Tomoko Fuke

402 total citations
15 papers, 282 citations indexed

About

Tomoko Fuke is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tomoko Fuke has authored 15 papers receiving a total of 282 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tomoko Fuke's work include Genetic Syndromes and Imprinting (13 papers), Prenatal Screening and Diagnostics (10 papers) and Epigenetics and DNA Methylation (9 papers). Tomoko Fuke is often cited by papers focused on Genetic Syndromes and Imprinting (13 papers), Prenatal Screening and Diagnostics (10 papers) and Epigenetics and DNA Methylation (9 papers). Tomoko Fuke collaborates with scholars based in Japan, United States and Germany. Tomoko Fuke's co-authors include Tsutomu Ogata, Keiko Matsubara, Masayo Kagami, Maki Fukami, Kazuhiko Nakabayashi, Shinichiro Sano, Seiji Mizuno, Kazuki Yamazawa, Akie Nakamura and Takanobu Inoue and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Journal of Medical Genetics.

In The Last Decade

Tomoko Fuke

14 papers receiving 281 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Tomoko Fuke Japan 10 245 202 141 24 15 15 282
Margaret Lever United Kingdom 6 246 1.0× 193 1.0× 153 1.1× 16 0.7× 17 1.1× 12 284
Fabienne Danton France 4 537 2.2× 519 2.6× 394 2.8× 16 0.7× 38 2.5× 5 612
Nadine Schönherr Germany 8 350 1.4× 299 1.5× 258 1.8× 6 0.3× 14 0.9× 14 398
Oluwakemi Lokulo‐Sodipe United Kingdom 7 263 1.1× 163 0.8× 111 0.8× 32 1.3× 57 3.8× 12 312
Shahrin Pereira United States 3 160 0.7× 82 0.4× 71 0.5× 9 0.4× 4 0.3× 3 201
L. Memo Italy 7 150 0.6× 131 0.6× 77 0.5× 13 0.5× 11 241
Marie-Paule Guillodo France 2 347 1.4× 257 1.3× 65 0.5× 70 2.9× 5 0.3× 3 380
Christian Pina United States 3 65 0.3× 108 0.5× 118 0.8× 8 0.3× 31 2.1× 9 194
Louise E Docherty United Kingdom 7 305 1.2× 244 1.2× 176 1.2× 15 0.6× 52 3.5× 7 362
Isabelle Oliver‐Petit France 4 95 0.4× 93 0.5× 60 0.4× 5 0.2× 46 3.1× 10 146

Countries citing papers authored by Tomoko Fuke

Since Specialization
Citations

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

Fields of papers citing papers by Tomoko Fuke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomoko Fuke

This figure shows the co-authorship network connecting the top 25 collaborators of Tomoko Fuke. A scholar is included among the top collaborators of Tomoko Fuke 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 Tomoko Fuke. Tomoko Fuke is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

15 of 15 papers shown
1.
Inoue, Takanobu, Akie Nakamura, Tomoko Fuke, et al.. (2025). Investigation of methylation profiles in Silver–Russell syndrome to explore episignatures. Clinical Epigenetics. 17(1). 184–184.
2.
Matsubara, Keiko, Akie Nakamura, Shinichiro Sano, et al.. (2023). Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes. Clinical Epigenetics. 15(1). 78–78. 3 indexed citations
3.
Fuke, Tomoko, Akie Nakamura, Takanobu Inoue, et al.. (2022). Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system. Journal of Human Genetics. 67(10). 607–611. 2 indexed citations
4.
Nakamura, Akie, Tomoko Fuke, Takanobu Inoue, et al.. (2022). Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting Disorders. The Journal of Clinical Endocrinology & Metabolism. 107(8). e3121–e3133. 6 indexed citations
5.
Matsubara, Keiko, Tomoko Fuke, Kazuki Yamazawa, et al.. (2020). Genome-wide methylation analysis in Silver–Russell syndrome, Temple syndrome, and Prader–Willi syndrome. Clinical Epigenetics. 12(1). 11 indexed citations
6.
Fuke, Tomoko, Akie Nakamura, Takanobu Inoue, et al.. (2020). Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum. The Journal of Clinical Endocrinology & Metabolism. 106(3). 802–813. 16 indexed citations
7.
Inoue, Takanobu, Akie Nakamura, Keiko Matsubara, et al.. (2020). Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients. Clinical Epigenetics. 12(1). 86–86. 33 indexed citations
8.
Inoue, Takanobu, Junko Nishioka, Akie Nakamura, et al.. (2018). Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology. Journal of Medical Genetics. 56(6). 413–418. 25 indexed citations
9.
Inoue, Takanobu, Akie Nakamura, Tomoko Fuke, et al.. (2017). Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defects. Clinical Epigenetics. 9(1). 52–52. 10 indexed citations
10.
Kagami, Masayo, Seiji Mizuno, Keiko Matsubara, et al.. (2014). Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver–Russell Syndrome-compatible phenotype. European Journal of Human Genetics. 23(8). 1062–1067. 49 indexed citations
11.
Fuke, Tomoko, Seiji Mizuno, Toshiro Nagai, et al.. (2013). Molecular and Clinical Studies in 138 Japanese Patients with Silver-Russell Syndrome. PLoS ONE. 8(3). e60105–e60105. 53 indexed citations
12.
Kato, Fumiko, Takashi Hamajima, Tomonobu Hasegawa, et al.. (2013). IMAGe syndrome: clinical and genetic implications based on investigations in three Japanese patients. Clinical Endocrinology. 80(5). 706–713. 13 indexed citations
13.
Higashimoto, Ken, Kosuke Jozaki, Tomoki Kosho, et al.. (2013). A novel de novo point mutation of the OCT‐binding site in the IGF2/H19‐imprinting control region in a Beckwith–Wiedemann syndrome patient. Clinical Genetics. 86(6). 539–544. 22 indexed citations
14.
Kagami, Masayo, Kentaro Matsuoka, Toshiro Nagai, et al.. (2012). Paternal uniparental disomy 14 and related disorders. Epigenetics. 7(10). 1142–1150. 30 indexed citations
15.
Mori, Tetsuya, Kenichi Sugita, Kyoko Kimura, et al.. (2003). Isolated Central Nervous System (CNS) Relapse in a Case of Childhood Systemic Anaplastic Large Cell Lymphoma Without Initial CNS Involvement. Journal of Pediatric Hematology/Oncology. 25(12). 975–977. 9 indexed citations

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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2026