Hiroyuki Mishima (H Mishima)

Scopus Author ID Researcher Name Resolver ID ORCID

Publication Activity (10 Years)

Years Active: 2014-2023
Publications (10 Years): 26

Top Venues

Journal of human genetics

Medicina (Kaunas, Lithuania)

Human genome variation

Translational psychiatry

Nagasaki University

Hokkaido University (PHD)

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

Affiliation History

Nagasaki University

Japan

Assistant Professor :: Human Genetics

Education History

Hokkaido University Apr 01 1998 - Mar 31 2001

Japan

PHD :: Graduate Schoole of Dental Medicine

Publications

Akari Niiya, Yo Hamaguchi, Hiroyuki Mishima, Shoko Miura, Nahoko Komatsu, Koh Nagata, Yuri Hasegawa, Kiyonori Miura, Koh-Ichiro Yoshiura
Four conserved amino acids on human papillomavirus E6 predict clinical high-risk types. Journal of medical virology 95 (8) (2023)
Hideki Kosako, Yusuke Yamashita, Ken Tanaka, Hiroyuki Mishima, Ryuta Iwamoto, Akira Kinoshita, Shin-Ichi Murata, Koichi Ohshima, Koh-Ichiro Yoshiura, Takashi Sonoki, Shinobu Tamura
Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma Transforming into Diffuse Large B-Cell Lymphoma in a Young Adult Patient with Neurofibromatosis Type 1: A Case Report. Medicina (Kaunas, Lithuania) 58 (12) (2022)
Hideki Kosako, Yusuke Yamashita, Ken Tanaka, Hiroyuki Mishima, Ryuta Iwamoto, Akira Kinoshita, Shin-Ichi Murata, Koichi Ohshima, Koh-Ichiro Yoshiura, Takashi Sonoki, Shinobu Tamura
Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma Transforming into Diffuse Large B-Cell Lymphoma in a Young Adult Patient with Neurofibromatosis Type 1: A Case Report. Medicina (Kaunas, Lithuania) 58 (12) (2022)
Hideki Kosako, Yusuke Yamashita, Ken Tanaka, Hiroyuki Mishima, Ryuta Iwamoto, Akira Kinoshita, Shin-Ichi Murata, Koichi Ohshima, Koh-Ichiro Yoshiura, Takashi Sonoki, Shinobu Tamura
Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma Transforming into Diffuse Large B-Cell Lymphoma in a Young Adult Patient with Neurofibromatosis Type 1: A Case Report. Medicina (Kaunas, Lithuania) 58 (12) (2022)
Hideki Kosako, Yusuke Yamashita, Ken Tanaka, Hiroyuki Mishima, Ryuta Iwamoto, Akira Kinoshita, Shin-Ichi Murata, Koichi Ohshima, Koh-Ichiro Yoshiura, Takashi Sonoki, Shinobu Tamura
Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma Transforming into Diffuse Large B-Cell Lymphoma in a Young Adult Patient with Neurofibromatosis Type 1: A Case Report. Medicina (Kaunas, Lithuania) 58 (12) (2022)
Yo Hamaguchi, Hiroyuki Mishima, Tomoko Kawai, Shinji Saitoh, Kenichiro Hata, Akira Kinoshita, Koh-Ichiro Yoshiura
Identification of unique DNA methylation sites in Kabuki syndrome using whole genome bisulfite sequencing and targeted hybridization capture followed by enzymatic methylation sequencing. Journal of human genetics 67 (12) (2022)
Kojima-Ishii Kanako, Nana Sakakibara, Kei Murayama, Koji Nagatani, Satoshi Murata, Akira Otake, Yasutoshi Koga, Hisato Suzuki, Tomoko Uehara, Kenjiro Kosaki, Koh-Ichiro Yoshiura, Hiroyuki Mishima, Yuko Ichimiya, Yuichi Mushimoto, Tomoko Horinouchi, China Nagano, Tomohiko Yamamura, Kazumoto Iijima, Kandai Nozu
BCS1L mutations produce Fanconi syndrome with developmental disability. Journal of human genetics (2021)
Nobuo Kanazawa, Hiroaki Hemmi, Noriko Kinjo, Hidenori Ohnishi, Jun Hamazaki, Hiroyuki Mishima, Akira Kinoshita, Tsunehiro Mizushima, Satoru Hamada, Kazuya Hamada, Norio Kawamoto, Saori Kadowaki, Yoshitaka Honda, Kazushi Izawa, Ryuta Nishikomori, Miyuki Tsumura, Yusuke Yamashita, Shinobu Tamura, Takashi Orimo, Toshiya Ozasa, Takashi Kato, Izumi Sasaki, Yuri Fukuda-Ohta, Naoko Wakaki-Nishiyama, Yutaka Inaba, Kayo Kunimoto, Satoshi Okada, Takeshi Taketani, Koichi Nakanishi, Shigeo Murata, Koh-Ichiro Yoshiura, Tsuneyasu Kaisho
Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency. Nature communications 12 (1) (2021)
M Asai, Yuta Koike, Yutaka Kuwatsuka, Y Yagi, K Kashiyama, K Tanaka, Hiroyuki Mishima, K Yoshiura, A Utani, Hiroyuki Murota
Multifaceted array-based keloidal gene expression profiling reveals specific MDFI upregulation in keloid lesions. Clinical and experimental dermatology 46 (7) (2021)
Akira Kinoshita, Kaname Ohyama, Susumu Tanimura, Katsuya Matsuda, Tatsuya Kishino, Yutaka Negishi, Naoko Asahina, Hideaki Shiraishi, Kana Hosoki, Kiyotaka Tomiwa, Naoko Ishihara, Hiroyuki Mishima, Ryoichi Mori, Masahiro Nakashima, Shinji Saitoh, Koh-Ichiro Yoshiura
Itpr1 regulates the formation of anterior eye segment tissues derived from neural crest cells. Development (Cambridge, England) 148 (16) (2021)
Yoshiro Morimoto, Shinji Ono, Shintaro Yoshida, Hiroyuki Mishima, Akira Kinoshita, Takeshi Tanaka, Yoshihiro Komohara, Naohiro Kurotaki, Tatsuya Kishino, Yuji Okazaki, Hiroki Ozawa, Koh-Ichiro Yoshiura, Akira Imamura
A unique missense variant in the E1A-binding protein P400 gene is implicated in schizophrenia by whole-exome sequencing and mutant mouse models. Translational psychiatry 11 (1) (2021)
Yusuke Yamashita, Shuhei Morita, Hiroki Hosoi, Hiroshi Kobata, Shohei Kishimoto, Tatsuya Ishibashi, Hiroyuki Mishima, Akira Kinoshita, Bradley J Backes, Koh-Ichiro Yoshiura, Feroz R Papa, Takashi Sonoki, Shinobu Tamura
Targeting Adaptive IRE1α Signaling and PLK2 in Multiple Myeloma: Possible Anti-Tumor Mechanisms of KIRA8 and Nilotinib. International journal of molecular sciences 21 (17) (2020)
Sumito Dateki, Satoshi Watanabe, Hiroyuki Mishima, Toshihiko Shirakawa, Minoru Morikawa, Eiichi Kinoshita, Koh-Ichiro Yoshiura, Hiroyuki Moriuchi
A homozygous splice site ROBO1 mutation in a patient with a novel syndrome with combined pituitary hormone deficiency. Journal of human genetics 64 (4) (2019)
Hitomi Shimizu, Satoshi Watanabe, Akira Kinoshita, Hiroyuki Mishima, Gen Nishimura, Hiroyuki Moriuchi, Koh-Ichiro Yoshiura, Sumito Dateki
Identification of a homozygous frameshift variant in RFLNA in a patient with a typical phenotype of spondylocarpotarsal synostosis syndrome. Journal of human genetics 64 (5) (2019)
Masayasu Shibano, Akira Watanabe, Nobuo Takano, Hiroyuki Mishima, Akira Kinoshita, Koh-Ichiro Yoshiura, Takahiko Shibahara
Target Capture/Next-Generation Sequencing for Nonsyndromic Cleft Lip and Palate in the Japanese Population. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 57 (1) (2019)
Hiroyuki Mishima, Hisato Suzuki, Michiko Doi, Mutsuko Miyazaki, Satoshi Watanabe, Tadashi Matsumoto, Kanako Morifuji, Hiroyuki Moriuchi, Koh-Ichiro Yoshiura, Tatsuro Kondoh, Kenjiro Kosaki
Evaluation of Face2Gene using facial images of patients with congenital dysmorphic syndromes recruited in Japan. Journal of human genetics 64 (8) (2019)
Yo Hamaguchi, Mikihiro Aoki, Satoshi Watanabe, Hiroyuki Mishima, Koh-Ichiro Yoshiura, Hiroyuki Moriuchi, Sumito Dateki
KAT6B-related disorder in a patient with a novel frameshift variant (c.3925dup). Human genome variation 6 (2019)
Yoshiro Morimoto, Shintaro Yoshida, Akira Kinoshita, Chisei Satoh, Hiroyuki Mishima, Naohiro Yamaguchi, Katsuya Matsuda, Miako Sakaguchi, Takeshi Tanaka, Yoshihiro Komohara, Akira Imamura, Hiroki Ozawa, Masahiro Nakashima, Naohiro Kurotaki, Tatsuya Kishino, Koh-Ichiro Yoshiura, Shinji Ono
Nonsense mutation in CFAP43 causes normal-pressure hydrocephalus with ciliary abnormalities. Neurology 92 (20) (2019)
Shohei Matsuno, Hiroto Furuta, Kitaro Kosaka, Asako Doi, Tohru Yorifuji, Takuya Fukuda, Takafumi Senmaru, Shinsuke Uraki, Norihiko Matsutani, Machi Furuta, Hiroyuki Mishima, Hiroshi Iwakura, Masahiro Nishi, Kohichiro Yoshiura, Michiaki Fukui, Takashi Akamizu
Identification of a variant associated with early-onset diabetes in the intron of the insulin gene with exome sequencing. Journal of diabetes investigation 10 (4) (2018)
Yoshiro Morimoto, Mihoko Shimada-Sugimoto, Takeshi Otowa, Shintaro Yoshida, Akira Kinoshita, Hiroyuki Mishima, Naohiro Yamaguchi, Takatoshi Mori, Akira Imamura, Hiroki Ozawa, Naohiro Kurotaki, Christiane Ziegler, Katharina Domschke, Jürgen Deckert, Tadashi Umekage, Mamoru Tochigi, Hisanobu Kaiya, Yuji Okazaki, Katsushi Tokunaga, Tsukasa Sasaki, Koh-Ichiro Yoshiura, Shinji Ono
Whole-exome sequencing and gene-based rare variant association tests suggest that PLA2G4E might be a risk gene for panic disorder. Translational psychiatry 8 (1) (2018)
Takashi Kikuiri, Hiroyuki Mishima, Hideto Imura, Satoshi Suzuki, Yusuke Matsuzawa, Takashi Nakamura, Satoshi Fukumoto, Yoshitaka Yoshimura, Satoshi Watanabe, Akira Kinoshita, Takahiro Yamada, Masanobu Shindoh, Yoshihiko Sugita, Hatsuhiko Maeda, Yasutaka Yawaka, Tadashi Mikoya, Nagato Natsume, Koh-Ichiro Yoshiura
Patients with SATB2-associated syndrome exhibiting multiple odontomas. American journal of medical genetics. Part A 176 (12) (2018)
Makiko Horai, Hiroyuki Mishima, Chisa Hayashida, Akira Kinoshita, Yoshibumi Nakane, Tatsuki Matsuo, Kazuto Tsuruda, Katsunori Yanagihara, Shinya Sato, Daisuke Imanishi, Yoshitaka Imaizumi, Tomoko Hata, Yasushi Miyazaki, Koh-Ichiro Yoshiura
Detection of de novo single nucleotide variants in offspring of atomic-bomb survivors close to the hypocenter by whole-genome sequencing. Journal of human genetics 63 (3) (2017)
Chisei Satoh, Ryuta Maekawa, Akira Kinoshita, Hiroyuki Mishima, Michiko Doi, Mutsuko Miyazaki, Masafumi Fukuda, Haruo Takahashi, Tatsuro Kondoh, Koh-Ichiro Yoshiura
Three brothers with a nonsense mutation in KAT6A caused by parental germline mosaicism. Human genome variation 4 (2017)
Yoshiro Morimoto, Shinji Ono, Akira Imamura, Yuji Okazaki, Akira Kinoshita, Hiroyuki Mishima, Hideyuki Nakane, Hiroki Ozawa, Koh-Ichiro Yoshiura, Naohiro Kurotaki
Deep sequencing reveals variations in somatic cell mosaic mutations between monozygotic twins with discordant psychiatric disease. Human genome variation 4 (2017)
Kiyonori Miura, Hiroyuki Mishima, Michio Yasunami, Masanori Kaneuchi, Michio Kitajima, Shuhei Abe, Ai Higashijima, Naoki Fuchi, Shoko Miura, Koh-Ichiro Yoshiura, Hideaki Masuzaki
A significant association between rs8067378 at 17q12 and invasive cervical cancer originally identified by a genome-wide association study in Han Chinese is replicated in a Japanese population. Journal of human genetics 61 (9) (2016)
Koichi Tomoshige, Keitaro Matsumoto, Tomoshi Tsuchiya, Masahiro Oikawa, Takuro Miyazaki, Naoya Yamasaki, Hiroyuki Mishima, Akira Kinoshita, Toru Kubo, Kiyoyasu Fukushima, Koh-Ichiro Yoshiura, Takeshi Nagayasu
Germline mutations causing familial lung cancer. Journal of human genetics 60 (10) (2015)
Shuhei Abe, Kiyonori Miura, Akira Kinoshita, Hiroyuki Mishima, Shoko Miura, Kentaro Yamasaki, Yuri Hasegawa, Ai Higashijima, Ozora Jo, Atsushi Yoshida, Masanori Kaneuchi, Koh-Ichiro Yoshiura, Hideaki Masuzaki
Single human papillomavirus 16 or 52 infection and later cytological findings in Japanese women with NILM or ASC-US. Journal of human genetics 59 (5) (2014)

Hiroyuki Mishima.css-eqlu8i{font-size:small;padding-left:4px;} (H Mishima)

Publication Activity (10 Years)

Top Topics

Top Venues

Hiroyuki Mishima (H Mishima)