Moriah Sandy

1.8k total citations
20 papers, 1.3k citations indexed

About

Moriah Sandy is a scholar working on Molecular Biology, Pharmacology and Plant Science. According to data from OpenAlex, Moriah Sandy has authored 20 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 5 papers in Pharmacology and 5 papers in Plant Science. Recurrent topics in Moriah Sandy's work include Microbial Natural Products and Biosynthesis (5 papers), Genomics and Phylogenetic Studies (4 papers) and Bacterial Genetics and Biotechnology (3 papers). Moriah Sandy is often cited by papers focused on Microbial Natural Products and Biosynthesis (5 papers), Genomics and Phylogenetic Studies (4 papers) and Bacterial Genetics and Biotechnology (3 papers). Moriah Sandy collaborates with scholars based in United States, Brazil and New Zealand. Moriah Sandy's co-authors include Alison Butler, Margo G. Haygood, Zhe Rui, Peter J. Turnbaugh, Wenjun Zhang, Katherine S. Pollard, Bing Zhang, Susan V. Lynch, Margaret Alexander and Annamarie E. Bustion and has published in prestigious journals such as Nature, Chemical Reviews and Journal of the American Chemical Society.

In The Last Decade

Moriah Sandy

20 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Moriah Sandy United States 14 668 235 191 185 175 20 1.3k
Eric Eichhorn Switzerland 13 697 1.0× 147 0.6× 148 0.8× 175 0.9× 273 1.6× 22 1.3k
Lesley A. Mitchenall United Kingdom 23 1.1k 1.6× 148 0.6× 168 0.9× 106 0.6× 154 0.9× 42 1.8k
M.A. Mazid Bangladesh 22 293 0.4× 106 0.5× 229 1.2× 92 0.5× 342 2.0× 139 1.8k
Nils Oberg United States 8 662 1.0× 230 1.0× 109 0.6× 78 0.4× 55 0.3× 10 1.0k
Kuniaki Hosono Japan 18 694 1.0× 217 0.9× 155 0.8× 54 0.3× 193 1.1× 61 1.2k
Jesús Sánchez Spain 23 722 1.1× 565 2.4× 129 0.7× 46 0.2× 172 1.0× 39 1.3k
J.H. Pereira United States 30 1.5k 2.3× 142 0.6× 154 0.8× 55 0.3× 200 1.1× 71 2.2k
De‐Feng Li China 20 690 1.0× 107 0.5× 69 0.4× 35 0.2× 135 0.8× 101 1.6k
Masatoshi Goto Japan 26 1.3k 1.9× 186 0.8× 101 0.5× 95 0.5× 584 3.3× 116 2.4k
Bing Tian China 30 1.6k 2.5× 80 0.3× 121 0.6× 164 0.9× 247 1.4× 135 2.8k

Countries citing papers authored by Moriah Sandy

Since Specialization
Citations

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

Fields of papers citing papers by Moriah Sandy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Moriah Sandy

This figure shows the co-authorship network connecting the top 25 collaborators of Moriah Sandy. A scholar is included among the top collaborators of Moriah Sandy 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 Moriah Sandy. Moriah Sandy 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.
Kyaw, Than S., Chen Zhang, Moriah Sandy, et al.. (2024). Human gut Actinobacteria boost drug absorption by secreting P-glycoprotein ATPase inhibitors. iScience. 27(6). 110122–110122. 5 indexed citations
2.
Sandy, Moriah, et al.. (2022). Plant Host Traits Mediated by Foliar Fungal Symbionts and Secondary Metabolites. Microbial Ecology. 86(1). 408–418. 3 indexed citations
3.
Spanogiannopoulos, Peter, Than S. Kyaw, Patrick H. Bradley, et al.. (2022). Host and gut bacteria share metabolic pathways for anti-cancer drug metabolism. Nature Microbiology. 7(10). 1605–1620. 64 indexed citations
4.
Kyaw, Than S., et al.. (2022). Human Gut Actinobacteria Boost Drug Absorption by Secreting P-Glycoprotein ATPase Inhibitors. SSRN Electronic Journal. 1 indexed citations
5.
Alexander, Margaret, Qi Yan Ang, Renuka R. Nayak, et al.. (2021). Human gut bacterial metabolism drives Th17 activation and colitis. Cell Host & Microbe. 30(1). 17–30.e9. 165 indexed citations
6.
Gallman, Antonia E., David N. Nguyen, Moriah Sandy, et al.. (2021). Abcc1 and Ggt5 support lymphocyte guidance through export and catabolism of S -geranylgeranyl- l -glutathione. Science Immunology. 6(60). 6 indexed citations
7.
Sandy, Moriah, et al.. (2017). Microbial Tools in Agriculture Require an Ecological Context: Stress‐Dependent Non‐Additive Symbiont Interactions. Agronomy Journal. 109(3). 917–926. 21 indexed citations
8.
Reitz, Zachary L., Moriah Sandy, & Alison Butler. (2017). Biosynthetic considerations of triscatechol siderophores framed on serine and threonine macrolactone scaffolds. Metallomics. 9(7). 824–839. 29 indexed citations
9.
Haygood, Margo G., Marvin A. Altamia, Sherif I. Elshahawi, et al.. (2015). Versatile bacterial symbionts of shipworms contribute to wood digestion, fix nitrogen and produce secondary metabolites. Planta Medica. 81(11). 1 indexed citations
10.
Zane, Hannah K., Hiroaki Naka, Federico Rosconi, et al.. (2014). Biosynthesis of Amphi-enterobactin Siderophores by Vibrio harveyi BAA-1116: Identification of a Bifunctional Nonribosomal Peptide Synthetase Condensation Domain. Journal of the American Chemical Society. 136(15). 5615–5618. 49 indexed citations
11.
Rui, Zhe, et al.. (2013). Tandem Enzymatic Oxygenations in Biosynthesis of Epoxyquinone Pharmacophore of Manumycin-type Metabolites. Chemistry & Biology. 20(7). 879–887. 6 indexed citations
12.
Han, Andrew, Moriah Sandy, Amaro E. Trindade‐Silva, et al.. (2013). Turnerbactin, a Novel Triscatecholate Siderophore from the Shipworm Endosymbiont Teredinibacter turnerae T7901. PLoS ONE. 8(10). e76151–e76151. 53 indexed citations
13.
Sandy, Moriah, Xuejun Zhu, Zhe Rui, & Wenjun Zhang. (2013). Characterization of AntB, a Promiscuous Acyltransferase Involved in Antimycin Biosynthesis. Organic Letters. 15(13). 3396–3399. 24 indexed citations
14.
Sandy, Moriah, Zhe Rui, Joe Gallagher, & Wenjun Zhang. (2012). Enzymatic Synthesis of Dilactone Scaffold of Antimycins. ACS Chemical Biology. 7(12). 1956–1961. 55 indexed citations
15.
Sandy, Moriah, et al.. (2011). Vanadium bromoperoxidase from Delisea pulchra: enzyme-catalyzed formation of bromofuranone and attendant disruption of quorum sensing. Chemical Communications. 47(44). 12086–12086. 49 indexed citations
16.
Sandy, Moriah & Alison Butler. (2011). Chrysobactin Siderophores Produced by Dickeya chrysanthemi EC16. Journal of Natural Products. 74(5). 1207–1212. 38 indexed citations
17.
Sandy, Moriah, Andrew Han, John W. Blunt, et al.. (2010). Vanchrobactin and Anguibactin Siderophores Produced by Vibrio sp. DS40M4. Journal of Natural Products. 73(6). 1038–1043. 43 indexed citations
18.
Butler, Alison & Moriah Sandy. (2009). Mechanistic considerations of halogenating enzymes. Nature. 460(7257). 848–854. 266 indexed citations
19.
Sandy, Moriah & Alison Butler. (2009). Microbial Iron Acquisition: Marine and Terrestrial Siderophores. Chemical Reviews. 109(10). 4580–4595. 374 indexed citations
20.
Sandy, Moriah, et al.. (2009). Loihichelins A−F, a Suite of Amphiphilic Siderophores Produced by the Marine Bacterium Halomonas LOB-5. Journal of Natural Products. 72(5). 884–888. 83 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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