Mathilde Lachia

690 total citations
21 papers, 573 citations indexed

About

Mathilde Lachia is a scholar working on Plant Science, Ecology, Evolution, Behavior and Systematics and Organic Chemistry. According to data from OpenAlex, Mathilde Lachia has authored 21 papers receiving a total of 573 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Plant Science, 10 papers in Ecology, Evolution, Behavior and Systematics and 7 papers in Organic Chemistry. Recurrent topics in Mathilde Lachia's work include Plant Parasitism and Resistance (12 papers), Plant and animal studies (10 papers) and Allelopathy and phytotoxic interactions (6 papers). Mathilde Lachia is often cited by papers focused on Plant Parasitism and Resistance (12 papers), Plant and animal studies (10 papers) and Allelopathy and phytotoxic interactions (6 papers). Mathilde Lachia collaborates with scholars based in Switzerland, United Kingdom and Türkiye. Mathilde Lachia's co-authors include Alain De Mesmaeker, Christopher J. Moody, Claudio Screpanti, Pierre M. J. Jung, Alexandre Lumbroso, Raymonde Fonné‐Pfister, Stefano Rendine, Cyril Poriel, Philippe Renaud and F. Dénès and has published in prestigious journals such as Chemical Communications, The Journal of Organic Chemistry and Organic Letters.

In The Last Decade

Mathilde Lachia

21 papers receiving 571 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mathilde Lachia Switzerland 14 291 262 180 67 35 21 573
Carlton L. Campbell United States 11 207 0.7× 165 0.6× 45 0.3× 100 1.5× 48 1.4× 13 446
Yuanqiong Huang China 12 339 1.2× 74 0.3× 50 0.3× 130 1.9× 14 0.4× 22 450
Jin Dong China 12 137 0.5× 106 0.4× 48 0.3× 146 2.2× 9 0.3× 21 370
Christopher M. Glinkerman United States 12 271 0.9× 210 0.8× 26 0.1× 224 3.3× 18 0.5× 16 596
Zili Ren China 15 249 0.9× 126 0.5× 109 0.6× 109 1.6× 9 0.3× 22 432
Bai‐Ping Ying United States 12 144 0.5× 129 0.5× 44 0.2× 278 4.1× 23 0.7× 23 473
Ren-Xuan Wang China 8 148 0.5× 142 0.5× 159 0.9× 89 1.3× 8 0.2× 8 344
Tommaso A. Foderaro United States 11 151 0.5× 117 0.4× 72 0.4× 197 2.9× 19 0.5× 14 399
José Coll Spain 14 173 0.6× 152 0.6× 54 0.3× 181 2.7× 9 0.3× 20 479
Sara J. Phythian United Kingdom 11 258 0.9× 50 0.2× 39 0.2× 99 1.5× 16 0.5× 12 450

Countries citing papers authored by Mathilde Lachia

Since Specialization
Citations

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

Fields of papers citing papers by Mathilde Lachia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mathilde Lachia

This figure shows the co-authorship network connecting the top 25 collaborators of Mathilde Lachia. A scholar is included among the top collaborators of Mathilde Lachia 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 Mathilde Lachia. Mathilde Lachia 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.
Quinodoz, Pierre, Alexandre Lumbroso, Mathilde Lachia, et al.. (2023). Stereoselective Synthesis and Biological Profile of All Stereoisomers of Lactam Analogues of Strigolactones GR24 and GR18. Helvetica Chimica Acta. 106(1). 4 indexed citations
2.
Borghi, Lorenzo, et al.. (2021). Efficiency and bioavailability of new synthetic strigolactone mimics with potential for sustainable agronomical applications. Plant and Soil. 465(1-2). 109–123. 13 indexed citations
3.
Mesmaeker, Alain De, Claudio Screpanti, Raymonde Fonné‐Pfister, et al.. (2019). Design, Synthesis and Biological Evaluation of Strigolactone and Strigolactam Derivatives for Potential Crop Enhancement Applications in Modern Agriculture. CHIMIA International Journal for Chemistry. 73(7-8). 549–549. 18 indexed citations
4.
Elzinga, Dezi, Erin L. Sternburg, Davide Sabbadin, et al.. (2019). Defining and Exploiting Hypersensitivity Hotspots to Facilitate Abscisic Acid Agonist Optimization. ACS Chemical Biology. 14(3). 332–336. 14 indexed citations
5.
Lachia, Mathilde, Raymonde Fonné‐Pfister, Claudio Screpanti, et al.. (2018). New and Scalable Access to Karrikin (KAR1) and Evaluation of Its Potential Application on Corn Germination. Helvetica Chimica Acta. 101(8). 13 indexed citations
6.
Lachia, Mathilde, F. Richard, Raphael Bigler, et al.. (2018). An improved procedure for the Beckmann rearrangement of cyclobutanones. Tetrahedron Letters. 59(20). 1896–1901. 15 indexed citations
7.
Wendeborn, Sebastian, Mathilde Lachia, Pierre M. J. Jung, et al.. (2017). Biological Activity of Brassinosteroids – Direct Comparison of Known and New Analogs in planta. Helvetica Chimica Acta. 100(2). 8 indexed citations
8.
Screpanti, Claudio, Raymonde Fonné‐Pfister, Alexandre Lumbroso, et al.. (2016). Strigolactone derivatives for potential crop enhancement applications. Bioorganic & Medicinal Chemistry Letters. 26(10). 2392–2400. 51 indexed citations
9.
Lachia, Mathilde, et al.. (2015). Strigolactam: New potent strigolactone analogues for the germination of Orobanche cumana. Bioorganic & Medicinal Chemistry Letters. 25(10). 2184–2188. 46 indexed citations
10.
Lachia, Mathilde, Pierre M. J. Jung, Claudio Screpanti, et al.. (2014). Chemicals Inducing Seed Germination and Early Seedling Development. CHIMIA International Journal for Chemistry. 68(9). 654–654. 24 indexed citations
11.
Lachia, Mathilde, et al.. (2014). Synthesis of strigolactones analogues by intramolecular [2+2] cycloaddition of ketene-iminium salts to olefins and their activity on Orobanche cumana seeds. Bioorganic & Medicinal Chemistry Letters. 24(9). 2123–2128. 39 indexed citations
12.
13.
Lachia, Mathilde, et al.. (2014). Asymmetric synthesis of the four stereoisomers of 5-deoxystrigol. Tetrahedron Letters. 55(48). 6577–6581. 22 indexed citations
14.
Çatak, Şaron, et al.. (2014). 6π/10π-Electrocyclization of ketene-iminium salts for the synthesis of substituted naphthylamines. Tetrahedron Letters. 55(15). 2446–2449. 20 indexed citations
15.
Lachia, Mathilde, Pierre M. J. Jung, & Alain De Mesmaeker. (2012). A novel approach toward the synthesis of strigolactones through intramolecular [2+2] cycloaddition of ketenes and ketene-iminiums to olefins. Application to the asymmetric synthesis of GR-24. Tetrahedron Letters. 53(34). 4514–4517. 52 indexed citations
16.
17.
Lachia, Mathilde & Christopher J. Moody. (2008). The synthetic challenge of diazonamide A, a macrocyclic indole bis-oxazole marine natural product. Natural Product Reports. 25(2). 227–227. 100 indexed citations
18.
Poriel, Cyril, Mathilde Lachia, Claire Wilson, James R. Davies, & Christopher J. Moody. (2007). Oxidative Rearrangement of Indoles:  A New Approach to the EFHG-Tetracyclic Core of Diazonamide A. The Journal of Organic Chemistry. 72(8). 2978–2987. 40 indexed citations
19.
Lachia, Mathilde, Cyril Poriel, Alexandra M. Z. Slawin, & Christopher J. Moody. (2006). The remarkable effect of the 7-substituent in the diastereoselective oxidative rearrangement of indoles: Asymmetric synthesis of 3,3-disubstituted oxindoles. Chemical Communications. 286–288. 13 indexed citations
20.
Lachia, Mathilde, F. Dénès, Florent Beaufils, & Philippe Renaud. (2005). Highly Diastereoselective Formation of Spirocyclic Compounds via 1,5-Hydrogen Transfer:  A Total Synthesis of (−)-Erythrodiene. Organic Letters. 7(19). 4103–4106. 41 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Carlton L. Campbell Breakdown of academic impact, for papers by Yuanqiong Huang Breakdown of academic impact, for papers by Jin Dong Breakdown of academic impact, for papers by Christopher M. Glinkerman Breakdown of academic impact, for papers by Zili Ren Breakdown of academic impact, for papers by Bai‐Ping Ying Breakdown of academic impact, for papers by Ren-Xuan Wang Breakdown of academic impact, for papers by Tommaso A. Foderaro Breakdown of academic impact, for papers by José Coll Breakdown of academic impact, for papers by Sara J. Phythian
Rankless by CCL
2026