Rune R. Frants
Leiden, ZH, Netherlands
Last Updated: 09/26/2026
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Found 10 publications
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations.
Journal: Brain : a journal of neurology
Published: December 25, 2015
Early-onset facioscapulohumeral muscular dystrophy type 1 with some atypical features.
Journal: Journal of child neurology
Published: April 11, 2014
RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice.
Journal: Cephalalgia : an international journal of headache
Published: August 30, 2013
Dysferlin regulates cell adhesion in human monocytes.
Journal: The Journal of biological chemistry
Published: April 06, 2013
Migraine is not associated with enhanced atherosclerosis.
Journal: Cephalalgia : an international journal of headache
Published: November 14, 2012
Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Journal: Nature genetics
Published: November 07, 2012
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2.
Journal: Nature genetics
Published: May 24, 2012
Genome-wide association analysis identifies susceptibility loci for migraine without aura.
Journal: Nature genetics
Published: December 13, 2011
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.
Journal: PLoS genetics
Published: September 30, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026