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T

Tomohiro Ebihara

kagoshima university
H指数:8
被引数:178

个人简介

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教育背景

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工作经历

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荣誉奖项

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Pleiotropic effects of MORC2 derive from its epigenetic signature

MORC2的多种表型效应源于其表观遗传特征

BRAIN
IF11.7
2025-12-011
OAAI
Peymani, Fatemeh; Ebihara, Tomohiro; Smirnov, Dmitrii; Kopajtich, Robert; Ando, Masahiro; Bertini, Enrico; Carrozzo, Rosalba; Diodato, Daria; Distelmaier, Felix; Fang, Fang; Ghezzi, Daniele; Hempel, Maja; Iwanicka-Pronicka, Katarzyna; Klopstock, Thomas; Stenton, Sarah L.; Lamperti, Costanza; Liu, Zhimei; Murtazina, Aysylu; Okamoto, Yuji; Okazaki, Yasushi; Piekutowska-Abramczuk, Dorota; Rotig, Agnes; Ryzhkova, Oxana; Schlein, Christian; Shagina, Olga; Takashima, Hiroshi; Tsygankova, Polina; Zech, Michael; Meitinger, Thomas; Shimura, Masaru; Murayama, Kei; Prokisch, Holger
Strategic validation of variants of uncertain significance in ECHS1 genetic testing

ECHS1基因检测中不确定意义变异的策略性验证

JOURNAL OF MEDICAL GENETICS
IF3.7
2023-04-132
PRE
Kishita, Yoshihito; Sugiura, Ayumu; Onuki, Takanori; Ebihara, Tomohiro; Matsuhashi, Tetsuro; Shimura, Masaru; Fushimi, Takuya; Ichino, Noriko; Nagatakidani, Yoshie; Nishihata, Hitomi; Nitta, Kazuhiro R.; Yatsuka, Yukiko; Imai-Okazaki, Atsuko; Wu, Yibo; Osaka, Hitoshi; Ohtake, Akira; Murayama, Kei; Okazaki, Yasushi
Development of Leigh syndrome with a high probability of cardiac manifestations in infantile-onset patients with m.14453G > A

在患有m.14453G> a的婴儿发作患者中，Leigh综合征的发展具有很高的心脏表现的可能性

Mitochondrion
IF4.5
2022-03-016
OAAI
Shimura, Masaru; Onuki, Takanori; Sugiyama, Yohei; Matsuhashi, Tetsuro; Ebihara, Tomohiro; Fushimi, Takuya; Tajika, Makiko; Ichimoto, Keiko; Matsunaga, Ayako; Tsuruoka, Tomoko; Nitta, Kazuhiro R.; Imai-Okazaki, Atsuko; Yatsuka, Yukiko; Kishita, Yoshihito; Ohtake, Akira; Okazaki, Yasushi; Murayama, Kei
Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan (vol 11, 3531, 2021)

核基因缺陷引起的严重线粒体疾病的产前诊断: 日本的一项研究 (第11卷，3531，2021)

SCIENTIFIC REPORTS
IF3.9
2021-11-160
OAAI
Akiyama, Nana; Shimura, Masaru; Yamazaki, Taro; Harashima, Hiroko; Fushimi, Takuya; Tsuruoka, Tomoko; Ebihara, Tomohiro; Ichimoto, Keiko; Matsunaga, Ayako; Saito-Tsuruoka, Megumi; Yatsuka, Yukiko; Kishita, Yoshihito; Kohda, Masakazu; Namba, Akira; Kamei, Yoshimasa; Okazaki, Yasushi; Kosugi, Shinji; Ohtake, Akira; Murayama, Kei
Neonatal-onset mitochondrial disease: clinical features, molecular diagnosis and prognosis

新生儿发病线粒体病的临床特征、分子诊断及预后

ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION
IF3.6
2021-10-0714
OAAI
Ebihara, Tomohiro; Nagatomo, Taro; Sugiyama, Yohei; Tsuruoka, Tomoko; Osone, Yoshiteru; Shimura, Masaru; Tajika, Makiko; Matsuhashi, Tetsuro; Ichimoto, Keiko; Matsunaga, Ayako; Akiyama, Nana; Ogawa-Tominaga, Minako; Yatsuka, Yukiko; Nitta, Kazuhiro R.; Kishita, Yoshihito; Fushimi, Takuya; Imai-Okazaki, Atsuko; Ohtake, Akira; Okazaki, Yasushi; Murayama, Kei
Long-term prognosis and genetic background of cardiomyopathy in 223 pediatric mitochondrial disease patients

223例儿童线粒体病患者心肌病的长期预后和遗传背景

INTERNATIONAL JOURNAL OF CARDIOLOGY
IF3.2
2021-10-0112
OAAI
Imai-Okazaki, Atsuko; Matsunaga, Ayako; Yatsuka, Yukiko; Nitta, Kazuhiro R.; Kishita, Yoshihito; Sugiura, Ayumu; Sugiyama, Yohei; Fushimi, Takuya; Shimura, Masaru; Ichimoto, Keiko; Tajika, Makiko; Ogawa-Tominaga, Minako; Ebihara, Tomohiro; Matsuhashi, Tetsuro; Tsuruoka, Tomoko; Kohda, Masakazu; Hirata, Tomoko; Harashima, Hiroko; Nojiri, Shuko; Takeda, Atsuhito; Nakaya, Akihiro; Kogaki, Shigetoyo; Sakata, Yasushi; Ohtake, Akira; Murayama, Kei; Okazaki, Yasushi
Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan

核基因缺陷引起的严重线粒体疾病的产前诊断: 日本的一项研究

SCIENTIFIC REPORTS
IF3.9
2021-02-113
OAAI
Akiyama, Nana; Shimura, Masaru; Yamazaki, Taro; Harashima, Hiroko; Fushimi, Takuya; Tsuruoka, Tomoko; Ebihara, Tomohiro; Ichimoto, Keiko; Matsunaga, Ayako; Saito-Tsuruoka, Megumi; Yatsuka, Yukiko; Kishita, Yoshihito; Kohda, Masakazu; Namba, Akira; Kamei, Yoshimasa; Okazaki, Yasushi; Kosugi, Shinji; Ohtake, Akira; Murayama, Kei
Clinical and molecular basis of hepatocerebral mitochondrial DNA depletion syndrome in Japan: evaluation of outcomes after liver transplantation

日本肝脑线粒体DNA耗竭综合征的临床和分子基础: 肝移植后结果的评估

ORPHANET JOURNAL OF RARE DISEASES
IF3.5
2020-07-2437
OAAI
Shimura, Masaru; Kuranobu, Naomi; Ogawa-Tominaga, Minako; Akiyama, Nana; Sugiyama, Yohei; Ebihara, Tomohiro; Fushimi, Takuya; Ichimoto, Keiko; Matsunaga, Ayako; Tsuruoka, Tomoko; Kishita, Yoshihito; Umetsu, Shuichiro; Inui, Ayano; Fujisawa, Tomoo; Tanikawa, Ken; Ito, Reiko; Fukuda, Akinari; Murakami, Jun; Kaji, Shunsaku; Kasahara, Mureo; Shiraki, Kazuo; Ohtake, Akira; Okazaki, Yasushi; Murayama, Kei

研究方向

暂未获取到该数据
K
Kei Murayama
H 指数:37论文数:297被引数:5,306
M
Masaru Shimura
H 指数:22论文数:130被引数:2,392
Y
Yasushi Okazaki
H 指数:65论文数:697被引数:2.7万
T
Takuya Fushimi
H 指数:14论文数:45被引数:846
A
Akira Ohtake
H 指数:43论文数:250被引数:6,014
Y
Yoshihito Kishita
H 指数:25论文数:78被引数:2,289
T
Tomoko Tsuruoka
H 指数:11论文数:30被引数:417
A
Ayako Matsunaga
H 指数:11论文数:34被引数:415
K
Keiko Ichimoto
H 指数:13论文数:36被引数:794
Y
Yukiko Yatsuka
H 指数:11论文数:44被引数:659