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Citation: Sk. Service et al., The genome-wide distribution of background linkage disequilibrium in a population isolate, HUM MOL GEN, 10(5), 2001, pp. 545-551

Authors: Terwindt, GM Ophoff, RA van Eijk, R Vergouwe, MN Haan, J Frants, RR Sandkuijl, LA Ferrari, MD

Citation: Gm. Terwindt et al., Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura, NEUROLOGY, 56(8), 2001, pp. 1028-1032

Authors: Ophoff, RA van den Maagdenberg, AMJM Roon, KI Ferrari, MD Frants, RR

Citation: Ra. Ophoff et al., The impact of pharmacogenetics for migraine, EUR J PHARM, 413(1), 2001, pp. 1-10

Authors: Ophoff, RA DeYoung, J Service, SK Joose, M Caffo, NA Sandkuijl, LA Terwindt, GM Haan, J van den Maagdenberg, AMJM Jen, J Baloh, RW Barilla-LaBarca, ML Saccone, NL Atkinson, JP Ferrari, MD Freimer, NB Frants, RR

Citation: Ra. Ophoff et al., Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3, AM J HU GEN, 69(2), 2001, pp. 447-453

Authors: Guida, S Trettel, F Pagnutti, S Mantuano, E Tottene, A Veneziano, L Fellin, T Spadaro, M Stauderman, KA Williams, ME Volsen, S Ophoff, RA Frants, RR Jodice, C Frontali, M Pietrobon, D

Citation: S. Guida et al., Complete loss of P/Q calcium channel activity caused by a CACNA1A missensemutation carried by patients with episodic ataxia type 2, AM J HU GEN, 68(3), 2001, pp. 759-764

Authors: Haan, J Kors, EE Terwindt, GM Vermeulen, FLMG Vergouwe, MN van den Maagdenberg, AMJM Gill, DS Pascual, J Ophoff, RA Frants, RR Ferrari, MD

Citation: J. Haan et al., Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene, CEPHALALGIA, 20(8), 2000, pp. 696-700