Audrey Putoux

1.9k total citations
32 papers, 369 citations indexed

About

Audrey Putoux is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Audrey Putoux has authored 32 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 20 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Audrey Putoux's work include RNA modifications and cancer (8 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Genetic and Kidney Cyst Diseases (6 papers). Audrey Putoux is often cited by papers focused on RNA modifications and cancer (8 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Genetic and Kidney Cyst Diseases (6 papers). Audrey Putoux collaborates with scholars based in France, United States and Switzerland. Audrey Putoux's co-authors include Tania Attié‐Bitach, Marie-Claire Gübler, Jelena Martinović, Damien Sanlaville, Patrick Edery, Audrey Labalme, Gaëtan Lesca, Christelle Rougeot, Estelle Dubruc and Laurent Guibaud and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Brain.

In The Last Decade

Audrey Putoux

26 papers receiving 354 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Audrey Putoux France 11 236 215 72 36 22 32 369
Bret L. Bostwick United States 9 225 1.0× 215 1.0× 29 0.4× 35 1.0× 22 1.0× 17 414
Jane Juusola United States 13 218 0.9× 192 0.9× 33 0.5× 34 0.9× 28 1.3× 22 390
Mónica Rosello Spain 14 295 1.3× 360 1.7× 95 1.3× 15 0.4× 25 1.1× 41 535
Yline Capri France 12 222 0.9× 181 0.8× 56 0.8× 16 0.4× 22 1.0× 33 381
Simone Gana Italy 9 125 0.5× 151 0.7× 50 0.7× 24 0.7× 12 0.5× 34 255
Luis Rohena United States 12 192 0.8× 154 0.7× 46 0.6× 47 1.3× 52 2.4× 27 383
Zhengjun Jia China 9 106 0.4× 112 0.5× 86 1.2× 29 0.8× 10 0.5× 23 262
Eva‐Christina Prott Germany 7 160 0.7× 199 0.9× 96 1.3× 17 0.5× 27 1.2× 9 283
Sanne M. C. Savelberg Netherlands 10 246 1.0× 257 1.2× 31 0.4× 40 1.1× 40 1.8× 11 443
Claudia Ciaccio Italy 11 184 0.8× 221 1.0× 25 0.3× 22 0.6× 13 0.6× 30 347

Countries citing papers authored by Audrey Putoux

Since Specialization
Citations

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

Fields of papers citing papers by Audrey Putoux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Audrey Putoux

This figure shows the co-authorship network connecting the top 25 collaborators of Audrey Putoux. A scholar is included among the top collaborators of Audrey Putoux 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 Putoux. Audrey Putoux 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.
Boutaud, Lucile, Virginie Hamel, Sophie Thomas, et al.. (2024). A Taybi-Linder syndrome-related RTTN variant impedes neural rosette formation in human cortical organoids. PLoS Genetics. 20(12). e1011517–e1011517.
2.
Quēlin, Chloé, Laurent Pasquier, Philippe Loget, et al.. (2023). PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serine biosynthesis defect. European Journal of Medical Genetics. 66(11). 104852–104852.
3.
Janin, Alexandre, Audrey Putoux, Philippe Chevalier, et al.. (2023). Biallelic PRKAG2 Truncating Variants Are Associated with Severe Neonatal Cardiomyopathies. Circulation Genomic and Precision Medicine. 16(3). 277–279.
4.
Quartier, Angélique, Nathalie Drouot, Damien Plassard, et al.. (2023). Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome. Molecular Psychiatry. 29(2). 287–296. 4 indexed citations
5.
Putoux, Audrey, et al.. (2023). Prenatal diagnosis of microcephaly with simplified gyral pattern: series of eight cases. Ultrasound in Obstetrics and Gynecology. 63(2). 271–275. 2 indexed citations
6.
Arzimanoglou, Alexis, et al.. (2022). STAG2 microduplication in a patient with eyelid myoclonia and absences and a review of EMA-related reported genes. European Journal of Medical Genetics. 65(12). 104636–104636. 3 indexed citations
7.
Delous, Marion, Audrey Putoux, Anne‐Louise Leutenegger, et al.. (2022). Mutations in the non-codingRNU4ATACgene affect the homeostasis and function of the Integrator complex. Nucleic Acids Research. 51(2). 712–727. 3 indexed citations
8.
Putoux, Audrey, et al.. (2021). Sensenbrenner syndrome: a further challenge in evaluating sagittal synostosis and a need for a multidisciplinary approach. Child s Nervous System. 37(5). 1695–1701. 5 indexed citations
9.
Bozon, Muriel, Valérie Castellani, Renaud Touraine, et al.. (2021). X-linked partial corpus callosum agenesis with mild intellectual disability: identification of a novel L1CAM pathogenic variant. Neurogenetics. 22(1). 43–51. 4 indexed citations
10.
Hanna, Nadine, Sophie Dupuis‐Girod, Marianne Till, et al.. (2020). A Case of Trisomy 13 Mosaicism Presenting with a Severe Aortic Root Dilatation and Marfanoid Habitus due to an Unpredictable Cytogenetic Mechanism. Cytogenetic and Genome Research. 160(2). 72–79.
11.
Benoit‐Pilven, Clara, Audrey Putoux, Claire Benetollo, et al.. (2020). Clinical interpretation of variants identified in RNU4ATAC, a non-coding spliceosomal gene. PLoS ONE. 15(7). e0235655–e0235655. 10 indexed citations
12.
Chatron, Nicolas, Michel Pugeat, Marianne Till, et al.. (2020). Follow-up of two adult brothers with homozygous CEP57 pathogenic variants expands the phenotype of Mosaic Variegated Aneuploidy Syndrome. European Journal of Medical Genetics. 63(11). 104044–104044. 8 indexed citations
13.
Zech, Jean‐Christophe, Audrey Putoux, Évelyne Decullier, et al.. (2020). Classifying Ectopia Lentis in Marfan Syndrome into Five Grades of Increasing Severity. Journal of Clinical Medicine. 9(3). 721–721. 5 indexed citations
14.
Benoit‐Pilven, Clara, Audrey Putoux, Amandine Campan-Fournier, et al.. (2019). New insights into minor splicing—a transcriptomic analysis of cells derived from TALS patients. RNA. 25(9). 1130–1149. 26 indexed citations
15.
Putoux, Audrey, Maryline Carneiro, Audrey Labalme, et al.. (2019). A novel truncating variant p.(Arg297*) in the GRM1 gene causing autosomal-recessive cerebellar ataxia with juvenile-onset. European Journal of Medical Genetics. 62(10). 103726–103726. 8 indexed citations
16.
Dimassi, Sarra, Thomas Simonet, Audrey Jalabert, et al.. (2015). Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA. PubMed. 7. 19–25. 19 indexed citations
17.
Dubruc, Estelle, Audrey Putoux, Audrey Labalme, et al.. (2014). A new intellectual disability syndrome caused by CTNNB1 haploinsufficiency. American Journal of Medical Genetics Part A. 164(6). 1571–1575. 49 indexed citations
18.
Putoux, Audrey, Audrey Labalme, Jean‐Marie André, et al.. (2013). Jacobsen and Beckwith–Wiedemann syndromes in a child with mosaicism for partial 11pter trisomy and partial 11qter monosomy. American Journal of Medical Genetics Part A. 161(2). 331–337. 13 indexed citations
19.
Putoux, Audrey, Tania Attié‐Bitach, Jelena Martinović, & Marie-Claire Gübler. (2011). Phenotypic variability of Bardet-Biedl syndrome: focusing on the kidney. Pediatric Nephrology. 27(1). 7–15. 65 indexed citations
20.
Putoux, Audrey, Soumaya Mougou-Zerelli, Sophie Thomas, et al.. (2010). BBS10 mutations are common in ‘Meckel’-type cystic kidneys. Journal of Medical Genetics. 47(12). 848–852. 20 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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