihiro Kawamura, Toshiya Matsuzaki, Keiko Matsubara, Hiroko Ogata-Kawata, Kenichiro Hata, Yuko Kato-Fukui, Maki Fukami
Exome-based genome-wide screening of rare variants associated with the risk of polycystic ovary syndrome. Reproductive medicine and biology 22 (1) (2023)
Satoshi Tamaoka, Kazuki Saito, Tomoko Yoshida, Kazuhiko Nakabayashi, Kenichi Tatsumi, Toshihiro Kawamura, Toshiya Matsuzaki, Keiko Matsubara, Hiroko Ogata-Kawata, Kenichiro Hata, Yuko Kato-Fukui, Maki Fukami
Exome-based genome-wide screening of rare variants associated with the risk of polycystic ovary syndrome. Reproductive medicine and biology 22 (1) (2023)
Taijun Hana, Hideki Ogiwara, Ohsuke Migita, Kazuhiko Nakabayashi, Kenichiro Hata, Nobuhito Morota
Deleterious fibronectin type III-related gene variants may induce a spinal extradural arachnoid cyst: an exome sequencing study of identical twin cases. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 37 (7) (2021)
Noriko Ito, Kazuhiro Tsukamoto, Kosuke Taniguchi, Ken Takahashi, Aikou Okamoto, Hiroaki Aoki, Yuka Otera-Takahashi, Michihiro Kitagawa, Hiroko Ogata-Kawata, Hideaki Morita, Kenichiro Hata, Kazuhiko Nakabayashi
Isolation and characterization of fetal nucleated red blood cells from maternal blood as a target for single cell sequencing-based non-invasive genetic testing. Reproductive medicine and biology 20 (3) (2021)
Asuka Hori, Hiroko Ogata-Kawata, Aiko Sasaki, Ken Takahashi, Kosuke Taniguchi, Ohsuke Migita, Akihiro Kawashima, Aikou Okamoto, Akihiko Sekizawa, Haruhiko Sago, Fumio Takada, Kazuhiko Nakabayashi, Kenichiro Hata
Improved library preparation protocols for amplicon sequencing-based noninvasive fetal genotyping for RHD-positive D antigen-negative alleles. BMC research notes 14 (1) (2021)
Mitsuko Nakashima, Jun Tohyama, Eiji Nakagawa, Yoshihiro Watanabe, Ch'ng Gaik Siew, Chieng Siik Kwong, Kaori Yamoto, Takuya Hiraide, Tokiko Fukuda, Tadashi Kaname, Kazuhiko Nakabayashi, Kenichiro Hata, Tsutomu Ogata, Hirotomo Saitsu, Naomichi Matsumoto
Identification of de novo CSNK2A1 and CSNK2B variants in cases of global developmental delay with seizures. Journal of human genetics 64 (4) (2019)
Yuko Yamaguchi, Chiharu Tayama, Junko Tomikawa, Rina Akaishi, Hiromi Kamura, Kentaro Matsuoka, Norio Wake, Hisanori Minakami, Kiyoko Kato, Takahiro Yamada, Kazuhiko Nakabayashi, Kenichiro Hata
Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2. Clinical epigenetics 11 (1) (2019)
Hiroyuki Ono, Hirotomo Saitsu, Reiko Horikawa, Shinichi Nakashima, Yumiko Ohkubo, Kumiko Yanagi, Kazuhiko Nakabayashi, Maki Fukami, Yasuko Fujisawa, Tsutomu Ogata
Partial androgen insensitivity syndrome caused by a deep intronic mutation creating an alternative splice acceptor site of the AR gene. Scientific reports 8 (1) (2018)
Tomoo Osumi, Shin-Ichi Tsujimoto, Moe Tamura, Meri Uchiyama, Kazuhiko Nakabayashi, Kohji Okamura, Masanori Yoshida, Daisuke Tomizawa, Akihiro Watanabe, Hiroyuki Takahashi, Tsukasa Hori, Shohei Yamamoto, Kazuko Hamamoto, Masahiro Migita, Hiroko Ogata-Kawata, Toru Uchiyama, Hiroe Kizawa, Hitomi Ueno-Yokohata, Ryota Shirai, Masafumi Seki, Kentaro Ohki, Junko Takita, Takeshi Inukai, Seishi Ogawa, Toshio Kitamura, Kimikazu Matsumoto, Kenichiro Hata, Nobutaka Kiyokawa, Susumu Goyama, Motohiro Kato
Recurrent RARB Translocations in Acute Promyelocytic Leukemia Lacking RARA Translocation. Cancer research 78 (16) (2018)
Wataru Yoshida, Hiroki Saikyo, Kazuhiko Nakabayashi, Hitomi Yoshioka, Daniyah Habiballah Bay, Keisuke Iida, Tomoko Kawai, Kenichiro Hata, Kazunori Ikebukuro, Kazuo Nagasawa, Isao Karube
Identification of G-quadruplex clusters by high-throughput sequencing of whole-genome amplified products with a G-quadruplex ligand. Scientific reports 8 (1) (2018)
Karin Sasaki, Kosei Abe, Takahide Mori, Kazunori Hashimoto, Kazuhiko Nakabayashi
Salvage of fetal karyotype information from SNP array data obtained from products of conception with maternal cell contamination. Prenatal diagnosis 37 (8) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Kazuhiko Nakabayashi