Rie Kawamura

613 total citations
26 papers, 283 citations indexed

About

Rie Kawamura is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Rie Kawamura has authored 26 papers receiving a total of 283 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 10 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Rie Kawamura's work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Connective tissue disorders research (3 papers). Rie Kawamura is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Connective tissue disorders research (3 papers). Rie Kawamura collaborates with scholars based in Japan, Taiwan and Norway. Rie Kawamura's co-authors include Keiko Wakui, Tomoki Kosho, Yoshimitsu Fukushima, Akira Aoki, Norihito Saito, Yuichi Izumi, Taichen Lin, Naomichi Matsumoto, Yasuhiko Igawa and Atsushi Hatamochi and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and Biomedical Optics Express.

In The Last Decade

Rie Kawamura

23 papers receiving 272 citations

Peers

Rie Kawamura
Colleen D’Arcy Australia
Fassil B. Mesfin United States
Audrey Desgrange France
George C. Gabriel United States
S. Lee South Korea
Jean H. Flockhart United Kingdom
Cassandra R. Farthing United Kingdom
Marie‐Pierre Cordier France
Kahei Sato Japan
La‐ongsri Atchaneeyasakul Thailand
Colleen D’Arcy Australia
Rie Kawamura
Citations per year, relative to Rie Kawamura Rie Kawamura (= 1×) peers Colleen D’Arcy

Countries citing papers authored by Rie Kawamura

Since Specialization
Citations

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

Fields of papers citing papers by Rie Kawamura

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rie Kawamura

This figure shows the co-authorship network connecting the top 25 collaborators of Rie Kawamura. A scholar is included among the top collaborators of Rie Kawamura 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 Rie Kawamura. Rie Kawamura 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.
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.
2.
3.
Kawamura, Rie, et al.. (2021). A Turner syndrome case associated with dic(Y;22). Molecular Cytogenetics. 14(1). 34–34. 1 indexed citations
4.
Kawamura, Rie, Koji Mizutani, Taichen Lin, et al.. (2020). Ex Vivo Evaluation of Gingival Ablation with Various Laser Systems and Electroscalpel. Photobiomodulation Photomedicine and Laser Surgery. 38(6). 364–373. 13 indexed citations
5.
Kawamura, Rie, Takema Kato, Fumihiko Suzuki, et al.. (2020). A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia. Journal of Human Genetics. 65(8). 705–709. 13 indexed citations
6.
Suzuki, Fumihiko, Takema Kato, Rie Kawamura, et al.. (2019). Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome. Case Reports in Obstetrics and Gynecology. 2019. 1–5. 2 indexed citations
7.
Koitabashi, Norimichi, Tomomi Yamaguchi, Daisuke Fukui, et al.. (2018). Peripartum Iliac Arterial Aneurysm and Rupture in a Patient with Vascular Ehlers-Danlos Syndrome Diagnosed by Next-Generation Sequencing. International Heart Journal. 59(5). 1180–1185. 7 indexed citations
8.
Saito, Norihito, Taichen Lin, Rie Kawamura, et al.. (2018). High-energy, nanosecond pulsed Cr:CdSe laser with a 225–308 μm tuning range for laser biomaterial processing. Biomedical Optics Express. 9(11). 5645–5645. 23 indexed citations
9.
Nishi, Eriko, Rie Kawamura, Soichi Shibuya, et al.. (2018). Clinical courses of children with trisomy 13 receiving intensive neonatal and pediatric treatment. American Journal of Medical Genetics Part A. 176(9). 1941–1949. 15 indexed citations
10.
Takano, Kyoko, Mitsuo Motobayashi, Keiko Wakui, et al.. (2017). Early manifestations of epileptic encephalopathy, brain atrophy, and elevation of serum neuron specific enolase in a boy with beta-propeller protein-associated neurodegeneration. European Journal of Medical Genetics. 60(10). 521–526. 14 indexed citations
11.
Lin, Taichen, Rie Kawamura, Akira Aoki, et al.. (2016). Energy output reduction and surface alteration of quartz tips following Er:YAG laser contact irradiation on soft and hard tissues <i>in vitro </i>. Dental Materials Journal. 35(1). 51–62. 1 indexed citations
12.
Kawamura, Rie, Hideyuki Tanabe, Takahito Wada, et al.. (2012). Visualization of the spatial positioning of the SNRPN, UBE3A, and GABRB3 genes in the normal human nucleus by three-color 3D fluorescence in situ hybridization. Chromosome Research. 20(6). 659–672. 11 indexed citations
13.
Narumi, Yoko, Tomoki Kosho, Masaaki Shiohara, et al.. (2010). Genital abnormalities in Pallister–Hall syndrome: Report of two patients and review of the literature. American Journal of Medical Genetics Part A. 152A(12). 3143–3147. 19 indexed citations
14.
Kosho, Tomoki, Noriko Miyake, Atsushi Hatamochi, et al.. (2010). A new Ehlers–Danlos syndrome with craniofacial characteristics, multiple congenital contractures, progressive joint and skin laxity, and multisystem fragility‐related manifestations. American Journal of Medical Genetics Part A. 152A(6). 1333–1346. 63 indexed citations
15.
Yamazaki, Masanori, Tomoki Kosho, Shigeo Kawachi, et al.. (2010). Cold‐induced sweating syndrome with neonatal features of Crisponi syndrome: Longitudinal observation of a patient homozygous for a CRLF1 mutation. American Journal of Medical Genetics Part A. 152A(3). 764–769. 12 indexed citations
16.
Kosho, Tomoki, Masatoki Ito, Chizuko Suzuki, et al.. (2010). Progressive aortic root and pulmonary artery aneurysms in a neonate with Loeys–Dietz syndrome type 1B. American Journal of Medical Genetics Part A. 152A(2). 417–421. 21 indexed citations
17.
Saito, Shoji, Rie Kawamura, Tomoki Kosho, et al.. (2008). Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5–11.1 Mb terminal deletion of 1p36. American Journal of Medical Genetics Part A. 146A(22). 2891–2897. 18 indexed citations
18.
Matsuda, Masako, et al.. (2002). Prevention of ventilatory disturbance while in the face‐down position after macular hole surgery. Nursing and Health Sciences. 4(3). 85–88. 5 indexed citations
19.
Kawamura, Rie, et al.. (2002). Operation and crystalline properties of electromagnetic casting. 2. 1652–1655.
20.
Kawamura, Rie, Niro Tayama, Atsushi Matsunaga, et al.. (1992). Retrospective Study of 971 Cases Undergone Laryngomicrosurgery for 9 Years.. Nihon Kikan Shokudoka Gakkai Kaiho. 43(5). 419–426.

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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