Aurélien Perrin

744 total citations
13 papers, 349 citations indexed

About

Aurélien Perrin is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Aurélien Perrin has authored 13 papers receiving a total of 349 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Cardiology and Cardiovascular Medicine and 3 papers in Genetics. Recurrent topics in Aurélien Perrin's work include Cardiomyopathy and Myosin Studies (4 papers), Ubiquitin and proteasome pathways (3 papers) and Epigenetics and DNA Methylation (3 papers). Aurélien Perrin is often cited by papers focused on Cardiomyopathy and Myosin Studies (4 papers), Ubiquitin and proteasome pathways (3 papers) and Epigenetics and DNA Methylation (3 papers). Aurélien Perrin collaborates with scholars based in France, United Kingdom and United States. Aurélien Perrin's co-authors include Dimitris P. Xirodimas, Robert Feil, David Llères, Aymeric Bailly, Chantal Maghames, Philippe Marin, Serge Urbach, Andrea Riccio, Édouard Bertrand and Florence Rage and has published in prestigious journals such as Nature Communications, Oncogene and International Journal of Molecular Sciences.

In The Last Decade

Aurélien Perrin

12 papers receiving 347 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aurélien Perrin France	9	291	86	47	45	43	13	349
Boubou Diagouraga France	7	414 1.4×	78 0.9×	46 1.0×	38 0.8×	55 1.3×	8	537
Simina Ticau United States	11	454 1.6×	129 1.5×	45 1.0×	14 0.3×	86 2.0×	22	572
Abhijit Shukla United States	16	1.2k 4.0×	99 1.2×	55 1.2×	61 1.4×	43 1.0×	20	1.2k
Erwan Delbarre Norway	16	880 3.0×	68 0.8×	35 0.7×	17 0.4×	90 2.1×	22	997
Adriana Gonzalez‐Sandoval Switzerland	8	637 2.2×	80 0.9×	23 0.5×	21 0.5×	47 1.1×	10	694
Arielle Yablonovitch United States	7	331 1.1×	36 0.4×	55 1.2×	63 1.4×	32 0.7×	15	439
Rocío Sierra Spain	5	289 1.0×	34 0.4×	51 1.1×	35 0.8×	177 4.1×	8	438
Elizabeth T. Wiles United States	9	347 1.2×	32 0.4×	37 0.8×	44 1.0×	49 1.1×	12	468
Sandra S. de Vries Netherlands	7	612 2.1×	209 2.4×	55 1.2×	101 2.2×	41 1.0×	7	773
Samuel C. Griffiths United Kingdom	8	224 0.8×	57 0.7×	43 0.9×	35 0.8×	26 0.6×	14	330

Countries citing papers authored by Aurélien Perrin

Since Specialization

Citations

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

Fields of papers citing papers by Aurélien Perrin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aurélien Perrin

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

All Works

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13 of 13 papers shown

Perrin, Aurélien, Tanya Stojkovic, Céline Tard, et al.. (2024). Congenital Titinopathies Linked to Mutations in TTN Metatranscript-Only Exons. International Journal of Molecular Sciences. 25(23). 12994–12994. 1 indexed citations

Cossée, Mireille, Martin Krahn, Tanya Stojkovic, et al.. (2022). A National French Consensus on Gene List for the Diagnosis of Charcot–Marie–Tooth Disease and Related Disorders Using Next-Generation Sequencing. Genes. 13(2). 318–318. 5 indexed citations

Perrin, Aurélien, Raúl Juntas Morales, Françoise Chapon, et al.. (2021). Novel dominant distal titinopathy phenotype associated with copy number variation. Annals of Clinical and Translational Neurology. 8(9). 1906–1912. 2 indexed citations

Perrin, Aurélien, Corinne Métay, Marcello Villanova, et al.. (2020). A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency. Annals of Clinical and Translational Neurology. 7(5). 846–854. 9 indexed citations

Perrin, Aurélien, Raúl Juntas‐Morales, François Rivier, et al.. (2020). The importance of an integrated genotype-phenotype strategy to unravel the molecular bases of titinopathies. Neuromuscular Disorders. 30(11). 877–887. 14 indexed citations

Juntas‐Morales, Raúl, Aurélien Perrin, & Mireille Cossée. (2020). Corrélations phénotype-génotype dans les titinopathies. Springer Link (Chiba Institute of Technology). 16–20.

Bailly, Aymeric, Aurélien Perrin, Marina Serrano‐Maciá, et al.. (2019). The Balance between Mono- and NEDD8-Chains Controlled by NEDP1 upon DNA Damage Is a Regulatory Module of the HSP70 ATPase Activity. Cell Reports. 29(1). 212–224.e8. 40 indexed citations

Llères, David, Benoît Moindrot, Rakesh Pathak, et al.. (2019). CTCF modulates allele-specific sub-TAD organization and imprinted gene activity at the mouse Dlk1-Dio3 and Igf2-H19 domains. Genome biology. 20(1). 272–272. 59 indexed citations

Lalevée, Sébastien, M Cammisa, Aurélien Perrin, et al.. (2018). Meg3 Non-coding RNA Expression Controls Imprinting by Preventing Transcriptional Upregulation in cis. Cell Reports. 23(2). 337–348. 51 indexed citations

10.

Maghames, Chantal, et al.. (2018). NEDDylation promotes nuclear protein aggregation and protects the Ubiquitin Proteasome System upon proteotoxic stress. Nature Communications. 9(1). 4376–4376. 69 indexed citations

11.

Llères, David, Aymeric Bailly, Aurélien Perrin, et al.. (2017). Quantitative FLIM-FRET Microscopy to Monitor Nanoscale Chromatin Compaction In Vivo Reveals Structural Roles of Condensin Complexes. Cell Reports. 18(7). 1791–1803. 38 indexed citations

12.

Bailly, Aymeric, Aurélien Perrin, Emmanuelle Pion, et al.. (2015). The NEDD8 inhibitor MLN4924 increases the size of the nucleolus and activates p53 through the ribosomal-Mdm2 pathway. Oncogene. 35(4). 415–426. 37 indexed citations

13.

Galet, Colette, et al.. (2001). Expression of a single βα chain protein of equine LH/CG in milk of transgenic rabbits and its biological activity. Molecular and Cellular Endocrinology. 174(1-2). 31–40. 24 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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