Aurélien Trimouille
Impact in
- Cell Biology top 10%
- melanin and skin pigmentation
-
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Genomics and Rare Diseases
Papers in
-
- Mitochondrial Function and Pathology 4
- Ion channel regulation and function 3
- Genetics 11
- Connective tissue disorders research 3
- Craniofacial Disorders and Treatments 3
- Genomic variations and chromosomal abnormalities 3
- Cleft Lip and Palate Research 2
- Co-authors
- Didier Lacombe (16 shared papers)Caroline Rooryck (9 shared papers)Benoı̂t Arveiler (11 shared papers)Eulalie Lasseaux (8 shared papers)Claudio Plaisant (6 shared papers)Vincent Michaud (5 shared papers)Angèle Tingaud‐Sequeira (6 shared papers)Perrine Pennamen (5 shared papers)
- Journals
- Clinical Genetics (4 papers)European Journal of Medical Genetics (3 papers)Clinical Kidney Journal (1 paper)Scientific Reports (1 paper)Acta Neuropathologica Communications (1 paper)
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
Aurélien Trimouille
23 papers receiving 423 citations
Peers
Comparison fields: 5 of 63
- Cell Biology 143
- Genetics 121
- Nutrition and Dietetics 65
- Sensory Systems 19
- Molecular Biology 237
Countries citing papers authored by Aurélien Trimouille
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
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-authors
The 25 scholars most cited alongside Aurélien Trimouille, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 98 | |
| 2 | 2020 | 55 | |
| 3 | 2017 | 43 | |
| 4 | 2018 | 30 | |
| 5 | 2018 | 26 | |
| 6 | 2022 | 25 | |
| 7 | 2020 | 20 | |
| 8 | 2021 | 16 | |
| 9 | 2019 | 14 | |
| 10 | 2020 | 12 | |
| 11 | 2019 | 12 | |
| 12 | 2021 | 11 | |
| 13 | 2020 | 10 | |
| 14 | 2022 | 9 | |
| 15 | 2018 | 7 | |
| 16 | 2015 | 7 | |
| 17 | 2020 | 7 | |
| 18 | 2020 | 6 | |
| 19 | 2022 | 5 | |
| 20 | 2019 | 5 |
About Aurélien Trimouille
Aurélien Trimouille is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Clinical Biochemistry and Pathology and Forensic Medicine, having authored 25 papers that have together received 427 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (4 papers), Mitochondrial Function and Pathology (4 papers), Connective tissue disorders research (3 papers), Craniofacial Disorders and Treatments (3 papers), Ion channel regulation and function (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Cleft Lip and Palate Research (2 papers) and Genetic Neurodegenerative Diseases (2 papers). The work is most often cited by research in Cell Biology (143 citations), Genetics (121 citations), Nutrition and Dietetics (65 citations), Sensory Systems (19 citations) and Molecular Biology (237 citations). Aurélien Trimouille has collaborated with scholars based in France, United States and Germany. Frequent 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. Their work appears in journals such as Clinical Genetics, European Journal of Medical Genetics, Clinical Kidney Journal, Scientific Reports and Acta Neuropathologica Communications.
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.