Identification of a novel mutation in GYS1 (muscle-specific glycogen synthase) resulting in sudden cardiac death, that is diagnosable from skin fibroblastsJessie M. Cameron, Brian H. Robinson, David A. Chiasson et al.|Molecular Genetics and Metabolism|2009Cited by 81
Disruption of a mitochondrial RNA-binding protein gene results in decreased cytochrome <i>b</i> expression and a marked reduction in ubiquinol–cytochrome <i>c</i> reductase activity in mouse heart mitochondriaFenghao Xu, Brian H. Robinson, Jisoo Lee et al.|Biochemical Journal|2008Cited by 80
Genome-Wide Association Analysis Identifies a Mutation in the Thiamine Transporter 2 (SLC19A3) Gene Associated with Alaskan Husky EncephalopathyKaren M. Vernau, Danika L. Bannasch, Jonathan A. Runstadler et al.|PLoS ONE|2013Cited by 65
Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganizationJessie M. Cameron, Brian H. Robinson, Valeriy Levandovskiy et al.|Mitochondrion|2010Cited by 45
Mitochondrial citrate synthase crystals: Novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutationsKomudi Siriwardena, Jessie M. Cameron, Nevena MacKay et al.|Molecular Genetics and Metabolism|2012Cited by 41