Sinead B. Heavin
Dublin, L, Ireland
Last Updated: 09/26/2026
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Found 10 publications
A comparison of genomic diagnostics in adults and children with epilepsy and comorbid intellectual disability.
Journal: European journal of human genetics : EJHG
Published: August 06, 2019
Genomic and clinical predictors of lacosamide response in refractory epilepsies.
Journal: Epilepsia open
Published: February 19, 2019
Development of a genomics module within an epilepsy-specific electronic health record: Toward genomic medicine in epilepsy care.
Journal: Epilepsia
Published: October 31, 2018
CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures.
Journal: Neurology
Published: February 13, 2015
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis.
Journal: Human molecular genetics
Published: January 28, 2014
Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients.
Journal: Neurology
Published: October 11, 2013
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Journal: Nature genetics
Published: December 28, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
Journal: Nature genetics
Published: April 16, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026