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Epileptic Disorders : International Epilepsy Journal with Videotape|September 14, 2016
GOSR2: a progressive myoclonus epilepsy geneLeanne M Dibbens, Guido Rubboli
Genome Medicine|April 4, 2009
Chipping away at the common epilepsies with complex genetics: the 15q13.3 microdeletion shows the wayJohn C Mulley, Leanne M Dibbens
Journal of Medical Genetics|January 25, 2013
Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropySarah E Heron, Leanne M Dibbens
The Application of Clinical Genetics|June 19, 2013
Genetic variations and associated pathophysiology in the management of epilepsyJohn C Mulley, Leanne M Dibbens
American Journal of Medical Genetics. Part A|August 3, 2016
BRAT1-associated neurodegeneration: Intra-familial phenotypic differences in siblingsNicholas J Smith, Jill Lipsett, Leanne M Dibbens, et al.
Journal of Medical Genetics|January 8, 2016
KCNT1 mutations in seizure disorders: the phenotypic spectrum and functional effectsChiao Xin Lim, Michael G Ricos, Leanne M Dibbens, et al.
Journal of Molecular Neuroscience : MN|May 1, 2024
Aneuploidy is Linked to Neurological Phenotypes Through Oxidative StressAnowarul Islam, Zeeshan Shaukat, Rashid Hussain, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 31, 2007
Channelopathies in idiopathic epilepsySarah E Heron, Ingrid E Scheffer, Samuel F Berkovic, et al.
Human Molecular Genetics|October 26, 2005
Susceptibility genes for complex epilepsyJohn C Mulley, Ingrid E Scheffer, Louise A Harkin, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 22, 2022
Investigating genetic variants in microRNA regulators of Neurokinin-1 receptor in sudden infant death syndromeZeeshan Shaukat, Roger W Byard, Robert Vink, et al.
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