Aurélien Trimouille

1.6k total citations
25 papers, 427 citations indexed

About

Aurélien Trimouille is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Aurélien Trimouille has authored 25 papers receiving a total of 427 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 11 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Aurélien Trimouille's work include Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (4 papers) and Connective tissue disorders research (3 papers). Aurélien Trimouille is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (4 papers) and Connective tissue disorders research (3 papers). Aurélien Trimouille collaborates with scholars based in France, United States and Germany. Aurélien Trimouille's co-authors include Didier Lacombe, Caroline Rooryck, Benoı̂t Arveiler, Eulalie Lasseaux, Claudio Plaisant, Vincent Michaud, Angèle Tingaud‐Sequeira, Perrine Pennamen, Fanny Morice‐Picard and Cyril Goizet and has published in prestigious journals such as Scientific Reports, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease and Journal of Medical Genetics.

In The Last Decade

Aurélien Trimouille

23 papers receiving 423 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aurélien Trimouille France 12 237 143 121 65 33 25 427
Keren Bismuth France 9 251 1.1× 116 0.8× 39 0.3× 42 0.6× 43 1.3× 14 466
Ruth Sheffer Israel 14 417 1.8× 118 0.8× 156 1.3× 43 0.7× 39 1.2× 22 627
Patricio Barros‐Núñez Mexico 15 359 1.5× 99 0.7× 302 2.5× 19 0.3× 28 0.8× 71 688
Hartmut Engel Germany 9 380 1.6× 69 0.5× 182 1.5× 18 0.3× 71 2.2× 15 518
Serena Giuliano France 12 313 1.3× 109 0.8× 21 0.2× 26 0.4× 20 0.6× 16 482
Shehla Mohammed United Kingdom 12 497 2.1× 57 0.4× 248 2.0× 18 0.3× 42 1.3× 25 680
Janine Altmueller Germany 11 477 2.0× 39 0.3× 43 0.4× 22 0.3× 42 1.3× 14 605
Keren I. Hilgendorf United States 9 443 1.9× 107 0.7× 339 2.8× 26 0.4× 87 2.6× 16 679
Lauren Brady Canada 17 360 1.5× 57 0.4× 120 1.0× 10 0.2× 26 0.8× 40 558
Paola Origone Italy 16 190 0.8× 57 0.4× 38 0.3× 15 0.2× 28 0.8× 47 584

Countries citing papers authored by Aurélien Trimouille

Since Specialization
Citations

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

Fields of papers citing papers by Aurélien Trimouille

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aurélien Trimouille

This figure shows the co-authorship network connecting the top 25 collaborators of Aurélien Trimouille. A scholar is included among the top collaborators of Aurélien Trimouille 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 Aurélien Trimouille. Aurélien Trimouille 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.
2.
Courtois, Sarah, Nívea Dias Amoêdo, Elodie Dumon, et al.. (2023). Mutation on MT-CO2 gene induces mitochondrial disease associated with neurodegeneration and intracerebral iron accumulation (NBIA). Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1870(1). 166856–166856. 2 indexed citations
3.
Trimouille, Aurélien, Cyril Goizet, Guilhem Solé, et al.. (2022). Renal involvement is frequent in adults with primary mitochondrial disorders: an observational study. Clinical Kidney Journal. 16(1). 100–110. 5 indexed citations
4.
Lacombe, Didier, Julien Van‐Gils, Marine Lebrun, et al.. (2022). Hemidystonia with polymicrogyria is part of ATP1A3-related disorders. Brain and Development. 44(8). 567–570.
5.
Michaud, Vincent, et al.. (2022). Whole-exome sequencing confirms implication of VPS13D as a potential cause of progressive spastic ataxia. BMC Neurology. 22(1). 53–53. 9 indexed citations
6.
Tingaud‐Sequeira, Angèle, Aurélien Trimouille, Rachel Stapleton, et al.. (2021). A recurrent missense variant in EYA3 gene is associated with oculo-auriculo-vertebral spectrum. Human Genetics. 140(6). 933–944. 16 indexed citations
7.
Schimpf, Johannes, Jean‐Paul di Rago, Déborah Tribouillard‐Tanvier, et al.. (2021). Biochemical consequences of two clinically relevant ND-gene mutations in Escherichia coli respiratory complex I. Scientific Reports. 11(1). 12641–12641. 11 indexed citations
8.
Trimouille, Aurélien, Benoı̂t Arveiler, Caroline Espil‐Taris, et al.. (2021). CHN1 and duane retraction syndrome: Expanding the phenotype to cranial nerves development disease. European Journal of Medical Genetics. 64(4). 104188–104188. 4 indexed citations
9.
Trimouille, Aurélien, Angèle Tingaud‐Sequeira, Didier Lacombe, et al.. (2020). Description of a family with X‐linked oculo‐auriculo‐vertebral spectrum associated with polyalanine tract expansion in ZIC3 . Clinical Genetics. 98(4). 384–389. 12 indexed citations
10.
Pennamen, Perrine, Linh Le, Angèle Tingaud‐Sequeira, et al.. (2020). BLOC1S5 pathogenic variants cause a new type of Hermansky–Pudlak syndrome. Genetics in Medicine. 22(10). 1613–1622. 55 indexed citations
11.
Trimouille, Aurélien, Florent Marguet, Eulalie Lasseaux, et al.. (2020). Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelination. Acta Neuropathologica Communications. 8(1). 48–48. 6 indexed citations
12.
Tingaud‐Sequeira, Angèle, Aurélien Trimouille, Sandrine Marlin, et al.. (2020). Functional and genetic analyses of ZYG11B provide evidences for its involvement in OAVS. Molecular Genetics & Genomic Medicine. 8(10). e1375–e1375. 20 indexed citations
13.
Trimouille, Aurélien, Cyril Goizet, Romain Boulestreau, et al.. (2019). Adult onset tubulo‐interstitial nephropathy in MT‐ND5‐related phenotypes. Clinical Genetics. 97(4). 628–633. 14 indexed citations
14.
Trimouille, Aurélien, et al.. (2019). Severe Thoracic and Spinal Bone Abnormalities in neurofibromatosis type 1. European Journal of Medical Genetics. 63(4). 103815–103815. 12 indexed citations
15.
Brischoux‐Boucher, Elise, Aurélien Trimouille, Geneviève Baujat, et al.. (2018). IL11RA‐related Crouzon‐like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differences. Clinical Genetics. 94(3-4). 373–380. 26 indexed citations
16.
Trimouille, Aurélien, Émilie Obre, Guillaume Banneau, et al.. (2018). An in-frame deletion in BICD2 associated with a non-progressive form of SMALED. Clinical Neurology and Neurosurgery. 166. 1–3. 7 indexed citations
17.
Lasseaux, Eulalie, Claudio Plaisant, Vincent Michaud, et al.. (2018). Molecular characterization of a series of 990 index patients with albinism. Pigment Cell & Melanoma Research. 31(4). 466–474. 98 indexed citations
18.
Van‐Gils, Julien, Antoine Bigourdan, Pierre‐Simon Jouk, et al.. (2018). Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variant. European Journal of Medical Genetics. 62(6). 103530–103530. 30 indexed citations
19.
Trimouille, Aurélien, Angèle Tingaud‐Sequeira, Perrine Pennamen, et al.. (2018). Deletion in 2q35 excluding the IHH gene leads to fetal severe limb anomalies and suggests a disruption of chromatin architecture. European Journal of Human Genetics. 27(3). 384–388. 3 indexed citations
20.
Trimouille, Aurélien, Eulalie Lasseaux, Pascal Barat, et al.. (2017). Further delineation of the phenotype caused by biallelic variants in the WDR4 gene. Clinical Genetics. 93(2). 374–377. 43 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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