Laura Addis
Gunnels Wood Road
Stevenage, ENG, United Kingdom
Stevenage, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 14 publications
GWAS of extended prescription analgesic use identifies genetic loci in chronic pain.
Journal: Nature communications
Published: February 06, 2025
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures.
Journal: Epilepsia
Published: August 07, 2019
Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses.
Journal: Journal of medical genetics
Published: February 08, 2018
Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency - molecular profiling and functional rescue.
Journal: Scientific reports
Published: September 29, 2016
Idiopathic focal epilepsies: the "lost tribe".
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: July 21, 2016
A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy.
Journal: Annals of clinical and translational neurology
Published: April 21, 2016
Analysis of rare copy number variation in absence epilepsies.
Journal: Neurology. Genetics
Published: August 31, 2015
Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic.
Journal: Bioinformatics (Oxford, England)
Published: April 16, 2014
Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci.
Journal: Genes, brain, and behavior
Published: September 04, 2013
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.
Journal: Nature genetics
Published: November 20, 2012
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.
Journal: Nature genetics
Published: November 01, 2012
Last Updated: 09/26/2026