Aude Beyens

494 total citations
15 papers, 146 citations indexed

About

Aude Beyens is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Aude Beyens has authored 15 papers receiving a total of 146 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Aude Beyens's work include Connective tissue disorders research (12 papers), Dermatological and Skeletal Disorders (6 papers) and Skin and Cellular Biology Research (2 papers). Aude Beyens is often cited by papers focused on Connective tissue disorders research (12 papers), Dermatological and Skeletal Disorders (6 papers) and Skin and Cellular Biology Research (2 papers). Aude Beyens collaborates with scholars based in Belgium, Canada and Türkiye. Aude Beyens's co-authors include Bert Callewaert, Sofie Symoens, Annekatrien Boel, Andrea L. Rideout, Anthony Vandersteen, Dirk Hubmacher, John D. Dickinson, Riet De Rycke, Frank Plasschaert and Piet Hoebeke and has published in prestigious journals such as International Journal of Molecular Sciences, Human Molecular Genetics and Antioxidants and Redox Signaling.

In The Last Decade

Aude Beyens

14 papers receiving 142 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aude Beyens Belgium	8	88	58	21	20	20	15	146
Maha Faden Saudi Arabia	6	100 1.1×	93 1.6×	22 1.0×	17 0.8×	4 0.2×	9	178
Elsa C. Bik Netherlands	5	69 0.8×	83 1.4×	12 0.6×	15 0.8×	14 0.7×	6	270
F. Dicső Hungary	5	19 0.2×	44 0.8×	21 1.0×	35 1.8×	33 1.6×	9	178
Magdalena Socha Poland	10	113 1.3×	143 2.5×	26 1.2×	39 1.9×	5 0.3×	24	260
Ali Awaji Saudi Arabia	4	170 1.9×	178 3.1×	18 0.9×	3 0.1×	10 0.5×	6	265
Huy Huynh Australia	4	16 0.2×	84 1.4×	22 1.0×	13 0.7×	7 0.3×	5	201
Biao Xie China	9	154 1.8×	169 2.9×	24 1.1×	25 1.3×	4 0.2×	13	329
Francisco J. Perea Mexico	10	86 1.0×	55 0.9×	14 0.7×	29 1.4×	8 0.4×	53	303
Celeste Owen Canada	7	28 0.3×	118 2.0×	18 0.9×	6 0.3×	7 0.3×	8	180
Fabienne Parente France	8	60 0.7×	76 1.3×	14 0.7×	39 1.9×	2 0.1×	12	174

Countries citing papers authored by Aude Beyens

Since Specialization

Citations

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

Fields of papers citing papers by Aude Beyens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aude Beyens

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

All Works

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15 of 15 papers shown

Beyens, Aude, et al.. (2025). Ocular Manifestations in Congenital Cutis Laxa: A Case Series. Cornea. 44(9). 1107–1112. 1 indexed citations

Beyens, Aude, Kathleen Claes, Elfride De Baere, et al.. (2023). HRAS ‐related epidermal nevus syndromes: Expansion of the spectrum with first branchial arch defects. Clinical Genetics. 103(6). 709–713. 1 indexed citations

Beyens, Aude, et al.. (2023). ATP7A‐related copper transport disorders: A systematic review and definition of the clinical subtypes. Journal of Inherited Metabolic Disease. 46(2). 163–173. 12 indexed citations

Beyens, Aude, Hilde Brems, Sandra Janssens, et al.. (2022). Identification of Codon 146 KRAS Variants in Isolated Epidermal Nevus and Multiple Lesions in Oculoectodermal Syndrome: Confirmation of the Phenotypic Continuum of Mosaic RASopathies. International Journal of Molecular Sciences. 23(7). 4036–4036. 5 indexed citations

McKenzie, F. Ellis, Kym Mina, Bert Callewaert, et al.. (2021). Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families. Clinical Genetics. 100(2). 168–175. 1 indexed citations

Beyens, Aude, et al.. (2021). Clinical and Molecular Delineation of Cutis Laxa Syndromes: Paradigms for Elastic Fiber Homeostasis. Advances in experimental medicine and biology. 1348. 273–309. 2 indexed citations

Beyens, Aude, et al.. (2021). Loss-of-Function Variants in EFEMP1 Cause a Recognizable Connective Tissue Disorder Characterized by Cutis Laxa and Multiple Herniations. Genes. 12(4). 510–510. 4 indexed citations

Boel, Annekatrien, Aude Beyens, Marjolijn Renard, et al.. (2020). Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects. Human Molecular Genetics. 29(9). 1476–1488. 4 indexed citations

Beyens, Aude, Annekatrien Boel, Sofie Symoens, & Bert Callewaert. (2020). Cutis laxa: A comprehensive overview of clinical characteristics and pathophysiology. Clinical Genetics. 99(1). 53–66. 16 indexed citations

10.

Boel, Annekatrien, Csilla Németh, Aude Beyens, et al.. (2019). Arterial Tortuosity Syndrome: An Ascorbate Compartmentalization Disorder?. Antioxidants and Redox Signaling. 34(11). 875–889. 8 indexed citations

11.

Beyens, Aude, Sofie Symoens, Anthony Vandersteen, et al.. (2019). A novel ADAMTS17 variant that causes Weill-Marchesani syndrome 4 alters fibrillin-1 and collagen type I deposition in the extracellular matrix. Matrix Biology. 88. 1–18. 34 indexed citations

12.

Beyens, Aude, Riet De Rycke, Michiel De Bruyne, et al.. (2019). Defining the Clinical, Molecular and Ultrastructural Characteristics in Occipital Horn Syndrome: Two New Cases and Review of the Literature. Genes. 10(7). 528–528. 23 indexed citations

13.

Beyens, Aude, Wouter Steyaert, Riet De Rycke, et al.. (2019). Myhre syndrome: A first familial recurrence and broadening of the phenotypic spectrum. American Journal of Medical Genetics Part A. 179(12). 2494–2499. 16 indexed citations

14.

Beyens, Aude, et al.. (2018). Arterial tortuosity syndrome: 40 new families and literature review. Genetics in Medicine. 20(10). 1236–1245. 9 indexed citations

15.

Beyens, Aude, Christine Bodemer, Helen Cox, et al.. (2018). ATP6V0A2‐related cutis laxa in 10 novel patients: Focus on clinical variability and expansion of the phenotype. Experimental Dermatology. 28(10). 1142–1145. 10 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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