Rika Fujimaru

1.2k total citations
21 papers, 542 citations indexed

About

Rika Fujimaru is a scholar working on Surgery, Molecular Biology and Nephrology. According to data from OpenAlex, Rika Fujimaru has authored 21 papers receiving a total of 542 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Surgery, 6 papers in Molecular Biology and 6 papers in Nephrology. Recurrent topics in Rika Fujimaru's work include Complement system in diseases (6 papers), Pancreatic function and diabetes (6 papers) and Renal Diseases and Glomerulopathies (5 papers). Rika Fujimaru is often cited by papers focused on Complement system in diseases (6 papers), Pancreatic function and diabetes (6 papers) and Renal Diseases and Glomerulopathies (5 papers). Rika Fujimaru collaborates with scholars based in Japan, United States and Iran. Rika Fujimaru's co-authors include Kazumoto Iijima, Yuki Hosokawa, Tohru Yorifuji, Rie Kawakita, Hironori Nagasaka, Kandai Nozu, Jun Inatomi, Tomohiko Yamamura, Atsuko Nakagawa and Tatsuhiko Urakami and has published in prestigious journals such as Journal of Medical Genetics, Clinical Endocrinology and Diabetic Medicine.

In The Last Decade

Rika Fujimaru

21 papers receiving 532 citations

Peers

Rika Fujimaru

SURGE

GENET

NEPHR

EDM

Giuseppe Loffredo Italy

Whitney Besse United States

Karen L. Imfeld United States

Marika Kvarnström Sweden

Masahiro Muto Japan

Antónia Szántó Hungary

Sladjana Andrejević Serbia

J P Grünfeld France

Ikuyo Miyake Japan

Elena Gallo MacFarlane United States

Giuseppe Loffredo Italy

Rika Fujimaru

88 ×0.5

68 ×0.4

SURGE

86 ×0.5

GENET

37 ×0.3

NEPHR

71 ×0.7

EDM

Citations per year, relative to Rika Fujimaru Rika Fujimaru (= 1×) peers Giuseppe Loffredo

Countries citing papers authored by Rika Fujimaru

Since Specialization

Citations

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

Fields of papers citing papers by Rika Fujimaru

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rika Fujimaru

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

All Works

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20 of 20 papers shown

Ashida, Akira, Hideki Matsumura, Toshihiro Sawai, et al.. (2018). Clinical features in a series of 258 Japanese pediatric patients with thrombotic microangiopathy. Clinical and Experimental Nephrology. 22(4). 924–930. 8 indexed citations

Nozu, Kandai, Koichi Nakanishi, Yoshifusa Abe, et al.. (2018). A review of clinical characteristics and genetic backgrounds in Alport syndrome. Clinical and Experimental Nephrology. 23(2). 158–168. 127 indexed citations

Yamamura, Tomohiko, Kandai Nozu, Hiroaki Ueda, et al.. (2018). Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes. Journal of Human Genetics. 63(6). 755–759. 7 indexed citations

Yamamura, Tomohiko, Kandai Nozu, Keita Nakanishi, et al.. (2017). An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis. BMC Nephrology. 18(1). 353–353. 13 indexed citations

Kato, Hideki, Masaomi Nangaku, Hiroshi Hataya, et al.. (2016). Clinical guides for atypical hemolytic uremic syndrome in Japan. Clinical and Experimental Nephrology. 20(4). 536–543. 40 indexed citations

Hashimoto, Yukiko, Rie Kawakita, Yuki Hosokawa, et al.. (2015). Focal form of congenital hyperinsulinism clearly detectable by contrast-enhanced computed tomography imaging. International Journal of Pediatric Endocrinology. 2015(1). 20–20. 2 indexed citations

Yorifuji, Tohru, Keiko Matsubara, Yukiko Hashimoto, et al.. (2015). Abnormalities in chromosome 6q24 as a cause of early‐onset, non‐obese, non‐autoimmune diabetes mellitus without history of neonatal diabetes. Diabetic Medicine. 32(7). 963–967. 16 indexed citations

Yorifuji, Tohru, Yukiko Hashimoto, Rie Kawakita, et al.. (2014). Relapsing 6q24-related transient neonatal diabetes mellitus successfully treated with a dipeptidyl peptidase-4 inhibitor: a case report. Pediatric Diabetes. 15(8). 606–610. 11 indexed citations

Kawakita, Rie, Yuki Hosokawa, Rika Fujimaru, et al.. (2014). Molecular and clinical characterization of glucokinase maturity‐onset diabetes of the young (GCK‐MODY) in Japanese patients. Diabetic Medicine. 31(11). 1357–1362. 22 indexed citations

10.

Sawai, Toshihiro, Masaomi Nangaku, Akira Ashida, et al.. (2013). Diagnostic criteria for atypical hemolytic uremic syndrome proposed by the joint committee of the Japanese society of nephrology and the Japan pediatric society. Clinical and Experimental Nephrology. 18(1). 4–9. 22 indexed citations

11.

Nakano, Yoshiko, Rika Fujimaru, Hiroaki Sakamoto, et al.. (2013). Childhood pheochromocytoma in a survivor of central primitive neuroectodermal tumor. Pediatrics International. 55(4). e100–2. 2 indexed citations

12.

Kagami, Shoji, Hirokazu Okada, Shinya Kaname, et al.. (2012). [Diagnostic criteria of atypical hemolytic uremic syndrome].. PubMed. 2(2). 91–3. 3 indexed citations

13.

Yorifuji, Tohru, Rie Kawakita, Yuki Hosokawa, et al.. (2012). Efficacy and safety of long‐term, continuous subcutaneous octreotide infusion for patients with different subtypes of K_ATP‐channel hyperinsulinism. Clinical Endocrinology. 78(6). 891–897. 34 indexed citations

14.

Yorifuji, Tohru, et al.. (2012). Dominantly inherited diabetes mellitus caused by GATA6 haploinsufficiency: variable intrafamilial presentation. Journal of Medical Genetics. 49(10). 642–643. 33 indexed citations

15.

Yorifuji, Tohru, Yuki Hosokawa, Rika Fujimaru, et al.. (2011). Lasting <sup>18</sup>F-DOPA PET Uptake after Clinical Remission of the Focal Form of Congenital Hyperinsulinism. Hormone Research in Paediatrics. 76(4). 286–290. 16 indexed citations

16.

Yorifuji, Tohru, Rika Fujimaru, Yuki Hosokawa, et al.. (2011). Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus. Pediatric Diabetes. 13(1). 26–32. 71 indexed citations

17.

Kosaki, Rika, Rika Fujimaru, Hiroshi Yamada, et al.. (2007). Wide phenotypic variations within a family with SALL1 mutations: Isolated external ear abnormalities to Goldenhar syndrome. American Journal of Medical Genetics Part A. 143A(10). 1087–1090. 20 indexed citations

18.

Inatomi, Jun, Kentaro Matsuoka, Rika Fujimaru, Atsuko Nakagawa, & Kazumoto Iijima. (2006). Mechanisms of development and progression of cyanotic nephropathy. Pediatric Nephrology. 21(10). 1440–1445. 41 indexed citations

19.

Okada, Michiyo, Rika Fujimaru, Noriko Morimoto, et al.. (2006). EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditions. Pediatric Nephrology. 21(4). 475–481. 22 indexed citations

20.

Inatomi, Jun, Osamu Miyazaki, Rika Fujimaru, & Kazumoto Iijima. (2005). Renovascular hypertension complicated with VATER association. Pediatric Nephrology. 20(8). 1174–1176. 3 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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