Kana Hosoki

747 total citations
13 papers, 490 citations indexed

About

Kana Hosoki is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Kana Hosoki has authored 13 papers receiving a total of 490 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Kana Hosoki's work include Genetic Syndromes and Imprinting (4 papers), Epigenetics and DNA Methylation (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Kana Hosoki is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Epigenetics and DNA Methylation (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Kana Hosoki collaborates with scholars based in Japan, Canada and Australia. Kana Hosoki's co-authors include Shinji Saitoh, Naoki Goshima, Archa H. Fox, Danny M. Hatters, K. Swaminathan Iyer, Tetsuya Kawaguchi, Geraldine Kong, Simon Kobelke, Gavin J. Knott and Tetsuro Hirose and has published in prestigious journals such as The Journal of Cell Biology, Development and Scientific Reports.

In The Last Decade

Kana Hosoki

12 papers receiving 485 citations

Peers

Kana Hosoki

GENET

PPCH

GENET

Siren Berland Norway

Sarah Vergult Belgium

Maïlys Daniau France

Flavia Palombo Italy

Alice Abdel Aleem Egypt

Isabel Aznarez Canada

Christapher S. Morrissey United States

Jonatan Halvardson Sweden

Jenny Blechingberg Denmark

Shelagh Joss United Kingdom

Siren Berland Norway

Kana Hosoki

360 ×0.9

207 ×1.5

GENET

51 ×1.0

PPCH

34 ×0.7

38 ×0.8

GENET

Citations per year, relative to Kana Hosoki Kana Hosoki (= 1×) peers Siren Berland

Countries citing papers authored by Kana Hosoki

Since Specialization

Citations

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

Fields of papers citing papers by Kana Hosoki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kana Hosoki

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

All Works

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13 of 13 papers shown

Fujimoto, Masanori, Y. Nakamura, Kana Hosoki, et al.. (2024). Genotype-phenotype correlation over time in Angelman syndrome: Researching 134 patients. Human Genetics and Genomics Advances. 5(4). 100342–100342. 3 indexed citations

Nishi, Eriko, Noriko Miyake, Rie Kawamura, et al.. (2023). Craniosynostosis in molecularly diagnosed Kabuki syndrome: Prevalence and clinical implications. American Journal of Medical Genetics Part A. 194(2). 268–278.

Kinoshita, Akira, Kaname Ohyama, Susumu Tanimura, et al.. (2021). Itpr1 regulates the formation of anterior eye segment tissues derived from neural crest cells. Development. 148(16). 9 indexed citations

Hosoki, Kana, et al.. (2018). A novel human muscle cell model of Duchenne muscular dystrophy created by CRISPR/Cas9 and evaluation of antisense-mediated exon skipping. Journal of Human Genetics. 63(3). 365–375. 21 indexed citations

Maruyama, Rika, et al.. (2017). LNA/DNA mixmer-based antisense oligonucleotides correct alternative splicing of the SMN2 gene and restore SMN protein expression in type 1 SMA fibroblasts. Scientific Reports. 7(1). 3672–3672. 39 indexed citations

Hennig, Sven, Geraldine Kong, Taro Mannen, et al.. (2015). Prion-like domains in RNA binding proteins are essential for building subnuclear paraspeckles. The Journal of Cell Biology. 210(4). 529–539. 249 indexed citations

Hosoki, Kana, Tohru Ohta, Jun Natsume, et al.. (2012). Clinical phenotype and candidate genes for the 5q31.3 microdeletion syndrome. American Journal of Medical Genetics Part A. 158A(8). 1891–1896. 25 indexed citations

Hosoki, Kana, Tohru Ohta, Keinosuke Fujita, et al.. (2012). Hand‐foot‐genital syndrome with a 7p15 deletion: Clinically recognizable syndrome. Pediatrics International. 54(3). 5 indexed citations

Takahashi, Yumi, Kana Hosoki, Masafumi Matsushita, et al.. (2011). A loss‐of‐function mutation in the SLC9A6 gene causes X‐linked mental retardation resembling Angelman syndrome. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(7). 799–807. 29 indexed citations

10.

Sudo, Akira, et al.. (2011). Successful cochlear implantation in a patient with mitochondrial hearing loss and m.625G>A transition. The Journal of Laryngology & Otology. 125(12). 1282–1285. 13 indexed citations

11.

Tohyama, Jun, Toshiyuki Yamamoto, Kana Hosoki, et al.. (2011). West syndrome associated with mosaic duplication of FOXG1 in a patient with maternal uniparental disomy of chromosome 14. American Journal of Medical Genetics Part A. 155(10). 2584–2588. 27 indexed citations

12.

Hosoki, Kana, Masayo Kagami, Masaya Kubota, et al.. (2009). Maternal Uniparental Disomy 14 Syndrome Demonstrates Prader-Willi Syndrome-Like Phenotype. The Journal of Pediatrics. 155(6). 900–903.e1. 41 indexed citations

13.

Hosoki, Kana, et al.. (2008). Epimutation (hypomethylation) affecting the chromosome 14q32.2 imprinted region in a girl with upd(14)mat-like phenotype. European Journal of Human Genetics. 16(8). 1019–1023. 29 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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