E. E. Kors

1.4k total citations
18 papers, 1.1k citations indexed

About

E. E. Kors is a scholar working on Psychiatry and Mental health, Cellular and Molecular Neuroscience and Endocrine and Autonomic Systems. According to data from OpenAlex, E. E. Kors has authored 18 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Psychiatry and Mental health, 6 papers in Cellular and Molecular Neuroscience and 6 papers in Endocrine and Autonomic Systems. Recurrent topics in E. E. Kors's work include Migraine and Headache Studies (16 papers), Neuroscience of respiration and sleep (6 papers) and Genetic Neurodegenerative Diseases (6 papers). E. E. Kors is often cited by papers focused on Migraine and Headache Studies (16 papers), Neuroscience of respiration and sleep (6 papers) and Genetic Neurodegenerative Diseases (6 papers). E. E. Kors collaborates with scholars based in Netherlands, United States and United Kingdom. E. E. Kors's co-authors include Michel D. Ferrari, Rune R. Frants, Arn M. J. M. van den Maagdenberg, Joost Haan, Gisela M. Terwindt, Kaate R. J. Vanmolkot, J. Haan, David F. Black, Lodewijk A. Sandkuijl and W.A.J. Hoefnagels and has published in prestigious journals such as Neurology, Annals of Neurology and Neurobiology of Disease.

In The Last Decade

E. E. Kors

17 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E. E. Kors Netherlands	14	745	334	251	228	220	18	1.1k
G.M. Terwindt Netherlands	10	799 1.1×	107 0.3×	329 1.3×	71 0.3×	118 0.5×	20	956
Nanna Arngrim Denmark	16	426 0.6×	107 0.3×	189 0.8×	128 0.6×	102 0.5×	25	725
José Pereira‐Monteiro Portugal	15	390 0.5×	141 0.4×	114 0.5×	94 0.4×	110 0.5×	36	594
Kenneth Silver Canada	18	311 0.4×	326 1.0×	76 0.3×	99 0.4×	54 0.2×	32	1.0k
Lars Lykke Thomsen Denmark	13	717 1.0×	102 0.3×	333 1.3×	108 0.5×	151 0.7×	21	1.0k
L. L. Thomsen Denmark	11	713 1.0×	133 0.4×	381 1.5×	66 0.3×	140 0.6×	11	853
Anine H Stam Netherlands	12	341 0.5×	158 0.5×	107 0.4×	139 0.6×	73 0.3×	15	513
Laura Pierguidi Italy	12	472 0.6×	65 0.2×	100 0.4×	108 0.5×	94 0.4×	15	808
LH Lassen Denmark	10	1.4k 1.9×	115 0.3×	782 3.1×	267 1.2×	288 1.3×	10	1.6k
Hashmat Ghanizada Denmark	17	624 0.8×	113 0.3×	301 1.2×	202 0.9×	134 0.6×	28	781

Countries citing papers authored by E. E. Kors

Since Specialization

Citations

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

Fields of papers citing papers by E. E. Kors

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. E. Kors

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

All Works

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18 of 18 papers shown

Graves, Tracey D., Paola Imbrici, E. E. Kors, et al.. (2008). Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2. Neurobiology of Disease. 32(1). 10–15. 22 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

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

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

Schoenen, Jean, Anna Ambrosini, Alain Maertens de Noordhout, et al.. (2005). Single-fiber EMG in familial hemiplegic migraine [5] (multiple letters). 64(9). 1666–1667. 1 indexed citations

Haan, Joost, E. E. Kors, Arn M. J. M. van den Maagdenberg, et al.. (2004). Toward a molecular genetic classification of familial hemiplegic migraine. Current Pain and Headache Reports. 8(3). 238–243. 10 indexed citations

Kors, E. E., Kaate R. J. Vanmolkot, J. Haan, et al.. (2004). Alternating Hemiplegia of Childhood: No Mutations in the Second Familial Hemiplegic Migraine GeneATP1A2. Neuropediatrics. 35(5). 293–296. 21 indexed citations

Kors, E. E., Kaate R. J. Vanmolkot, J. Haan, et al.. (2004). [From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene].. PubMed. 148(39). 1919–20.

Kors, E. E., Kaate R. J. Vanmolkot, Joost Haan, et al.. (2004). Recent findings in headache genetics. Current Opinion in Neurology. 17(3). 283–288. 46 indexed citations

10.

Kors, E. E., Atle Melberg, Kaate R. J. Vanmolkot, et al.. (2004). Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation. Neurology. 63(6). 1136–1137. 94 indexed citations

11.

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

12.

Kors, E. E., Joost Haan, & Michel D. Ferrari. (2003). Migraine genetics. Current Pain and Headache Reports. 7(3). 212–217. 21 indexed citations

13.

Kors, E. E., J. Haan, Nicola Giffin, et al.. (2003). Expanding the Phenotypic Spectrum of the CACNA1A Gene T666M Mutation. Archives of Neurology. 60(5). 684–684. 69 indexed citations

14.

Terwindt, G.M., et al.. (2003). Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine.. Headache The Journal of Head and Face Pain. 43(3). 303–303. 3 indexed citations

15.

Kors, E. E., Arn M. J. M. van den Maagdenberg, Jaap J. Plomp, Rune R. Frants, & Michel D. Ferrari. (2002). Calcium channel mutations and migraine. Current Opinion in Neurology. 15(3). 311–316. 26 indexed citations

16.

Maagdenberg, Arn M. J. M. van den, E. E. Kors, E. R. Brunt, et al.. (2002). Episodic ataxia type 2. Journal of Neurology. 249(11). 1515–1519. 28 indexed citations

17.

Kors, E. E., Gisela M. Terwindt, Robin B. Fitzsimons, et al.. (2001). Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine. Annals of Neurology. 49(6). 753–760. 269 indexed citations

18.

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