Fumiaki Kamada

1.3k total citations · 1 hit paper
12 papers, 853 citations indexed

About

Fumiaki Kamada is a scholar working on Molecular Biology, Clinical Biochemistry and Sensory Systems. According to data from OpenAlex, Fumiaki Kamada has authored 12 papers receiving a total of 853 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 3 papers in Sensory Systems. Recurrent topics in Fumiaki Kamada's work include Metabolism and Genetic Disorders (4 papers), Ion Channels and Receptors (3 papers) and RNA modifications and cancer (2 papers). Fumiaki Kamada is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Ion Channels and Receptors (3 papers) and RNA modifications and cancer (2 papers). Fumiaki Kamada collaborates with scholars based in Japan, Israel and Germany. Fumiaki Kamada's co-authors include Shigeo Kure, Yoko Aoki, Yoichi Matsubara, Ayumi Narisawa, Junko Kanno, Tetsuya Niihori, Shigeru Tsuchiya, Shoko Komatsuzaki, Akira Hata and Atsuo Kikuchi and has published in prestigious journals such as Annals of Neurology, American Journal of Physiology-Renal Physiology and Journal of Medical Genetics.

In The Last Decade

Fumiaki Kamada

12 papers receiving 846 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A genome-wide association study identifies RNF213 as the first Moyamoya disease gene

2010 514 citations Fumiaki Kamada, Yoko Aoki et al. Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fumiaki Kamada Japan	10	483	328	249	238	160	12	853
Junko Kanno Japan	12	487 1.0×	329 1.0×	264 1.1×	240 1.0×	139 0.9×	33	850
Shoko Komatsuzaki Germany	8	469 1.0×	333 1.0×	148 0.6×	240 1.0×	138 0.9×	13	664
David Kronn United States	15	274 0.6×	284 0.9×	362 1.5×	66 0.3×	79 0.5×	35	1.0k
Yoichi Mashimo Japan	12	481 1.0×	331 1.0×	127 0.5×	252 1.1×	201 1.3×	24	835
Ting‐Rong Hsu Taiwan	16	178 0.4×	89 0.3×	201 0.8×	113 0.5×	32 0.2×	53	780
Mislen Bauer United States	10	208 0.4×	109 0.3×	143 0.6×	63 0.3×	73 0.5×	19	561
Argirios Dinopoulos Greece	14	40 0.1×	153 0.5×	410 1.6×	89 0.4×	65 0.4×	43	998
James D. Weisfeld‐Adams United States	14	286 0.6×	50 0.2×	284 1.1×	40 0.2×	20 0.1×	27	663
Thorsten Rosenbaum Germany	19	167 0.3×	582 1.8×	237 1.0×	38 0.2×	190 1.2×	39	899
Guilhem Solé France	15	107 0.2×	176 0.5×	250 1.0×	37 0.2×	95 0.6×	62	731

Countries citing papers authored by Fumiaki Kamada

Since Specialization

Citations

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

Fields of papers citing papers by Fumiaki Kamada

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fumiaki Kamada

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

All Works

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12 of 12 papers shown

Isobe, Kiyoshi, Takayasu Mori, Takako Asano, et al.. (2013). Development of enzyme-linked immunosorbent assays for urinary thiazide-sensitive Na-Cl cotransporter measurement. American Journal of Physiology-Renal Physiology. 305(9). F1374–F1381. 32 indexed citations

Kamada, Fumiaki, Yoko Aoki, Ayumi Narisawa, et al.. (2010). A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. Journal of Human Genetics. 56(1). 34–40. 514 indexed citations breakdown →

Hino‐Fukuyo, Naomi, Kazuhiro Haginoya, Mitsugu Uematsu, et al.. (2009). Smith-Magenis Syndrome With West Syndrome in a 5-Year-Old Girl: A Long-Term Follow-Up Study. Journal of Child Neurology. 24(7). 868–873. 5 indexed citations

Kure, Shigeo, Akiko Ichinohe, Toshikatsu Shinka, et al.. (2008). Model Mice for Mild-Form Glycine Encephalopathy: Behavioral and Biochemical Characterizations and Efficacy of Antagonists for the Glycine Binding Site of N-Methyl D-Aspartate Receptor. Pediatric Research. 64(3). 228–233. 7 indexed citations

Takano, Kyoko, Eiji Nakagawa, Ken Inoue, et al.. (2007). A loss‐of‐function mutation in the FTSJ1 gene causes nonsyndromic X‐linked mental retardation in a japanese family. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(4). 479–484. 36 indexed citations

Kanno, Junko, Shigeo Kure, Ayumi Narisawa, et al.. (2007). Allelic and non-allelic heterogeneities in pyridoxine dependent seizures revealed by ALDH7A1 mutational analysis. Molecular Genetics and Metabolism. 91(4). 384–389. 36 indexed citations

Kanno, Jun, Tim Hutchin, Fumiaki Kamada, et al.. (2007). Genomic deletion within GLDC is a major cause of non-ketotic hyperglycinaemia. Journal of Medical Genetics. 44(3). e69–e69. 44 indexed citations

Kure, Shigeo, Stanley H. Korman, Junko Kanno, et al.. (2006). Rapid diagnosis of glycine encephalopathy by ¹³C‐glycine breath test. Annals of Neurology. 59(5). 862–867. 14 indexed citations

Kamada, Fumiaki, Shigeo Kure, Takayuki Kudo, et al.. (2006). A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype–phenotype correlation. Journal of Human Genetics. 51(5). 455–460. 40 indexed citations

10.

Hasegawa, Koichi, Mayumi Tamari, Makiko Shimizu, et al.. (2004). Variations in the C3, C3a receptor, and C5 genes affect susceptibility to bronchial asthma. Human Genetics. 115(4). 295–301. 74 indexed citations

11.

Kojima, Kanako, Shigeo Kure, Fumiaki Kamada, et al.. (2004). Genetic testing of glycogen storage disease type Ib in Japan: five novel G6PT1 mutations and a rapid detection method for a prevalent mutation W118R. Molecular Genetics and Metabolism. 81(4). 343–346. 11 indexed citations

12.

Kamada, Fumiaki, Yoichi Suzuki, Mayumi Tamari, et al.. (2004). Association of the hCLCA1 gene with childhood and adult asthma. Genes and Immunity. 5(7). 540–547. 40 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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