Hiroko Morisaki

5.8k total citations
105 papers, 2.4k citations indexed

About

Hiroko Morisaki is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Hiroko Morisaki has authored 105 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Genetics, 37 papers in Molecular Biology and 37 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Hiroko Morisaki's work include Connective tissue disorders research (32 papers), Aortic Disease and Treatment Approaches (23 papers) and Aortic aneurysm repair treatments (13 papers). Hiroko Morisaki is often cited by papers focused on Connective tissue disorders research (32 papers), Aortic Disease and Treatment Approaches (23 papers) and Aortic aneurysm repair treatments (13 papers). Hiroko Morisaki collaborates with scholars based in Japan, United States and Indonesia. Hiroko Morisaki's co-authors include Takayuki Morisaki, Tsunehiro Mukai, Akira Nabetani, Izuho Hatada, E W Holmes, Itaru Yamanaka, Yoshihiro Miyamoto, Yoshihiro Kokubo, Keiko Toyama and Yoshimitsu Fukushima and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Hiroko Morisaki

102 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hiroko Morisaki Japan 25 1.1k 814 488 423 302 105 2.4k
Takayuki Morisaki Japan 34 2.1k 2.0× 747 0.9× 501 1.0× 645 1.5× 399 1.3× 154 3.7k
Katsuhiko Asanuma Japan 29 1.5k 1.4× 668 0.8× 180 0.4× 189 0.4× 392 1.3× 89 4.0k
Lorenz Sellin Germany 28 1.5k 1.3× 739 0.9× 320 0.7× 198 0.5× 64 0.2× 59 2.8k
May Christine V. Malicdan United States 29 1.5k 1.3× 544 0.7× 130 0.3× 309 0.7× 744 2.5× 126 2.6k
Kálmán Tory Hungary 25 1.4k 1.3× 538 0.7× 499 1.0× 106 0.3× 136 0.5× 68 2.2k
Céline Schaeffer Italy 20 1.3k 1.2× 544 0.7× 224 0.5× 109 0.3× 255 0.8× 32 2.0k
Finian Martin Ireland 37 2.5k 2.3× 653 0.8× 379 0.8× 127 0.3× 157 0.5× 75 4.0k
Lin Zuo China 19 1.4k 1.3× 376 0.5× 122 0.3× 398 0.9× 206 0.7× 42 3.0k
Frédérique Savagner France 24 1.0k 0.9× 298 0.4× 120 0.2× 260 0.6× 147 0.5× 58 2.2k
Billie M. Moats‐Staats United States 24 796 0.7× 342 0.4× 366 0.8× 122 0.3× 175 0.6× 46 2.1k

Countries citing papers authored by Hiroko Morisaki

Since Specialization
Citations

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

Fields of papers citing papers by Hiroko Morisaki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hiroko Morisaki

This figure shows the co-authorship network connecting the top 25 collaborators of Hiroko Morisaki. A scholar is included among the top collaborators of Hiroko Morisaki 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 Hiroko Morisaki. Hiroko Morisaki 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.
Morisaki, Hiroko. (2024). Hereditary Aortic Aneurysms and Dissections: Clinical Diagnosis and Genetic Testing. Annals of Vascular Diseases. 17(2). 128–134. 1 indexed citations
2.
Iwasa, Toru, Akihiro Urasaki, Soichi Takeda, et al.. (2023). Computational and Experimental Analyses for Pathogenicity Prediction of ACVRL1 Missense Variants in Hereditary Hemorrhagic Telangiectasia. Journal of Clinical Medicine. 12(15). 5002–5002. 1 indexed citations
3.
Wang, Qiang, Wei Yu, De Xie, et al.. (2023). AMPD2 plays important roles in regulating hepatic glucose and lipid metabolism. Molecular and Cellular Endocrinology. 577. 112039–112039. 3 indexed citations
4.
Shimokawa, Osamu, et al.. (2023). Aortic Dissection and a Previously Unreported ACTA2 Missense Variant Mutation in a Young Patient: A Case Report. Pediatric and Developmental Pathology. 26(5). 494–498. 1 indexed citations
5.
Seike, Yoshimasa, Koki Yokawa, Shigeki Koizumi, et al.. (2022). Long-term durability of a reimplantation valve-sparing aortic root replacement can be expected in both Marfan syndrome and Loeys-Dietz syndrome. European Journal of Cardio-Thoracic Surgery. 61(6). 1318–1325. 2 indexed citations
6.
Yokota, Takashi, Shouji Matsushima, Shingo Tsujinaga, et al.. (2021). Loeys-Dietz Cardiomyopathy? Long-term Follow-up After Onset of Acute Decompensated Heart Failure. Canadian Journal of Cardiology. 38(3). 389–391. 3 indexed citations
7.
Seike, Yoshimasa, Kenji Minatoya, Hitoshi Matsuda, et al.. (2019). Histologic differences between the ascending and descending aortas in young adults with fibrillin-1 mutations. Journal of Thoracic and Cardiovascular Surgery. 159(4). 1214–1220.e1. 1 indexed citations
8.
Takasawa, Kei, Hiroko Morisaki, Takashi Ito, et al.. (2019). A Nonsense <b><i>SMAD3</i></b> Mutation in a Girl with Familial Thoracic Aortic Aneurysm and Dissection without Joint Abnormality. Cardiology. 144(1-2). 53–59. 1 indexed citations
9.
Fujiki, Ryoji, Akiko Yoshida, Akiko Maeda, et al.. (2018). Assessing the Accuracy of Variant Detection in Cost-Effective Gene Panel Testing by Next-Generation Sequencing. Journal of Molecular Diagnostics. 20(5). 572–582. 34 indexed citations
10.
Matsuura, N., et al.. (2017). A case of fulminant type 1 diabetes masquerading acute pancreatitis. Journal of General and Family Medicine. 18(1). 32–34. 1 indexed citations
11.
Akazawa, Yohei, Yuji Inaba, Akira Hachiya, et al.. (2015). Reversible cerebral vasoconstriction syndrome and posterior reversible encephalopathy syndrome in a boy with Loeys‐Dietz syndrome. American Journal of Medical Genetics Part A. 167(10). 2435–2439. 15 indexed citations
12.
Morisaki, Hiroko & Takayuki Morisaki. (2014). Loeys-Dietz Syndrome. 30(3). 232–238. 3 indexed citations
13.
Kono, Atsushi K., Masahiro Higashi, Hiroko Morisaki, et al.. (2013). Prevalence of Dural Ectasia in Loeys-Dietz Syndrome: Comparison with Marfan Syndrome and Normal Controls. PLoS ONE. 8(9). e75264–e75264. 14 indexed citations
14.
Iwasa, Toru, et al.. (2011). Neonatal Marfan Syndrome and Review of 12 Cases in Japan. 27(6). 262–269.
15.
Hidaka, Koushi, Hiroko Morisaki, Manabu Shirai, et al.. (2004). Serine–arginine-rich nuclear protein Luc7l regulates myogenesis in mice. Gene. 341. 41–47. 13 indexed citations
16.
Ito, Toshikazu, Suenori Chiku, Eisuke Inoue, et al.. (2003). Estimation of Haplotype Frequencies, Linkage-Disequilibrium Measures, and Combination of Haplotype Copies in Each Pool by Use of Pooled DNA Data. The American Journal of Human Genetics. 72(2). 384–398. 46 indexed citations
17.
Morisaki, Takayuki, Hiroko Morisaki, I. Higuchi, Mitsuhiro Osame, & Mayumi Abé. (1999). Real defect of AMPD1 accompanied with myopathy: new missense mutations found in a Japanese patient. Cellular & Molecular Biology Letters. 4(3). 1 indexed citations
18.
Bhuiyan, Zahurul A., Hitomi Yatsuki, Toshiyuki Sasaguri, et al.. (1999). Functional analysis of the p57 KIP2 gene mutation in Beckwith-Wiedemann syndrome. Human Genetics. 104(3). 205–210. 26 indexed citations
19.
Nagabukuro, Akira, Yoichi Matsuda, Hiroko Morisaki, et al.. (1997). Genomic organization of Ampd3, heart-type AMPD gene, located in mouse Chromosome 7. Mammalian Genome. 8(10). 767–769. 6 indexed citations
20.
Hatada, Izuho, Hirofumi Ohashi, Yoshimitsu Fukushima, et al.. (1996). An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome. Nature Genetics. 14(2). 171–173. 287 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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