Keiko Matsubara

6.5k total citations
142 papers, 4.9k citations indexed

About

Keiko Matsubara is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Keiko Matsubara has authored 142 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Molecular Biology, 74 papers in Genetics and 37 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Keiko Matsubara's work include Genetic Syndromes and Imprinting (53 papers), Prenatal Screening and Diagnostics (34 papers) and Epigenetics and DNA Methylation (27 papers). Keiko Matsubara is often cited by papers focused on Genetic Syndromes and Imprinting (53 papers), Prenatal Screening and Diagnostics (34 papers) and Epigenetics and DNA Methylation (27 papers). Keiko Matsubara collaborates with scholars based in Japan, Iran and United Kingdom. Keiko Matsubara's co-authors include Toshiki Tsurimoto, Tsutomu Ogata, Maki Fukami, Masayo Kagami, Eiko Ohtsuka, S Matsuki, Hiroshi Shiono, Takashi Tokino, K Toyoshima and Kentaro Semba and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Keiko Matsubara

138 papers receiving 4.8k citations

Peers

Countries citing papers authored by Keiko Matsubara

Since Specialization

Citations

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

Fields of papers citing papers by Keiko Matsubara

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Keiko Matsubara

This figure shows the co-authorship network connecting the top 25 collaborators of Keiko Matsubara. A scholar is included among the top collaborators of Keiko Matsubara 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 Keiko Matsubara. Keiko Matsubara 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	Investigation of methylation profiles in Silver–Russell syndrome to explore episignatures 2025 ·Clinical Epigenetics ·(unknown), Takanobu Inoue, Akie Nakamura, Tomoko Fuke, Kazuki Yamazawa, Keiko Matsubara, Maki Fukami, (unknown), Tomoko Kawai, Masayo Kagami	0
2	Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance 2024 ·Clinical Epigenetics ·(unknown), Hidenobu Soejima, (unknown), (unknown), Akie Nakamura, Sayaka Kawashima, (unknown), Rika Kosaki, Yutaka Nishimura, Kazuki Yamazawa, Tetsuo Hattori, (unknown), Takanobu Inoue, Keiko Matsubara, Maki Fukami, Shinji Saitoh, Tsutomu Ogata, Masayo Kagami	4
3	Temple Syndrome: Comprehensive Clinical Study in Genetically Confirmed 60 Japanese Patients 2024 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), (unknown), Keisuke Nagasaki, Rika Kosaki, Yasuhiro Naiki, Michihiko Aramaki, Keiko Matsubara, Akie Nakamura, Maki Fukami, Tsutomu Ogata, Masayo Kagami	1
4	Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes 2023 ·Clinical Epigenetics ·(unknown), Keiko Matsubara, Akie Nakamura, Shinichiro Sano, Takanobu Inoue, Sayaka Kawashima, Tomoko Fuke, Kazuki Yamazawa, Maki Fukami, Tsutomu Ogata, Masayo Kagami	3
5	(Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B 2023 ·European Journal of Endocrinology ·(unknown), Shinichiro Sano, Sayaka Kawashima, Akie Nakamura, Hirohito Shima, (unknown), Yuki Yamada, (unknown), (unknown), Yoshiaki Ohtsu, Keiko Matsubara, Sumito Dateki, Yoshihiro Maruo, Maki Fukami, Tsutomu Ogata, Masayo Kagami	1
6	A boy with overgrowth caused by multi-locus imprinting disturbance including hypomethylation of MEST:alt-TSS-DMR 2022 ·European Journal of Medical Genetics ·(unknown), (unknown), (unknown), Keiko Matsubara, Maki Fukami, Keisuke Nagasaki, Masayo Kagami	3
7	Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system 2022 ·Journal of Human Genetics ·Tomoko Fuke, Akie Nakamura, Takanobu Inoue, Sayaka Kawashima, (unknown), Keiko Matsubara, Shinichiro Sano, Kazuki Yamazawa, Maki Fukami, Tsutomu Ogata, Masayo Kagami	2
8	Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting Disorders 2022 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Akie Nakamura, Tomoko Fuke, Takanobu Inoue, Sayaka Kawashima, Keiko Matsubara, Shinichiro Sano, Kazuki Yamazawa, Maki Fukami, Tsutomu Ogata, Masayo Kagami	6
9	Methylation status of genes escaping from X-chromosome inactivation in patients with X-chromosome rearrangements 2021 ·Clinical Epigenetics ·Sayaka Kawashima, Atsushi Hattori, Erina Suzuki, Keiko Matsubara, (unknown), Rika Kosaki, Yukihiro Hasegawa, Kazuhiko Nakabayashi, Maki Fukami, Masayo Kagami	1
10	ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance 2021 ·Clinical Epigenetics ·Masayo Kagami, (unknown), Keiko Matsubara, Kazuhiko Nakabayashi, Satoshi Narumi, Maki Fukami, (unknown), Hirotomo Saitsu, Shuji Takada, Tsutomu Ogata	17
11	Genome-wide methylation analysis in Silver–Russell syndrome, Temple syndrome, and Prader–Willi syndrome 2020 ·Clinical Epigenetics ·(unknown), Keiko Matsubara, Tomoko Fuke, Kazuki Yamazawa, Kazuhito Satou, Nobuyuki Murakami, Shinji Saitoh, Kazuhiko Nakabayashi, Kenichiro Hata, Tsutomu Ogata, Maki Fukami, Masayo Kagami	11
12	Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum 2020 ·The Journal of Clinical Endocrinology & Metabolism ·Tomoko Fuke, Akie Nakamura, Takanobu Inoue, Sayaka Kawashima, Kaori Hara, Keiko Matsubara, Shinichiro Sano, Kazuki Yamazawa, Maki Fukami, Tsutomu Ogata, Masayo Kagami	16
13	Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome 2020 ·Journal of Medical Genetics ·Kazuki Yamazawa, Takanobu Inoue, (unknown), (unknown), Hiroharu Yamashita, (unknown), Hideki Fujita, Keisuke Enomoto, Kazuhiko Nakabayashi, Kenichiro Hata, (unknown), Tatsuo Matsunaga, Akie Nakamura, Keiko Matsubara, Tsutomu Ogata, Masayo Kagami	7
14	Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients 2020 ·Clinical Epigenetics ·Takanobu Inoue, Akie Nakamura, (unknown), (unknown), Keiko Matsubara, Junko Nishioka, Yoshihiro Maruo, Yukihiro Hasegawa, Hiroshi Suzumura, Seiji Sato, Yoshiyuki Kobayashi, Nobuyuki Murakami, Kazuhiko Nakabayashi, Kazuki Yamazawa, Tomoko Fuke, Satoshi Narumi, Akira Oka, Tsutomu Ogata, Maki Fukami, Masayo Kagami	33
15	Coffin‐Lowry syndrome in a girl with 46,XX,t(X;11)(p22;p15)dn: Identification of RPS6KA3 disruption by whole genome sequencing 2020 ·SHILAP Revista de lepidopterología ·(unknown), Hirotomo Saitsu, Yasuko Fujisawa, Fumiko Kato, Keiko Matsubara, Maki Fukami, Masayo Kagami, Tsutomu Ogata	7
16	Assisted reproductive technology represents a possible risk factor for development of epimutation-mediated imprinting disorders for mothers aged ≥ 30 years 2020 ·Clinical Epigenetics ·(unknown), Keiko Matsubara, Masashi Mikami, Takahiro Arima, Tsutomu Ogata, Maki Fukami, Masayo Kagami	10
17	Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR 2019 ·Clinical Epigenetics ·Masayo Kagami, (unknown), Miyuki Ota, Kentaro Matsuoka, Akie Nakamura, Keiko Matsubara, Kazuhiko Nakabayashi, Shuji Takada, Maki Fukami, Tsutomu Ogata	18
18	Frequency of Common Copy-Number Variations at 15q11.2q13 in Sperm of Healthy Men 2019 ·Cytogenetic and Genome Research ·Takahiro Kinoshita, Masashi Mikami, Tadayuki Ayabe, Keiko Matsubara, Hiromi Ono, Kentaro Ohki, Maki Fukami, Yûkô Fukui	3
19	Temple syndrome diagnosed in an adult patient with clinical autism spectrum disorder 2018 ·Clinical Case Reports ·(unknown), Masayo Kagami, Keiko Matsubara, Shuichi Yatsuga, (unknown), (unknown), (unknown), Yasutoshi Koga	5
20	Electron Spin Resonance of Natural Graphite Powder Different in Grinding Method and Diameter 1996 ·TANSO ·Keiko Matsubara, (unknown), Kiyoshi Kawamura, (unknown)	4

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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