Mary N. Burtnick

2.7k total citations
63 papers, 2.2k citations indexed

About

Mary N. Burtnick is a scholar working on Epidemiology, Biomedical Engineering and Small Animals. According to data from OpenAlex, Mary N. Burtnick has authored 63 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Epidemiology, 16 papers in Biomedical Engineering and 11 papers in Small Animals. Recurrent topics in Mary N. Burtnick's work include Burkholderia infections and melioidosis (59 papers), Chemical Looping and Thermochemical Processes (16 papers) and Brucella: diagnosis, epidemiology, treatment (11 papers). Mary N. Burtnick is often cited by papers focused on Burkholderia infections and melioidosis (59 papers), Chemical Looping and Thermochemical Processes (16 papers) and Brucella: diagnosis, epidemiology, treatment (11 papers). Mary N. Burtnick collaborates with scholars based in United States, Thailand and United Kingdom. Mary N. Burtnick's co-authors include Paul J. Brett, Donald E. Woods, David DeShazer, Frank C. Gherardini, Narisara Chantratita, Parastoo Azadi, Vinod Nair, Christian Heiß, Sharon J. Peacock and David P. AuCoin and has published in prestigious journals such as Nature Communications, PLoS ONE and Scientific Reports.

In The Last Decade

Mary N. Burtnick

61 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mary N. Burtnick United States	30	1.5k	417	291	257	254	63	2.2k
Timothy P. Atkins United Kingdom	25	1.1k 0.8×	283 0.7×	374 1.3×	165 0.6×	173 0.7×	44	1.8k
Apichai Tuanyok United States	29	1.6k 1.1×	413 1.0×	312 1.1×	128 0.5×	168 0.7×	79	2.2k
Jay E. Gee United States	28	1.3k 0.8×	349 0.8×	766 2.6×	102 0.4×	509 2.0×	74	2.7k
David DeShazer United States	40	3.3k 2.2×	563 1.4×	959 3.3×	639 2.5×	329 1.3×	90	5.0k
Joann L. Prior United Kingdom	23	602 0.4×	147 0.4×	602 2.1×	125 0.5×	111 0.4×	43	1.5k
Rasana W. Sermswan Thailand	26	672 0.4×	178 0.4×	218 0.7×	44 0.2×	511 2.0×	81	1.9k
Mitali Sarkar‐Tyson United Kingdom	23	591 0.4×	121 0.3×	438 1.5×	77 0.3×	68 0.3×	51	1.2k
Helen S. Atkins United Kingdom	22	460 0.3×	68 0.2×	518 1.8×	170 0.7×	246 1.0×	61	1.4k
Wilson J. Ribot United States	16	365 0.2×	91 0.2×	627 2.2×	279 1.1×	37 0.1×	27	1.2k
David J. Mead United States	23	704 0.5×	68 0.2×	858 2.9×	228 0.9×	40 0.2×	32	2.4k

Countries citing papers authored by Mary N. Burtnick

Since Specialization

Citations

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

Fields of papers citing papers by Mary N. Burtnick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary N. Burtnick. 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 Mary N. Burtnick. The network helps show where Mary N. Burtnick may publish in the future.

Co-authorship network of co-authors of Mary N. Burtnick

This figure shows the co-authorship network connecting the top 25 collaborators of Mary N. Burtnick. A scholar is included among the top collaborators of Mary N. Burtnick 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 Mary N. Burtnick. Mary N. Burtnick 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

Cote, Christopher K., Christopher P. Klimko, Michael L. Davies, et al.. (2025). Comparison of homologous and heterologous vaccination strategies for combating disease caused by Burkholderia pseudomallei. Frontiers in Immunology. 16. 1596265–1596265.

Tandhavanant, Sarunporn, Thatcha Yimthin, Andrey A. Lebedev, et al.. (2025). Genetic variation of hemolysin co-regulated protein 1 affects the immunogenicity and pathogenicity of Burkholderia pseudomallei. PLoS neglected tropical diseases. 19(1). e0012758–e0012758. 1 indexed citations

Burtnick, Mary N., David A. B. Dance, Manivanh Vongsouvath, et al.. (2024). Identification of Burkholderia cepacia strains that express a Burkholderia pseudomallei -like capsular polysaccharide. Microbiology Spectrum. 12(3). e0332123–e0332123. 6 indexed citations

Cote, Christopher K., Christopher P. Klimko, Jennifer L. Shoe, et al.. (2022). Evaluation of two different vaccine platforms for immunization against melioidosis and glanders. Frontiers in Microbiology. 13. 13 indexed citations

Amornchai, Premjit, Viriya Hantrakun, Gumphol Wongsuvan, et al.. (2021). Evaluation of antigen-detecting and antibody-detecting diagnostic test combinations for diagnosing melioidosis. PLoS neglected tropical diseases. 15(11). e0009840–e0009840. 13 indexed citations

Chantratita, Narisara, et al.. (2019). Melioidosis patient serum-reactive synthetic tetrasaccharides bearing the predominant epitopes ofBurkholderia pseudomalleiandBurkholderia malleiO-antigens. Organic & Biomolecular Chemistry. 17(39). 8878–8901. 14 indexed citations

Ekchariyawat, Peeraya, Ekkachai Thiansukhon, Nicholas Day, et al.. (2019). Distinct classes and subclasses of antibodies to hemolysin co-regulated protein 1 and O-polysaccharide and correlation with clinical characteristics of melioidosis patients. Scientific Reports. 9(1). 13972–13972. 16 indexed citations

Dunachie, Susanna, Kemajittra Jenjaroen, Kitisak Sintiprungrat, et al.. (2017). Comparison of O-polysaccharide and hemolysin co-regulated protein as target antigens for serodiagnosis of melioidosis. PLoS neglected tropical diseases. 11(3). e0005499–e0005499. 48 indexed citations

Mazur, Marcelina, Jérôme Marrot, Roberta Marchetti, et al.. (2017). Deciphering minimal antigenic epitopes associated with Burkholderia pseudomallei and Burkholderia mallei lipopolysaccharide O-antigens. Nature Communications. 8(1). 115–115. 35 indexed citations

10.

Norris, Michael H., Apichai Tuanyok, Paul J. Brett, et al.. (2016). Development of Immunoassays for Burkholderia pseudomallei Typical and Atypical Lipopolysaccharide Strain Typing. American Journal of Tropical Medicine and Hygiene. 96(2). 358–367. 10 indexed citations

11.

Thorkildson, Peter, et al.. (2016). In vivo Distribution and Clearance of Purified Capsular Polysaccharide from Burkholderia pseudomallei in a Murine Model. PLoS neglected tropical diseases. 10(12). e0005217–e0005217. 21 indexed citations

12.

Marlenee, Nicole L., Mary N. Burtnick, Paul J. Brett, et al.. (2016). Thermoregulation of Biofilm Formation in Burkholderia pseudomallei Is Disrupted by Mutation of a Putative Diguanylate Cyclase. Journal of Bacteriology. 199(5). 25 indexed citations

13.

Burtnick, Mary N., Paul J. Brett, & David DeShazer. (2014). Proteomic Analysis of the Burkholderia pseudomallei Type II Secretome Reveals Hydrolytic Enzymes, Novel Proteins, and the Deubiquitinase TssM. Infection and Immunity. 82(8). 3214–3226. 50 indexed citations

14.

Houghton, Raymond L., Mark Hubbard, Michael J. Dillon, et al.. (2014). Development of a Prototype Lateral Flow Immunoassay (LFI) for the Rapid Diagnosis of Melioidosis. PLoS neglected tropical diseases. 8(3). e2727–e2727. 107 indexed citations

15.

Burtnick, Mary N. & Paul J. Brett. (2013). Burkholderia mallei and Burkholderia pseudomallei Cluster 1 Type VI Secretion System Gene Expression Is Negatively Regulated by Iron and Zinc. PLoS ONE. 8(10). e76767–e76767. 40 indexed citations

16.

Burtnick, Mary N., Christian Heiß, Rosemary A. Roberts, et al.. (2012). Development of capsular polysaccharide-based glycoconjugates for immunization against melioidosis and glanders. Frontiers in Cellular and Infection Microbiology. 2. 108–108. 52 indexed citations

17.

Burtnick, Mary N., et al.. (2012). Development of novel O-polysaccharide based glycoconjugates for immunization against glanders. Frontiers in Cellular and Infection Microbiology. 2. 148–148. 23 indexed citations

18.

Shanks, John, Mary N. Burtnick, Paul J. Brett, et al.. (2009). Burkholderia mallei tssM Encodes a Putative Deubiquitinase That Is Secreted and Expressed inside Infected RAW 264.7 Murine Macrophages. Infection and Immunity. 77(4). 1636–1648. 46 indexed citations

19.

Jewett, Mollie W., Rebecca Byram, Aaron Bestor, et al.. (2007). Genetic basis for retention of a critical virulence plasmid of Borrelia burgdorferi. Molecular Microbiology. 66(4). 975–990. 56 indexed citations

20.

Burtnick, Mary N., Jennifer S. Downey, Paul J. Brett, et al.. (2007). Insights into the complex regulation of rpoS in Borrelia burgdorferi. Molecular Microbiology. 65(2). 277–293. 99 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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