S. Aramaki

538 total citations
18 papers, 436 citations indexed

About

S. Aramaki is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, S. Aramaki has authored 18 papers receiving a total of 436 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 2 papers in Genetics. Recurrent topics in S. Aramaki's work include Metabolism and Genetic Disorders (10 papers), Enzyme function and inhibition (5 papers) and Ion Transport and Channel Regulation (5 papers). S. Aramaki is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Enzyme function and inhibition (5 papers) and Ion Transport and Channel Regulation (5 papers). S. Aramaki collaborates with scholars based in Japan, United States and Canada. S. Aramaki's co-authors include William L. Nyhan, Georg F. Hoffmann, Lawrence Sweetman, K. Michael Gibson, A. Hodson, C. Jakobs, Ichiro Yoshida, D. C. DeVivo, Makoto Yoshino and Hirohisa Kato and has published in prestigious journals such as Clinical Chemistry, Acta Neuropathologica and Human Mutation.

In The Last Decade

S. Aramaki

18 papers receiving 424 citations

Peers

Countries citing papers authored by S. Aramaki

Since Specialization

Citations

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

Fields of papers citing papers by S. Aramaki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Aramaki

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Complications in patients with neurological impairment after gastrostomy 2021 ·Pediatrics International ·(unknown), Naoki Hashizume, Suguru Fukahori, (unknown), (unknown), (unknown), S. Aramaki, (unknown), Eiko Takeshita, Yoshiaki Tanaka, Yushiro Yamashita, Minoru Yagi	3
2	Dietary chloride deficiency due to new liquid nutritional products 2008 ·Pediatrics International ·(unknown), S. Aramaki, Kenji Yokochi	1
3	Inter- and/or Intra-organ distribution of mitochondrial C3303T or A3243G mutation in mitochondrial cytopathy 2001 ·Acta Neuropathologica ·(unknown), Yasutoshi Koga, S. Aramaki, Seiya Kato, (unknown)	7
4	Two novel gene mutations (Glu174→Lys, Phe383→Tyr) causing the "hepatic" form of carnitine palmitoyltransferase II deficiency 1996 ·Human Genetics ·Shogo Yamamoto, Hiroki Abe, (unknown), (unknown), Akira Ohtake, Hidemasa Hayashibe, Hitoshi Sakuraba, Yoshiyuki Suzuki, S. Aramaki, Masaki Takayanagi, Shuji Hasegawa, Hiroo Niimi	34
5	A point mutation in exon 3 (His 107→Tyr) in two unrelated Japanese patients with carbonic anhydrase II deficiency with central nervous system involvement 1996 ·Human Genetics ·(unknown), (unknown), Ichiro Yoshida, Yasutoshi Koga, S. Aramaki, Hirohisa Kato	2
6	A point mutation in exon 3 (His 107→Tyr) in two unrelated Japanese patients with carbonic anhydrase II deficiency with central nervous system involvement 1996 ·Human Genetics ·(unknown), (unknown), Ichiro Yoshida, Yasutoshi Koga, S. Aramaki, Hirohisa Kato	17
7	Carbonic anhydrase II deficiency in a Japanese patient produced by a nonsense mutation (TAT →TAG) at Tyr-40 in exon 2, (Y40X) 1995 ·Human Mutation ·(unknown), (unknown), Ichiro Yoshida, S. Aramaki, Hirohisa Kato	12
8	Prenatal diagnosis and therapy for a patient with vitamin B₁₂‐responsive methylmalonic acidaemia 1994 ·Journal of Inherited Metabolic Disease ·(unknown), T. Ohura, Ichiro Yoshida, S. Aramaki, Kazuhiro Aoki, Takashi Inokuchi, Hitoshi Mikami, K. Narisawa	6
9	Carbonic Anhydrase II Deficiency. A Report of Two Cases. 1994 ·Orthopedics & Traumatology ·(unknown), (unknown), Ken Kusaba, (unknown), (unknown), (unknown), Akira Fujiwara, (unknown), (unknown), S. Aramaki	1
10	Carbonic anhydrase II deficiency in three unrelated Japanese patients 1993 ·Journal of Inherited Metabolic Disease ·S. Aramaki, Ichiro Yoshida, Makoto Yoshino, (unknown), Yoshihiro Satō, Kohei Noda, (unknown), (unknown), (unknown), Fumiyoshi Yamashita	26
11	Erythematous skin lesions and partial deficiency of 3‐methylcrotonyl‐CoA carboxylase in peripheral lymphocytes in a patient with propionic acidaemia 1991 ·Journal of Inherited Metabolic Disease ·Makoto Yoshino, S. Aramaki, Fumio Yamashita, Kanji Sato, Yoshito Inoue, Tomiko Kuhara, I. Matsumoto	3
12	Stable isotope dilution analysis of 4-hydroxybutyric acid: An accurate method for quantification in physiological fluids and the prenatal diagnosis of 4-hydroxybutyric aciduria 1990 ·Journal of Mass Spectrometry ·K. Michael Gibson, S. Aramaki, Lawrence Sweetman, William L. Nyhan, D. C. DeVivo, A. Hodson, C. Jakobs	82
13	Urinary excretion of 2‐methylacetoacetate, 2‐methyl‐3‐hydroxybutyrate and tiglylglycine after isoleucine loading in the diagnosis of 2‐methylacetoacetyl‐CoA thiolase deficiency 1990 ·Journal of Inherited Metabolic Disease ·S. Aramaki, Denis C. Lehotay, Lawrence Sweetman, William L. Nyhan, Susan Winter, B. Middleton	21
14	Quantitative analysis for organic acids in biological samples: batch isolation followed by gas chromatographic-mass spectrometric analysis. 1989 ·Clinical Chemistry ·Georg F. Hoffmann, S. Aramaki, (unknown), William L. Nyhan, (unknown)	173
15	4-Hydroxybutyric aciduria in a patient without ataxia or convulsions 1988 ·European Journal of Pediatrics ·K. Michael Gibson, Georg F. Hoffmann, William L. Nyhan, S. Aramaki, J. Thompson, Stephen I. Goodman, Debra Johnson, (unknown)	12
16	Methylcitrate in maternal urine during a pregnancy with a fetus affected with propionic acidaemia 1988 ·Journal of Inherited Metabolic Disease ·S. Aramaki, Denis C. Lehotay, William L. Nyhan, Patrick MacLeod, Lawrence Sweetman	3
17	New Diagnostic Techniques for the Detection of OrganicAcidemias 1987 ·Enzyme ·Lawrence Sweetman, Georg F. Hoffmann, S. Aramaki	8
18	Dihydrolipoyl dehydrogenase deficiency: a therapeutic trial with branched-chain amino acid restriction 1986 ·European Journal of Pediatrics ·Yuriko Sakaguchi, Makoto Yoshino, S. Aramaki, Ichiro Yoshida, Fumiyoshi Yamashita, Tomiko Kuhara, I. Matsumoto, Tokishi Hayashi	25

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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