Joost Haan

10.2k total citations · 1 hit paper
118 papers, 6.0k citations indexed

About

Joost Haan is a scholar working on Psychiatry and Mental health, Neurology and Physiology. According to data from OpenAlex, Joost Haan has authored 118 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Psychiatry and Mental health, 44 papers in Neurology and 35 papers in Physiology. Recurrent topics in Joost Haan's work include Migraine and Headache Studies (63 papers), Cerebrovascular and genetic disorders (26 papers) and Trigeminal Neuralgia and Treatments (25 papers). Joost Haan is often cited by papers focused on Migraine and Headache Studies (63 papers), Cerebrovascular and genetic disorders (26 papers) and Trigeminal Neuralgia and Treatments (25 papers). Joost Haan collaborates with scholars based in Netherlands, United States and United Kingdom. Joost Haan's co-authors include Michel D. Ferrari, Gisela M. Terwindt, Rune R. Frants, Arn M. J. M. van den Maagdenberg, Roel A. Ophoff, Ronald van Eijk, Dick Lindhout, Jane E. Lamerdin, Gert‐Jan B. van Ommen and Dennis E. Bulman and has published in prestigious journals such as New England Journal of Medicine, Cell and Neurology.

In The Last Decade

Joost Haan

116 papers receiving 5.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

1996 1.8k citations Roel A. Ophoff, Gisela M. Terwindt et al. Cell profile →

Peers

Joost Haan

PMH

NEURO

PFM

PHYSI

Anne Ducros France

Gisela M. Terwindt Netherlands

Jan Erik Hardebo Sweden

J. Haan Netherlands

Wouter Kamphorst Netherlands

Daniel D. Mikol United States

Tobias Freilinger Germany

Paolo Aridon Italy

Johannes Woitzik Germany

Robert Lenz United States

Anne Ducros France

Joost Haan

4.1k ×1.3

PMH

3.0k ×1.5

NEURO

1.3k ×0.8

1.1k ×0.8

PFM

671 ×0.5

PHYSI

Citations per year, relative to Joost Haan Joost Haan (= 1×) peers Anne Ducros

Countries citing papers authored by Joost Haan

Since Specialization

Citations

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

Fields of papers citing papers by Joost Haan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joost Haan

This figure shows the co-authorship network connecting the top 25 collaborators of Joost Haan. A scholar is included among the top collaborators of Joost Haan 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 Joost Haan. Joost Haan 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

Brandt, Roemer B., Leopoldine A. Wilbrink, Joost Haan, et al.. (2023). A prospective open label 2–8 year extension of the randomised controlled ICON trial on the long-term efficacy and safety of occipital nerve stimulation in medically intractable chronic cluster headache. EBioMedicine. 98. 104895–104895. 7 indexed citations

Brandt, Roemer B., et al.. (2020). Pharmacotherapy for Cluster Headache. CNS Drugs. 34(2). 171–184. 33 indexed citations

Wilbrink, Leopoldine A., Mark A. Louter, Onno Teernstra, et al.. (2017). Allodynia in cluster headache. Pain. 158(6). 1113–1117. 23 indexed citations

Rutten, Julie W., Joost Haan, Gisela M. Terwindt, et al.. (2014). Interpretation ofNOTCH3mutations in the diagnosis of CADASIL. Expert Review of Molecular Diagnostics. 14(5). 593–603. 88 indexed citations

Haan, Joost & Peter J. Koehler. (2014). Traces of Hysteria in Novels. Monographs in clinical neuroscience/Frontiers of neurology and neuroscience/Monographs in neural sciences. 35. 99–108. 2 indexed citations

Haan, Joost. (2013). Locked-in. Progress in brain research. 206. 19–34. 6 indexed citations

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

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

Vanmolkot, Kaate R. J., E. E. Kors, Ülkü Türk Börü, et al.. (2006). Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine. European Journal of Human Genetics. 14(5). 555–560. 54 indexed citations

10.

Vanmolkot, Kaate R. J., E. E. Kors, Jouke‐Jan Hottenga, et al.. (2003). Novel mutations in the Na⁺, K⁺‐ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. Annals of Neurology. 54(3). 360–366. 270 indexed citations

11.

Bornebroek, Marjolijn, Chris De Jonghe, Joost Haan, et al.. (2003). Hereditary cerebral hemorrhage with amyloidosis dutch type (AβPP 693): decreased plasma amyloid-β 42 concentration. Neurobiology of Disease. 14(3). 619–623. 26 indexed citations

12.

Kors, E. E., Joost Haan, & Michel D. Ferrari. (1999). Genetics of primary headaches. Current Opinion in Neurology. 12(3). 249–254. 18 indexed citations

13.

Bornebroek, Marjolijn, Peter A. von dem Borne, Joost Haan, et al.. (1998). Binding of amyloid β precursor protein to coagulation factor XIa in vivo may favour haemorrhagic stroke. Journal of Neurology. 245(2). 111–115. 5 indexed citations

14.

Terwindt, G.M., et al.. (1998). Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. European Journal of Human Genetics. 6(4). 297–307. 66 indexed citations

15.

Maat–Schieman, Marion L. C., et al.. (1997). Association of Vascular Amyloid β and Cells of the Mononuclear Phagocyte System in Hereditary Cerebral Hemorrhage with Amyloidosis (Dutch) and Alzheimer Disease. Journal of Neuropathology & Experimental Neurology. 56(3). 273–284. 58 indexed citations

16.

Ophoff, Roel A., Gisela M. Terwindt, Monique N. Vergouwe, et al.. (1996). Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4. Cell. 87(3). 543–552. 1758 indexed citations breakdown →

17.

May, Arne, Roel A. Ophoff, Gisela M. Terwindt, et al.. (1995). Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura. Human Genetics. 96(5). 604–608. 133 indexed citations

18.

Ophoff, Roel A., Ronald van Eijk, Lodewijk A. Sandkuijl, et al.. (1994). Genetic Heterogeneity of Familial Hemiplegic Migraine. Genomics. 22(1). 21–26. 117 indexed citations

19.

Wagner, Steven L., et al.. (1992). Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis–dutch type share a decrease in cerebrospinal fluid levels of amyloid β‐protein precursor. Annals of Neurology. 32(2). 215–218. 26 indexed citations

20.

Roos, Raymund A.C., Joost Haan, & Christine Van Broeckhoven. (1991). Hereditary Cerebral Hemorrhage with Amyloidosis—Dutch Type: A Congophilic Angiopathy. Annals of the New York Academy of Sciences. 640(1). 155–160. 7 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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