Marjatta Son

815 total citations
20 papers, 647 citations indexed

About

Marjatta Son is a scholar working on Molecular Biology, Neurology and Ecology. According to data from OpenAlex, Marjatta Son has authored 20 papers receiving a total of 647 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Neurology and 8 papers in Ecology. Recurrent topics in Marjatta Son's work include Amyotrophic Lateral Sclerosis Research (9 papers), Bacteriophages and microbial interactions (8 papers) and Neurological diseases and metabolism (5 papers). Marjatta Son is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (9 papers), Bacteriophages and microbial interactions (8 papers) and Neurological diseases and metabolism (5 papers). Marjatta Son collaborates with scholars based in United States, Uruguay and Australia. Marjatta Son's co-authors include Jeffrey L. Elliott, Krishna Puttaparthi, Philip Serwer, Giovanni Manfredi, Philip J. Boyer, Hibiki Kawamata, William L. Gitomer, Valeria Culotta, Robert H. Watson and Shirley J. Hayes and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Marjatta Son

19 papers receiving 634 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marjatta Son United States 12 351 253 205 153 118 20 647
Barbara M. Ross United States 12 123 0.4× 364 1.4× 508 2.5× 120 0.8× 18 0.2× 17 1.0k
E. Danciger Israel 10 75 0.2× 284 1.1× 112 0.5× 54 0.4× 34 0.3× 11 540
Edwin M. Labut United States 9 76 0.2× 129 0.5× 112 0.5× 57 0.4× 29 0.2× 11 370
Stefanie D. Boyd United States 10 66 0.2× 126 0.5× 176 0.9× 53 0.3× 18 0.2× 14 369
Małgorzata Goralska United States 12 40 0.1× 242 1.0× 111 0.5× 41 0.3× 35 0.3× 19 411
Marco Rimoldi Italy 13 31 0.1× 621 2.5× 26 0.1× 128 0.8× 20 0.2× 17 908
Hilda Brown United States 15 305 0.9× 289 1.1× 32 0.2× 81 0.5× 135 1.1× 24 498
Joy Mitra United States 19 497 1.4× 777 3.1× 33 0.2× 108 0.7× 221 1.9× 39 1.2k
Stéphanie Delga France 8 19 0.1× 132 0.5× 107 0.5× 58 0.4× 175 1.5× 10 493

Countries citing papers authored by Marjatta Son

Since Specialization
Citations

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

Fields of papers citing papers by Marjatta Son

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marjatta Son

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

All Works

20 of 20 papers shown
1.
Trías, Emiliano, Nathan I. Lopez, Edwin M. Labut, et al.. (2016). Copper delivery to the CNS by CuATSM effectively treats motor neuron disease in SODG93A mice co-expressing the Copper-Chaperone-for-SOD. Neurobiology of Disease. 89. 1–9. 122 indexed citations
2.
Son, Marjatta & Jeffrey L. Elliott. (2013). Mitochondrial defects in transgenic mice expressing Cu,Zn Superoxide Dismutase mutations, the role of Copper Chaperone for SOD1. Journal of the Neurological Sciences. 336(1-2). 1–7. 21 indexed citations
3.
Son, Marjatta, et al.. (2011). Biochemical properties and in vivo effects of the SOD1 zinc‐binding site mutant (H80G). Journal of Neurochemistry. 118(5). 891–901. 9 indexed citations
4.
Son, Marjatta, et al.. (2009). Redox susceptibility of SOD1 mutants is associated with the differential response to CCS over-expression in vivo. Neurobiology of Disease. 34(1). 155–162. 28 indexed citations
5.
Son, Marjatta, Scot C. Leary, Nadine Romain, et al.. (2008). Isolated Cytochrome c Oxidase Deficiency in G93A SOD1 Mice Overexpressing CCS Protein. Journal of Biological Chemistry. 283(18). 12267–12275. 42 indexed citations
6.
Son, Marjatta, et al.. (2008). Biological effects of CCS in the absence of SOD1 enzyme activation: implications for disease in a mouse model for ALS. Human Molecular Genetics. 17(12). 1728–1737. 56 indexed citations
7.
Son, Marjatta, Krishna Puttaparthi, Hibiki Kawamata, et al.. (2007). Overexpression of CCS in G93A-SOD1 mice leads to accelerated neurological deficits with severe mitochondrial pathology. Proceedings of the National Academy of Sciences. 104(14). 6072–6077. 133 indexed citations
8.
Son, Marjatta, et al.. (2006). Novel Mutations that Enhance or Repress the Aggregation Potential of SOD1. Molecular and Cellular Biochemistry. 287(1-2). 201–211. 11 indexed citations
9.
Son, Marjatta, et al.. (2003). Aggregate Formation in Cu,Zn Superoxide Dismutase-related Proteins. Journal of Biological Chemistry. 278(16). 14331–14336. 35 indexed citations
10.
Serwer, Philip, Robert H. Watson, & Marjatta Son. (2003). In-Gel Detection of DNA: Application to Study of Viral DNA Metabolism by Use of Pulsed-Field Agarose Gel Electrophoresis. Humana Press eBooks. 12. 333–344.
11.
Puttaparthi, Krishna, et al.. (2002). Disease Progression in a Transgenic Model of Familial Amyotrophic Lateral Sclerosis Is Dependent on Both Neuronal and Non-Neuronal Zinc Binding Proteins. Journal of Neuroscience. 22(20). 8790–8796. 96 indexed citations
12.
Sun, Mao, Marjatta Son, & Philip Serwer. (1997). Formation and Cleavage of a DNA Network during in Vitro Bacteriophage T7 DNA Packaging:  Light Microscopy of DNA Metabolism. Biochemistry. 36(42). 13018–13026. 6 indexed citations
13.
Son, Marjatta, et al.. (1995). c-fos and HSP70 gene expression in rat brains in high gravitation-induced cerebral ischemia. Neuroscience Letters. 200(2). 81–84. 5 indexed citations
14.
15.
Son, Marjatta, Robert H. Watson, & Philip Serwer. (1993). The Direction and Rate of Bacteriophage T7 DNA Packaging in Vitro. Virology. 196(1). 282–289. 13 indexed citations
16.
Son, Marjatta & Philip Serwer. (1992). Role of exonuclease in the specificity of bacteriophage T7 DNA packaging. Virology. 190(2). 824–833. 10 indexed citations
17.
Serwer, Philip, Robert H. Watson, & Marjatta Son. (1990). Role of gene 6 exonuclease in the replication and packaging of bacteriophage T7 DNA. Journal of Molecular Biology. 215(2). 287–299. 16 indexed citations
18.
Son, Marjatta, Robert H. Watson, & Philip Serwer. (1990). In-gel hybridization of DNA separated by pulsed field agarose gel electrophoresis. Nucleic Acids Research. 18(10). 3098–3098. 9 indexed citations
19.
Son, Marjatta, Shirley J. Hayes, & Philip Serwer. (1989). Optimization of the in vitro packaging efficiency of bacteriophage T7 DNA: effects of neutral polymers. Gene. 82(2). 321–325. 9 indexed citations
20.

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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