J. Haan

4.4k total citations
90 papers, 3.1k citations indexed

About

J. Haan is a scholar working on Psychiatry and Mental health, Neurology and Physiology. According to data from OpenAlex, J. Haan has authored 90 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Psychiatry and Mental health, 36 papers in Neurology and 23 papers in Physiology. Recurrent topics in J. Haan's work include Migraine and Headache Studies (41 papers), Cerebrovascular and genetic disorders (19 papers) and Amyloidosis: Diagnosis, Treatment, Outcomes (17 papers). J. Haan is often cited by papers focused on Migraine and Headache Studies (41 papers), Cerebrovascular and genetic disorders (19 papers) and Amyloidosis: Diagnosis, Treatment, Outcomes (17 papers). J. Haan collaborates with scholars based in Netherlands, United Kingdom and United States. J. Haan's co-authors include Michel D. Ferrari, R. A. C. Roos, Egbert Bakker, Rune R. Frants, GM Terwindt, Christine Van Broeckhoven, Wim Van Hul, Mark A. van Buchem, Arn M. J. M. van den Maagdenberg and John Hardy and has published in prestigious journals such as Science, The Lancet and Brain.

In The Last Decade

J. Haan

89 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. Haan Netherlands	31	1.4k	1.0k	939	783	524	90	3.1k
M.G. Bousser France	24	1.9k 1.4×	830 0.8×	696 0.7×	224 0.3×	1.1k 2.1×	51	2.8k
Tobias Freilinger Germany	24	1.4k 1.0×	560 0.6×	390 0.4×	655 0.8×	490 0.9×	59	2.6k
Jürgen Herzog Germany	20	945 0.7×	1.0k 1.0×	291 0.3×	473 0.6×	357 0.7×	29	2.3k
G D’Andrea Italy	31	1.4k 1.0×	395 0.4×	628 0.7×	252 0.3×	879 1.7×	154	3.1k
I. Jansen Sweden	32	952 0.7×	395 0.4×	1.0k 1.1×	697 0.9×	552 1.1×	79	3.0k
Joost Haan Netherlands	41	3.1k 2.2×	1.9k 1.9×	1.3k 1.4×	1.6k 2.1×	1.4k 2.6×	118	6.0k
Silvana Archetti Italy	33	746 0.5×	1.2k 1.2×	1.1k 1.2×	532 0.7×	73 0.1×	106	3.2k
Marek Gawel Canada	30	1.6k 1.1×	819 0.8×	786 0.8×	221 0.3×	904 1.7×	75	2.8k
Christina Kruuse Denmark	28	1.6k 1.1×	334 0.3×	743 0.8×	495 0.6×	717 1.4×	130	3.1k
Francesco Perini Italy	24	811 0.6×	323 0.3×	457 0.5×	525 0.7×	463 0.9×	62	1.9k

Countries citing papers authored by J. Haan

Since Specialization

Citations

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

Fields of papers citing papers by J. Haan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Haan

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

Wilbrink, Leopoldine A., et al.. (2013). Co-Occurrence of Cluster Headache and Trigeminal Neuralgia : Cluster-Tic Syndrome in the LUCA Population. Cephalalgia. 33. 6–7. 1 indexed citations

Haan, J., Peter J. Koehler, & Julien Bogousslavsky. (2012). Neurology and surrealism: Andre Breton and Joseph Babinski. Brain. 135(12). 3830–3838. 10 indexed citations

Koppen, Hille, Gisela M. Terwindt, J. Haan, Sebastiaan F.T.M. de Bruijn, & Jeroen J. Bax. (2010). Strong association between right-to-left shunt and migraine. Netherlands Heart Journal. 18(5). 275–276. 1 indexed citations

Haan, J., Marion L. C. Maat–Schieman, Sjoerd G. van Duinen, et al.. (2009). Co-localization of β/A4 and cystatin C in cortical blood vessels in Dutch, but not in Icelandic hereditary cerebral hemorrhage with amyloidosis. Acta Neurologica Scandinavica. 89(5). 367–371. 11 indexed citations

Liem, Michael, Saskia A.J. Lesnik Oberstein, J. Haan, et al.. (2009). Cerebrovascular Reactivity Is a Main Determinant of White Matter Hyperintensity Progression in CADASIL. American Journal of Neuroradiology. 30(6). 1244–1247. 42 indexed citations

Haan, J., et al.. (2008). A review of the genetic relation between migraine and epilepsy.. PubMed. 28(2). 105–13. 45 indexed citations

Vanmolkot, Kaate R. J., Hans Stroink, Jan B. Koenderink, et al.. (2006). Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation. Annals of Neurology. 59(2). 310–314. 70 indexed citations

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

Haan, J., E. E. Kors, Kaate R. J. Vanmolkot, et al.. (2005). Migraine genetics: An update. Current Pain and Headache Reports. 9(3). 213–220. 40 indexed citations

10.

Ferrari, Michel D. & J. Haan. (2002). The genetics of migraine: implication for treatment approaches. PubMed. 111–127. 7 indexed citations

11.

Oberstein, Saskia A.J. Lesnik, Michel D. Ferrari, Egbert Bakker, et al.. (1999). Diagnostic Notch3 sequence analysis in CADASIL: Three new mutations in Dutch patients. Neurology. 52(9). 1913–1913. 63 indexed citations

12.

Bornebroek, Marjolijn, J. Haan, Sjoerd G. van Duinen, et al.. (1997). Dutch hereditary cerebral amyloid angiopathy: Structural lesions and apolipoprotein E genotype. Annals of Neurology. 41(5). 695–698. 36 indexed citations

13.

Bornebroek, Marjolijn, J. Haan, H. Backhovens, et al.. (1997). Presenilin‐I polymorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch type. Annals of Neurology. 42(1). 108–110. 5 indexed citations

14.

Bornebroek, Marjolijn, J. Haan, Mark A. van Buchem, et al.. (1996). White Matter Lesions and Cognitive Deterioration in Presymptomatic Carriers of the Amyloid Precursor Protein Gene Codon 693 Mutation. Archives of Neurology. 53(1). 43–48. 21 indexed citations

15.

Bornebroek, Marjolijn, Roel A. Ophoff, H.A.O. Winter-Warnars, et al.. (1995). A four-generation Dutch family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), linked to chromosome 19p13. Clinical Neurology and Neurosurgery. 97(4). 307–313. 12 indexed citations

16.

Weinstein, H. C., J. Haan, M.M.A. Derix, et al.. (1991). SPECT in the diagnosis of Alzheimer's disease and multi-infarct-dementia. Clinical Neurology and Neurosurgery. 93(1). 39–43. 28 indexed citations

17.

Haan, J., et al.. (1990). Dementia in Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type. Archives of Neurology. 47(9). 965–967. 62 indexed citations

18.

Bloem, Bastiaan R., A. Margot Lagaay, Wessel van Beek, et al.. (1990). Prevalence of subjective dysphagia in community residents aged over 87.. BMJ. 300(6726). 721–722. 152 indexed citations

19.

Haan, J., et al.. (1988). Spinal epidural hematoma visualized by magnetic resonance imaging. Neuroradiology. 30(3). 280–280. 35 indexed citations

20.

Haan, J., Michel D. Ferrari, & Oebele F. Brouwer. (1988). Acute confusional migraine. Clinical Neurology and Neurosurgery. 90(3). 275–278. 19 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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