Christopher J. Marx

7.2k total citations · 1 hit paper
85 papers, 4.6k citations indexed

About

Christopher J. Marx is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Christopher J. Marx has authored 85 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 38 papers in Genetics and 13 papers in Ecology. Recurrent topics in Christopher J. Marx's work include Microbial Metabolic Engineering and Bioproduction (36 papers), Evolution and Genetic Dynamics (26 papers) and Microbial metabolism and enzyme function (19 papers). Christopher J. Marx is often cited by papers focused on Microbial Metabolic Engineering and Bioproduction (36 papers), Evolution and Genetic Dynamics (26 papers) and Microbial metabolism and enzyme function (19 papers). Christopher J. Marx collaborates with scholars based in United States, France and Canada. Christopher J. Marx's co-authors include Mary E. Lidstrom, Hsin-Hung Chou, Nigel F. Delaney, Ming‐Chun Lee, Daniel Segrè, Nicholas Leiby, William R. Harcombe, Hsuan-Chao Chiu, Julia A. Vorholt and Sean M. Carroll and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Christopher J. Marx

83 papers receiving 4.5k citations

Hit Papers

Metabolic Resource Allocation in Individual Microbes Dete... 2014 2026 2018 2022 2014 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher J. Marx United States 37 3.2k 1.6k 677 567 482 85 4.6k
Thomas Ferenci Australia 50 4.4k 1.4× 3.3k 2.2× 1.0k 1.5× 372 0.7× 377 0.8× 133 6.4k
Lawrence J. Shimkets United States 40 3.2k 1.0× 1.9k 1.2× 1.5k 2.2× 491 0.9× 118 0.2× 89 4.6k
Haeyoung Jeong South Korea 29 2.2k 0.7× 1.0k 0.7× 600 0.9× 414 0.7× 208 0.4× 111 3.5k
Stéphane Cruveiller France 33 2.5k 0.8× 1.2k 0.8× 888 1.3× 226 0.4× 200 0.4× 71 4.4k
Ákos T. Kovács Denmark 39 2.9k 0.9× 1.1k 0.7× 1.4k 2.0× 365 0.6× 192 0.4× 161 5.0k
Jihyun F. Kim South Korea 42 3.0k 0.9× 1.3k 0.8× 884 1.3× 331 0.6× 219 0.5× 102 6.3k
Jared R. Leadbetter United States 31 2.6k 0.8× 1.4k 0.9× 966 1.4× 817 1.4× 83 0.2× 61 4.9k
Yuki Takai Japan 12 5.0k 1.6× 3.1k 2.0× 930 1.4× 487 0.9× 53 0.1× 50 6.7k
Esteban Martínez‐García Spain 29 2.7k 0.8× 1.3k 0.9× 749 1.1× 520 0.9× 81 0.2× 64 3.7k
Tomoya Baba Japan 24 6.6k 2.1× 4.3k 2.8× 1.2k 1.8× 688 1.2× 64 0.1× 43 9.3k

Countries citing papers authored by Christopher J. Marx

Since Specialization
Citations

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

Fields of papers citing papers by Christopher J. Marx

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher J. Marx. 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 Christopher J. Marx. The network helps show where Christopher J. Marx may publish in the future.

Co-authorship network of co-authors of Christopher J. Marx

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher J. Marx. A scholar is included among the top collaborators of Christopher J. Marx 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 Christopher J. Marx. Christopher J. Marx 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
3.
Leducq, Jean‐Baptiste, Geneviève Bourret, N. Cecilia Martínez-Gómez, et al.. (2022). Comprehensive Phylogenomics of Methylobacterium Reveals Four Evolutionary Distinct Groups and Underappreciated Phyllosphere Diversity. Genome Biology and Evolution. 14(8). 17 indexed citations
4.
Le, Thomas K., et al.. (2022). Methylothon: a Versatile Course-Based High School Research Experience in Microbiology and Bioinformatics with Pink Bacteria. Journal of Microbiology and Biology Education. 23(2). 2 indexed citations
5.
Leducq, Jean‐Baptiste, Geneviève Bourret, James A. Foster, et al.. (2022). Fine-Scale Adaptations to Environmental Variation and Growth Strategies Drive Phyllosphere Methylobacterium Diversity. mBio. 13(1). e0317521–e0317521. 9 indexed citations
6.
Nayak, Dipti D., M.G. Davlieva, Jessica A. Lee, et al.. (2021). EfgA is a conserved formaldehyde sensor that leads to bacterial growth arrest in response to elevated formaldehyde. PLoS Biology. 19(5). e3001208–e3001208. 20 indexed citations
7.
Hardy, Ronald W., et al.. (2018). Partial replacement of soybean meal with Methylobacterium extorquens single-cell protein in feeds for rainbow trout (Oncorhynchus mykiss Walbaum). Aquaculture Research. 49(6). 2218–2224. 58 indexed citations
8.
Dalia, Ankur B., Chelsea Hayes, Sergey Stolyar, Christopher J. Marx, & James B. McKinlay. (2017). Multiplex Genome Editing by Natural Transformation (MuGENT) for Synthetic Biology in Vibrio natriegens. ACS Synthetic Biology. 6(9). 1650–1655. 108 indexed citations
9.
Michener, Joshua K., Stéphane Vuilleumier, Françoise Bringel, & Christopher J. Marx. (2016). Transfer of a Catabolic Pathway for Chloromethane in Methylobacterium Strains Highlights Different Limitations for Growth with Chloromethane or with Dichloromethane. Frontiers in Microbiology. 7. 1116–1116. 10 indexed citations
10.
Nayak, Dipti D., Deepa Agashe, Ming‐Chun Lee, & Christopher J. Marx. (2016). Selection Maintains Apparently Degenerate Metabolic Pathways due to Tradeoffs in Using Methylamine for Carbon versus Nitrogen. Current Biology. 26(11). 1416–1426. 15 indexed citations
11.
Savir, Yonatan, Sean M. Carroll, John Ingraham, et al.. (2015). Galactose metabolic genes in yeast respond to a ratio of galactose and glucose. Proceedings of the National Academy of Sciences. 112(5). 1636–1641. 92 indexed citations
12.
Plucain, Jessica, Thomas Hindré, Mickaël Le Gac, et al.. (2014). Epistasis and Allele Specificity in the Emergence of a Stable Polymorphism in Escherichia coli. Science. 343(6177). 1366–1369. 88 indexed citations
13.
Nayak, Dipti D. & Christopher J. Marx. (2014). Genetic and Phenotypic Comparison of Facultative Methylotrophy between Methylobacterium extorquens Strains PA1 and AM1. PLoS ONE. 9(9). e107887–e107887. 29 indexed citations
14.
Michener, Joshua K., Stéphane Vuilleumier, Françoise Bringel, & Christopher J. Marx. (2014). Phylogeny Poorly Predicts the Utility of a Challenging Horizontally Transferred Gene in Methylobacterium Strains. Journal of Bacteriology. 196(11). 2101–2107. 21 indexed citations
15.
Lee, Ming‐Chun & Christopher J. Marx. (2013). Synchronous Waves of Failed Soft Sweeps in the Laboratory: Remarkably Rampant Clonal Interference of Alleles at a Single Locus. Genetics. 193(3). 943–952. 36 indexed citations
16.
Delaney, Nigel F., Susan L. Balenger, Camille Bonneaud, et al.. (2012). Correction: Ultrafast Evolution and Loss of CRISPRs Following a Host Shift in a Novel Wildlife Pathogen, Mycoplasma gallisepticum. PLoS Genetics. 8(3). 28 indexed citations
17.
Agashe, Deepa, N. Cecilia Martínez-Gómez, D. Allan Drummond, & Christopher J. Marx. (2012). Good Codons, Bad Transcript: Large Reductions in Gene Expression and Fitness Arising from Synonymous Mutations in a Key Enzyme. Molecular Biology and Evolution. 30(3). 549–560. 106 indexed citations
18.
Marx, Christopher J.. (2012). Recovering from a bad start: rapid adaptation and tradeoffs to growth below a threshold density. BMC Evolutionary Biology. 12(1). 109–109. 11 indexed citations
19.
Gudelj, Ivana, Joshua S. Weitz, M. Claire Horner‐Devine, et al.. (2010). An integrative approach to understanding microbial diversity: from intracellular mechanisms to community structure. Ecology Letters. 13(9). 1073–1084. 71 indexed citations
20.
Chou, Hsin-Hung, Julia Hicks‐Berthet, & Christopher J. Marx. (2009). Fast Growth Increases the Selective Advantage of a Mutation Arising Recurrently during Evolution under Metal Limitation. PLoS Genetics. 5(9). e1000652–e1000652. 74 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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