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Meta-analysis of genome-wide association for migraine in six population-based European cohorts.
Ligthart L, de Vries B, Smith AV, Ikram MA, Amin N, Hottenga JJ, Koelewijn SC, Kattenberg VM, de Moor MH, Janssens AC, Aulchenko YS, Oostra BA, de Geus EJ, Smit JH, Zitman FG, Uitterlinden AG, Hofman A, Willemsen G, Nyholt DR, Montgomery GW, Terwindt GM, Gudnason V, Penninx BW, Breteler M, Ferrari MD, Launer LJ, van Duijn CM, van den Maagdenberg AM, Boomsma DI. Ligthart L, et al. Among authors: koelewijn sc. Eur J Hum Genet. 2011 Aug;19(8):901-7. doi: 10.1038/ejhg.2011.48. Epub 2011 Mar 30. Eur J Hum Genet. 2011. PMID: 21448238 Free PMC article.
Two novel SCN1A mutations identified in families with familial hemiplegic migraine.
Weller CM, Pelzer N, de Vries B, López MA, De Fàbregues O, Pascual J, Arroyo MA, Koelewijn SC, Stam AH, Haan J, Ferrari MD, Terwindt GM, van den Maagdenberg AM. Weller CM, et al. Among authors: koelewijn sc. Cephalalgia. 2014 Nov;34(13):1062-9. doi: 10.1177/0333102414529195. Epub 2014 Apr 4. Cephalalgia. 2014. PMID: 24707016
PRRT2 mutation causes benign familial infantile convulsions.
de Vries B, Callenbach PM, Kamphorst JT, Weller CM, Koelewijn SC, ten Houten R, de Coo IF, Brouwer OF, van den Maagdenberg AM. de Vries B, et al. Among authors: koelewijn sc. Neurology. 2012 Nov 20;79(21):2154-5. doi: 10.1212/WNL.0b013e3182752c30. Epub 2012 Oct 17. Neurology. 2012. PMID: 23077019
Noradrenergic and Cholinergic Modulation of Belief Updating.
Jepma M, Brown SBRE, Murphy PR, Koelewijn SC, de Vries B, van den Maagdenberg AM, Nieuwenhuis S. Jepma M, et al. Among authors: koelewijn sc. J Cogn Neurosci. 2018 Dec;30(12):1803-1820. doi: 10.1162/jocn_a_01317. Epub 2018 Jul 31. J Cogn Neurosci. 2018. PMID: 30063180 Clinical Trial.
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
Heinzen EL, Swoboda KJ, Hitomi Y, Gurrieri F, Nicole S, de Vries B, Tiziano FD, Fontaine B, Walley NM, Heavin S, Panagiotakaki E; European Alternating Hemiplegia of Childhood (AHC) Genetics Consortium; Biobanca e Registro Clinico per l'Emiplegia Alternante (I.B.AHC) Consortium; European Network for Research on Alternating Hemiplegia (ENRAH) for Small and Medium-sized Enterpriese (SMEs) Consortium; Fiori S, Abiusi E, Di Pietro L, Sweney MT, Newcomb TM, Viollet L, Huff C, Jorde LB, Reyna SP, Murphy KJ, Shianna KV, Gumbs CE, Little L, Silver K, Ptáček LJ, Haan J, Ferrari MD, Bye AM, Herkes GK, Whitelaw CM, Webb D, Lynch BJ, Uldall P, King MD, Scheffer IE, Neri G, Arzimanoglou A, van den Maagdenberg AM, Sisodiya SM, Mikati MA, Goldstein DB. Heinzen EL, et al. Nat Genet. 2012 Sep;44(9):1030-4. doi: 10.1038/ng.2358. Epub 2012 Jul 29. Nat Genet. 2012. PMID: 22842232 Free PMC article.