Pauline Arnaud

1.4k total citations
36 papers, 609 citations indexed

About

Pauline Arnaud is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Pauline Arnaud has authored 36 papers receiving a total of 609 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 15 papers in Pulmonary and Respiratory Medicine and 10 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Pauline Arnaud's work include Connective tissue disorders research (24 papers), Aortic Disease and Treatment Approaches (14 papers) and Cardiac Valve Diseases and Treatments (9 papers). Pauline Arnaud is often cited by papers focused on Connective tissue disorders research (24 papers), Aortic Disease and Treatment Approaches (14 papers) and Cardiac Valve Diseases and Treatments (9 papers). Pauline Arnaud collaborates with scholars based in France, United States and United Kingdom. Pauline Arnaud's co-authors include Cathérine Boileau, Guillaume Jondeau, Nadine Hanna, Laurent Gouya, Olivier Milleron, Dianna M. Milewicz, Ellen S. Regalado, Suzanne M. Leal, Ellen M. Hostetler and Maud Langeois and has published in prestigious journals such as Journal of the American College of Cardiology, Circulation Research and Arteriosclerosis Thrombosis and Vascular Biology.

In The Last Decade

Pauline Arnaud

34 papers receiving 603 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pauline Arnaud France 13 363 350 175 148 58 36 609
Andrea L. Lafont United States 6 520 1.4× 586 1.7× 204 1.2× 253 1.7× 109 1.9× 6 907
M. Boxer United Kingdom 14 277 0.8× 146 0.4× 137 0.8× 131 0.9× 52 0.9× 18 493
Van Tran‐Fadulu United States 11 535 1.5× 658 1.9× 254 1.5× 135 0.9× 115 2.0× 12 862
Albert J Pedroza United States 12 199 0.5× 263 0.8× 75 0.4× 151 1.0× 49 0.8× 34 437
Thomas Cullup United Kingdom 15 130 0.4× 73 0.2× 164 0.9× 434 2.9× 42 0.7× 24 615
R.F. Suijkerbuijk Netherlands 12 139 0.4× 68 0.2× 75 0.4× 274 1.9× 94 1.6× 14 465
Darrell Wu United States 9 86 0.2× 423 1.2× 130 0.7× 200 1.4× 189 3.3× 13 622
Stoyan N. Angelov United States 7 148 0.4× 200 0.6× 57 0.3× 138 0.9× 67 1.2× 11 380
Cathy J. Hatcher United States 13 97 0.3× 142 0.4× 221 1.3× 481 3.3× 158 2.7× 22 710
Henrike Liptau Germany 6 99 0.3× 99 0.3× 210 1.2× 229 1.5× 23 0.4× 6 426

Countries citing papers authored by Pauline Arnaud

Since Specialization
Citations

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

Fields of papers citing papers by Pauline Arnaud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pauline Arnaud

This figure shows the co-authorship network connecting the top 25 collaborators of Pauline Arnaud. A scholar is included among the top collaborators of Pauline Arnaud 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 Pauline Arnaud. Pauline Arnaud 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.
Arnaud, Pauline, Geneviève Baujat, Valérie Drouin‐Garraud, et al.. (2024). Pathogenic variants affecting the TB5 domain of the fibrillin-1 protein: not only in geleophysic/acromicric dysplasias but also in Marfan syndrome. Journal of Medical Genetics. 61(5). 469–476.
2.
Callier, Patrick, Renaud Touraine, Antonio Vitobello, et al.. (2024). De Novo Balanced Translocations Disrupting the FBN1 Gene Diagnosed by Genome Sequencing: An Uncommon Cause of Marfan Syndrome Modifying Genetic Counseling. American Journal of Medical Genetics Part A. 197(4). e63923–e63923. 1 indexed citations
3.
Arnaud, Pauline, Carine Le Goff, Sébastien Perbet, et al.. (2023). Early-Onset Aortic Dissection: Characterization of a New Pathogenic Splicing Variation in the MYH11 Gene with Several In-Frame Abnormal Transcripts. Human Mutation. 2023. 1–7. 1 indexed citations
4.
Delsart, Pascal, Clémence Vanlerberghe, Françis Juthier, et al.. (2021). The natural history of a family with aortic dissection associated with a novel ACTA2 variant. Annals of Vascular Surgery. 77. 348.e7–348.e11. 5 indexed citations
5.
Arnaud, Pauline, Olivier Milleron, Nadine Hanna, et al.. (2021). Clinical relevance of genotype–phenotype correlations beyond vascular events in a cohort study of 1500 Marfan syndrome patients with FBN1 pathogenic variants. Genetics in Medicine. 23(7). 1296–1304. 69 indexed citations
6.
Filippetti, Laura, Virginie Dufrost, Nadine Hanna, et al.. (2021). A Giant Abdominal Aortic Aneurysm Revealing a Marfan Syndrome With a New FBN1 Mutation. Canadian Journal of Cardiology. 37(11). 1870–1872. 1 indexed citations
7.
Arnaud, Pauline, et al.. (2021). Cooperative Mechanism of ADAMTS/ ADAMTSL and Fibrillin-1 in the Marfan Syndrome and Acromelic Dysplasias. Frontiers in Genetics. 12. 734718–734718. 2 indexed citations
8.
Arnaud, Pauline, Hélène Morel, Olivier Milleron, et al.. (2021). Unsuspected somatic mosaicism for FBN1 gene contributes to Marfan syndrome. Genetics in Medicine. 23(5). 865–871. 18 indexed citations
9.
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.
10.
Milleron, Olivier, Florence Arnoult, G Delorme, et al.. (2020). Pathogenic FBN1 Genetic Variation and Aortic Dissection in Patients With Marfan Syndrome. Journal of the American College of Cardiology. 75(8). 843–853. 31 indexed citations
11.
Arnaud, Pauline, Nadine Hanna, Julien Thévenon, et al.. (2020). A new mutational hotspot in the SKI gene in the context of MFS/TAA molecular diagnosis. Human Genetics. 139(4). 461–472. 6 indexed citations
12.
Hansen, Jens, Josephine Galatioto, Cristina I. Caescu, et al.. (2019). Systems pharmacology–based integration of human and mouse data for drug repurposing to treat thoracic aneurysms. JCI Insight. 4(11). 19 indexed citations
13.
Aubart, Mélodie, Steven Gazal, Pauline Arnaud, et al.. (2018). Association of modifiers and other genetic factors explain Marfan syndrome clinical variability. European Journal of Human Genetics. 26(12). 1759–1772. 59 indexed citations
14.
Wallace, Stephanie E, Ellen S. Regalado, Limin Gong, et al.. (2018). MYLK pathogenic variants aortic disease presentation, pregnancy risk, and characterization of pathogenic missense variants. Genetics in Medicine. 21(1). 144–151. 30 indexed citations
15.
Benarroch, Louise, Mélodie Aubart, Marie‐Sylvie Gross, et al.. (2018). Marfan Syndrome Variability: Investigation of the Roles of Sarcolipin and Calcium as Potential Transregulator of FBN1 Expression. Genes. 9(9). 421–421. 6 indexed citations
16.
Guo, Dongchuan, Ellen S. Regalado, Limin Gong, et al.. (2016). LOX Mutations Predispose to Thoracic Aortic Aneurysms and Dissections. Circulation Research. 118(6). 928–934. 156 indexed citations
17.
Gloan, Laurianne Le, Albert David, Nadine Hanna, et al.. (2015). Neonatal Marfan Syndrome: Report of a Case with an Inherited Splicing Mutation outside the Neonatal Domain. Molecular Syndromology. 6(6). 281–286. 7 indexed citations
18.
Arnaud, Pauline. (2015). Le broyage des comprimés, l’ouverture des capsules, quelles responsabilités ?. Le Pharmacien Hospitalier et Clinicien. 50(3). 309–311. 2 indexed citations
19.
Purrello, Michele, Becky Alhadeff, K.E. Buckton, et al.. (1987). Comparison of cytologic and genetic distances between long arm subtelomeric markers of human autosome 14 suggests uneven distribution of crossing-over. Cytogenetic and Genome Research. 44(1). 32–40. 21 indexed citations
20.
Arnaud, Pauline, et al.. (1957). Sclérodermie et anachlorhydrie.. 89(9). 197–203. 2 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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