Audrey Letourneau

2.7k total citations
20 papers, 622 citations indexed

About

Audrey Letourneau is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Audrey Letourneau has authored 20 papers receiving a total of 622 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Audrey Letourneau's work include Down syndrome and intellectual disability research (5 papers), Lymphoma Diagnosis and Treatment (5 papers) and Congenital heart defects research (4 papers). Audrey Letourneau is often cited by papers focused on Down syndrome and intellectual disability research (5 papers), Lymphoma Diagnosis and Treatment (5 papers) and Congenital heart defects research (4 papers). Audrey Letourneau collaborates with scholars based in Switzerland, France and United States. Audrey Letourneau's co-authors include Stylianos E. Antonarakis, Federico Santoni, Michel Guipponi, M. Reza Sailani, Youssef Hibaoui, Anis Féki, Frédérique Béna, Iwona Grad, Christelle Borel and Laurence de Leval and has published in prestigious journals such as Nature Communications, Molecular Cell and PLoS ONE.

In The Last Decade

Audrey Letourneau

19 papers receiving 610 citations

Peers

Audrey Letourneau
Randall L. Given United States
Michail Spiliopoulos United States
Laurence Loubière United Kingdom
Christopher Allen United Kingdom
Audrey Letourneau
Citations per year, relative to Audrey Letourneau Audrey Letourneau (= 1×) peers Periklis Makrythanasis

Countries citing papers authored by Audrey Letourneau

Since Specialization
Citations

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

Fields of papers citing papers by Audrey Letourneau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Audrey Letourneau

This figure shows the co-authorship network connecting the top 25 collaborators of Audrey Letourneau. A scholar is included among the top collaborators of Audrey Letourneau 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 Audrey Letourneau. Audrey Letourneau 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.
Poullot, Elsa, François Lemonnier, Bettina Bisig, et al.. (2023). Angioimmunoblastic T‐cell lymphoma and Kaposi sarcoma: A fortuitous collision?. Histopathology. 84(3). 556–564. 1 indexed citations
2.
Nicolae, Alina, Justine Bouilly, Virginie Fataccioli, et al.. (2022). Nodal cytotoxic peripheral T-cell lymphoma occurs frequently in the clinical setting of immunodysregulation and is associated with recurrent epigenetic alterations. Modern Pathology. 35(8). 1126–1136. 24 indexed citations
3.
Letourneau, Audrey, Edoardo Missiaglia, Bernard De Prijck, et al.. (2021). Angioimmunoblastic T-Cell Lymphoma and Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma. The American Journal of Surgical Pathology. 45(6). 773–786. 13 indexed citations
4.
Tomita, Sakura, Yara Yukie Kikuti, Joaquim Carreras, et al.. (2020). Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma in Asia Frequently Shows SETD2 Alterations. Cancers. 12(12). 3539–3539. 20 indexed citations
5.
Stamoulis, Georgios, Marco Garieri, Periklis Makrythanasis, et al.. (2019). Single cell transcriptome in aneuploidies reveals mechanisms of gene dosage imbalance. Nature Communications. 10(1). 4495–4495. 28 indexed citations
6.
Letourneau, Audrey, et al.. (2018). Dual JAK1 and STAT3 mutations in a breast implant-associated anaplastic large cell lymphoma. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 473(4). 505–511. 48 indexed citations
7.
Popadin, Konstantin, Stephan Peischl, Marco Garieri, et al.. (2017). Slightly deleterious genomic variants and transcriptome perturbations in Down syndrome embryonic selection. Genome Research. 28(1). 1–10. 15 indexed citations
8.
Letourneau, Audrey, Gilda Cobellis, Alexandre Fort, et al.. (2015). HSA21 Single-Minded 2 (Sim2) Binding Sites Co-Localize with Super-Enhancers and Pioneer Transcription Factors in Pluripotent Mouse ES Cells. PLoS ONE. 10(5). e0126475–e0126475. 9 indexed citations
9.
Sailani, M. Reza, Federico Santoni, Audrey Letourneau, et al.. (2015). DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins. PLoS ONE. 10(8). e0135555–e0135555. 41 indexed citations
10.
Bosman, Alexis, Audrey Letourneau, Laura Sartiani, et al.. (2015). Perturbations of Heart Development and Function in Cardiomyocytes from Human Embryonic Stem Cells with Trisomy 21. Stem Cells. 33(5). 1434–1446. 28 indexed citations
11.
Letourneau, Audrey, Laura Sartiani, Martina Del Lungo, et al.. (2015). Perturbations of Heart Development and Function in Cardiomyocytes from hESC with Trisomy 21. 1 indexed citations
12.
Hibaoui, Youssef, Iwona Grad, Audrey Letourneau, et al.. (2014). Data in brief: Transcriptome analysis of induced pluripotent stem cells from monozygotic twins discordant for trisomy 21. Genomics Data. 2. 226–229. 9 indexed citations
13.
Texari, Lorane, Guennaëlle Dieppois, Patrizia Vinciguerra, et al.. (2013). The Nuclear Pore Regulates GAL1 Gene Transcription by Controlling the Localization of the SUMO Protease Ulp1. Molecular Cell. 51(6). 807–818. 62 indexed citations
14.
Hibaoui, Youssef, Iwona Grad, Audrey Letourneau, et al.. (2013). Modelling and rescuing neurodevelopmental defect of D own syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21. EMBO Molecular Medicine. 6(2). 259–277. 132 indexed citations
15.
Borel, Christelle, Eugenia Migliavacca, Audrey Letourneau, et al.. (2012). Tandem repeat sequence variation as causative Cis-eQTLs for protein-coding gene expression variation: The case of CSTB. Human Mutation. 33(8). 1302–1309. 25 indexed citations
16.
Letourneau, Audrey & Stylianos E. Antonarakis. (2012). Genomic determinants in the phenotypic variability of Down syndrome. Progress in brain research. 197. 15–28. 20 indexed citations
17.
Borel, Christelle, Samuel Deutsch, Audrey Letourneau, et al.. (2010). Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts. Genome Research. 21(1). 68–73. 52 indexed citations
18.
Failly, Mike, Lucia Bartoloni, Audrey Letourneau, et al.. (2009). Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesia. Journal of Medical Genetics. 46(4). 281–286. 55 indexed citations
19.
Rosenstiel, Philip, Tina Gruosso, Audrey Letourneau, et al.. (2008). HIV-1 Vpr inhibits cytokinesis in human proximal tubule cells. Kidney International. 74(8). 1049–1058. 39 indexed citations
20.
Doré, D., et al.. (2007). Delayed neutrons measurement at the MEGAPIE target. Springer Link (Chiba Institute of Technology).

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

Rankless by CCL
2026