Kate M. Lawrence
Heidelberg, VIC 3084, Australia
Last Updated: 09/26/2026
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Found 11 publications
SUDEP risk is influenced by longevity genomics: a polygenic risk score study.
Journal: EBioMedicine
Published: February 19, 2025
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy.
Journal: Annals of clinical and translational neurology
Published: April 10, 2015
Genetics of epilepsy: The testimony of twins in the molecular era.
Journal: Neurology
Published: August 10, 2014
Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26.
Journal: Neurology
Published: April 17, 2013
Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency.
Journal: Epilepsia
Published: October 31, 2012
Genetics of febrile seizure subtypes and syndromes: a twin study.
Journal: Epilepsy research
Published: August 31, 2012
Evidence for genetic factors in vasovagal syncope: a twin-family study.
Journal: Neurology
Published: August 08, 2012
Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locus.
Journal: Archives of neurology
Published: April 12, 2012
Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.
Journal: Annals of neurology
Published: December 20, 2011
Showing 1-11 of 11
Last Updated: 09/26/2026