浜之上はるか

ハマノウエハルカ | Hamanoue Haruka

所属機関・部署：
職名：講師
ホームページURL (1件)： http://www.yokohama-cu.ac.jp/fukuhp/section/central_section/genetic/index.html

研究分野 (1件)：産婦人科学

研究キーワード (6件)：生殖 , 発生 , 先天異常 , 遺伝子 , 葉酸 , 胚

MISC (11件)：

Haruhiko Sago, Akihiko Sekizawa. Nationwide demonstration project of next-generation sequencing of cell-free DNA in maternal plasma in Japan: 1-year experience. PRENATAL DIAGNOSIS. 2015. 35. 4. 331-336
Shinnosuke Kuroda, Yasushi Yumura, Haruka Hamanoue, Kengo Yasuda, Hiroyuki Yamanaka, Hiroyuki Sanjo, Teppei Takeshima, Masataka Kobayashi, Yoshitake Kato, Akira Iwasaki, et al. A case of azoospermia patient with a chromosomal abnormality considered a ring Y chromosome. Acta Urologica Japonica. 2014. 60. 11. 583-586
Yukiko Kondo, Eriko Koshimizu, Andre Megarbane, Haruka Hamanoue, Ippei Okada, Kiyomi Nishiyama, Hirofumi Kodera, Satoko Miyatake, Yoshinori Tsurusaki, Mitsuko Nakashima, et al. Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2013. 161A. 7. 1543-1546
Yoshinori Tsurusaki, Hitoshi Osaka, Haruka Hamanoue, Hiroko Shimbo, Megumi Tsuji, Hiroshi Doi, Hirotomo Saitsu, Naomichi Matsumoto, Noriko Miyake. Rapid detection of a mutation causing X-linked leucoencephalopathy by exome sequencing. JOURNAL OF MEDICAL GENETICS. 2011. 48. 9. 606-609
Akira Nishimura-Tadaki, Takahito Wada, Gul Bano, Karen Gough, Janet Warner, Tomoki Kosho, Noriko Ando, Haruka Hamanoue, Hideya Sakakibara, Gen Nishimura, et al. Breakpoint determination of X;autosome balanced translocations in four patients with premature ovarian failure. JOURNAL OF HUMAN GENETICS. 2011. 56. 2. 156-160

学位 (1件)：

医学博士(甲号) (横浜市立大学大学院)

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浜之上 はるか

浜之上はるか