Aude Tessier

660 total citations
11 papers, 246 citations indexed

About

Aude Tessier is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Aude Tessier has authored 11 papers receiving a total of 246 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Aude Tessier's work include Congenital heart defects research (4 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Aude Tessier is often cited by papers focused on Congenital heart defects research (4 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Aude Tessier collaborates with scholars based in France, Belgium and Japan. Aude Tessier's co-authors include Scott Zeitlin, Sophie Lenoir, Monia Barnat, Mariacristina Capizzi, Barbara Y. Braz, Radhia Kacher, Alexandra Dürr, Sandrine Humbert, Charles Duyckaerts and Marc Dommergues and has published in prestigious journals such as Science, Kidney International and American Journal of Obstetrics and Gynecology.

In The Last Decade

Aude Tessier

10 papers receiving 245 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aude Tessier France 5 152 144 58 28 27 11 246
Lúcia Inês Macedo‐Souza Brazil 10 143 0.9× 90 0.6× 49 0.8× 56 2.0× 41 1.5× 18 338
Tyrone DeSpenza United States 10 156 1.0× 77 0.5× 31 0.5× 79 2.8× 26 1.0× 13 293
Samantha L. Sison United States 9 272 1.8× 109 0.8× 100 1.7× 21 0.8× 19 0.7× 10 412
Michiel R. Fokkens Netherlands 9 206 1.4× 176 1.2× 64 1.1× 25 0.9× 17 0.6× 11 312
Cinzia Bertolin Italy 10 191 1.3× 105 0.7× 105 1.8× 37 1.3× 22 0.8× 21 317
J. Benjamin Kacerovsky Canada 5 129 0.8× 83 0.6× 26 0.4× 9 0.3× 24 0.9× 5 281
Juan José Casañas Spain 7 265 1.7× 115 0.8× 28 0.5× 37 1.3× 66 2.4× 9 355
Lauren M. Watson United Kingdom 10 251 1.7× 185 1.3× 33 0.6× 30 1.1× 19 0.7× 13 355
Nan Min United States 8 96 0.6× 163 1.1× 20 0.3× 38 1.4× 15 0.6× 17 317
Jana Haberlová Czechia 11 105 0.7× 156 1.1× 48 0.8× 31 1.1× 45 1.7× 24 297

Countries citing papers authored by Aude Tessier

Since Specialization
Citations

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

Fields of papers citing papers by Aude Tessier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aude Tessier

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

All Works

11 of 11 papers shown
1.
Cassart, Marie, et al.. (2024). An unusual presentation of de novo RAC3 variation in prenatal diagnosis. Child s Nervous System. 40(5). 1597–1602. 3 indexed citations
2.
Tessier, Aude, et al.. (2023). Prenatal diagnosis of recurrent hypoplastic left heart syndrome associated with MYH6 variants: a case report. BMC Cardiovascular Disorders. 23(1). 116–116. 1 indexed citations
3.
Patat, Olivier, Renaud Touraine, Thomas Édouard, et al.. (2023). Clinical heterogeneity of NADSYN1 ‐associated VCRL syndrome. Clinical Genetics. 104(1). 114–120. 4 indexed citations
4.
Tessier, Aude, Lucile Boutaud, Mélanie Parisot, et al.. (2023). Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla. Acta Neuropathologica Communications. 11(1). 29–29. 7 indexed citations
5.
Tessier, Aude, Roman Hossein Khonsari, Yukiko Kurihara, et al.. (2023). Biallelic truncating variants in VGLL2 cause syngnathia in humans. Journal of Medical Genetics. 60(11). 1084–1091.
6.
Marguet, Florent, Fabien Guimiot, Jelena Martinović, et al.. (2021). Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndrome. European Journal of Medical Genetics. 64(9). 104282–104282. 7 indexed citations
7.
Barnat, Monia, Mariacristina Capizzi, Radhia Kacher, et al.. (2020). Huntington’s disease alters human neurodevelopment. Science. 369(6505). 787–793. 188 indexed citations
8.
Lœuillet, Laurence, Jean–Paul Duong Van Huyen, Bettina Bessières, et al.. (2020). Severe and progressive neuronal loss in myelomeningocele begins before 16 weeks of pregnancy. American Journal of Obstetrics and Gynecology. 223(2). 256.e1–256.e9. 20 indexed citations
9.
Arrondel, Christelle, Bettina Bessières, Aude Tessier, et al.. (2020). Bi-allelic pathogenic variations in DNAJB11 cause Ivemark II syndrome, a renal-hepatic-pancreatic dysplasia. Kidney International. 99(2). 405–409. 11 indexed citations
10.
Tessier, Aude, Patrick Callier, Nathalie Le Meur, et al.. (2018). Postmortem Diagnosis of Heart-hand Syndrome Associated With a 7p22.1p22.3 Deletion in a 16-week-old Fetus. Pediatric and Developmental Pathology. 22(2). 146–151. 1 indexed citations
11.
Gordon, Christopher T., Aude Tessier, Zeynep Demir, et al.. (2017). The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C function. Clinical Genetics. 93(2). 356–359. 4 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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