1. Cardiac arrest in a mother and daughter and the identification of a novel RYR2 variant, predisposing to low penetrant catecholaminergic polymorphic ventricular tachycardia in a four‐generation Canadian family. Issue 4 (28th January 2020) Authors: Tung, Matthew; Van Petegem, Filip; Lauson, Samantha; Collier, Ashley; Hodgkinson, Kathy; Fernandez, Bridget; Connors, Sean; Leather, Rick; Sanatani, Shubhayan; Arbour, Laura Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 4(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Commentary on "Opportunities for Participation: A Mapping Review of Inclusive Physical Activity for Youth With Disabilities". Issue 1 (January 2023) Authors: Gosselin, Dora; Collier, Ashley Journal: Pediatric physical therapy Issue: Volume 35:Issue 1(2023) Page Start: 84 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Long-Term Clinical Outcome of Arrhythmogenic Right Ventricular Cardiomyopathy in Individuals With a p.S358L Mutation in TMEM43 Following Implantable Cardioverter Defibrillator Therapy. (March 2016) Authors: Hodgkinson, Kathleen A.; Howes, A.J.; Boland, Paul; Shen, Xiou Seegar; Stuckless, Susan; Young, Terry-Lynn; Curtis, Fiona; Collier, Ashley; Parfrey, Patrick S.; Connors, Sean P. Journal: Circulation Issue: Volume 9:Number 3(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Novel pathogenic COX20 variants causing dysarthria, ataxia, and sensory neuropathy. Issue 1 (9th November 2018) Authors: Otero, Maria G.; Tiongson, Emmanuelle; Diaz, Frank; Haude, Katrina; Panzer, Karin; Collier, Ashley; Kim, Jaemin; Adams, David; Tifft, Cynthia J.; Cui, Hong; Millian Zamora, Francisca; Au, Margaret G.; Graham, John M.; Buckley, David J.; Lewis, Richard; Toro, Camilo; Bai, Renkui; Turner, Lesley; M... Journal: Annals of clinical and translational neurology Issue: Volume 6:Issue 1(2019) Page Start: 154 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. On the persistence and detectability of ancient Beothuk mitochondrial DNA genomes in living First Nations peoples. (2nd January 2019) Authors: Collier, Ashley; Carr, Steven M. Journal: Mitochondrial DNA Issue: Volume 30:Number 1(2019) Page Start: 68 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum. (15th December 2021) Authors: Johannesen, Katrine M.; Gardella, Elena; Gjerulfsen, Cathrine E.; Bayat, Allan; Rouhl, Rob P.W.; Reijnders, Margot; Whalen, Sandra; Keren, Boris; Buratti, Julien; Courtin, Thomas; Wierenga, Klaas J.; Isidor, Bertrand; Piton, Amélie; Faivre, Laurence; Garde, Aurore; Moutton, Sébastien; Tran-Mau-Th... Journal: Neurology Issue: Volume 7:Number 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum. (December 2021) Authors: Johannesen, Katrine M.; Gardella, Elena; Gjerulfsen, Cathrine E.; Bayat, Allan; Rouhl, Rob P.W.; Reijnders, Margot; Whalen, Sandra; Keren, Boris; Buratti, Julien; Courtin, Thomas; Wierenga, Klaas J.; Isidor, Bertrand; Piton, Amélie; Faivre, Laurence; Garde, Aurore; Moutton, Sébastien; Tran-Mau-Th... Journal: Neurology Issue: Volume 7:Number 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗