M. David Marks

11.4k total citations · 3 hit papers
84 papers, 8.7k citations indexed

About

M. David Marks is a scholar working on Plant Science, Molecular Biology and Genetics. According to data from OpenAlex, M. David Marks has authored 84 papers receiving a total of 8.7k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Plant Science, 66 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in M. David Marks's work include Plant Reproductive Biology (42 papers), Plant Molecular Biology Research (40 papers) and Plant tissue culture and regeneration (20 papers). M. David Marks is often cited by papers focused on Plant Reproductive Biology (42 papers), Plant Molecular Biology Research (40 papers) and Plant tissue culture and regeneration (20 papers). M. David Marks collaborates with scholars based in United States, United Kingdom and Japan. M. David Marks's co-authors include Kenneth A. Feldmann, Daniel B. Szymanski, David G Oppenheimer, Jeffrey J. Esch, John C. Larkin, Brian A. Larkins, Patricia L. Herman, Alan Lloyd, Karl Pedersen and Susan M. Wick and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

M. David Marks

81 papers receiving 8.4k citations

Hit Papers

The TRANSPARENT TESTA GLABRA1 Locus, Which Regulates Tric... 1991 2026 2002 2014 1999 1991 1994 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. David Marks United States 50 7.0k 6.6k 358 342 340 84 8.7k
Tomohiko Kato Japan 47 9.0k 1.3× 7.1k 1.1× 349 1.0× 388 1.1× 186 0.5× 77 10.6k
Kirankumar S. Mysore United States 67 12.4k 1.8× 5.8k 0.9× 531 1.5× 401 1.2× 745 2.2× 274 14.0k
Xiping Wang China 46 5.5k 0.8× 4.2k 0.6× 496 1.4× 183 0.5× 253 0.7× 191 7.4k
Nobutaka Mitsuda Japan 54 9.0k 1.3× 7.2k 1.1× 179 0.5× 406 1.2× 265 0.8× 166 10.4k
Zheng‐Hua Ye United States 61 11.4k 1.6× 9.7k 1.5× 606 1.7× 250 0.7× 841 2.5× 120 14.0k
Mark J. Guiltinan United States 42 4.1k 0.6× 3.0k 0.5× 335 0.9× 159 0.5× 483 1.4× 116 5.6k
Dominique Roby France 47 5.7k 0.8× 2.9k 0.4× 520 1.5× 211 0.6× 311 0.9× 80 6.5k
Alain Jauneau France 47 6.0k 0.8× 2.8k 0.4× 490 1.4× 599 1.8× 407 1.2× 118 7.2k
José Ramón Botella Australia 49 5.2k 0.7× 4.4k 0.7× 353 1.0× 129 0.4× 357 1.1× 154 6.9k
George W. Haughn Canada 57 7.8k 1.1× 6.5k 1.0× 111 0.3× 540 1.6× 237 0.7× 97 9.1k

Countries citing papers authored by M. David Marks

Since Specialization
Citations

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

Fields of papers citing papers by M. David Marks

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. David Marks. 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 M. David Marks. The network helps show where M. David Marks may publish in the future.

Co-authorship network of co-authors of M. David Marks

This figure shows the co-authorship network connecting the top 25 collaborators of M. David Marks. A scholar is included among the top collaborators of M. David Marks 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 M. David Marks. M. David Marks 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.
Marks, M. David, et al.. (2023). Impact of extraction conditions and seed variety on the characteristics of pennycress (Thlaspi arvense) protein: a structure and function approach. Journal of the American Oil Chemists Society. 100(11). 869–888. 8 indexed citations
2.
Sun, Xiao, et al.. (2023). Fungal Bioprocessing to Improve Quality of Pennycress Meal as a Potential Feeding Ingredient for Monogastric Animals. Fermentation. 9(8). 732–732. 10 indexed citations
3.
Hampton, Marshall, et al.. (2017). The pennycress (Thlaspi arvense L.) nectary: structural and transcriptomic characterization. BMC Plant Biology. 17(1). 201–201. 18 indexed citations
4.
Dorn, Kevin, Johnathon D. Fankhauser, Dominic Wyse, & M. David Marks. (2015). A draft genome of field pennycress (Thlaspi arvense) provides tools for the domestication of a new winter biofuel crop. DNA Research. 22(2). 121–131. 78 indexed citations
5.
Sedbrook, John C., Winthrop B. Phippen, & M. David Marks. (2014). New approaches to facilitate rapid domestication of a wild plant to an oilseed crop: Example pennycress (Thlaspi arvense L.). Plant Science. 227. 122–132. 111 indexed citations
6.
Gilding, Edward K. & M. David Marks. (2010). Analysis of purified glabra3-shapeshifter trichomes reveals a role for NOECK in regulating early trichome morphogenic events. The Plant Journal. 64(2). 304–317. 49 indexed citations
7.
Shi, Feng, et al.. (2009). Distortion of trichome morphology by the hairless mutation of tomato affects leaf surface chemistry. Journal of Experimental Botany. 61(4). 1053–1064. 144 indexed citations
9.
Wenger, Jonathan P. & M. David Marks. (2008). E2F and retinoblastoma related proteins may regulateGL1expression in developing Arabidopsis trichomes. Plant Signaling & Behavior. 3(6). 420–422. 5 indexed citations
10.
Marks, M. David, Edward K. Gilding, & Jonathan P. Wenger. (2007). Genetic interaction between glabra3‐shapeshifter and siamese in Arabidopsis thaliana converts trichome precursors into cells with meristematic activity. The Plant Journal. 52(2). 352–361. 13 indexed citations
11.
Marks, M. David, et al.. (2004). Influence of medium soil cultivation methods and meteorological conditions on weeds infestation in horse bean. Polish Journal of Natural Science. 16. 67–75.
12.
Wada, Takuji, Tetsuya Kurata, Rumi Tominaga, et al.. (2002). Role of a positive regulator of root hair development, CAPRICE ,in Arabidopsis root epidermal cell differentiation. Development. 129(23). 5409–5419. 259 indexed citations
13.
Qiu, Jin‐Long, et al.. (2002). The Arabidopsis SPIKE1 Gene Is Required for Normal Cell Shape Control and Tissue Development. The Plant Cell. 14(1). 101–118. 171 indexed citations
14.
Szymanski, Daniel B., Alan Lloyd, & M. David Marks. (2000). Progress in the molecular genetic analysis of trichome initiation and morphogenesis in Arabidopsis. Trends in Plant Science. 5(5). 214–219. 206 indexed citations
15.
Esch, Jeffrey J., David G Oppenheimer, & M. David Marks. (1994). Characterization of a weak allele of the GL1 gene of Arabidopsis thaliana. Plant Molecular Biology. 24(1). 203–207. 33 indexed citations
16.
Marks, M. David. (1994). Plant Development: The making of a plant hair. Current Biology. 4(7). 621–623. 16 indexed citations
17.
Marks, M. David, Joanne West, & Donald P. Weeks. (1987). The relatively large beta-tubulin gene family of Arabidopsis contains a member with an unusual transcribed 5? noncoding sequence. Plant Molecular Biology. 10(2). 91–104. 75 indexed citations
18.
Jonas, Adam J., et al.. (1987). Nephropathic cystinosis with central nervous system involvement. The American Journal of Medicine. 83(5). 966–970. 54 indexed citations
19.
Garger, Stephen J., et al.. (1987). Molecular cloning and physical characterization of a Brassica linear mitochondrial plasmid. Molecular and General Genetics MGG. 209(2). 227–233. 24 indexed citations
20.
Marks, M. David, et al.. (1985). Assignment of the temperature-sensitive lesion in the replication mutant A1 of vesicular stomatitis virus to the N gene. Journal of Virology. 53(1). 44–51. 4 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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