Alexandre Mathieu

1.3k total citations
7 papers, 156 citations indexed

About

Alexandre Mathieu is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Alexandre Mathieu has authored 7 papers receiving a total of 156 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 1 paper in Surgery. Recurrent topics in Alexandre Mathieu's work include Genomic variations and chromosomal abnormalities (5 papers), Congenital heart defects research (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Alexandre Mathieu is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Congenital heart defects research (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Alexandre Mathieu collaborates with scholars based in France, United Kingdom and United States. Alexandre Mathieu's co-authors include Thomas Bourgeron, Claire S. Leblond, Guillaume Huguet, Freddy Cliquet, Nathalie Lemière, Christopher Gillberg, Richard Delorme, Thomas Kergrohen, Thierry Bienvenu and Jean‐François Deleuze and has published in prestigious journals such as JAMA Psychiatry, Translational Psychiatry and American Journal of Medical Genetics Part A.

In The Last Decade

Alexandre Mathieu

6 papers receiving 155 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alexandre Mathieu France	6	97	81	48	16	16	7	156
Aurora Arghir Romania	7	87 0.9×	78 1.0×	31 0.6×	10 0.6×	24 1.5×	30	187
Marta Codina‐Solà Spain	7	125 1.3×	96 1.2×	72 1.5×	10 0.6×	11 0.7×	21	210
Tianyun Wang China	8	97 1.0×	71 0.9×	89 1.9×	12 0.8×	29 1.8×	15	205
Gérald Bussy France	8	80 0.8×	70 0.9×	31 0.6×	10 0.6×	15 0.9×	17	176
Nathan P. Achilly United States	6	74 0.8×	132 1.6×	37 0.8×	16 1.0×	14 0.9×	6	204
Daniel L Rice United Kingdom	2	122 1.3×	76 0.9×	41 0.9×	8 0.5×	9 0.6×	2	187
Crina M. Floruta United States	4	65 0.7×	92 1.1×	62 1.3×	33 2.1×	17 1.1×	5	166
Anna Mikhailov Canada	7	104 1.1×	102 1.3×	40 0.8×	24 1.5×	14 0.9×	16	194
Gail Reiner United States	6	66 0.7×	101 1.2×	71 1.5×	21 1.3×	10 0.6×	9	207
Emily Hansen‐Kiss United States	5	46 0.5×	89 1.1×	36 0.8×	24 1.5×	6 0.4×	9	150

Countries citing papers authored by Alexandre Mathieu

Since Specialization

Citations

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

Fields of papers citing papers by Alexandre Mathieu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexandre Mathieu

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

All Works

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7 of 7 papers shown

Moreau, Clara, Christopher R. K. Ching, Alexandre Mathieu, et al.. (2025). Neuroimaging insights into brain mechanisms of early-onset restrictive eating disorders. Nature Mental Health. 3(7). 780–788.

Leblond, Claire S., Thomas Rolland, Freddy Cliquet, et al.. (2023). Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndrome. European Journal of Medical Genetics. 66(5). 104732–104732. 14 indexed citations

Pagan, Cécile, Claire S. Leblond, Freddy Cliquet, et al.. (2021). Decreased phenol sulfotransferase activities associated with hyperserotonemia in autism spectrum disorders. Translational Psychiatry. 11(1). 23–23. 18 indexed citations

Leblond, Claire S., Freddy Cliquet, Guillaume Huguet, et al.. (2019). Both rare and common genetic variants contribute to autism in the Faroe Islands. npj Genomic Medicine. 4(1). 1–1. 52 indexed citations

Leblond, Claire S., Béatrice Regnault, Alexandre Mathieu, et al.. (2018). Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology. Journal of Applied Genetics. 60(1). 49–56. 10 indexed citations

Huguet, Guillaume, Catherine Schramm, Élise Douard, et al.. (2018). Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples. JAMA Psychiatry. 75(5). 447–447. 45 indexed citations

Maruani, Anna, Guillaume Huguet, Anita Beggiato, et al.. (2015). 11q24.2‐25 micro‐rearrangements in autism spectrum disorders: Relation to brain structures. American Journal of Medical Genetics Part A. 167(12). 3019–3030. 17 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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