Ryoko Fukai

1.1k total citations
23 papers, 368 citations indexed

About

Ryoko Fukai is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Ryoko Fukai has authored 23 papers receiving a total of 368 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Genetics and 5 papers in Neurology. Recurrent topics in Ryoko Fukai's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Ryoko Fukai is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Ryoko Fukai collaborates with scholars based in Japan, Israel and Egypt. Ryoko Fukai's co-authors include Naomichi Matsumoto, Noriko Miyake, Hirotomo Saitsu, Mitsuko Nakashima, Yoshinori Tsurusaki, Fumiaki Tanaka, Wei Chen, Yasunari Sakai, Yoko Hiraki and Nobuhiko Okamoto and has published in prestigious journals such as Journal of neurosurgery, American Journal Of Pathology and Frontiers in Immunology.

In The Last Decade

Ryoko Fukai

22 papers receiving 351 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ryoko Fukai Japan 11 190 148 53 53 38 23 368
Roberto Micheli Italy 9 217 1.1× 69 0.5× 81 1.5× 80 1.5× 21 0.6× 16 387
Lincon A. Stamp Australia 14 227 1.2× 69 0.5× 56 1.1× 16 0.3× 10 0.3× 40 784
Alice Abdel Aleem Egypt 13 216 1.1× 119 0.8× 57 1.1× 17 0.3× 48 1.3× 24 376
Vivek Sudhakar United States 11 228 1.2× 127 0.9× 148 2.8× 84 1.6× 14 0.4× 21 512
Lucy Crompton United Kingdom 9 488 2.6× 120 0.8× 66 1.2× 24 0.5× 32 0.8× 17 660
Nadia Sachewsky Canada 9 210 1.1× 26 0.2× 169 3.2× 24 0.5× 34 0.9× 14 544
Katrin Linda Netherlands 11 277 1.5× 110 0.7× 198 3.7× 13 0.2× 8 0.2× 12 511
M. Pike United Kingdom 6 284 1.5× 47 0.3× 30 0.6× 68 1.3× 9 0.2× 6 524
Raquel Vaz Sweden 10 211 1.1× 41 0.3× 47 0.9× 6 0.1× 23 0.6× 21 392
Martin Belle France 4 123 0.6× 24 0.2× 107 2.0× 16 0.3× 14 0.4× 7 265

Countries citing papers authored by Ryoko Fukai

Since Specialization
Citations

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

Fields of papers citing papers by Ryoko Fukai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ryoko Fukai

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

All Works

20 of 20 papers shown
1.
Takada, Sanami, Ghada M. H. Abdel‐Salam, Mohamed S. Abdel‐Hamid, et al.. (2024). Biallelic loss-of-function variants in GON4L cause microcephaly and brain structure abnormalities. npj Genomic Medicine. 9(1). 55–55.
2.
Takahashi, Keita, Hideyuki Takeuchi, Ryoko Fukai, et al.. (2021). Case Report: Anti-MOG Antibody Seroconversion Accompanied by Dimethyl Fumarate Treatment. Frontiers in Immunology. 12. 625465–625465. 1 indexed citations
3.
Doi, Hiroshi, Shigeru Koyano, Kenichi Tanaka, et al.. (2021). SGTA associates with intracellular aggregates in neurodegenerative diseases. Molecular Brain. 14(1). 59–59. 3 indexed citations
4.
Fukai, Ryoko, Keita Takahashi, Hiroyuki Abé, et al.. (2019). Non-traumatic Acute Epidural Hematoma in Multiple Sclerosis Treated With Fingolimod. Frontiers in Neurology. 10. 763–763. 2 indexed citations
5.
Fukai, Ryoko, Noriko Miyake, Soo-Young Lee, et al.. (2018). An acute encephalopathy with reduced diffusion in BRAF-associated cardio-facio-cutaneous syndrome. Brain and Development. 41(4). 378–381. 3 indexed citations
6.
Akamine, Satoshi, Yoshito Ishizaki, Yasunari Sakai, et al.. (2018). A male case with CDKL5-associated encephalopathy manifesting transient methylmalonic acidemia. European Journal of Medical Genetics. 61(8). 451–454. 5 indexed citations
7.
Takahashi, Keita, Hideyuki Takeuchi, Yuji Kurihara, et al.. (2018). Cerebrospinal fluid level of Nogo receptor 1 antagonist lateral olfactory tract usher substance (LOTUS) correlates inversely with the extent of neuroinflammation. Journal of Neuroinflammation. 15(1). 46–46. 6 indexed citations
8.
Fukai, Ryoko, Kenichi Tanaka, Mikiko Tada, et al.. (2018). A Case of McLeod Syndrome with A Novel XK Missense Mutation. Movement Disorders Clinical Practice. 5(3). 333–336. 1 indexed citations
9.
Tada, Mikiko, Hiroshi Doi, Shigeru Koyano, et al.. (2017). Matrin 3 Is a Component of Neuronal Cytoplasmic Inclusions of Motor Neurons in Sporadic Amyotrophic Lateral Sclerosis. American Journal Of Pathology. 188(2). 507–514. 37 indexed citations
10.
Monden, Yukifumi, Ryoko Fukai, Noriko Miyake, et al.. (2017). A case of severe movement disorder with GNAO1 mutation responsive to topiramate. Brain and Development. 39(5). 439–443. 22 indexed citations
11.
Fukai, Ryoko, Yasunari Sakai, Michiko Torio, et al.. (2016). De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis. BMC Neurology. 16(1). 174–174. 20 indexed citations
12.
Fukai, Ryoko, Hirotomo Saitsu, Nobuhiko Okamoto, et al.. (2016). De novo missense mutations in NALCN cause developmental and intellectual impairment with hypotonia. Journal of Human Genetics. 61(5). 451–455. 23 indexed citations
13.
Fukai, Ryoko, Hirotomo Saitsu, Yoshinori Tsurusaki, et al.. (2016). De novo KCNH1 mutations in four patients with syndromic developmental delay, hypotonia and seizures. Journal of Human Genetics. 61(5). 381–387. 38 indexed citations
14.
Sakai, Yasunari, Ryoko Fukai, Yuki Matsushita, et al.. (2016). De Novo Truncating Mutation of TRIM8 Causes Early‐Onset Epileptic Encephalopathy. Annals of Human Genetics. 80(4). 235–240. 21 indexed citations
15.
Miyatake, Satoko, Eriko Koshimizu, Atsushi Fujita, et al.. (2015). Detecting copy-number variations in whole-exome sequencing data using the eXome Hidden Markov Model: an ‘exome-first’ approach. Journal of Human Genetics. 60(4). 175–182. 41 indexed citations
16.
Imagawa, Eri, Ryoko Fukai, Mahdiyeh Behnam, et al.. (2015). Two novel homozygous RAB3GAP1 mutations cause Warburg micro syndrome. Human Genome Variation. 2(1). 15034–15034. 8 indexed citations
17.
Afifi, Hanan H., Ryoko Fukai, Noriko Miyake, et al.. (2015). De Novo 17q24.2–q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features. American Journal of Medical Genetics Part A. 167(10). 2418–2424. 5 indexed citations
18.
Fukai, Ryoko, Yoko Hiraki, Yoshinori Tsurusaki, et al.. (2015). A case of autism spectrum disorder arising from a de novo missense mutation in POGZ. Journal of Human Genetics. 60(5). 277–279. 31 indexed citations
19.
Fukai, Ryoko, Nobuhiko Ochi, Akira Murakami, et al.. (2013). Co‐occurrence of 22q11 deletion syndrome and hdr syndrome. American Journal of Medical Genetics Part A. 161(10). 2576–2581. 6 indexed citations
20.
Fukai, Ryoko, et al.. (2004). Strategies toward biocompatible artificial implants: Grafting of functionalized poly(ethylene glycol)s to poly(ethylene terephthalate) surfaces. Journal of Polymer Science Part A Polymer Chemistry. 42(21). 5389–5400. 37 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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