Melissa E. Bell

990 total citations
26 papers, 524 citations indexed

About

Melissa E. Bell is a scholar working on Epidemiology, Endocrinology and Molecular Biology. According to data from OpenAlex, Melissa E. Bell has authored 26 papers receiving a total of 524 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Epidemiology, 9 papers in Endocrinology and 7 papers in Molecular Biology. Recurrent topics in Melissa E. Bell's work include Actinomycetales infections and treatment (7 papers), Infections and bacterial resistance (6 papers) and Mycobacterium research and diagnosis (6 papers). Melissa E. Bell is often cited by papers focused on Actinomycetales infections and treatment (7 papers), Infections and bacterial resistance (6 papers) and Mycobacterium research and diagnosis (6 papers). Melissa E. Bell collaborates with scholars based in United States, Germany and United Kingdom. Melissa E. Bell's co-authors include John R. McQuiston, Ben W. Humrighouse, Brent A. Lasker, Ainsley Nicholson, Christopher A. Gulvik, Anne M. Whitney, Wun‐Ju Shieh, Rita M. Traxler, Hans‐Peter Klenk and Dhwani Batra and has published in prestigious journals such as Gastroenterology, PLoS ONE and Clinical Microbiology Reviews.

In The Last Decade

Melissa E. Bell

26 papers receiving 514 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Melissa E. Bell United States 12 187 178 133 130 109 26 524
Gema Carrasco Spain 13 168 0.9× 115 0.6× 92 0.7× 186 1.4× 70 0.6× 28 562
C. PASCUAL United Kingdom 10 153 0.8× 231 1.3× 128 1.0× 76 0.6× 20 0.2× 12 503
Dorothy M. W. Tam Hong Kong 8 254 1.4× 156 0.9× 73 0.5× 40 0.3× 25 0.2× 8 489
Carine Couderc France 16 231 1.2× 512 2.9× 96 0.7× 28 0.2× 35 0.3× 38 817
Lisa R. McTaggart Canada 15 508 2.7× 85 0.5× 31 0.2× 164 1.3× 98 0.9× 27 706
Michal Slaný Czechia 17 440 2.4× 172 1.0× 46 0.3× 17 0.1× 17 0.2× 43 754
Sirlei Garcia Marques Brazil 16 331 1.8× 102 0.6× 57 0.4× 25 0.2× 77 0.7× 38 582
M M Henton South Africa 11 44 0.2× 66 0.4× 61 0.5× 28 0.2× 24 0.2× 29 335
Berit Sjödén Sweden 17 335 1.8× 280 1.6× 140 1.1× 60 0.5× 7 0.1× 21 709
M. J. Gevaudan France 9 385 2.1× 114 0.6× 34 0.3× 22 0.2× 25 0.2× 19 567

Countries citing papers authored by Melissa E. Bell

Since Specialization
Citations

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

Fields of papers citing papers by Melissa E. Bell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Melissa E. Bell. 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 Melissa E. Bell. The network helps show where Melissa E. Bell may publish in the future.

Co-authorship network of co-authors of Melissa E. Bell

This figure shows the co-authorship network connecting the top 25 collaborators of Melissa E. Bell. A scholar is included among the top collaborators of Melissa E. Bell 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 Melissa E. Bell. Melissa E. Bell 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.
Sabin, Susanna, Cari A. Beesley, Chung K. Marston, et al.. (2024). Investigating Anthrax-Associated Virulence Genes among Archival and Contemporary Bacillus cereus Group Genomes. Pathogens. 13(10). 884–884. 1 indexed citations
2.
Traxler, Rita M., et al.. (2022). Updated Review onNocardiaSpecies: 2006–2021. Clinical Microbiology Reviews. 35(4). e0002721–e0002721. 71 indexed citations
5.
Pillai, Segaran P., Jason G. Ramage, Jawad Sarwar, et al.. (2019). Rapid Presumptive Identification of Bacillus anthracis Isolates Using the Tetracore RedLine Alert™ Test. Health Security. 17(4). 334–343. 12 indexed citations
6.
Kelly, Aubree J., Sandor E. Karpathy, Christopher A. Gulvik, et al.. (2019). A Real-Time Multiplex PCR Assay for Detection ofElizabethkingiaSpecies and Differentiation betweenElizabethkingia anophelisandE. meningoseptica. Journal of Clinical Microbiology. 57(4). 7 indexed citations
7.
Gulvik, Christopher A., John R. McQuiston, Ben W. Humrighouse, et al.. (2018). Genotypic differences between strains of the opportunistic pathogen Corynebacterium bovis isolated from humans, cows, and rodents. PLoS ONE. 13(12). e0209231–e0209231. 16 indexed citations
8.
Johnson, William L., Akhilesh Ramachandran, Ainsley Nicholson, et al.. (2018). The draft genomes of Elizabethkingia anophelis of equine origin are genetically similar to three isolates from human clinical specimens. PLoS ONE. 13(7). e0200731–e0200731. 11 indexed citations
9.
Bonwitt, Jesse, et al.. (2018). Fly Reservoir Associated with Wohlfahrtiimonas Bacteremia in a Human. Emerging infectious diseases. 24(2). 370–373. 13 indexed citations
11.
Pei, Dong, Ainsley Nicholson, Jinjin Jiang, et al.. (2017). Complete Circularized Genome Sequences of Four Strains of Elizabethkingia anophelis, Including Two Novel Strains Isolated from Wild-Caught Anopheles sinensis. Genome Announcements. 5(47). 4 indexed citations
12.
Bell, Melissa E., Brent A. Lasker, Hans‐Peter Klenk, et al.. (2016). Kroppenstedtia pulmonis sp. nov. and Kroppenstedtia sanguinis sp. nov., isolated from human patients. Antonie van Leeuwenhoek. 109(5). 603–610. 6 indexed citations
13.
Ercibengoa, María, et al.. (2016). Nocardia donostiensis sp. nov., isolated from human respiratory specimens. Antonie van Leeuwenhoek. 109(5). 653–660. 12 indexed citations
14.
Girard, Victoria, Sandrine Mailler, Martin Welker, et al.. (2016). Identification of mycobacterium spp. and nocardia spp. from solid and liquid cultures by matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS). Diagnostic Microbiology and Infectious Disease. 86(3). 277–283. 36 indexed citations
15.
Bell, Melissa E., Kathryn Bernard, Susan M. Harrington, et al.. (2016). Lawsonella clevelandensis gen. nov., sp. nov., a new member of the suborder Corynebacterineae isolated from human abscesses. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 66(8). 2929–2935. 37 indexed citations
16.
Nicholson, Ainsley, Anne M. Whitney, Brian Emery, et al.. (2016). Complete Genome Sequences of Four Strains from the 2015-2016 Elizabethkingia anophelis Outbreak. Genome Announcements. 4(3). 10 indexed citations
17.
Lasker, Brent A., Melissa E. Bell, Hans‐Peter Klenk, Peter Schümann, & June M. Brown. (2015). Nocardia arizonensis sp. nov., obtained from human respiratory specimens. Antonie van Leeuwenhoek. 108(5). 1129–1137. 8 indexed citations
18.
Harrington, Susan M., Melissa E. Bell, Kathryn Bernard, et al.. (2013). Novel Fastidious, Partially Acid-Fast, Anaerobic Gram-Positive Bacillus Associated with Abscess Formation and Recovered from Multiple Medical Centers. Journal of Clinical Microbiology. 51(11). 3903–3907. 21 indexed citations
19.
Theodore, M. Jordan, Raydel Anderson, Xin Wang, et al.. (2012). Evaluation of New Biomarker Genes for Differentiating Haemophilus influenzae from Haemophilus haemolyticus. Journal of Clinical Microbiology. 50(4). 1422–1424. 28 indexed citations
20.
Suerbaum, Sebastian, Christine Josenhans, Matthias Frosch, et al.. (2001). Determining the whole genome sequence of Helicobacter hepaticus ATCC 51449. Gastroenterology. 120(5). A655–A655. 1 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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