Aurore Devos

733 total citations
14 papers, 267 citations indexed

About

Aurore Devos is a scholar working on Molecular Biology, Epidemiology and Infectious Diseases. According to data from OpenAlex, Aurore Devos has authored 14 papers receiving a total of 267 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Epidemiology and 2 papers in Infectious Diseases. Recurrent topics in Aurore Devos's work include Retinal Development and Disorders (3 papers), Biochemical and Molecular Research (2 papers) and Cytomegalovirus and herpesvirus research (2 papers). Aurore Devos is often cited by papers focused on Retinal Development and Disorders (3 papers), Biochemical and Molecular Research (2 papers) and Cytomegalovirus and herpesvirus research (2 papers). Aurore Devos collaborates with scholars based in France, Tunisia and United States. Aurore Devos's co-authors include Marco Fiore, Gary Horwith, Paul R. Pentel, Douglas E. Jorenby, Stephen I. Rennard, Franck Broly, François Glowacki, Delphine Allorge, Christelle Cauffiez and Christian L. Lino Cardenas and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Aurore Devos

14 papers receiving 257 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aurore Devos France	7	153	78	55	38	31	14	267
Sharat Chandra India	13	209 1.4×	64 0.8×	42 0.8×	53 1.4×	35 1.1×	25	387
Sammy R. Shaver United States	11	188 1.2×	27 0.3×	85 1.5×	19 0.5×	12 0.4×	12	467
E Jacotot France	5	290 1.9×	36 0.5×	53 1.0×	14 0.4×	42 1.4×	5	415
Riccardo Graber Switzerland	9	239 1.6×	53 0.7×	26 0.5×	34 0.9×	47 1.5×	17	450
Ieva Vasiliauskaité-Brooks France	6	197 1.3×	77 1.0×	101 1.8×	43 1.1×	12 0.4×	7	317
Preethi Chander United States	13	195 1.3×	23 0.3×	21 0.4×	17 0.4×	29 0.9×	17	349
R.J. Warren United Kingdom	9	161 1.1×	37 0.5×	21 0.4×	18 0.5×	36 1.2×	14	362
Lanĕ United States	10	181 1.2×	107 1.4×	29 0.5×	14 0.4×	29 0.9×	23	417
Matthew L. Fowler United States	8	135 0.9×	243 3.1×	53 1.0×	25 0.7×	35 1.1×	9	424

Countries citing papers authored by Aurore Devos

Since Specialization

Citations

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

Fields of papers citing papers by Aurore Devos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aurore Devos

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

All Works

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14 of 14 papers shown

Vaclavik, Veronika, Isabelle Meunier, Isabelle Drumare, et al.. (2022). Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants. International Journal of Molecular Sciences. 23(8). 4294–4294. 9 indexed citations

Dessein, Anne‐Frédérique, Jòseph Vamecq, Aurore Devos, et al.. (2022). A novel HADHA variant associated with an atypical moderate and late-onset LCHAD deficiency. Molecular Genetics and Metabolism Reports. 31. 100860–100860. 4 indexed citations

Muller, Jean, Christina Zeitz, Carolin D. Obermaier, et al.. (2021). Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy. International Journal of Molecular Sciences. 22(12). 6410–6410. 10 indexed citations

Khan, Mubeen, Stéphanie S. Cornelis, Muhammad Imran Khan, et al.. (2019). Cost‐effective molecular inversion probe‐based ABCA4 sequencing reveals deep‐intronic variants in Stargardt disease. Human Mutation. 40(10). 1749–1759. 37 indexed citations

Pagin, A., et al.. (2016). Applicability and Efficiency of NGS in Routine Diagnosis: In-Depth Performance Analysis of a Complete Workflow for CFTR Mutation Analysis. PLoS ONE. 11(2). e0149426–e0149426. 14 indexed citations

Cardenas, Christian L. Lino, Aurore Devos, Aminata Touré, et al.. (2011). Arachidonic acid ω-hydroxylase CYP4A11: inter-ethnic variations in the 8590T>C loss-of-function variant. Molecular Biology Reports. 39(2). 1503–1508. 6 indexed citations

Devos, Aurore, Christian L. Lino Cardenas, François Glowacki, et al.. (2010). Genetic polymorphism of CYP2U1, a cytochrome P450 involved in fatty acids hydroxylation. Prostaglandins Leukotrienes and Essential Fatty Acids. 83(2). 105–110. 22 indexed citations

Garat, Anne, Christian L. Lino Cardenas, Arnaud Lionet, et al.. (2010). Inter-ethnic variability of three functional polymorphisms affecting the IMPDH2 gene. Molecular Biology Reports. 38(8). 5185–5188. 4 indexed citations

Garat, Anne, Christelle Cauffiez, François Glowacki, et al.. (2009). IMPDH2 Genetic Polymorphism: A Promoter Single-Nucleotide Polymorphism Disrupts a Cyclic Adenosine Monophosphate Responsive Element. Genetic Testing and Molecular Biomarkers. 13(6). 841–847. 11 indexed citations

10.

Rennard, Stephen I., Douglas E. Jorenby, Marco Fiore, et al.. (2005). Safety and immunogenicity of a nicotine conjugate vaccine in current smokers. Clinical Pharmacology & Therapeutics. 78(5). 456–467. 142 indexed citations

11.

Messiaen, Ludwine, Manfred Stuhrmann, Gert Matthijs, et al.. (2002). Multicenter validation of a new reverse hybridization assay for CFTR mutation analysis. The American Journal of Human Genetics. 71(4). 386–386. 1 indexed citations

12.

Ja, Gruwez, et al.. (1970). [Gastroinestinal complications of kidney transplantation].. PubMed. 69(6). 440–9. 2 indexed citations

13.

Devos, Aurore. (1969). Post-mortem findings in rabbits.. Vlaams Diergeneeskundig Tijdschrift. 38. 275–280. 2 indexed citations

14.

Vandeplassche, M., et al.. (1960). Ulcerative balanoposthitis in bulls.. Vlaams Diergeneeskundig Tijdschrift. 29. 171–186. 3 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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