Haruka Hamanoue

777 total citations
23 papers, 220 citations indexed

About

Haruka Hamanoue is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Haruka Hamanoue has authored 23 papers receiving a total of 220 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Haruka Hamanoue's work include Prenatal Screening and Diagnostics (6 papers), Sexual Differentiation and Disorders (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Haruka Hamanoue is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Sexual Differentiation and Disorders (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Haruka Hamanoue collaborates with scholars based in Japan, Indonesia and Lebanon. Haruka Hamanoue's co-authors include Naomichi Matsumoto, Hirotomo Saitsu, Noriko Miyake, Hiroko Shimbo, Hitoshi Osaka, Yoshinori Tsurusaki, Fumiki Hirahara, Takeshi Mizuguchi, Hiroshi Doi and Kenji Kurosawa and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Neurology and Journal of Medical Genetics.

In The Last Decade

Haruka Hamanoue

23 papers receiving 215 citations

Peers

Countries citing papers authored by Haruka Hamanoue

Since Specialization

Citations

This map shows the geographic impact of Haruka Hamanoue's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Haruka Hamanoue with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Haruka Hamanoue more than expected).

Fields of papers citing papers by Haruka Hamanoue

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Haruka Hamanoue. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Haruka Hamanoue. The network helps show where Haruka Hamanoue may publish in the future.

Co-authorship network of co-authors of Haruka Hamanoue

This figure shows the co-authorship network connecting the top 25 collaborators of Haruka Hamanoue. A scholar is included among the top collaborators of Haruka Hamanoue based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Haruka Hamanoue. Haruka Hamanoue is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Inconsistent embryo selection across polygenic score methods 2024 ·Nature Human Behaviour ·Shinichi Namba, Masato Akiyama, Haruka Hamanoue, Yoshihiro Kato, Minae Kawashima, Itaru Kushima, Koichi Matsuda, Masahiro Nakatochi, Soichi Ogishima, Kyuto Sonehara, Ken Suzuki, Atsushi Takata, (unknown), Chizu Tanikawa, Kenichi Yamamoto, Natsuko Yamamoto, (unknown), (unknown), Norio Ozaki, (unknown)	1
2	Mitochondrial DNA mutations can influence the post-implantation development of human mosaic embryos 2023 ·Frontiers in Cell and Developmental Biology ·(unknown), (unknown), Tomonari Hayama, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Haruka Hamanoue, Teppei Takeshima, Yasushi Yumura, (unknown), Hiroki Kurahashi, Hideya Sakakibara, (unknown)	1
3	Periodic paralysis due to cumulative effects of rare variants in SCN4A with small functional alterations 2022 ·Muscle & Nerve ·(unknown), Tomoya Kubota, Norito Kokubun, (unknown), (unknown), Yuzuru Ito, Haruka Hamanoue, Masanori Takahashi	4
4	Changes in the number of babies born with Down syndrome in Japan 2022 ·Journal of obstetrics and gynaecology research ·(unknown), Kentaro Kurasawa, Yusuke Saigusa, Haruka Hamanoue, Fumiki Hirahara, Etsuko Miyagi	2
5	Attitudes of clinical geneticists and certified genetic counselors to genome editing and its clinical applications: A nation-wide questionnaire survey in Japan 2019 ·Journal of Human Genetics ·(unknown), Takahiro Yamada, Rina Akaishi, Issei Imoto, Kenji Kurosawa, Kaname Nakatani, Fumio Nomura, Haruka Hamanoue, (unknown), Hiromi Murakami, Hiroshi Yoshihashi, Junko Yotsumoto, Shinji Kosugi	9
6	An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis 2018 ·Daehan saengsik uihak hoeji/Clinical and experimental reproductive medicine ·Shinnosuke Kuroda, Kimitsugu Usui, Kohei Mori, Kengo Yasuda, (unknown), Hiroyuki Sanjo, (unknown), Teppei Takeshima, Takashi Kawahara, Haruka Hamanoue, Yoshitake Kato, Yasuhide Miyoshi, Hiroji Uemura, Akira Iwasaki, Yasushi Yumura	2
7	Distribution of PAPP-A and total hCG between 11 and 13 weeks of gestation in Japanese pregnant women 2018 ·The Journal of Maternal-Fetal & Neonatal Medicine ·Junichi Hasegawa, Seiji Wada, Atsushi Kasamatsu, (unknown), Haruka Hamanoue, Eriko Iwata, Jun Murotsuki, (unknown), Yoko Tateishi, (unknown), Atsushi Tajima, Susumu MURATA, Keiichi Matsubara, Masahiko Nakata, Akane Kondo, (unknown), A. Sasaki, Akihiko Sekizawa, Haruhiko Sago, Yoshimasa Kamei	2
8	A case of a rare variant of Klinefelter syndrome, 47,XY,i(X)(q10) 2018 ·Andrologia ·Takuya Kondo, Shinnosuke Kuroda, Kimitsugu Usui, Keiichiro Mori, Tohru Asai, Teppei Takeshima, Takashi Kawahara, Haruka Hamanoue, Hiroji Uemura, Yasushi Yumura	6
9	Multicenter experience with large panel next-generation sequencing in patients with advanced solid cancers in Japan 2018 ·Japanese Journal of Clinical Oncology ·Shingo Kato, Takuo Hayashi, Yoshiyuki Suehara, Haruka Hamanoue, Shoji Yamanaka, Yasushi Ichikawa, Takuma Higurashi, Kenichi Ohashi, Shigeo Yamaguchi, (unknown), Yasuhisa Terao, Tsuyoshi Saito	5
10	Clinical features of Birt–Hogg–Dubé syndrome: A Japanese case with pulmonary cysts, fibrofolliculomas and renal cell carcinoma 2016 ·The Journal of Dermatology ·(unknown), Yukie Yamaguchi, Haruka Hamanoue, Masahiro Yao, Mitsuko Furuya, Michiko Aihara	1
11	Peran Mutasi Gen CRELD1 pada Defek Septum Ventrikel dan Hubungannya dengan Manifestasi Klinis 2016 ·SHILAP Revista de lepidopterología ·(unknown), Haruka Hamanoue, Naomichi Matsumoto	1
12	[Case of azoospermia patient with a chromosomal abnormality considered a ring Y chromosome]. 2014 ·PubMed ·Shinnosuke Kuroda, Yasushi Yumura, Haruka Hamanoue, Kengo Yasuda, Hiroyuki Yamanaka, Hiroyuki Sanjo, Teppei Takeshima, (unknown), Yoshitake Kato, Akira Iwasaki, Kazumi Noguchi	2
13	Whole‐exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies 2013 ·American Journal of Medical Genetics Part A ·Yukiko Kondo, Eriko Koshimizu, André Mégarbané, Haruka Hamanoue, Ippei Okada, Kiyomi Nishiyama, Hirofumi Kodera, Satoko Miyatake, Yoshinori Tsurusaki, Mitsuko Nakashima, Hiroshi Doi, Noriko Miyake, Hirotomo Saitsu, Naomichi Matsumoto	15
14	Rapid detection of a mutation causing X-linked leucoencephalopathy by exome sequencing 2011 ·Journal of Medical Genetics ·Yoshinori Tsurusaki, Hitoshi Osaka, Haruka Hamanoue, Hiroko Shimbo, Megumi Tsuji, Hiroshi Doi, Hirotomo Saitsu, Naomichi Matsumoto, Noriko Miyake	33
15	Disrupted SOX10 regulation of GJC2 transcription causes Pelizaeus‐Merzbacher‐like disease 2010 ·Annals of Neurology ·Hitoshi Osaka, Haruka Hamanoue, Ryoko Yamamoto, Atsuo Nezu, Megumi Sasaki, Hirotomo Saitsu, Kenji Kurosawa, Hiroko Shimbo, Naomichi Matsumoto, Ken Inoue	31
16	Breakpoint determination of X;autosome balanced translocations in four patients with premature ovarian failure 2010 ·Journal of Human Genetics ·(unknown), Takahito Wada, Gul Bano, (unknown), Janet Warner, Tomoki Kosho, Noriko Ando, Haruka Hamanoue, Hideya Sakakibara, Gen Nishimura, Yoshinori Tsurusaki, Hiroshi Doi, Noriko Miyake, Keiko Wakui, Hirotomo Saitsu, Yoshimitsu Fukushima, Fumiki Hirahara, Naomichi Matsumoto	15
17	Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects 2009 ·Cardiology in the Young ·Haruka Hamanoue, (unknown), (unknown), (unknown), Utako Yokoyama, Takeshi Mizuguchi, Hirotomo Saitsu, Noriko Miyake, Fumiki Hirahara, Naomichi Matsumoto	23
18	A locus for ophthalmo‐acromelic syndrome mapped to 10p11.23 2009 ·American Journal of Medical Genetics Part A ·Haruka Hamanoue, André Mégarbané, Takaya Tohma, Akira Nishimura, Takeshi Mizuguchi, Hirotomo Saitsu, Haruya Sakai, Shoko Miura, Tatsushi Toda, Noriko Miyake, Norio Niikawa, Ko–ichiro Yoshiura, Fumiki Hirahara, Naomichi Matsumoto	10
19	A −16C>T substitution in the 5′ UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano 2006 ·Journal of Human Genetics ·(unknown), Kunihiro Yoshida, Haruya Sakai, Haruka Hamanoue, Takeshi Mizuguchi, Yusaku Shimizu, (unknown), Fumio Takada, Kinya Ishikawa, Hidehiro Mizusawa, Ko–ichiro Yoshiura, Yoshimitsu Fukushima, Shu‐ichi Ikeda, Naomichi Matsumoto	23
20	Complete hydatidiform mole and normal live birth following intracytoplasmic sperm injection 2006 ·Journal of Human Genetics ·Haruka Hamanoue, (unknown), Mika Okuda, Naoki Harada, (unknown), Haruya Sakai, Takeshi Mizuguchi, Hiroshi Ishikawa, Tsuneo Takahashi, Kiyonori Miura, Fumiki Hirahara, Naomichi Matsumoto	15

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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