Jun Akanuma

480 total citations
14 papers, 335 citations indexed

About

Jun Akanuma is a scholar working on Molecular Biology, Clinical Biochemistry and Organic Chemistry. According to data from OpenAlex, Jun Akanuma has authored 14 papers receiving a total of 335 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 4 papers in Organic Chemistry. Recurrent topics in Jun Akanuma's work include Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (6 papers) and Carbohydrate Chemistry and Synthesis (4 papers). Jun Akanuma is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (6 papers) and Carbohydrate Chemistry and Synthesis (4 papers). Jun Akanuma collaborates with scholars based in Japan, United States and Italy. Jun Akanuma's co-authors include Hirofumi Komaki, Yoichi Matsubara, Shigeo Kure, Kuniaki Narisawa, Ikuya Nonaka, Kunihiro Fujii, Yu‐ichi Goto, Kazutoshi Takahashi, Kazuie Iinuma and Takao Takahashi and has published in prestigious journals such as Pediatric Research, Human Mutation and American Journal of Medical Genetics.

In The Last Decade

Jun Akanuma

13 papers receiving 326 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jun Akanuma Japan	9	233	142	58	56	47	14	335
Lara Abulhoul United Kingdom	8	155 0.7×	135 1.0×	55 0.9×	52 0.9×	113 2.4×	12	311
Aline Cano France	13	288 1.2×	160 1.1×	85 1.5×	44 0.8×	79 1.7×	27	485
Ali Alasmari Saudi Arabia	10	222 1.0×	69 0.5×	69 1.2×	21 0.4×	26 0.6×	28	334
Ramona Salvarinova Canada	8	109 0.5×	80 0.6×	40 0.7×	24 0.4×	46 1.0×	18	202
Daisy Castiñeiras Spain	11	224 1.0×	265 1.9×	69 1.2×	111 2.0×	70 1.5×	16	438
Sonia Clavero United States	12	286 1.2×	165 1.2×	55 0.9×	59 1.1×	21 0.4×	15	351
Mohammad Arif Hossain Japan	12	113 0.5×	54 0.4×	34 0.6×	42 0.8×	196 4.2×	24	307
Ken Momosaki Japan	10	102 0.4×	47 0.3×	63 1.1×	77 1.4×	163 3.5×	22	286
Jean Larochelle Canada	5	95 0.4×	166 1.2×	56 1.0×	28 0.5×	66 1.4×	7	248
Celia Medrano Spain	7	100 0.4×	38 0.3×	67 1.2×	41 0.7×	30 0.6×	9	191

Countries citing papers authored by Jun Akanuma

Since Specialization

Citations

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

Fields of papers citing papers by Jun Akanuma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jun Akanuma

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

All Works

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14 of 14 papers shown

Tanaka, Noriko, Yu‐ichi Goto, Jun Akanuma, et al.. (2009). Mitochondrial DNA variants in a Japanese population of patients with Alzheimer’s disease. Mitochondrion. 10(1). 32–37. 36 indexed citations

Komaki, Hirofumi, Jun Akanuma, Hideki Iwata, et al.. (2003). A novel mtDNA C11777A mutation in Leigh syndrome. Mitochondrion. 2(4). 293–304. 43 indexed citations

Mimaki, Masakazu, et al.. (2003). A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy. Journal of Human Genetics. 48(1). 47–50. 27 indexed citations

Akanuma, Jun, et al.. (2000). Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene. Journal of Human Genetics. 45(6). 337–341. 33 indexed citations

Fujii, Kunihiro, Yoichi Matsubara, Jun Akanuma, et al.. (2000). Mutation detection by TaqMan-allele specific amplification: Application to molecular diagnosis of glycogen storage disease type Ia and medium-chain acyl-CoA dehydrogenase deficiency. Human Mutation. 15(2). 189–196. 51 indexed citations

Takahashi, Kazutoshi, Jun Akanuma, Yoichi Matsubara, et al.. (2000). Heterogeneous mutations in the glucose-6-phosphatase gene in Japanese patients with glycogen storage disease type Ia. American Journal of Medical Genetics. 92(2). 90–94. 12 indexed citations

Matsubara, Yoichi, Jun Akanuma, Kazutoshi Takahashi, et al.. (2000). Mutation detection by TaqMan-allele specific amplification: Application to molecular diagnosis of glycogen storage disease type Ia and medium-chain acyl-CoA dehydrogenase deficiency. Human Mutation. 15(2). 189–189. 1 indexed citations

Akanuma, Jun, Toshinori Nishigaki, Yoichi Matsubara, et al.. (2000). Glycogen storage disease type Ia: Molecular diagnosis of 51 Japanese patients and characterization of splicing mutations by analysis of ectopically transcribed mRNA from lymphoblastoid cells. American Journal of Medical Genetics. 91(2). 107–107.

Yoshida, Yukie, et al.. (2000). Slowly Progressive Dystonia Following Central Pontine and Extrapontine Myelinolysis.. Internal Medicine. 39(11). 956–960. 7 indexed citations

10.

Akanuma, Jun, Kunihiro Fujii, Koji Inui, et al.. (2000). Glycogen storage disease type Ia: Molecular diagnosis of 51 Japanese patients and characterization of splicing mutations by analysis of ectopically transcribed mRNA from lymphoblastoid cells. American Journal of Medical Genetics. 91(2). 107–112. 35 indexed citations

11.

Nagasaki, Yutaka, Yoichi Matsubara, Hideaki Takano, et al.. (1999). Reversal of Hypopigmentation in Phenylketonuria Mice by Adenovirus-Mediated Gene Transfer. Pediatric Research. 45(4, Part 1 of 2). 465–473. 39 indexed citations

12.

Akanuma, Jun, Patrizia Cavadini, Yoko Aoki, et al.. (1998). TwoCPT2 mutations in three Japanese patients with carnitine palmitoyltransferase II deficiency: Functional analysis and association with polymorphic haplotypes and two clinical phenotypes. Human Mutation. 11(5). 377–386. 49 indexed citations

13.

Akanuma, Jun, et al.. (1997). [Identification of missense mutations and haplotyping of carnitine palmitoyltransferase II gene].. PubMed. 55(12). 3297–301. 1 indexed citations

14.

Akanuma, Jun, Naoshi Saito, Masashi Aoki, Kazumichi Abe, & Toshiyuki Yamamoto. (1995). [Chorea with prominent spasticity associated with an expansion of the CAG trinucleotide repeat in the IT15 gene: a case report].. PubMed. 35(11). 1253–5. 1 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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