Thomas Blein

3.9k total citations
37 papers, 2.2k citations indexed

About

Thomas Blein is a scholar working on Plant Science, Molecular Biology and Cancer Research. According to data from OpenAlex, Thomas Blein has authored 37 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Plant Science, 23 papers in Molecular Biology and 6 papers in Cancer Research. Recurrent topics in Thomas Blein's work include Plant Molecular Biology Research (25 papers), Plant Reproductive Biology (12 papers) and Plant nutrient uptake and metabolism (8 papers). Thomas Blein is often cited by papers focused on Plant Molecular Biology Research (25 papers), Plant Reproductive Biology (12 papers) and Plant nutrient uptake and metabolism (8 papers). Thomas Blein collaborates with scholars based in France, Argentina and Germany. Thomas Blein's co-authors include Patrick Laufs, Alexis Peaucelle, Krisztina Nikovics, Martín Crespi, Mitsuhiro Aida, Tetsuya Ishida, Halima Morin, Alice Hasson, Aurélie Christ and Miltos Tsiantis and has published in prestigious journals such as Science, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Thomas Blein

36 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Blein France 19 1.9k 1.5k 148 145 81 37 2.2k
Arthur Chun-Chieh Shih Taiwan 16 782 0.4× 926 0.6× 118 0.8× 25 0.2× 68 0.8× 34 1.6k
Chun Liang United States 22 586 0.3× 1.2k 0.8× 214 1.4× 32 0.2× 8 0.1× 75 1.7k
Klaus Richter Germany 26 1.3k 0.7× 506 0.3× 70 0.5× 12 0.1× 16 0.2× 106 2.2k
Han Jiang China 22 657 0.3× 784 0.5× 173 1.2× 5 0.0× 40 0.5× 68 1.4k
Hideyuki Takahashi Japan 31 2.7k 1.4× 1.4k 0.9× 27 0.2× 7 0.0× 7 0.1× 103 3.0k
Na Cui China 19 638 0.3× 359 0.2× 17 0.1× 13 0.1× 90 1.1× 65 1.0k
Rongzhi Zhang China 15 795 0.4× 411 0.3× 47 0.3× 12 0.1× 38 0.5× 34 1.0k
Guanglei Yang China 13 415 0.2× 215 0.1× 103 0.7× 160 1.1× 240 3.0× 27 847
Xiangchao Gan Germany 18 881 0.5× 1.0k 0.7× 29 0.2× 4 0.0× 45 0.6× 40 1.6k

Countries citing papers authored by Thomas Blein

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Blein

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Blein

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Blein. A scholar is included among the top collaborators of Thomas Blein 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 Thomas Blein. Thomas Blein 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.
Mansilla, Natanael, Thomas Blein, Céline Sorin, et al.. (2025). The transcription factor NFYA10 determines the area explored by Arabidopsis thaliana roots and directly regulates LAZY genes. The Plant Journal. 121(5). e70016–e70016. 1 indexed citations
2.
Elmayan, Taline, Thomas Blein, Emilie Elvira‐Matelot, et al.. (2025). Arabidopsis SGS3 is recruited to chromatin by CHR11 to select RNA that initiate siRNA production. Nature Communications. 16(1). 2978–2978. 2 indexed citations
3.
Charon, Céline, et al.. (2024). From environmental responses to adaptation: the roles of plant lncRNAs. PLANT PHYSIOLOGY. 195(1). 232–244. 18 indexed citations
4.
Bazin, Jérémie, Emilie Elvira‐Matelot, Thomas Blein, et al.. (2023). Synergistic action of the Arabidopsis spliceosome components PRP39a and SmD1b in promoting posttranscriptional transgene silencing. The Plant Cell. 35(6). 1917–1935. 5 indexed citations
5.
Roulé, Thomas, et al.. (2023). The long intergenic noncoding RNA ARES modulates root architecture in Arabidopsis. IUBMB Life. 75(10). 880–892. 2 indexed citations
6.
Fonouni‐Farde, Camille, Aurélie Christ, Thomas Blein, et al.. (2022). The Arabidopsis APOLO and human UPAT sequence-unrelated long noncoding RNAs can modulate DNA and histone methylation machineries in plants. Genome biology. 23(1). 181–181. 35 indexed citations
7.
Ariel, Federico, Thomas Roulé, Diego H. Milone, et al.. (2021). ChronoRoot: High-throughput phenotyping by deep segmentation networks reveals novel temporal parameters of plant root system architecture. GigaScience. 10(7). 33 indexed citations
8.
Bazin, Jérémie, Natali Romero-Barrios, Michaël Moison, et al.. (2020). The Arabidopsis lnc RNA ASCO modulates the transcriptome through interaction with splicing factors. EMBO Reports. 21(5). e48977–e48977. 71 indexed citations
9.
Blein, Thomas, Coline Balzergue, Thomas Roulé, et al.. (2020). Landscape of the Noncoding Transcriptome Response of Two Arabidopsis Ecotypes to Phosphate Starvation. PLANT PHYSIOLOGY. 183(3). 1058–1072. 26 indexed citations
10.
Ariel, Federico, Leandro Lucero, Aurélie Christ, et al.. (2020). R-Loop Mediated trans Action of the APOLO Long Noncoding RNA. Molecular Cell. 77(5). 1055–1065.e4. 194 indexed citations
11.
Bazin, Jérémie, Kiruthiga Mariappan, Yunhe Jiang, et al.. (2020). Role of MPK4 in pathogen-associated molecular pattern-triggered alternative splicing in Arabidopsis. PLoS Pathogens. 16(4). e1008401–e1008401. 45 indexed citations
13.
Gonçalves, Beatriz, Aude Maugarny-Calès, Bernard Adroher, et al.. (2017). GDP-L-fucose is required for boundary definition in plants. Journal of Experimental Botany. 68(21-22). 5801–5811. 12 indexed citations
14.
Jégu, Teddy, Séverine Domenichini, Thomas Blein, et al.. (2015). A SWI/SNF Chromatin Remodelling Protein Controls Cytokinin Production through the Regulation of Chromatin Architecture. PLoS ONE. 10(10). e0138276–e0138276. 26 indexed citations
15.
Sorin, Céline, Aurélie Christ, Thomas Blein, et al.. (2014). A miR169 isoform regulates specific NFYA targets and root architecture in Arabidopsis. New Phytologist. 202(4). 1197–1211. 183 indexed citations
17.
Schmidt, Thorsten, et al.. (2013). Variational attenuation correction in two-view confocal microscopy. BMC Bioinformatics. 14(1). 366–366. 1 indexed citations
18.
Blein, Thomas, Amada Pulido, Aurélie Vialette‐Guiraud, et al.. (2008). A Conserved Molecular Framework for Compound Leaf Development. Science. 322(5909). 1835–1839. 275 indexed citations
19.
Greb, Thomas, et al.. (2008). Interplay of miR164, CUP‐SHAPED COTYLEDON genes and LATERAL SUPPRESSOR controls axillary meristem formation in Arabidopsis thaliana. The Plant Journal. 55(1). 65–76. 242 indexed citations
20.
Nikovics, Krisztina, Thomas Blein, Alexis Peaucelle, et al.. (2006). The Balance between the MIR164A and CUC2 Genes Controls Leaf Margin Serration in Arabidopsis. The Plant Cell. 18(11). 2929–2945. 477 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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