Yoshihashi Hiroshi

ヨシハシヒロシ | Yoshihashi Hiroshi

Affiliation and department：

Research field (1)： Fetal medicine/Pediatrics

Research theme for competitive and other funds (3)：

2010 - 2012 The high resolution oligonucleotide microarray for the chromosomaland epigenetic alterations in Russell-Silver syndrome
2001 - 2002 先天異常とダイオキシン受容体関連蛋白の多型との相関:性腺機能障害と口蓋裂
2000 - 2001 子宮内発育遅延の分子遺伝学的研究:GRB10のimprinting異常・変異解析

Papers (65)：

Hiroshi Futagawa, Shiho Ito, Kenjiro Kosaki, Hiroshi Yoshihashi. Long-term clinical course of Heyn-Sproul-Jackson syndrome. Congenital anomalies. 2023. 63. 5. 174-175
Mamiko Yamada, Hisato Suzuki, Hiroshi Futagawa, Toshiki Takenouchi, Fuyuki Miya, Hiroshi Yoshihashi, Kenjiro Kosaki. Phenotypic overlap between cardioacrofacial dysplasia-2 and oral-facial-digital syndrome. European journal of medical genetics. 2022. 65. 6. 104512-104512
Yoh ichiro Iwasa, Shin ya Nishio, Hidekane Yoshimura, Akiko Sugaya, Yuko Kataoka, Yukihide Maeda, Yukihiko Kanda, Kyoko Nagai, Yasushi Naito, Hiroshi Yamazaki, et al. Correction to: Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan (Human Genetics, (2022), 141, 3-4, (865-875), 10.1007/s00439-021-02351-7). Human Genetics. 2022. 141. 3-4. 993-995
Yoh-Ichiro Iwasa, Shin-Ya Nishio, Hidekane Yoshimura, Akiko Sugaya, Yuko Kataoka, Yukihide Maeda, Yukihiko Kanda, Kyoko Nagai, Yasushi Naito, Hiroshi Yamazaki, et al. Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan. Human genetics. 2022. 141. 3-4. 865-875
Tomoya Kawazoe, Shinsuke Tobisawa, Keizo Sugaya, Akinori Uruha, Kazuhito Miyamoto, Takashi Komori, Yu-Ichi Goto, Ichizo Nishino, Hiroshi Yoshihashi, Takeshi Mizuguchi, et al. Myoclonic Epilepsy with Ragged-red Fibers with Intranuclear Inclusions. Internal medicine (Tokyo, Japan). 2022. 61. 4. 547-552

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MISC (137)：

Naoki Kajita, Hiroshi Futagawa, Hiroshi Yoshihashi, Koichi Yoshida, Masami Narita. Two cases of an infant with Down syndrome with solid food protein-induced enterocolitis syndrome. Pediatrics International. 2021
鈴木寿人, 野崎昌俊, 吉橋博史, 今川和生, 梶川大悟, 山田茉未子, 山口有, 森貞直哉, 江口麻優子, 大橋祥子, et al. 重症新生児85名における遺伝学的解析:構造変異の検出と精緻な新生児ゲノム医療の実現. 日本人類遺伝学会大会プログラム・抄録集. 2021. 66th (CD-ROM)
萩田美和, 宮田世羽, 中川栄二, 武田良淳, 吉橋博史, 本田雅敬, 武内俊樹, 小崎健次郎, 岡明, 岡明, et al. A case of early infantile epileptic encephalopathy type 7 with partial response to pyridoxal phosphate. 脳と発達. 2021. 53. 2
吉橋博史. 【診断・治療可能な遺伝性疾患を見逃さないために】遺伝学的検査どのような遺伝学的検査をどのような時に考えるか. 小児科臨床. 2020. 73. 5. 561-564
吉橋博史. 【NICUで経験する先天異常とその対応】未診断疾患イニシアチブの遺伝カウンセリングにおける情報提供の在り方. 日本新生児成育医学会雑誌. 2020. 32. 1. 36-40

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Education (1)：

Professional career (1)：

Work history (1)：

Association Membership(s) (6)：

日本新生児成育医学会 , 日本周産期・新生児医学会 , 日本小児遺伝学会 , 日本小児科学会 , 日本遺伝カウンセリング学会 , 日本人類遺伝学会

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