Anthony Vandersteen

3.7k total citations
21 papers, 448 citations indexed

About

Anthony Vandersteen is a scholar working on Genetics, Oncology and Molecular Biology. According to data from OpenAlex, Anthony Vandersteen has authored 21 papers receiving a total of 448 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 5 papers in Oncology and 4 papers in Molecular Biology. Recurrent topics in Anthony Vandersteen's work include Connective tissue disorders research (13 papers), Dermatological and Skeletal Disorders (6 papers) and Bone health and treatments (4 papers). Anthony Vandersteen is often cited by papers focused on Connective tissue disorders research (13 papers), Dermatological and Skeletal Disorders (6 papers) and Bone health and treatments (4 papers). Anthony Vandersteen collaborates with scholars based in United Kingdom, Canada and United States. Anthony Vandersteen's co-authors include Neeti Ghali, Cecilia Giunta, Angela F. Brady, Marianne Rohrbach, Tomoki Kosho, Fransiska Malfait, Johannes Zschocke, Serwet Demirdas, Tim Van Damme and Nicol C. Voermans and has published in prestigious journals such as PEDIATRICS, British Journal of Dermatology and Journal of Medical Genetics.

In The Last Decade

Anthony Vandersteen

20 papers receiving 440 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anthony Vandersteen United Kingdom 11 355 152 83 79 62 21 448
James J. Earley United States 9 189 0.5× 107 0.7× 39 0.5× 92 1.2× 44 0.7× 14 416
Markus S. Ladewig Germany 11 327 0.9× 170 1.1× 90 1.1× 40 0.5× 87 1.4× 19 547
Harikiran Nistala United States 8 218 0.6× 184 1.2× 58 0.7× 56 0.7× 23 0.4× 11 375
B Lee United States 5 279 0.8× 124 0.8× 36 0.4× 59 0.7× 41 0.7× 5 386
Mitzi L. Murray United States 10 314 0.9× 130 0.9× 35 0.4× 51 0.6× 43 0.7× 13 467
Antonella Sangalli Italy 13 133 0.4× 139 0.9× 61 0.7× 64 0.8× 31 0.5× 24 376
Clair A. Francomano United States 7 221 0.6× 197 1.3× 32 0.4× 43 0.5× 24 0.4× 7 351
Valerie M. Carlberg United States 8 199 0.6× 119 0.8× 45 0.5× 41 0.5× 35 0.6× 17 352
Kathleen E. Tumelty United States 5 100 0.3× 124 0.8× 31 0.4× 34 0.4× 30 0.5× 5 272
D. Sillence Australia 10 310 0.9× 181 1.2× 80 1.0× 116 1.5× 42 0.7× 22 451

Countries citing papers authored by Anthony Vandersteen

Since Specialization
Citations

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

Fields of papers citing papers by Anthony Vandersteen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anthony Vandersteen

This figure shows the co-authorship network connecting the top 25 collaborators of Anthony Vandersteen. A scholar is included among the top collaborators of Anthony Vandersteen 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 Anthony Vandersteen. Anthony Vandersteen 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.
Stringer, Elizabeth, Neil Warner, Johan Van Limbergen, et al.. (2021). Multisystem Autoimmune Inflammatory Disease, Including Colitis, Due to Inborn Error of Immunity. PEDIATRICS. 148(5). 3 indexed citations
2.
Ghali, Neeti, Duncan Baker, Jessica Bowen, et al.. (2020). Classical-like Ehlers–Danlos syndrome: a clinical description of 20 newly identified individuals with evidence of tissue fragility. Genetics in Medicine. 22(10). 1576–1582. 17 indexed citations
3.
Ghali, Neeti, Duncan Baker, Angela F. Brady, et al.. (2020). Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers‐Danlos syndrome. American Journal of Medical Genetics Part A. 182(5). 994–1007. 14 indexed citations
4.
Brady, Angela F., F. Michael Pope, Anthony Vandersteen, et al.. (2020). Arterial complications in classical Ehlers-Danlos syndrome: a case series. Journal of Medical Genetics. 57(11). 769–776. 8 indexed citations
5.
Ghali, Neeti, Duncan Baker, Angela F. Brady, et al.. (2019). Electron microscopy in the diagnosis of Ehlers–Danlos syndromes: correlation with clinical and genetic investigations. British Journal of Dermatology. 182(3). 698–707. 20 indexed citations
6.
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
7.
Rideout, Andrea L., Sara MacKay, Jill Beis, et al.. (2019). A family with Classical Ehlers-Danlos Syndrome (cEDS), mild bone fragility and without vascular complications, caused by the p.Arg312Cys mutation in COL1A1. European Journal of Medical Genetics. 63(2). 103730–103730. 9 indexed citations
8.
Ghali, Neeti, Duncan Baker, Angela F. Brady, et al.. (2019). Atypical COL3A1 variants (glutamic acid to lysine) cause vascular Ehlers–Danlos syndrome with a consistent phenotype of tissue fragility and skin hyperextensibility. Genetics in Medicine. 21(9). 2081–2091. 14 indexed citations
9.
Blackmore, Christopher, et al.. (2018). An Omental Lymphatic Malformation Mimicking Ascites in a 2‐Year‐Old Boy. Journal of Pediatric Gastroenterology and Nutrition. 67(1). e14–e15.
10.
Burca, Anna de, C. Ioannou, Anthony Vandersteen, F. Michael Pope, & Deirdre Cilliers. (2018). Intrafamilial variability of clinical features in distal arthrogryposis type 2B. Clinical Dysmorphology. 28(1). 35–37. 2 indexed citations
11.
Brady, Angela F., Serwet Demirdas, Sylvie Fournel‐Gigleux, et al.. (2017). The Ehlers–Danlos syndromes, rare types. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 175(1). 70–115. 163 indexed citations
12.
Weerakkody, Ruwan, Jana Vandrovcová, Michael Mueller, et al.. (2016). Targeted next-generation sequencing makes new molecular diagnoses and expands genotype–phenotype relationship in Ehlers–Danlos syndrome. Genetics in Medicine. 18(11). 1119–1127. 45 indexed citations
13.
George, Susannah, et al.. (2016). Two patients with Ehlers-Danlos syndrome type VIII with unexpected hoarseness. Clinical and Experimental Dermatology. 41(7). 771–774. 12 indexed citations
14.
McKenna, Caoimhe, Anthony Vandersteen, Emma Wakeling, F. Michael Pope, & Neeti Ghali. (2016). Recognizing vascular Ehlers–Danlos syndrome (type IV) in the newborn. Clinical Dysmorphology. 26(1). 50–57. 1 indexed citations
15.
Choong, Andrew M.T.L., Natalie Canham, Sophie Renton, et al.. (2015). A combined vascular surgical and clinical genetics approach to diffuse aneurysmal disease. Annals of The Royal College of Surgeons of England. 97(5). e73–e76. 3 indexed citations
16.
Rohrbach, Marianne, Anthony Vandersteen, Uluç Yiş, et al.. (2011). Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation. Orphanet Journal of Rare Diseases. 6(1). 46–46. 67 indexed citations
17.
Vandersteen, Anthony, Wajanat Jan, John Simpson, et al.. (2009). Cutaneous signs are important in the diagnosis of the rare neoplasia syndrome Carney complex. European Journal of Pediatrics. 168(11). 1401–1404. 15 indexed citations
18.
Walter, Edward, et al.. (2004). Hyperkalaemic ascending paralysis. Journal of the Royal Society of Medicine. 97(7). 330–331. 7 indexed citations
19.
Walter, Edward, et al.. (2004). Hyperkalaemic Ascending Paralysis. Journal of the Royal Society of Medicine. 97(7). 330–331. 2 indexed citations
20.
Illidge, Tim, Jamie Honeychurch, Anthony Vandersteen, & Mark S. Cragg. (2000). Radioimmunotherapy in the π-BCL 1 B cell Lymphoma Model: Efficacy Depends on More Than Targeted Irradiation Alone. Cancer Biotherapy and Radiopharmaceuticals. 15(6). 581–591. 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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