Kaate R. J. Vanmolkot
MRC Epidemiology Unit(GB)
Publications by Year
Research Areas
Migraine and Headache Studies, Neuroscience of respiration and sleep, Trigeminal Neuralgia and Treatments, Epilepsy research and treatment, Genetic Neurodegenerative Diseases
Most-Cited Works
- → C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy(2007)447 cited
- → p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation(2001)377 cited
- → Novel mutations in the Na+, K+‐ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions(2003)357 cited
- → Episodic Ataxia Associated With EAAT1 Mutation C186S Affecting Glutamate Reuptake(2009)145 cited
- → Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine(2007)120 cited
- → Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation(2004)116 cited
- → Shared genetic factors in migraine and depression(2010)109 cited
- → The novel p.L1649Q mutation in theSCN1Aepilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies(2007)105 cited
- → Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation(2006)83 cited
- → Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine(2006)71 cited