Laurian S. Robert

2.3k total citations
54 papers, 1.8k citations indexed

About

Laurian S. Robert is a scholar working on Molecular Biology, Plant Science and Biotechnology. According to data from OpenAlex, Laurian S. Robert has authored 54 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 39 papers in Plant Science and 14 papers in Biotechnology. Recurrent topics in Laurian S. Robert's work include Plant Reproductive Biology (24 papers), Photosynthetic Processes and Mechanisms (17 papers) and Plant tissue culture and regeneration (16 papers). Laurian S. Robert is often cited by papers focused on Plant Reproductive Biology (24 papers), Photosynthetic Processes and Mechanisms (17 papers) and Plant tissue culture and regeneration (16 papers). Laurian S. Robert collaborates with scholars based in Canada, United Kingdom and United States. Laurian S. Robert's co-authors include Illimar Altosaar, Richard D. Thompson, Diego Albani, R. B. Flavell, Paul G. Arnison, Constance Nozzolillo, Steven F. Fabijanski, Sharon Allard, Michael Bevan and Tony A. Kavanagh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The EMBO Journal and Nature Biotechnology.

In The Last Decade

Laurian S. Robert

53 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laurian S. Robert Canada 24 1.4k 1.1k 236 127 126 54 1.8k
Tuomas Sopanen Finland 22 968 0.7× 724 0.6× 240 1.0× 84 0.7× 181 1.4× 40 1.3k
Yong Weon Seo South Korea 23 1.3k 0.9× 721 0.6× 63 0.3× 123 1.0× 57 0.5× 124 1.6k
Yingkao Hu China 23 1.4k 1.0× 870 0.8× 39 0.2× 61 0.5× 98 0.8× 48 1.7k
Heidi F. Kaeppler United States 28 2.0k 1.4× 1.6k 1.4× 315 1.3× 268 2.1× 30 0.2× 58 2.4k
Linda Tabe Australia 14 991 0.7× 533 0.5× 220 0.9× 73 0.6× 86 0.7× 21 1.2k
Mercedes Díaz‐Mendoza Spain 20 1.1k 0.8× 872 0.8× 157 0.7× 38 0.3× 37 0.3× 27 1.4k
Jens Tiedemann Germany 13 1.8k 1.2× 1.2k 1.1× 93 0.4× 45 0.4× 38 0.3× 16 2.1k
Champa Sengupta‐Gopalan United States 24 1.5k 1.0× 988 0.9× 376 1.6× 39 0.3× 38 0.3× 47 1.8k
Vimla Vasil United States 37 3.9k 2.7× 3.9k 3.5× 1.3k 5.5× 141 1.1× 68 0.5× 63 4.6k
Hideyuki Funatsuki Japan 24 1.4k 1.0× 449 0.4× 87 0.4× 118 0.9× 50 0.4× 46 1.6k

Countries citing papers authored by Laurian S. Robert

Since Specialization
Citations

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

Fields of papers citing papers by Laurian S. Robert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laurian S. Robert. 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 Laurian S. Robert. The network helps show where Laurian S. Robert may publish in the future.

Co-authorship network of co-authors of Laurian S. Robert

This figure shows the co-authorship network connecting the top 25 collaborators of Laurian S. Robert. A scholar is included among the top collaborators of Laurian S. Robert 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 Laurian S. Robert. Laurian S. Robert 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.
Sprott, David E., et al.. (2023). The triticale mature pollen and stigma proteomes – assembling the proteins for a productive encounter. Journal of Proteomics. 278. 104867–104867. 2 indexed citations
2.
Zaidi, Mohsin Abbas, Stephen J. B. O’Leary, Denise Chabot, et al.. (2020). A triticale tapetal non-specific lipid transfer protein (nsLTP) is translocated to the pollen cell wall. Plant Cell Reports. 39(9). 1185–1197. 12 indexed citations
3.
4.
Zaidi, Mohsin Abbas, Stephen J. B. O’Leary, Shaobo Wu, et al.. (2016). Investigating Triticeae anther gene promoter activity in transgenic Brachypodium distachyon. Planta. 245(2). 385–396. 6 indexed citations
5.
Nazemof, Nazila, et al.. (2014). Proteomic profiling reveals insights into Triticeae stigma development and function. Journal of Experimental Botany. 65(20). 6069–6080. 8 indexed citations
6.
Zaidi, Mohsin Abbas, Stephen O’Leary, Shaobo Wu, et al.. (2012). A molecular and proteomic investigation of proteins rapidly released from triticale pollen upon hydration. Plant Molecular Biology. 79(1-2). 101–121. 17 indexed citations
7.
Harris, Linda J., Nancy J. Alexander, B. D. Blackwell, et al.. (2006). A novel gene cluster in Fusarium graminearum contains a gene that contributes to butenolide synthesis. Fungal Genetics and Biology. 44(4). 293–306. 42 indexed citations
8.
Robert, Laurian S.. (2006). Crop Ferality and Volunteerism. Crop Science. 46(3). 1418–1419. 109 indexed citations
9.
Albani, Diego, et al.. (2003). Expression of CCAAT-binding factor antisense transcripts in reproductive tissues affects plant fertility. Plant Cell Reports. 21(8). 804–808. 15 indexed citations
10.
Schneiderman, Danielle, et al.. (2002). Modifying the pollen coat protein composition in Brassica. The Plant Journal. 31(4). 477–486. 14 indexed citations
11.
Robert, Laurian S., et al.. (1998). Conserved structure and function of the Arabidopsis flowering time gene CONSTANS in Brassica napus. Plant Molecular Biology. 37(5). 763–772. 90 indexed citations
12.
Johnson‐Flanagan, Anne M., et al.. (1998). REDUCTION OF CHLOROPHYLL ACCUMULATION IN SEED OF TRANSGENIC BRASSICA NAPUS USING ANTISENSE TECHNOLOGY. Acta Horticulturae. 183–190.
13.
Datla, Raju, et al.. (1997). The promoter of aBrassica napus polygalacturonase gene directs pollen expression of?-glucuronidase in transgenicBrassica plants. Plant Cell Reports. 16(6). 373–378. 24 indexed citations
14.
Albani, Diego & Laurian S. Robert. (1995). Cloning and characterization of a Brassica napus gene encoding a homologue of the B subunit of a heteromeric CCAAT-binding factor. Gene. 167(1-2). 209–213. 34 indexed citations
15.
Robert, Laurian S., et al.. (1994). Molecular characterization of two Brassica napus genes related to oleosins which are highly expressed in the tapetum. The Plant Journal. 6(6). 927–933. 40 indexed citations
16.
Robert, Laurian S., et al.. (1994). Sequence and expression of endogenous S-locus glycoprotein genes in self-compatible Brassica napus. Molecular and General Genetics MGG. 242(2). 209–216. 20 indexed citations
17.
Robert, Laurian S., et al.. (1989). Antisense RNA inhibition of ?-glucuronidase gene expression in transgenic tobacco plants. Plant Molecular Biology. 13(4). 399–409. 36 indexed citations
18.
Colot, Vincent, Laurian S. Robert, Tony A. Kavanagh, Michael Bevan, & Richard D. Thompson. (1987). Localization of sequences in wheat endosperm protein genes which confer tissue-specific expression in tobacco. The EMBO Journal. 6(12). 3559–3564. 152 indexed citations
19.
Robert, Laurian S., Constance Nozzolillo, & Illimar Altosaar. (1983). Molecular weight and charge heterogeneity of prolamins (Avenins) from nine oat (Avena sativa L.) cultivars of different protein content and from developing seeds. Europe PMC (PubMed Central). 60(6). 438–442. 26 indexed citations
20.
Robert, Laurian S., et al.. (1983). Total Solubilization of Groat Proteins in High Protein Oat (Avena sativa L. cv. Hinoat): Evidence that Glutelins are a Minor Component. Canadian Institute of Food Science and Technology Journal. 16(3). 196–200. 30 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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