1. Case–Control and Family‐Based Association Study of Specific PTPRD Variants in Restless Legs Syndrome. Issue 5 (9th January 2016) Authors: Gan‐Or, Ziv; Zhou, Sirui; Johnson, Amelie; Montplaisir, Jacques Y.; Allen, Richard P.; Earley, Christopher J.; Desautels, Alex; Dion, Patrick A.; Xiong, Lan; Rouleau, Guy A. Journal: Movement disorders clinical practice Issue: Volume 3:Issue 5(2016) Page Start: 460 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical and genetic study of hereditary spastic paraplegia in Canada. (February 2017) Authors: Chrestian, Nicolas; Dupré, Nicolas; Gan-Or, Ziv; Szuto, Anna; Chen, Shiyi; Venkitachalam, Anil; Brisson, Jean-Denis; Warman-Chardon, Jodi; Ahmed, Sohnee; Ashtiani, Setareh; MacDonald, Heather; Mohsin, Noreen; Mourabit-Amari, Karim; Provencher, Pierre; Boycott, Kym M.; Stavropoulos, Dimitri J.; Di... Journal: Neurology Issue: Volume 3:Number 1(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Copy-number variants in the contactin-5 gene are a potential risk factor for autism spectrum disorder. (November 2022) Authors: Schmilovich, Zoe; Huguet, Guillaume; He, Qin; Musa-Johnson, Amélie; Douard, Elise; Loum, Mor Absa; Liao, Calwing; Ross, Jay P.; Dionne-Laporte, Alexandre; Spiegelman, Dan; Jean-Louis, Martineau; Saci, Zohra; Hayward, Caroline; Banaschewski, Tobias; Bokde, Arun; Desrivieres, Sylvane; Lemaitre, Her... Journal: Research in autism spectrum disorders Issue: Volume 99(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. CPT1A Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height in Greenlanders. (June 2017) Authors: Skotte, Line; Koch, Anders; Yakimov, Victor; Zhou, Sirui; Søborg, Bolette; Andersson, Mikael; Michelsen, Sascha W.; Navne, Johan E.; Mistry, Jacqueline M.; Dion, Patrick A.; Pedersen, Michael L.; Børresen, Malene L.; Rouleau, Guy A.; Geller, Frank; Melbye, Mads; Feenstra, Bjarke Journal: Circulation Issue: Volume 10:Number 3(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopia. (April 2016) Authors: Leblond, Claire S.; Webber, Alina; Gan-Or, Ziv; Moore, Fraser; Dagher, Alain; Dion, Patrick A.; Rouleau, Guy A. Journal: Neurology Issue: Volume 2:Number 2(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia?. Issue 1 (18th August 2022) Authors: Peretz, Isabelle; Ross, Jay; Bourassa, Cynthia V.; Perreault, Louis‐Philippe Lemieux; Dion, Patrick A.; Weiss, Michael W.; Felezeu, Mihaela; Rouleau, Guy A.; Dubé, Marie‐Pierre Journal: Annals of the New York Academy of Sciences Issue: Volume 1517:Issue 1(2022) Page Start: 279 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7. Issue 7 (17th February 2021) Authors: Estiar, Mehrdad A.; Yu, Eric; Haj Salem, Ikhlass; Ross, Jay P.; Mufti, Kheireddin; Akçimen, Fulya; Leveille, Etienne; Spiegelman, Dan; Ruskey, Jennifer A.; Asayesh, Farnaz; Dagher, Alain; Yoon, Grace; Tarnopolsky, Mark; Boycott, Kym M.; Dupre, Nicolas; Dion, Patrick A.; Suchowersky, Oksana; Tremp... Journal: Movement disorders Issue: Volume 36:Issue 7(2021) Page Start: 1664 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Exome-wide rare variant analysis in familial essential tremor. (January 2021) Authors: Diez-Fairen, Monica; Houle, Gabrielle; Ortega-Cubero, Sara; Bandres-Ciga, Sara; Alvarez, Ignacio; Carcel, Maria; Ibañez, Laura; Fernandez, Maria Victoria; Budde, John P.; Trotta, Jean-Rémi; Tonda, Raúl; Chong, Jessica X.; Bamshad, Michael J.; Nickerson, Deborah A.; Aguilar, Miquel; Tartari, Juan ... Journal: Parkinsonism & related disorders Issue: Volume 82(2021) Page Start: 109 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project. Issue 2 (7th November 2020) Authors: Akçimen, Fulya; Ross, Jay P.; Liao, Calwing; Spiegelman, Dan; Dion, Patrick A.; Rouleau, Guy A. Journal: Movement disorders Issue: Volume 36:Issue 2(2021) Page Start: 514 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder. Issue 6 (14th May 2018) Authors: Li, Jiao; Ruskey, Jennifer A.; Arnulf, Isabelle; Dauvilliers, Yves; Hu, Michele T.M.; Högl, Birgit; Leblond, Claire S.; Zhou, Sirui; Ambalavanan, Amirthagowri; Ross, Jay P.; Bourassa, Cynthia V.; Spiegelman, Dan; Laurent, Sandra B; Stefani, Ambra; Charley Monaca, Christelle; Cochen De Cock, Valér... Journal: Movement disorders Issue: Volume 33:Issue 6(2018) Page Start: 1016 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗