Arnaud Duchon

2.6k total citations
33 papers, 1.8k citations indexed

About

Arnaud Duchon is a scholar working on Public Health, Environmental and Occupational Health, Genetics and Molecular Biology. According to data from OpenAlex, Arnaud Duchon has authored 33 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Public Health, Environmental and Occupational Health, 22 papers in Genetics and 14 papers in Molecular Biology. Recurrent topics in Arnaud Duchon's work include Down syndrome and intellectual disability research (24 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Congenital heart defects research (8 papers). Arnaud Duchon is often cited by papers focused on Down syndrome and intellectual disability research (24 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Congenital heart defects research (8 papers). Arnaud Duchon collaborates with scholars based in France, United States and Spain. Arnaud Duchon's co-authors include Yann Hérault, Robert A. Floyd, John M. Carney, Mordechai Chevion, Véronique Brault, Valérie Nalesso, Claire Chevalier, Andrew J. Sharp, Matthieu Raveau and Nathalie Janel and has published in prestigious journals such as PLoS ONE, Scientific Reports and Genetics.

In The Last Decade

Arnaud Duchon

33 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Arnaud Duchon France	23	896	693	619	252	185	33	1.8k
James Stoll United States	20	235 0.3×	669 1.0×	203 0.3×	448 1.8×	240 1.3×	32	1.4k
Heather A. Ferris United States	19	113 0.1×	687 1.0×	150 0.2×	615 2.4×	323 1.7×	33	1.9k
Joan Rodríguez Spain	16	181 0.2×	588 0.8×	166 0.3×	267 1.1×	101 0.5×	24	1.3k
Roberta Lattanzi Italy	29	130 0.1×	861 1.2×	106 0.2×	697 2.8×	855 4.6×	103	2.4k
Emma S. Jones Australia	20	159 0.2×	617 0.9×	53 0.1×	161 0.6×	202 1.1×	28	1.8k
Meagan J. McManus United States	14	67 0.1×	1.2k 1.8×	114 0.2×	454 1.8×	159 0.9×	24	1.7k
Yang Du China	25	47 0.1×	680 1.0×	135 0.2×	121 0.5×	229 1.2×	69	1.5k
Pier Francesco Mannaioni Italy	24	264 0.3×	609 0.9×	31 0.1×	414 1.6×	192 1.0×	42	1.8k
Mohammad Reza Hojjati United States	17	36 0.0×	875 1.3×	238 0.4×	246 1.0×	233 1.3×	34	1.5k
Daiki Setoyama Japan	22	65 0.1×	724 1.0×	79 0.1×	243 1.0×	95 0.5×	64	1.5k

Countries citing papers authored by Arnaud Duchon

Since Specialization

Citations

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

Fields of papers citing papers by Arnaud Duchon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arnaud Duchon

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Lepagnol-Bestel, Aude-Marie, et al.. (2025). DYRK1A Up-Regulation Specifically Impairs a Presynaptic Form of Long-Term Potentiation. Life. 15(2). 149–149. 1 indexed citations

Lanzillotta, Chiara, Valérie Nalesso, Marzia Perluigi, et al.. (2024). Shaping down syndrome brain cognitive and molecular changes due to aging using adult animals from the Ts66Yah murine model. Neurobiology of Disease. 196. 106523–106523. 6 indexed citations

Duchon, Arnaud, Claire Chevalier, Valérie Nalesso, et al.. (2022). Ts66Yah, a mouse model of Down syndrome with improved construct and face validity. Disease Models & Mechanisms. 15(12). 26 indexed citations

Duchon, Arnaud, Claire Chevalier, Valérie Nalesso, et al.. (2021). Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse models. Human Molecular Genetics. 30(9). 771–788. 24 indexed citations

Guyot, Anne-Cécile, Clémence Disdier, Nassima Oumata, et al.. (2020). A Small Compound Targeting Prohibitin with Potential Interest for Cognitive Deficit Rescue in Aging mice and Tau Pathology Treatment. Scientific Reports. 10(1). 1143–1143. 23 indexed citations

Souchet, Benoît, Arnaud Duchon, Yuchen Gu, et al.. (2019). Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models. Scientific Reports. 9(1). 3914–3914. 38 indexed citations

Duchon, Arnaud & Yann Hérault. (2016). DYRK1A, a Dosage-Sensitive Gene Involved in Neurodevelopmental Disorders, Is a Target for Drug Development in Down Syndrome. Frontiers in Behavioral Neuroscience. 10. 104–104. 129 indexed citations

Maréchal, Damien, Patricia Lopes Pereira, Arnaud Duchon, & Yann Hérault. (2015). Dosage of the Abcg1-U2af1 Region Modifies Locomotor and Cognitive Deficits Observed in the Tc1 Mouse Model of Down Syndrome. PLoS ONE. 10(2). e0115302–e0115302. 12 indexed citations

Brault, Véronique, Arnaud Duchon, Caroline Romestaing, et al.. (2015). Opposite Phenotypes of Muscle Strength and Locomotor Function in Mouse Models of Partial Trisomy and Monosomy 21 for the Proximal Hspa13-App Region. PLoS Genetics. 11(3). e1005062–e1005062. 32 indexed citations

10.

Souchet, Benoît, Fayçal Guedj, Arnaud Duchon, et al.. (2015). Pharmacological correction of excitation/inhibition imbalance in Down syndrome mouse models. Frontiers in Behavioral Neuroscience. 9. 267–267. 56 indexed citations

11.

Souchet, Benoît, Fayçal Guedj, Ignasi Sahún, et al.. (2014). Excitation/inhibition balance and learning are modified by Dyrk1a gene dosage. Neurobiology of Disease. 69. 65–75. 91 indexed citations

12.

Noll, Christophe, Sandrine Middendorp, Arnaud Duchon, et al.. (2013). DYRK1A overexpression decreases plasma lecithin:cholesterol acyltransferase activity and apolipoprotein A-I levels. Molecular Genetics and Metabolism. 110(3). 371–377. 4 indexed citations

13.

Raveau, Matthieu, Valérie Nalesso, Arnaud Duchon, et al.. (2012). The App-Runx1 Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in a Down Syndrome Mouse Model. PLoS Genetics. 8(5). e1002724–e1002724. 22 indexed citations

14.

Delatour, Benoı̂t, Arnaud Duchon, Luce Dauphinot, et al.. (2011). Specific targeting of the GABA-A receptor α5 subtype by a selective inverse agonist restores cognitive deficits in Down syndrome mice. Journal of Psychopharmacology. 25(8). 1030–1042. 127 indexed citations

15.

Dauphinot, Luce, Arnaud Duchon, Robert H. Dodd, et al.. (2011). Chronic Treatment with a Promnesiant GABA-A -Selective Inverse Agonist Increases Immediate Early Genes Expression during Memory Processing in Mice and Rectifies Their Expression Levels in a Down Syndrome Mouse Model. Advances in Pharmacological Sciences. 2011. 1–11. 39 indexed citations

16.

Duchon, Arnaud, Stéphanie Pothion, Véronique Brault, et al.. (2010). The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndrome. Behavioural Brain Research. 217(2). 271–281. 25 indexed citations

17.

Pereira, Patricia Lopes, Laetitia Magnol, Ignasi Sahún, et al.. (2009). A new mouse model for the trisomy of the Abcg1–U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome. Human Molecular Genetics. 18(24). 4756–4769. 92 indexed citations

18.

Noll, Christophe, Chris Planque, Fayçal Guedj, et al.. (2009). DYRK1A, a Novel Determinant of the Methionine-Homocysteine Cycle in Different Mouse Models Overexpressing this Down-Syndrome-Associated Kinase. PLoS ONE. 4(10). e7540–e7540. 42 indexed citations

19.

Brault, Véronique, Vanessa Besson, Laetitia Magnol, Arnaud Duchon, & Yann Hérault. (2007). Cre/loxP-Mediated Chromosome Engineering of the Mouse Genome. Handbook of experimental pharmacology. 29–48. 39 indexed citations

20.

Besson, Vanessa, Véronique Brault, Arnaud Duchon, et al.. (2007). Modeling the monosomy for the telomeric part of human chromosome 21 reveals haploinsufficient genes modulating the inflammatory and airway responses. Human Molecular Genetics. 16(17). 2040–2052. 29 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