Shin Hayashi

5.4k total citations
113 papers, 3.9k citations indexed

About

Shin Hayashi is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Shin Hayashi has authored 113 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 39 papers in Genetics and 25 papers in Immunology. Recurrent topics in Shin Hayashi's work include Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Hematopoietic Stem Cell Transplantation (12 papers). Shin Hayashi is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Hematopoietic Stem Cell Transplantation (12 papers). Shin Hayashi collaborates with scholars based in Japan, United States and Canada. Shin Hayashi's co-authors include Kei Nakachi, Kaname Kawajiri, Kohsuke Imai, Johji Inazawa, Issei Imoto, Yoshiyuki Niho, Hisashi Gondo, Leonard D. Shultz, Shinobu Oguchi and Akio Inoue and has published in prestigious journals such as Journal of Biological Chemistry, Genes & Development and Blood.

In The Last Decade

Shin Hayashi

110 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shin Hayashi Japan 34 1.8k 865 738 725 469 113 3.9k
Gregory Hollis United States 36 2.7k 1.5× 548 0.6× 1.0k 1.4× 996 1.4× 454 1.0× 101 5.1k
Toshiyuki Fukao Japan 41 3.0k 1.7× 710 0.8× 497 0.7× 448 0.6× 192 0.4× 307 6.3k
Stefano Martinotti Italy 25 1.7k 0.9× 365 0.4× 899 1.2× 881 1.2× 226 0.5× 87 3.6k
Martin Pagé United Kingdom 36 2.0k 1.2× 781 0.9× 567 0.8× 392 0.5× 154 0.3× 100 3.7k
Aritoshi Iida Japan 33 2.1k 1.2× 1.5k 1.7× 789 1.1× 720 1.0× 94 0.2× 126 4.5k
Hermann Gram Switzerland 40 3.8k 2.1× 348 0.4× 763 1.0× 1.6k 2.2× 344 0.7× 74 6.1k
Izumi Hayashi Japan 40 1.9k 1.1× 591 0.7× 721 1.0× 619 0.9× 276 0.6× 152 5.0k
Sunil Nagpal United States 38 2.5k 1.4× 1.2k 1.4× 588 0.8× 1.0k 1.4× 226 0.5× 87 4.2k
Jacques Bertoglio France 41 3.1k 1.8× 350 0.4× 1.0k 1.4× 1.9k 2.6× 441 0.9× 118 6.1k
Masanobu Kobayashi Japan 36 1.8k 1.0× 282 0.3× 1.0k 1.4× 996 1.4× 536 1.1× 131 4.1k

Countries citing papers authored by Shin Hayashi

Since Specialization
Citations

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

Fields of papers citing papers by Shin Hayashi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shin Hayashi

This figure shows the co-authorship network connecting the top 25 collaborators of Shin Hayashi. A scholar is included among the top collaborators of Shin Hayashi 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 Shin Hayashi. Shin Hayashi 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.
Nishikawa, Masashi, Shin Hayashi, Hidenori Ito, et al.. (2024). Pathophysiological significance of the p.E31G variant in RAC1 responsible for a neurodevelopmental disorder with microcephaly. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1871(1). 167520–167520. 1 indexed citations
2.
Suzuki, Y., Noriko Nomura, Kenichiro Yamada, et al.. (2023). Pathogenicity evaluation of variants of uncertain significance at exon-intron junction by splicing assay in patients with Mowat–Wilson syndrome. European Journal of Medical Genetics. 66(12). 104882–104882.
3.
Muramatsu, Kazuhiro, et al.. (2022). Recurrent pneumonia in three patients with MECP2 duplication syndrome with aspiration as the possible cause. Brain and Development. 44(7). 486–491. 2 indexed citations
4.
Murata, Akihiko, Miya Yoshino, Kazuki Okuyama, et al.. (2014). An Evolutionary-Conserved Function of Mammalian Notch Family Members as Cell Adhesion Molecules. PLoS ONE. 9(9). e108535–e108535. 14 indexed citations
5.
Hayashi, Shin, Rika Kosaki, Tomoko Hasegawa, et al.. (2012). Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion. Journal of Human Genetics. 57(3). 191–196. 14 indexed citations
6.
Hayashi, Shin, Nobuhiko Okamoto, Yasutsugu Chinen, et al.. (2011). Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH). Human Genetics. 131(1). 99–110. 31 indexed citations
7.
Honda, Shozo, Koji Orii, Junya Kobayashi, et al.. (2010). Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation. Journal of Human Genetics. 55(4). 244–247. 23 indexed citations
8.
Matsumoto, Mitsuyo, Hiroko Sakamoto, Yuri Yamaguchi, et al.. (2009). 3-Dimensional microarray analysis of estrogen signal-related genes in breast cancer tissues.. PubMed. 29(10). 3971–5. 2 indexed citations
9.
Hayashi, Shin, Seiji Mizuno, Ohsuke Migita, et al.. (2008). The CASK gene harbored in a deletion detected by array‐CGH as a potential candidate for a gene causative of X‐linked dominant mental retardation. American Journal of Medical Genetics Part A. 146A(16). 2145–2151. 34 indexed citations
10.
Udaka, Toru, Issei Imoto, Yoshinori Aizu, et al.. (2007). Multiplex PCR/Liquid Chromatography Assay for Screening of Subtelomeric Rearrangements. Genetic Testing. 11(3). 241–248. 3 indexed citations
11.
Hayashi, Shin, Shozo Honda, Yoshio Makita, et al.. (2007). Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis. Journal of Human Genetics. 52(5). 397–405. 13 indexed citations
12.
Kamezaki, Kenjiro, Yoshikane Kikushige, Akihiko Numata, et al.. (2007). Rituximab does not compromise the mobilization and engraftment of autologous peripheral blood stem cells in diffuse-large B-cell lymphoma. Bone Marrow Transplantation. 39(9). 523–527. 18 indexed citations
13.
Hayashi, Shin, Kenji Kurosawa, Issei Imoto, Shuki Mizutani, & Johji Inazawa. (2005). Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array‐based comparative genomic hybridization. American Journal of Medical Genetics Part A. 139A(1). 32–36. 28 indexed citations
14.
Inoue, Akio, Nobuyuki Yoshida, Y Omoto, et al.. (2002). Development of cDNA microarray for expression profiling of estrogen-responsive genes. Journal of Molecular Endocrinology. 29(2). 175–192. 219 indexed citations
15.
Umeda, Syuji, Wesley G. Beamer, Katsumasa Takagi, et al.. (1999). Deficiency of SHP-1 Protein-Tyrosine Phosphatase Activity Results in Heightened Osteoclast Function and Decreased Bone Density. American Journal Of Pathology. 155(1). 223–233. 61 indexed citations
16.
Maeda, Yoshinobu, Takanori Teshima, Masao Yamada, et al.. (1999). Monitoring of human herpesviruses after allogeneic peripheral blood stem cell transplantation and bone marrow transplantation. British Journal of Haematology. 105(1). 295–302. 55 indexed citations
17.
Hayashi, Shin, Junko Watanabe, Kei Nakachi, et al.. (1994). Interindividual difference in expression of human Ah receptor and related P450 genes. Carcinogenesis. 15(5). 801–806. 89 indexed citations
18.
Teshima, Takanori, Masahiro Murakawa, Y Niho, et al.. (1993). A randomized phase II trial of low-dose aclarubicin vs very low-dose cytosine arabinoside for treatment of myelodysplastic syndromes. Leukemia Research. 17(8). 629–632. 6 indexed citations
19.
Kawajiri, Kaname, Kei Nakachi, Kazue Imai, Shin Hayashi, & Junko Watanabe. (1990). Individual differences in lung cancer susceptibility in relation to polymorphisms of P-450IA1 gene and cigarette dose.. PubMed. 21. 55–61. 25 indexed citations
20.
Nagafuchi, Seiho, Yasushi Takamatsu, Shin Hayashi, et al.. (1989). Treatment of disseminated herpes zoster in six severely immunocompromised patients. Acyclovir and vidarabine.. Japanese Journal of Medicine. 28(1). 100–104. 2 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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