Amybeth Cohen

1.1k total citations
19 papers, 816 citations indexed

About

Amybeth Cohen is a scholar working on Molecular Biology, Plant Science and Cellular and Molecular Neuroscience. According to data from OpenAlex, Amybeth Cohen has authored 19 papers receiving a total of 816 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Plant Science and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Amybeth Cohen's work include Photosynthetic Processes and Mechanisms (9 papers), Plant Stress Responses and Tolerance (6 papers) and Plant Molecular Biology Research (6 papers). Amybeth Cohen is often cited by papers focused on Photosynthetic Processes and Mechanisms (9 papers), Plant Stress Responses and Tolerance (6 papers) and Plant Molecular Biology Research (6 papers). Amybeth Cohen collaborates with scholars based in United States, Israel and Canada. Amybeth Cohen's co-authors include Stephen P. Mayfield, Christopher B. Yohn, Avihai Danon, Elizabeth A. Bray, Áine L. Plant, M.R. Kuchka, Darya Alizadeh, Ryozo Imai, Ekem T. Efuet and Richard K. Bruick and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and The Journal of Cell Biology.

In The Last Decade

Amybeth Cohen

19 papers receiving 775 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amybeth Cohen United States 15 597 433 143 83 42 19 816
Katia Wostrikoff France 16 1.1k 1.8× 455 1.1× 314 2.2× 89 1.1× 33 0.8× 21 1.2k
Chris J. Chastain United States 19 654 1.1× 433 1.0× 136 1.0× 38 0.5× 59 1.4× 32 868
Lisa Heins Germany 15 927 1.6× 274 0.6× 156 1.1× 103 1.2× 83 2.0× 16 981
Jeffrey P. Woessner United States 16 607 1.0× 263 0.6× 279 2.0× 52 0.6× 56 1.3× 18 827
Cristina Dal Bosco Germany 15 665 1.1× 585 1.4× 43 0.3× 50 0.6× 13 0.3× 17 820
Andrea L. Manuell United States 7 581 1.0× 146 0.3× 264 1.8× 25 0.3× 32 0.8× 8 683
Oskar Johansson Sweden 12 297 0.5× 288 0.7× 42 0.3× 28 0.3× 79 1.9× 26 520
Fabienne Cartieaux France 15 395 0.7× 755 1.7× 46 0.3× 28 0.3× 68 1.6× 21 979
James L. Lissemore United States 14 619 1.0× 505 1.2× 26 0.2× 52 0.6× 26 0.6× 21 773
Adi Zaltsman United States 15 1.2k 2.0× 901 2.1× 126 0.9× 33 0.4× 39 0.9× 20 1.4k

Countries citing papers authored by Amybeth Cohen

Since Specialization
Citations

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

Fields of papers citing papers by Amybeth Cohen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amybeth Cohen

This figure shows the co-authorship network connecting the top 25 collaborators of Amybeth Cohen. A scholar is included among the top collaborators of Amybeth Cohen 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 Amybeth Cohen. Amybeth Cohen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Golembo, Myriam, Sailaja Puttagunta, Urania Rappo, et al.. (2022). Development of a Topical Bacteriophage Gel Targeting Cutibacterium Acnes for Acne Prone Skin and Results of a Phase 1 Cosmetic Randomized Clinical Trial. SHILAP Revista de lepidopterología. 2(2). e93–e93. 24 indexed citations
2.
Stapp, Paul, et al.. (2010). Polymerase chain reaction (PCR) identification of rodent blood meals confirms host sharing by flea vectors of plague. Journal of Vector Ecology. 35(2). 363–371. 9 indexed citations
3.
Alizadeh, Darya & Amybeth Cohen. (2010). Red Light and Calmodulin Regulate the Expression of the psbA Binding Protein Genes in Chlamydomonas reinhardtii. Plant and Cell Physiology. 51(2). 312–322. 15 indexed citations
4.
Barnes, Dwight, Amybeth Cohen, Richard K. Bruick, et al.. (2004). Identification and Characterization of a Novel RNA Binding Protein That Associates with the 5‘-Untranslated Region of the Chloroplast psbA mRNA. Biochemistry. 43(26). 8541–8550. 30 indexed citations
5.
Cohen, Amybeth, Christopher B. Yohn, & Stephen P. Mayfield. (2001). Translation of the chloroplast-encoded psbD mRNA is arrested post-initiation in a nuclear mutant of Chlamydomonas reinhardtii. Journal of Plant Physiology. 158(8). 1069–1075. 4 indexed citations
6.
Cohen, Amybeth, et al.. (1999). Multiple mechanisms control the expression of abscisic acid (ABA)‐requiring genes in tomato plants exposed to soil water deficit. Plant Cell & Environment. 22(8). 989–998. 23 indexed citations
7.
Bray, Elizabeth A., et al.. (1999). Water-deficit induction of a tomato H1 histone requires abscisic acid. Plant Growth Regulation. 29(1-2). 35–46. 28 indexed citations
8.
Yohn, Christopher B., Amybeth Cohen, Avihai Danon, & Stephen P. Mayfield. (1998). A poly(A) binding protein functions in the chloroplast as a message-specific translation factor. Proceedings of the National Academy of Sciences. 95(5). 2238–2243. 81 indexed citations
9.
Yohn, Christopher B., et al.. (1998). Translation of the Chloroplast psbA mRNA Requires the Nuclear-encoded Poly(A)-binding Protein, RB47. The Journal of Cell Biology. 142(2). 435–442. 52 indexed citations
10.
Cohen, Amybeth & Stephen P. Mayfield. (1997). Translational regulation of gene expression in plants. Current Opinion in Biotechnology. 8(2). 189–194. 19 indexed citations
11.
Bray, Elizabeth A., et al.. (1997). Regulation of gene expression by endogenous ABA in tomato plants. Acta Physiologiae Plantarum. 19(4). 405–418. 3 indexed citations
12.
Yohn, Christopher B., Amybeth Cohen, Avihai Danon, & Stephen P. Mayfield. (1996). Altered mRNA Binding Activity and Decreased Translation Initiation in a Nuclear Mutant Lacking Translation of the Chloroplast psbA mRNA. Molecular and Cellular Biology. 16(7). 3560–3566. 59 indexed citations
13.
Mayfield, Stephen P., Christopher B. Yohn, Amybeth Cohen, & Avihai Danon. (1995). Regulation of Chloroplast Gene Expression. Annual Review of Plant Physiology and Plant Molecular Biology. 46(1). 147–166. 143 indexed citations
14.
Mayfield, Stephen P., Amybeth Cohen, Avihai Danon, & Christopher B. Yohn. (1994). Translation of the psbA mRNA of Chlamydomonas reinhardtii requires a structured RNA element contained within the 5' untranslated region.. The Journal of Cell Biology. 127(6). 1537–1545. 87 indexed citations
15.
Cohen, Amybeth & Elizabeth A. Bray. (1992). Nucleotide sequence of an ABA-induced tomato gene that is expressed in wilted vegetative organs and developing seeds. Plant Molecular Biology. 18(2). 411–413. 17 indexed citations
16.
Cohen, Amybeth, et al.. (1991). Organ-Specific and Environmentally Regulated Expression of Two Abscisic Acid-Induced Genes of Tomato. PLANT PHYSIOLOGY. 97(4). 1367–1374. 59 indexed citations
17.
Plant, Áine L., et al.. (1991). Nucleotide Sequence and Spatial Expression Pattern of a Drought- and Abscisic Acid-Induced Gene of Tomato. PLANT PHYSIOLOGY. 97(3). 900–906. 84 indexed citations
18.
Bray, Elizabeth A., Áine L. Plant, & Amybeth Cohen. (1990). Drought-and ABA-regulated gene expression in tomato leaves.. Plant Biology. 11. 315–322. 4 indexed citations
19.

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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