Mayra Eduardoff

1.3k total citations
20 papers, 936 citations indexed

About

Mayra Eduardoff is a scholar working on Genetics, Molecular Biology and Ecology. According to data from OpenAlex, Mayra Eduardoff has authored 20 papers receiving a total of 936 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 14 papers in Molecular Biology and 4 papers in Ecology. Recurrent topics in Mayra Eduardoff's work include Forensic and Genetic Research (13 papers), Molecular Biology Techniques and Applications (10 papers) and Genetic Associations and Epidemiology (8 papers). Mayra Eduardoff is often cited by papers focused on Forensic and Genetic Research (13 papers), Molecular Biology Techniques and Applications (10 papers) and Genetic Associations and Epidemiology (8 papers). Mayra Eduardoff collaborates with scholars based in Austria, United States and Spain. Mayra Eduardoff's co-authors include Walther Parson, Christopher Phillips, Christina Strobl, Catarina Xavier, M.V. Lareu, Carla Santos, Christian Ploner, Reinhard Kofler, Harald Niederegger and Johannes Rainer and has published in prestigious journals such as PLoS ONE, Leukemia and Genes.

In The Last Decade

Mayra Eduardoff

19 papers receiving 921 citations

Peers

Mayra Eduardoff

GENET

ECOLO

ARCHE

Dmitry Zubakov Netherlands

Yaran Yang China

Rachel Herndon Klein United States

Bjørnar Olaisen Norway

Dan Frumkin Israel

Adam Wasserstrom Israel

Raphael Sung United States

Lotte Henke Germany

Mark Barash Australia

Sofia B. Zuniga Netherlands

Dmitry Zubakov Netherlands

Mayra Eduardoff

853 ×1.3

435 ×0.7

GENET

118 ×0.8

ECOLO

270 ×2.6

36 ×0.4

ARCHE

Citations per year, relative to Mayra Eduardoff Mayra Eduardoff (= 1×) peers Dmitry Zubakov

Countries citing papers authored by Mayra Eduardoff

Since Specialization

Citations

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

Fields of papers citing papers by Mayra Eduardoff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mayra Eduardoff

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

Parsons, Thomas J., Andreas Tillmar, Mayra Eduardoff, et al.. (2025). Inter-platform evaluation of the MPSplex large-scale tri-allelic SNP panel for forensic identification. Forensic Science International Genetics. 77. 103233–103233.

Xavier, Catarina, Mayra Eduardoff, Barbara Bertoglio, et al.. (2021). Evaluation of DNA Extraction Methods Developed for Forensic and Ancient DNA Applications Using Bone Samples of Different Age. Genes. 12(2). 146–146. 33 indexed citations

Xavier, Catarina, M. de la Puente, Christopher Phillips, et al.. (2020). Forensic evaluation of the Asia Pacific ancestry-informative MAPlex assay. Forensic Science International Genetics. 48. 102344–102344. 16 indexed citations

Phillips, Christopher, et al.. (2019). Performance of ancestry-informative SNP and microhaplotype markers. Forensic Science International Genetics. 43. 102141–102141. 40 indexed citations

Phillips, Christopher, Dennis McNevin, Kenneth K. Kídd, et al.. (2019). MAPlex - A massively parallel sequencing ancestry analysis multiplex for Asia-Pacific populations. Forensic Science International Genetics. 42. 213–226. 43 indexed citations

Xavier, Catarina, Mayra Eduardoff, Christina Strobl, & Walther Parson. (2019). SD quants—Sensitive detection tetraplex-system for nuclear and mitochondrial DNA quantification and degradation inference. Forensic Science International Genetics. 42. 39–44. 20 indexed citations

Strobl, Christina, Mayra Eduardoff, Magdalena M. Buś, Marie Allen, & Walther Parson. (2018). Evaluation of the precision ID whole MtDNA genome panel for forensic analyses. Forensic Science International Genetics. 35. 21–25. 68 indexed citations

Parson, Walther, Mayra Eduardoff, Catarina Xavier, Barbara Bertoglio, & Maria Teschler‐Nicola. (2018). Resolving the matrilineal relationship of seven Late Bronze Age individuals from Stillfried, Austria. Forensic Science International Genetics. 36. 148–151. 8 indexed citations

Bleka, Øyvind, Mayra Eduardoff, Carla Santos, et al.. (2017). Open source software EuroForMix can be used to analyse complex SNP mixtures. Forensic Science International Genetics. 31. 105–110. 36 indexed citations

10.

Eduardoff, Mayra, et al.. (2017). Optimized mtDNA Control Region Primer Extension Capture Analysis for Forensically Relevant Samples and Highly Compromised mtDNA of Different Age and Origin. Genes. 8(10). 237–237. 44 indexed citations

11.

Bleka, Øyvind, Mayra Eduardoff, Carla Santos, et al.. (2017). Using EuroForMix to analyse complex SNP mixtures, up to six contributors. Forensic science international. Genetics supplement series. 6. e277–e279. 8 indexed citations

12.

Eduardoff, Mayra, T.E. Gross, Carla Santos, et al.. (2016). Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™. Forensic Science International Genetics. 23. 178–189. 50 indexed citations

13.

Pośpiech, Ewelina, Jeppe Dyrberg Andersen, M. van den Berge, et al.. (2015). Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness. PLoS ONE. 10(5). e0127852–e0127852. 50 indexed citations

14.

Eduardoff, Mayra, Carla Santos, M. de la Puente, et al.. (2015). Inter-laboratory evaluation of SNP-based forensic identification by massively parallel sequencing using the Ion PGM™. Forensic Science International Genetics. 17. 110–121. 106 indexed citations

15.

Gill, Peter, Hinda Haned, Mayra Eduardoff, et al.. (2015). The open-source software LRmix can be used to analyse SNP mixtures. Forensic science international. Genetics supplement series. 5. e50–e51. 12 indexed citations

16.

Phillips, Christopher, Walther Parson, Carla Santos, et al.. (2014). Building a forensic ancestry panel from the ground up: The EUROFORGEN Global AIM-SNP set. Forensic Science International Genetics. 11. 13–25. 101 indexed citations

17.

Parson, Walther, Gabriela Huber, Lilliana I. Moreno, et al.. (2014). Massively parallel sequencing of complete mitochondrial genomes from hair shaft samples. Forensic Science International Genetics. 15. 8–15. 82 indexed citations

18.

Eduardoff, Mayra, Gabriela Huber, Birgit Bayer, et al.. (2013). Mass spectrometric base composition profiling: Implications for forensic mtDNA databasing. Forensic Science International Genetics. 7(6). 587–592. 5 indexed citations

19.

Rainer, Johannes, Christian Ploner, Mayra Eduardoff, et al.. (2009). Glucocorticoid-regulated microRNAs and mirtrons in acute lymphoblastic leukemia. Leukemia. 23(4). 746–752. 102 indexed citations

20.

Ploner, Christian, Johannes Rainer, Harald Niederegger, et al.. (2007). The BCL2 rheostat in glucocorticoid-induced apoptosis of acute lymphoblastic leukemia. Leukemia. 22(2). 370–377. 112 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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