Anke Van Dijck

2.2k total citations
18 papers, 403 citations indexed

About

Anke Van Dijck is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Anke Van Dijck has authored 18 papers receiving a total of 403 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Molecular Biology and 6 papers in Cognitive Neuroscience. Recurrent topics in Anke Van Dijck's work include Genetics and Neurodevelopmental Disorders (12 papers), Autism Spectrum Disorder Research (6 papers) and Congenital heart defects research (4 papers). Anke Van Dijck is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Autism Spectrum Disorder Research (6 papers) and Congenital heart defects research (4 papers). Anke Van Dijck collaborates with scholars based in Belgium, United States and Israel. Anke Van Dijck's co-authors include R. Frank Kooy, Illana Gozes, Sandra Bedrosian‐Sermone, Zlatko Marušić, Jurica Vuković, Danh V. Nguyen, Olga Touloumi, Kathleen Angkustsiri, Gidon Karmon and David Hessl and has published in prestigious journals such as Scientific Reports, Gene and Frontiers in Endocrinology.

In The Last Decade

Anke Van Dijck

14 papers receiving 386 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anke Van Dijck Belgium 10 223 213 112 80 30 18 403
James Nguyen United States 7 205 0.9× 151 0.7× 114 1.0× 105 1.3× 28 0.9× 15 496
Gal Hacohen-Kleiman Israel 8 127 0.6× 162 0.8× 93 0.8× 114 1.4× 19 0.6× 12 368
Sheng Tang United States 10 204 0.9× 219 1.0× 43 0.4× 80 1.0× 30 1.0× 17 417
Wenjia Song United States 6 185 0.8× 228 1.1× 146 1.3× 73 0.9× 30 1.0× 13 427
Kathryn B. Garber United States 11 466 2.1× 392 1.8× 182 1.6× 70 0.9× 22 0.7× 19 700
Aia Elise Jønch Denmark 6 306 1.4× 230 1.1× 194 1.7× 69 0.9× 21 0.7× 11 396
Mustapha Rammal United States 4 354 1.6× 309 1.5× 239 2.1× 100 1.3× 17 0.6× 7 518
Matthieu Raveau Japan 10 229 1.0× 232 1.1× 99 0.9× 93 1.2× 70 2.3× 13 535
Elisabeth Gabau Spain 16 463 2.1× 336 1.6× 103 0.9× 39 0.5× 20 0.7× 36 675

Countries citing papers authored by Anke Van Dijck

Since Specialization
Citations

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

Fields of papers citing papers by Anke Van Dijck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anke Van Dijck. 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 Anke Van Dijck. The network helps show where Anke Van Dijck may publish in the future.

Co-authorship network of co-authors of Anke Van Dijck

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

All Works

18 of 18 papers shown
1.
Cappuyns, Elisa, et al.. (2025). ADNP Exhibits Methyltransferase Activity in Overexpression Systems and Modulates DNA and Histone Methylation. Autism Research. 18(11). 2174–2191.
2.
Jansen, Anna, An‐Sofie Schoonjans, Anke Van Dijck, et al.. (2025). Investigation of Gait Characteristics and Kinematic Deviations in Rare Genetic Disorders with Instrumented Gait Analysis. Journal of Intellectual Disability Research. 69(5). 383–392.
3.
Dijck, Anke Van, Ellen Elinck, Alexander J.M. Dingemans, et al.. (2025). A frameshift variant in activity-dependent neuroprotective protein (ADNP) causes nucleocytoskeletal alterations in a dizygotic male twin: a case study. Clinical Epigenetics. 17(1). 185–185.
4.
Gabriele, Michele, Alessandro Vitriolo, Giuseppe Testa, et al.. (2024). Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patients. Scientific Reports. 14(1). 14710–14710. 3 indexed citations
5.
Dijck, Anke Van, Joe Ibrahim, Ellen Elinck, et al.. (2024). ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel–Van der Aa syndrome autopsy case. Acta Neuropathologica Communications. 12(1). 62–62. 9 indexed citations
6.
Dijck, Anke Van, Alessandro Vitriolo, Giuseppe Testa, et al.. (2023). Chromatin remodeler Activity-Dependent Neuroprotective Protein (ADNP) contributes to syndromic autism. Clinical Epigenetics. 15(1). 45–45. 19 indexed citations
7.
8.
Ivashko‐Pachima, Yanina, Vlasta Korenková, Olga Touloumi, et al.. (2020). Tauopathy in the young autistic brain: novel biomarker and therapeutic target. Translational Psychiatry. 10(1). 228–228. 67 indexed citations
9.
Werf, Ilse M. van der, Sandra Jansen, Petra F. de Vries, et al.. (2020). Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurodevelopmental disorders. European Journal of Human Genetics. 28(12). 1726–1733. 4 indexed citations
10.
Dijck, Anke Van, Susana Barbosa, Olfa Khalfallah, et al.. (2020). Reduced serum levels of pro-inflammatory chemokines in fragile X syndrome. BMC Neurology. 20(1). 138–138. 14 indexed citations
11.
Leboucher, Antoine, Didier F. Pisani, Laura Martínez-Gili, et al.. (2019). The translational regulator FMRP controls lipid and glucose metabolism in mice and humans. Molecular Metabolism. 21. 22–35. 37 indexed citations
12.
Dijck, Anke Van, Danh V. Nguyen, Reymundo Lozano, et al.. (2017). A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome. Journal of Neurodevelopmental Disorders. 9(1). 26–26. 59 indexed citations
13.
Gozes, Illana, Anke Van Dijck, Gal Hacohen-Kleiman, et al.. (2017). Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children. Translational Psychiatry. 7(2). e1043–e1043. 59 indexed citations
14.
Gozes, Illana, Marc C. Patterson, Anke Van Dijck, et al.. (2017). The Eight and a Half Year Journey of Undiagnosed AD: Gene Sequencing and Funding of Advanced Genetic Testing Has Led to Hope and New Beginnings. Frontiers in Endocrinology. 8. 107–107. 31 indexed citations
15.
Dijck, Anke Van, Céline Helsmoortel, Geert Vandeweyer, & R. Frank Kooy. (2016). ADNP-Related Intellectual Disability and Autism Spectrum Disorder. 2 indexed citations
16.
Werf, Ilse M. van der, Anke Van Dijck, Edwin Reyniers, et al.. (2016). Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. Gene. 605. 92–98. 21 indexed citations
17.
Dijck, Anke Van, Ilse M. van der Werf, Edwin Reyniers, et al.. (2015). Five patients with a chromosome 1q21.1 triplication show macrocephaly, increased weight and facial similarities. European Journal of Medical Genetics. 58(10). 503–508. 21 indexed citations
18.
Vandeweyer, Geert, Céline Helsmoortel, Anke Van Dijck, et al.. (2014). The transcriptional regulatorADNPlinks the BAF (SWI/SNF) complexes with autism. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(3). 315–326. 56 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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