Noriko Miyake

19.0k total citations
321 papers, 7.1k citations indexed

About

Noriko Miyake is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Noriko Miyake has authored 321 papers receiving a total of 7.1k indexed citations (citations by other indexed papers that have themselves been cited), including 179 papers in Molecular Biology, 129 papers in Genetics and 34 papers in Cell Biology. Recurrent topics in Noriko Miyake's work include Genetics and Neurodevelopmental Disorders (37 papers), Genomic variations and chromosomal abnormalities (31 papers) and Genomics and Rare Diseases (29 papers). Noriko Miyake is often cited by papers focused on Genetics and Neurodevelopmental Disorders (37 papers), Genomic variations and chromosomal abnormalities (31 papers) and Genomics and Rare Diseases (29 papers). Noriko Miyake collaborates with scholars based in Japan, United States and China. Noriko Miyake's co-authors include Naomichi Matsumoto, Hirotomo Saitsu, Yoshinori Tsurusaki, Mitsuko Nakashima, Koichi Miyake, Satoko Miyatake, Takashi Shimada, Mitsuhiro Kato, Nobuhiko Okamoto and Takeshi Mizuguchi and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Noriko Miyake

312 papers receiving 7.0k citations

Peers

Countries citing papers authored by Noriko Miyake

Since Specialization

Citations

This map shows the geographic impact of Noriko Miyake'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 Noriko Miyake with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Noriko Miyake more than expected).

Fields of papers citing papers by Noriko Miyake

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Noriko Miyake. 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 Noriko Miyake. The network helps show where Noriko Miyake may publish in the future.

Co-authorship network of co-authors of Noriko Miyake

This figure shows the co-authorship network connecting the top 25 collaborators of Noriko Miyake. A scholar is included among the top collaborators of Noriko Miyake 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 Noriko Miyake. Noriko Miyake 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	A Unique Case of MBD5 and CCM2 Deletions Leading to a Severe Neurological Phenotype With Prolonged Status Epilepticus 2025 ·Clinical Genetics ·(unknown), Viviana Venegas, (unknown), (unknown), (unknown), (unknown), (unknown), Mariko Okubo, Sanami Takada, Noriko Miyake	1
2	Streptococcal toxic shock syndrome due to Streptococcus dysgalactiae subsp. equisimilis from retroperitoneal panniculitis during the treatment with anti-IL-6 receptor antibody: A case report 2024 ·Modern Rheumatology Case Reports ·(unknown), Yoshihiro Eriguchi, (unknown), (unknown), Akiko Yonekawa, Noriko Miyake, Nobuyuki Ono, Hiroaki Niiro	0
3	A novel molecular target, superoxide dismutase 1, in ALK inhibitor-resistant lung cancer cells, detected through proteomic analysis 2024 ·Experimental Cell Research ·Noriko Miyake, (unknown), Masami Takeyama, Hideko Isozaki, Eiki Ichihara, Hiromichi Yamane, Takuya Fukazawa, (unknown), (unknown), (unknown), Akio Hiraki, Katsuyuki Kiura, (unknown)	1
4	Breakthrough candidemia with hematological disease: Results from a single-center retrospective study in Japan, 2009–2020 2023 ·Medical Mycology ·(unknown), Yoshihiro Eriguchi, Noriko Miyake, Yoji Nagasaki, Akiko Yonekawa, Yasuo Mori, Koji Kato, Koichi Akashi, Nobuyuki Shimono	4
5	Reduction of pyrrolizidine alkaloids by cooking pre-treatment for the petioles and the young spikes of <i>Petasites japonicus</i> 2022 ·Food Science and Technology Research ·Makiko Takenaka, Noriko Miyake, Toshiyuki Kimura, Setsuko Todoriki, (unknown)	3
6	COG1‐ congenital disorders of glycosylation: Milder presentation and review 2021 ·Clinical Genetics ·(unknown), Noriko Miyake, (unknown), (unknown), (unknown), Carla Asteggiano, Naomichi Matsumoto	4
7	Expanding the phenotypic spectrum of cardiospondylocarpofacial syndrome: From a detailed clinical and radiological observation of a boy with a novel missense variant in MAP3K7 2021 ·American Journal of Medical Genetics Part A ·(unknown), Noriko Miyake, (unknown), Yuko Tanabe, Takamichi Uchiyama, Naomichi Matsumoto, Tomoki Kosho	2
8	Legg‐Calvé‐Perthes disease in a patient with Bardet‐Biedl syndrome: A case report of a novel MKKS/BBS6 mutation 2020 ·SHILAP Revista de lepidopterología ·Kenichi Mishima, Atsushi Fujita, Seiji Mizuno, Masaki Matsushita, (unknown), (unknown), Noriko Miyake, Naomichi Matsumoto, Shiro Imagama, Hiroshi Kitoh	2
9	Clinical significance of SARS‐CoV‐2‐specific IgG detection with a rapid antibody kit for COVID‐19 patients 2020 ·Influenza and Other Respiratory Viruses ·Yong Chong, Hideyuki Ikematsu, Naoki Tani, (unknown), (unknown), (unknown), Akiko Yonekawa, (unknown), (unknown), Yoshihiro Eriguchi, Noriko Miyake, Shinji Shimoda, Yoji Nagasaki, Nobuyuki Shimono, Koichi Akashi	5
10	A novel ITPA variant causes epileptic encephalopathy with multiple-organ dysfunction 2020 ·Journal of Human Genetics ·(unknown), (unknown), (unknown), (unknown), M. Troncoso, (unknown), (unknown), (unknown), Nobuhiko Okamoto, Kohei Hamanaka, Takeshi Mizuguchi, Satomi Mitsuhashi, Noriko Miyake, Naomichi Matsumoto	11
11	Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy 2020 ·Journal of Human Genetics ·(unknown), Kazuhiro Iwama, Futoshi Sekiguchi, (unknown), Satoko Kumada, Keiko Ishigaki, Nobuhiko Okamoto, Mahdiyeh Behnam, Mohsen Ghadami, Eriko Koshimizu, Satoko Miyatake, Satomi Mitsuhashi, Takeshi Mizuguchi, Atsushi Takata, Hirotomo Saitsu, Noriko Miyake, Naomichi Matsumoto	13
12	Wipi3 is essential for alternative autophagy and its loss causes neurodegeneration 2020 ·Nature Communications ·Hirofumi Yamaguchi, Shinya Honda, Satoru Torii, Kimiko Shimizu, Kaoru Katoh, Koichi Miyake, Noriko Miyake, Nobuhiro Fujikake, (unknown), Satoko Arakawa, Shigeomi Shimizu	37
13	Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet’s disease 2019 ·Arthritis Research & Therapy ·Naomi Tsuchida, Yohei Kirino, (unknown), Masafumi Onodera, Katsuhiro Arai, (unknown), Takashi Ishikawa, Toshinao Kawai, Toru Uchiyama, Shigeru Nomura, Daisuke Kobayashi, Masataka Taguri, Satomi Mitsuhashi, Takeshi Mizuguchi, Atsushi Takata, Noriko Miyake, Hideaki Nakajima, Satoko Miyatake, Naomichi Matsumoto	43
14	RALA mutation in a patient with autism spectrum disorder and Noonan syndrome‐like phenotype 2019 ·Congenital Anomalies ·Nobuhiko Okamoto, Atsushi Takata, Noriko Miyake, Naomichi Matsumoto	4
15	A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features 2018 ·Journal of Human Genetics ·Futoshi Sekiguchi, (unknown), Maryam Sedghi, Mansoor Salehi, Majid Hosseinzadeh, Nobuhiko Okamoto, Takeshi Mizuguchi, Mitsuko Nakashima, Satoko Miyatake, Atsushi Takata, Noriko Miyake, Naomichi Matsumoto	10
16	A novel CYCS mutation in the α‐helix of the CYCS C‐terminal domain causes non‐syndromic thrombocytopenia 2018 ·Clinical Genetics ·Yuri Uchiyama, (unknown), Shinji Kunishima, Masaaki Shiina, Yoshiyuki Ogawa, Mitsuko Nakashima, Junko Hirato, Eri Imagawa, Atsushi Fujita, Kohei Hamanaka, Satoko Miyatake, Satomi Mitsuhashi, Atsushi Takata, Noriko Miyake, Kazuhiro Ogata, Hiroshi Handa, Naomichi Matsumoto, Takeshi Mizuguchi	20
17	Three patients with Schaaf–Yang syndrome exhibiting arthrogryposis and endocrinological abnormalities 2018 ·American Journal of Medical Genetics Part A ·(unknown), Nobuhiko Okamoto, Yoshinori Iba, Tomoki Miyazawa, Mitsuru Okada, Shinobu Ida, Takuya Naruto, Issei Imoto, Atsushi Fujita, Noriko Miyake, Naomichi Matsumoto, Keisuke Sugimoto, Tsukasa Takemura	18
18	PRUNE1‐related disorder: Expanding the clinical spectrum 2018 ·Clinical Genetics ·Eri Imagawa, Yutaka Yamamoto, Satomi Mitsuhashi, Bertrand Isidor, Tetsuhiro Fukuyama, Mitsuhiro Kato, Masayuki Sasaki, Saori Tanabe, Satoko Miyatake, Takeshi Mizuguchi, Atsushi Takata, Noriko Miyake, Naomichi Matsumoto	8
19	SOFT syndrome in a patient from Chile 2018 ·American Journal of Medical Genetics Part A ·Ken Saida, (unknown), (unknown), Atsushi Fujita, Kohei Hamanaka, Satomi Mitsuhashi, Eriko Koshimizu, Takeshi Mizuguchi, Satoko Miyatake, Atsushi Takata, Noriko Miyake, Naomichi Matsumoto	10
20	Coffin‐Siris syndrome and cardiac anomaly with a novel SOX11 mutation 2017 ·Congenital Anomalies ·Nobuhiko Okamoto, Eiji Ehara, Yoshinori Tsurusaki, Noriko Miyake, 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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