Charles R. Dietrich

2.2k total citations
18 papers, 1.7k citations indexed

About

Charles R. Dietrich is a scholar working on Plant Science, Molecular Biology and Biochemistry. According to data from OpenAlex, Charles R. Dietrich has authored 18 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Plant Science, 10 papers in Molecular Biology and 5 papers in Biochemistry. Recurrent topics in Charles R. Dietrich's work include Plant Molecular Biology Research (8 papers), Plant Surface Properties and Treatments (5 papers) and Chromosomal and Genetic Variations (5 papers). Charles R. Dietrich is often cited by papers focused on Plant Molecular Biology Research (8 papers), Plant Surface Properties and Treatments (5 papers) and Chromosomal and Genetic Variations (5 papers). Charles R. Dietrich collaborates with scholars based in United States, France and United Kingdom. Charles R. Dietrich's co-authors include Edgar B. Cahoon, Patrick S. Schnable, Ming Chen, Basil J. Nikolau, Gongshe Han, Teresa Dunn, John M. Dyer, R. Howard Berg, Jan G. Jaworski and Sanzhen Liu and has published in prestigious journals such as PLoS ONE, The Plant Cell and PLANT PHYSIOLOGY.

In The Last Decade

Charles R. Dietrich

18 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Charles R. Dietrich United States	18	1.2k	1.1k	410	112	87	18	1.7k
Diego Breviario Italy	24	840 0.7×	1.0k 0.9×	104 0.3×	115 1.0×	77 0.9×	79	1.5k
Wilfred A. Keller Canada	16	1.2k 0.9×	970 0.9×	201 0.5×	35 0.3×	40 0.5×	22	1.5k
Kenichiro Maeo Japan	7	1.3k 1.0×	1.1k 1.0×	243 0.6×	26 0.2×	43 0.5×	11	1.6k
Raju Datla Canada	25	1.6k 1.3×	1.4k 1.3×	81 0.2×	81 0.7×	48 0.6×	54	2.0k
Hidemitsu Nakamura Japan	26	1.8k 1.5×	967 0.9×	90 0.2×	208 1.9×	47 0.5×	57	2.1k
Henrik Næsted Denmark	14	1.3k 1.0×	821 0.8×	125 0.3×	45 0.4×	128 1.5×	18	1.7k
Michael H. Luethy United States	20	843 0.7×	756 0.7×	154 0.4×	116 1.0×	154 1.8×	21	1.3k
Judy A. Schnurr United States	12	723 0.6×	734 0.7×	294 0.7×	18 0.2×	85 1.0×	14	1.1k
Inmaculada Hernández‐Pinzón United Kingdom	15	676 0.5×	544 0.5×	218 0.5×	71 0.6×	34 0.4×	27	1.0k
James S. Keddie United Kingdom	12	2.7k 2.2×	2.1k 1.9×	120 0.3×	100 0.9×	75 0.9×	14	3.2k

Countries citing papers authored by Charles R. Dietrich

Since Specialization

Citations

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

Fields of papers citing papers by Charles R. Dietrich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles R. Dietrich. 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 Charles R. Dietrich. The network helps show where Charles R. Dietrich may publish in the future.

Co-authorship network of co-authors of Charles R. Dietrich

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

All Works

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18 of 18 papers shown

Paciorek, Tomasz, Brandi J Chiapelli, Heping Yang, et al.. (2022). Targeted suppression of gibberellin biosynthetic genes ZmGA20ox3 and ZmGA20ox5 produces a short stature maize ideotype. Plant Biotechnology Journal. 20(6). 1140–1153. 42 indexed citations

Li, Li, Cheng He, Charles R. Dietrich, et al.. (2019). Maize glossy6 is involved in cuticular wax deposition and drought tolerance. Journal of Experimental Botany. 70(12). 3089–3099. 64 indexed citations

Li, Li, Delin Li, Sanzhen Liu, et al.. (2013). The Maize glossy13 Gene, Cloned via BSR-Seq and Seq-Walking Encodes a Putative ABC Transporter Required for the Normal Accumulation of Epicuticular Waxes. PLoS ONE. 8(12). e82333–e82333. 71 indexed citations

Saucedo‐García, Mariana, Arturo Guevara‐García, Ariadna González‐Solís, et al.. (2011). MPK6, sphinganine and the LCB2a gene from serine palmitoyltransferase are required in the signaling pathway that mediates cell death induced by long chain bases in Arabidopsis. New Phytologist. 191(4). 943–957. 104 indexed citations

Chao, Dai‐Yin, Kenneth Gable, Ming Chen, et al.. (2011). Sphingolipids in the Root Play an Important Role in Regulating the Leaf Ionome inArabidopsis thaliana . The Plant Cell. 23(3). 1061–1081. 100 indexed citations

Liu, Sanzhen, Irina Makarevitch, Scott Emrich, et al.. (2009). High-Throughput Genetic Mapping of Mutants via Quantitative Single Nucleotide Polymorphism Typing. Genetics. 184(1). 19–26. 54 indexed citations

Liu, Sanzhen, Charles R. Dietrich, & Patrick S. Schnable. (2009). DLA-Based Strategies for Cloning Insertion Mutants: Cloning the gl4 Locus of Maize Using Mu Transposon Tagged Alleles. Genetics. 183(4). 1215–1225. 37 indexed citations

Dietrich, Charles R., Gongshe Han, Ming Chen, et al.. (2008). Loss‐of‐function mutations and inducible RNAi suppression of Arabidopsis LCB2 genes reveal the critical role of sphingolipids in gametophytic and sporophytic cell viability. The Plant Journal. 54(2). 284–298. 88 indexed citations

Chen, Ming, Jennifer E. Markham, Charles R. Dietrich, Jan G. Jaworski, & Edgar B. Cahoon. (2008). Sphingolipid Long-Chain Base Hydroxylation Is Important for Growth and Regulation of Sphingolipid Content and Composition inArabidopsis . The Plant Cell. 20(7). 1862–1878. 134 indexed citations

10.

Cahoon, Edgar B., Jay Shockey, Charles R. Dietrich, et al.. (2007). Engineering oilseeds for sustainable production of industrial and nutritional feedstocks: solving bottlenecks in fatty acid flux. Current Opinion in Plant Biology. 10(3). 236–244. 159 indexed citations

11.

Chen, Ming, Gongshe Han, Charles R. Dietrich, Teresa Dunn, & Edgar B. Cahoon. (2006). The Essential Nature of Sphingolipids in Plants as Revealed by the Functional Identification and Characterization of theArabidopsisLCB1 Subunit of Serine Palmitoyltransferase. The Plant Cell. 18(12). 3576–3593. 134 indexed citations

12.

Cahoon, Edgar B., Charles R. Dietrich, Knut Meyer, et al.. (2006). Conjugated fatty acids accumulate to high levels in phospholipids of metabolically engineered soybean and Arabidopsis seeds. Phytochemistry. 67(12). 1166–1176. 119 indexed citations

13.

Dietrich, Charles R., Minoli A. Perera, Marna D. Yandeau‐Nelson, et al.. (2005). Characterization of two GL8 paralogs reveals that the 3‐ketoacyl reductase component of fatty acid elongase is essential for maize (Zea mays L.) development. The Plant Journal. 42(6). 844–861. 82 indexed citations

14.

Ge, Xiaochun, Charles R. Dietrich, Michiyo Matsuno, et al.. (2005). An Arabidopsis aspartic protease functions as an anti‐cell‐death component in reproduction and embryogenesis. EMBO Reports. 6(3). 282–288. 119 indexed citations

15.

Dietrich, Charles R., Feng Cui, Jin Li, et al.. (2002). Maize Mu Transposons Are Targeted to the 5′ Untranslated Region of the gl8 Gene and Sequences Flanking Mu Target-Site Duplications Exhibit Nonrandom Nucleotide Composition Throughout the Genome. Genetics. 160(2). 697–716. 94 indexed citations

16.

Xu, Xiaojie, Charles R. Dietrich, René Lessire, Basil J. Nikolau, & Patrick S. Schnable. (2002). The Endoplasmic Reticulum-Associated Maize GL8 Protein Is a Component of the Acyl-Coenzyme A Elongase Involved in the Production of Cuticular Waxes. PLANT PHYSIOLOGY. 128(3). 924–934. 57 indexed citations

17.

Frame, Bronwyn, Suzy M. Cocciolone, Л. В. Сидоренко, et al.. (2000). Production of transgenic maize from bombarded type II callus: Effect of gold particle size and callus morphology on transformation efficiency. In Vitro Cellular & Developmental Biology - Plant. 36(1). 21–29. 143 indexed citations

18.

Xu, Xiaojie, Charles R. Dietrich, Massimo Delledonne, et al.. (1997). Sequence Analysis of the Cloned glossy8 Gene of Maize Suggests That It May Code for a β-Ketoacyl Reductase Required for the Biosynthesis of Cuticular Waxes. PLANT PHYSIOLOGY. 115(2). 501–510. 85 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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