Fleur S. van Dijk

434 total citations
26 papers, 195 citations indexed

About

Fleur S. van Dijk is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Fleur S. van Dijk has authored 26 papers receiving a total of 195 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Rheumatology. Recurrent topics in Fleur S. van Dijk's work include Connective tissue disorders research (21 papers), Dermatological and Skeletal Disorders (7 papers) and Bone and Dental Protein Studies (3 papers). Fleur S. van Dijk is often cited by papers focused on Connective tissue disorders research (21 papers), Dermatological and Skeletal Disorders (7 papers) and Bone and Dental Protein Studies (3 papers). Fleur S. van Dijk collaborates with scholars based in United Kingdom, Netherlands and Canada. Fleur S. van Dijk's co-authors include Neeti Ghali, Angela F. Brady, Anton Franken, Guus Janus, F. Michael Pope, Duncan Baker, Anthony Vandersteen, Diana Johnson, Glenda Sobey and David Ferguson and has published in prestigious journals such as PLoS ONE, Journal Of Clinical Periodontology and Bone.

In The Last Decade

Fleur S. van Dijk

23 papers receiving 195 citations

Peers

Countries citing papers authored by Fleur S. van Dijk

Since Specialization

Citations

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

Fields of papers citing papers by Fleur S. van Dijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fleur S. van Dijk. 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 Fleur S. van Dijk. The network helps show where Fleur S. van Dijk may publish in the future.

Co-authorship network of co-authors of Fleur S. van Dijk

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome 2025 ·European Journal of Human Genetics ·(unknown), Shadi Albaba, Glenda Sobey, Jessica Bowen, Deirdre E. Donnelly, Marina Colombi, Marco Ritelli, (unknown), Neeti Ghali, Fleur S. van Dijk, Emma Hobson, (unknown), Esther Kinning, Abhijit Dixit, (unknown), Duncan Baker, Diana Johnson	0
2	Pleiotropic effects of a recessive Col1a2 mutation occurring in a mouse model of severe osteogenesis imperfecta 2025 ·PLoS ONE ·Michelangelo Corcelli, (unknown), (unknown), Mohammad Mehedi Hasan, Fleur S. van Dijk, Anna L. David, Pascale V. Guillot	0
3	Genetic diagnosis of the Ehlers-Danlos syndromes 2024 ·Medizinische Genetik ·Johannes Zschocke, Serwet Demirdas, Fleur S. van Dijk	1
4	Clinical diagnosis of the monogenic Ehlers-Danlos syndromes 2024 ·Medizinische Genetik ·Fleur S. van Dijk, (unknown), Serwet Demirdas, Neeti Ghali, Johannes Zschocke	0
5	The Natural History of Dermatosparaxis Ehlers Danlos Syndrome: An Adult Case Series 2024 ·American Journal of Medical Genetics Part A ·(unknown), Peter H. Byers, (unknown), Neeti Ghali, Juliette Harris, Ingrid Haußer, (unknown), Glenda Sobey, Fleur S. van Dijk	1
6	Vascular Ehlers-Danlos syndrome in children: evaluating the importance of diagnosis and follow-up during childhood 2024 ·European Journal of Human Genetics ·Nafisa Wilkinson, Elena Cervi, Bart Wagner, Déborah Morris-Rosendahl, Duncan Baker, (unknown), (unknown), Toby Andrew, Neeti Ghali, Fleur S. van Dijk	1
7	Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome 2023 ·Journal of Medical Genetics ·Anthony M. Vandersteen, Ruwan Weerakkody, David Parry, (unknown), (unknown), Jana Vandrovcová, Rebecca Darlay, Javier Santoyo‐López, Alison Meynert, (unknown), Hanadi Kazkaz, Rodney Grahame, (unknown), (unknown), Neeti Ghali, Angela F. Brady, F M Pope, Fleur S. van Dijk, Heather J. Cordell, Timothy J. Aitman	7
8	Ehlers-Danlos syndromes: importance of defining the type 2023 ·Practical Neurology ·Fleur S. van Dijk, Neeti Ghali, Arvind Chandratheva	3
9	An exemplary model of genetic counselling for highly specialised services 2023 ·Journal of Community Genetics ·Juliette Harris, (unknown), Duncan Baker, (unknown), Jessica Bowen, (unknown), (unknown), Claire Green, (unknown), (unknown), (unknown), (unknown), Clare L. Stacey, Jan M. Cobben, Neeti Ghali, Diana Johnson, Glenda Sobey, Fleur S. van Dijk	2
10	Amniotic band sequence in vascular Ehlers-Danlos Syndrome (EDS): Experience of the EDS National Diagnostic Services in the UK 2022 ·European Journal of Medical Genetics ·(unknown), Fleur S. van Dijk, Matthew Cauldwell, Rachel Harrison, Alison Kraus, Paul Brennan, Neeti Ghali, Nayana Lahiri, Diana Johnson, Glenda Sobey	4
11	Fractures following pregnancy in Osteogenesis imperfecta – A self-controlled case series using Danish Health Registers 2021 ·Bone ·(unknown), (unknown), Fleur S. van Dijk, Daniel Prieto‐Alhambra, Bo Abrahamsen, Lars Folkestad	7
12	Classical-like Ehlers–Danlos syndrome: a clinical description of 20 newly identified individuals with evidence of tissue fragility 2020 ·Genetics in Medicine ·(unknown), Neeti Ghali, (unknown), (unknown), Duncan Baker, (unknown), Jessica Bowen, Angela F. Brady, (unknown), (unknown), (unknown), Vivienne McConnell, (unknown), Hanadi Kazkaz, Diana Johnson, F. Michael Pope, Anthony Vandersteen, Glenda Sobey, Fleur S. van Dijk	17
13	Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers‐Danlos syndrome 2020 ·American Journal of Medical Genetics Part A ·(unknown), Neeti Ghali, (unknown), Duncan Baker, (unknown), Angela F. Brady, Maria Luisa Giovannucci Uzielli, Cecilia Giunta, Diana Johnson, Tomoki Kosho, Katherine Neas, F M Pope, Frank Rutsch, (unknown), Glenda Sobey, Anthony Vandersteen, Fleur S. van Dijk	14
14	Prospective clinical investigations of children with periodontal Ehlers–Danlos syndrome identify generalized lack of attached gingiva as a pathognomonic feature 2020 ·Genetics in Medicine ·Ines Kapferer‐Seebacher, (unknown), (unknown), Diana Johnson, Neeti Ghali, Angela F. Brady, Glenda Sobey, Johannes Zschocke, Fleur S. van Dijk	16
15	Fatigue in adults with Osteogenesis Imperfecta 2020 ·BMC Musculoskeletal Disorders ·(unknown), (unknown), Fleur S. van Dijk, (unknown), Anton Franken, (unknown), Guus Janus	16
16	Electron microscopy in the diagnosis of Ehlers–Danlos syndromes: correlation with clinical and genetic investigations 2019 ·British Journal of Dermatology ·(unknown), Neeti Ghali, Duncan Baker, Angela F. Brady, F. Michael Pope, Anthony Vandersteen, Bart Wagner, David Ferguson, Fleur S. van Dijk	20
17	Absence of Collagen Flowers on Electron Microscopy and Identification of (Likely) Pathogenic COL5A1 Variants in Two Patients 2019 ·Genes ·(unknown), Angela F. Brady, Marina Colombi, David Ferguson, Rebecca C. Pollitt, F. Michael Pope, Marco Ritelli, Sofie Symoens, Neeti Ghali, Fleur S. van Dijk	11
18	Amniotic band sequence in paternal half‐siblings with vascular Ehlers–Danlos syndrome 2019 ·American Journal of Medical Genetics Part A ·(unknown), Robert D. M. Hadden, (unknown), Katherine Lachlan, Fleur S. van Dijk, Peter D. Turnpenny	5
19	Adults with osteogenesis imperfecta: Clinical characteristics of 151 patients with a focus on bisphosphonate use and bone density measurements 2018 ·Bone Reports ·Luuk J.J. Scheres, Fleur S. van Dijk, (unknown), (unknown), (unknown), Guus Janus, Anton Franken	12
20	Ehlers Danlos syndrome, kyphoscoliotic type due to Lysyl Hydroxylase 1 deficiency in two children without congenital or early onset kyphoscoliosis 2017 ·European Journal of Medical Genetics ·Fleur S. van Dijk, Grazia M.S. Mancini, Alessandra Maugeri, Jan M. Cobben	9

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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