Boukje de Vries

6.0k total citations
36 papers, 1.3k citations indexed

About

Boukje de Vries is a scholar working on Psychiatry and Mental health, Endocrine and Autonomic Systems and Neurology. According to data from OpenAlex, Boukje de Vries has authored 36 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Psychiatry and Mental health, 10 papers in Endocrine and Autonomic Systems and 8 papers in Neurology. Recurrent topics in Boukje de Vries's work include Migraine and Headache Studies (30 papers), Neuroscience of respiration and sleep (10 papers) and Epilepsy research and treatment (6 papers). Boukje de Vries is often cited by papers focused on Migraine and Headache Studies (30 papers), Neuroscience of respiration and sleep (10 papers) and Epilepsy research and treatment (6 papers). Boukje de Vries collaborates with scholars based in Netherlands, United Kingdom and United States. Boukje de Vries's co-authors include Michel D. Ferrari, Arn M. J. M. van den Maagdenberg, Rune R. Frants, Gisela M. Terwindt, Joost Haan, Kaate R. J. Vanmolkot, Anine H Stam, Lisanne S. Vijfhuizen, Stephany C Koelewijn and Reinald Shyti and has published in prestigious journals such as Neurology, Scientific Reports and Pain.

In The Last Decade

Boukje de Vries

36 papers receiving 1.3k citations

Peers

Boukje de Vries
Boukje de Vries
Citations per year, relative to Boukje de Vries Boukje de Vries (= 1×) peers Kaate R. J. Vanmolkot

Countries citing papers authored by Boukje de Vries

Since Specialization
Citations

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

Fields of papers citing papers by Boukje de Vries

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Boukje de Vries. 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 Boukje de Vries. The network helps show where Boukje de Vries may publish in the future.

Co-authorship network of co-authors of Boukje de Vries

This figure shows the co-authorship network connecting the top 25 collaborators of Boukje de Vries. A scholar is included among the top collaborators of Boukje de Vries 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 Boukje de Vries. Boukje de Vries 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.
Eising, Else, Nadine Pelzer, Lisanne S. Vijfhuizen, et al.. (2017). Identifying a gene expression signature of cluster headache in blood. Scientific Reports. 7(1). 40218–40218. 15 indexed citations
2.
Eising, Else, Reinald Shyti, Peter A.C. ’t Hoen, et al.. (2016). Cortical Spreading Depression Causes Unique Dysregulation of Inflammatory Pathways in a Transgenic Mouse Model of Migraine. Molecular Neurobiology. 54(4). 2986–2996. 40 indexed citations
3.
Demirkan, Ayşe, Peter Henneman, Aswin Verhoeven, et al.. (2015). Insight in Genome-Wide Association of Metabolite Quantitative Traits by Exome Sequence Analyses. PLoS Genetics. 11(1). e1004835–e1004835. 41 indexed citations
4.
Tolner, Else A., Thijs Houben, Gisela M. Terwindt, et al.. (2015). From migraine genes to mechanisms. Pain. 156(Supplement 1). S64–S74. 59 indexed citations
5.
Eising, Else, Christiaan de Leeuw, Josine L. Min, et al.. (2015). Involvement of astrocyte and oligodendrocyte gene sets in migraine. Cephalalgia. 36(7). 640–647. 15 indexed citations
6.
Pelzer, Nadine, Boukje de Vries, Jessica T. Kamphorst, et al.. (2014). PRRT2 and hemiplegic migraine: A complex association. Neurology. 83(3). 288–290. 32 indexed citations
7.
Pelzer, Nadine, Anine H Stam, Johannes A. Carpay, et al.. (2014). Familial hemiplegic migraine treated by sodium valproate and lamotrigine. Cephalalgia. 34(9). 708–711. 15 indexed citations
8.
Weller, Claudia M, Nadine Pelzer, Boukje de Vries, et al.. (2014). Two novel SCN1A mutations identified in families with familial hemiplegic migraine. Cephalalgia. 34(13). 1062–1069. 24 indexed citations
9.
Fernández‐Morales, Jessica, Boukje de Vries, Bendik S. Winsvold, et al.. (2013). Genotyping the Risk of Migraine Chronification: The CHROMIG Study. Cephalalgia. 33. 153–153. 1 indexed citations
10.
Vries, Boukje de, et al.. (2013). Novel SCN1A mutation in the IFMT motif of the α1 subunit of the voltage-gated NaV1.1 channel causing familial hemiplegic migraine. The Journal of Headache and Pain. 14(S1). 1 indexed citations
11.
Shyti, Reinald, Boukje de Vries, & Arn van den Maagdenberg. (2011). Migraine Genes and the Relation to Gender. Headache The Journal of Head and Face Pain. 51(6). 880–890. 39 indexed citations
12.
Vries, Boukje de, Hafsa Mamsa, Anine H Stam, et al.. (2009). Episodic Ataxia Associated With EAAT1 Mutation C186S Affecting Glutamate Reuptake. Archives of Neurology. 66(1). 97–101. 99 indexed citations
13.
Vries, Boukje de, Rune R. Frants, Michel D. Ferrari, & Arn M. J. M. van den Maagdenberg. (2009). Molecular genetics of migraine. Human Genetics. 126(1). 115–132. 207 indexed citations
14.
Lemos, Carolina, Boukje de Vries, José Barros, et al.. (2008). First Mutation in the Voltage-Gated Nav1.1 Subunit Gene SCN1A with Co-Occurring Familial Hemiplegic Migraine and Epilepsy. Cephalalgia. 29(3). 308–313. 74 indexed citations
15.
Vries, Boukje de, Carolina Lemos, Teresa Temudo, et al.. (2007). Two novel functional mutations in the Na+,K+‐ATPase α2‐subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes. Clinical Genetics. 73(1). 37–43. 26 indexed citations
16.
Vanmolkot, Kaate R. J., Anine H Stam, Ashok Raman, et al.. (2007). First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine. European Journal of Human Genetics. 15(8). 884–888. 19 indexed citations
17.
Vanmolkot, Kaate R. J., Elena Babini, Boukje de Vries, et al.. (2007). The novel p.L1649Q mutation in theSCN1Aepilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Human Mutation. 28(5). 522–522. 81 indexed citations
18.
Vries, Boukje de, Joost Haan, Rune R. Frants, Arn M. J. M. van den Maagdenberg, & Michel D. Ferrari. (2006). Genetic Biomarkers for Migraine. Headache The Journal of Head and Face Pain. 46(7). 1059–1068. 33 indexed citations
19.
Loder, Elizabeth, et al.. (2006). Selected Confirmed, Probable, and Exploratory Migraine Biomarkers. Headache The Journal of Head and Face Pain. 46(7). 1108–1127. 12 indexed citations
20.
Vries, Boukje de, J. Haan, Kaate R. J. Vanmolkot, et al.. (2006). Alternating Hemiplegia of Childhood: No Mutations in the Glutamate Transporter EAAT1. Neuropediatrics. 37(5). 302–304. 11 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026