Jamiyan Purevsuren

683 total citations
25 papers, 513 citations indexed

About

Jamiyan Purevsuren is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jamiyan Purevsuren has authored 25 papers receiving a total of 513 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Clinical Biochemistry, 19 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jamiyan Purevsuren's work include Metabolism and Genetic Disorders (20 papers), Mitochondrial Function and Pathology (14 papers) and Neonatal Health and Biochemistry (4 papers). Jamiyan Purevsuren is often cited by papers focused on Metabolism and Genetic Disorders (20 papers), Mitochondrial Function and Pathology (14 papers) and Neonatal Health and Biochemistry (4 papers). Jamiyan Purevsuren collaborates with scholars based in Japan, United States and China. Jamiyan Purevsuren's co-authors include Seiji Yamaguchi, Yuki Hasegawa, Hironori Kobayashi, Seiji Fukuda, Takeshi Taketani, Yuichi Mushimoto, Hong Li, Toshiyuki Fukao, Kenji Yamada and Yosuke Shigematsu and has published in prestigious journals such as PLoS ONE, The Journal of Pediatrics and Analytical and Bioanalytical Chemistry.

In The Last Decade

Jamiyan Purevsuren

24 papers receiving 502 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jamiyan Purevsuren Japan	14	384	373	78	75	55	25	513
Darius J. Adams United States	10	328 0.9×	328 0.9×	76 1.0×	102 1.4×	64 1.2×	17	464
Keow Giak Sim Australia	12	399 1.0×	335 0.9×	112 1.4×	94 1.3×	105 1.9×	13	512
Vassiliki Konstantopoulou Austria	14	344 0.9×	288 0.8×	92 1.2×	90 1.2×	75 1.4×	33	484
Inga Knudsen Denmark	11	463 1.2×	448 1.2×	103 1.3×	90 1.2×	94 1.7×	13	588
W. Oostheim Netherlands	13	266 0.7×	398 1.1×	64 0.8×	60 0.8×	35 0.6×	16	550
A. Kimberly Iafolla United States	9	367 1.0×	298 0.8×	139 1.8×	104 1.4×	47 0.9×	13	517
Sunita Bijarnia‐Mahay India	13	241 0.6×	257 0.7×	133 1.7×	75 1.0×	65 1.2×	63	522
Gaetano Sabetta Italy	10	402 1.0×	340 0.9×	174 2.2×	125 1.7×	78 1.4×	11	631
Francjan van Spronsen Netherlands	10	253 0.7×	249 0.7×	56 0.7×	157 2.1×	74 1.3×	14	414
Vladimir Sarnavka Croatia	10	179 0.5×	272 0.7×	48 0.6×	52 0.7×	186 3.4×	25	445

Countries citing papers authored by Jamiyan Purevsuren

Since Specialization

Citations

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

Fields of papers citing papers by Jamiyan Purevsuren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jamiyan Purevsuren

This figure shows the co-authorship network connecting the top 25 collaborators of Jamiyan Purevsuren. A scholar is included among the top collaborators of Jamiyan Purevsuren 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 Jamiyan Purevsuren. Jamiyan Purevsuren 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

1.

Hasegawa, Yuki, Kenji Yamada, Hironori Kobayashi, et al.. (2018). Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening. Molecular Genetics and Metabolism Reports. 16. 5–10. 88 indexed citations

2.

Yamada, Kenji, Hironori Kobayashi, Jamiyan Purevsuren, et al.. (2017). Clinical and molecular investigation of 14 Japanese patients with complete TFP deficiency: a comparison with Caucasian cases. Journal of Human Genetics. 62(9). 809–814. 20 indexed citations

3.

Abe, Mariko, Louis M. Pelus, Pratibha Singh, et al.. (2016). Internal Tandem Duplication in FLT3 Attenuates Proliferation and Regulates Resistance to the FLT3 Inhibitor AC220 by Modulating p21Cdkn1a and Pbx1 in Hematopoietic Cells. PMC.

4.

Kobayashi, Hironori, Seiji Fukuda, Kenji Yamada, et al.. (2016). Clinical Features of Carnitine Deficiency Secondary to Pivalate-Conjugated Antibiotic Therapy. The Journal of Pediatrics. 173. 183–187. 19 indexed citations

5.

Yamada, Kenji, Hironori Kobayashi, Jamiyan Purevsuren, et al.. (2016). Efficacy of bezafibrate on fibroblasts of glutaric acidemia type II patients evaluated using an in vitro probe acylcarnitine assay. Brain and Development. 39(1). 48–57. 14 indexed citations

6.

Purevsuren, Jamiyan, et al.. (2016). The first Mongolian cases of phenylketonuria in selective screening of inborn errors of metabolism. Molecular Genetics and Metabolism Reports. 9. 71–74. 5 indexed citations

7.

Abe, Mariko, Louis M. Pelus, Pratibha Singh, et al.. (2016). Internal Tandem Duplication in FLT3 Attenuates Proliferation and Regulates Resistance to the FLT3 Inhibitor AC220 by Modulating p21Cdkn1a and Pbx1 in Hematopoietic Cells. PLoS ONE. 11(7). e0158290–e0158290. 11 indexed citations

8.

Ochi, Nobuhiko, Jamiyan Purevsuren, Kenichiro Yamada, et al.. (2014). Mutations in HADHB, which encodes the β‐subunit of mitochondrial trifunctional protein, cause infantile onset hypoparathyroidism and peripheral polyneuropathy. American Journal of Medical Genetics Part A. 164(5). 1180–1187. 26 indexed citations

9.

Yamaguchi, Seiji, Hong Li, Jamiyan Purevsuren, et al.. (2012). Bezafibrate can be a new treatment option for mitochondrial fatty acid oxidation disorders: Evaluation by in vitro probe acylcarnitine assay. Molecular Genetics and Metabolism. 107(1-2). 87–91. 40 indexed citations

10.

Purevsuren, Jamiyan, Yuki Hasegawa, Seiji Fukuda, et al.. (2012). Clinical and molecular aspects of Japanese children with medium chain acyl-CoA dehydrogenase deficiency. Molecular Genetics and Metabolism. 107(1-2). 237–240. 9 indexed citations

11.

Purevsuren, Jamiyan, Hironori Kobayashi, Yuki Hasegawa, et al.. (2012). Intracellular in vitro probe acylcarnitine assay for identifying deficiencies of carnitine transporter and carnitine palmitoyltransferase-1. Analytical and Bioanalytical Chemistry. 405(4). 1345–1351. 1 indexed citations

12.

Hasegawa, Yuki, Seiji Fukuda, Hironori Kobayashi, et al.. (2010). In vitro probe acylcarnitine profiling assay using cultured fibroblasts and electrospray ionization tandem mass spectrometry predicts severity of patients with glutaric aciduria type 2. Journal of Chromatography B. 878(20). 1673–1676. 6 indexed citations

13.

Mushimoto, Yuichi, Seiji Fukuda, Yuki Hasegawa, et al.. (2010). Clinical and molecular investigation of 19 Japanese cases of glutaric acidemia type 1. Molecular Genetics and Metabolism. 102(3). 343–348. 78 indexed citations

14.

Li, Hong, Seiji Fukuda, Yuki Hasegawa, et al.. (2010). Heat stress deteriorates mitochondrial β-oxidation of long-chain fatty acids in cultured fibroblasts with fatty acid β-oxidation disorders. Journal of Chromatography B. 878(20). 1669–1672. 11 indexed citations

15.

Li, Hong, Seiji Fukuda, Yuki Hasegawa, et al.. (2009). Effect of heat stress and bezafibrate on mitochondrial β-oxidation: Comparison between cultured cells from normal and mitochondrial fatty acid oxidation disorder children using in vitro probe acylcarnitine profiling assay. Brain and Development. 32(5). 362–370. 21 indexed citations

16.

Mushimoto, Yuichi, Yuki Hasegawa, Hironori Kobayashi, et al.. (2009). Enzymatic evaluation of glutaric acidemia type 1 by an in vitro probe assay of acylcarnitine profiling using fibroblasts and electrospray ionization/tandem mass spectrometry (MS/MS). Journal of Chromatography B. 877(25). 2648–2651. 2 indexed citations

17.

Purevsuren, Jamiyan, Toshiyuki Fukao, Yuki Hasegawa, et al.. (2009). Clinical and molecular aspects of Japanese patients with mitochondrial trifunctional protein deficiency. Molecular Genetics and Metabolism. 98(4). 372–377. 26 indexed citations

18.

Purevsuren, Jamiyan, Hironori Kobayashi, Yuki Hasegawa, et al.. (2008). A novel molecular aspect of Japanese patients with medium-chain acyl-CoA dehydrogenase deficiency (MCADD): c.449-452delCTGA is a common mutation in Japanese patients with MCADD. Molecular Genetics and Metabolism. 96(2). 77–79. 21 indexed citations

19.

Purevsuren, Jamiyan, et al.. (2008). Urinary organic metabolite screening of children with influenza-associated encephalopathy for inborn errors of metabolism using GC/MS. Brain and Development. 30(8). 520–526. 11 indexed citations

20.

Kobayashi, Hironori, et al.. (2007). ESI–MS/MS study of acylcarnitine profiles in urine from patients with organic acidemias and fatty acid oxidation disorders. Journal of Chromatography B. 855(1). 80–87. 20 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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