1. A multi‐informant and multi‐polygenic approach to understanding predictors of peer victimisation in childhood and adolescence. Issue 1 (23rd February 2022) Authors: Armitage, Jessica M.; Morneau‐Vaillancourt, Geneviève; Pingault, Jean‐Baptiste; Andlauer, Till F. M.; Paquin, Stéphane; Langevin, Stéphanie; Brendgen, Mara; Dionne, Ginette; Séguin, Jean; Rouleau, Guy; Vitaro, Frank; Ouellet‐Morin, Isabelle; Boivin, Michel Journal: JCPP advances Issue: Volume 2:Issue 1(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of LMNB1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele‐Specific Expression. Issue 1 (28th October 2013) Authors: Giorgio, Elisa; Rolyan, Harshvardhan; Kropp, Laura; Chakka, Anish Baswanth; Yatsenko, Svetlana; Gregorio, Eleonora Di; Lacerenza, Daniela; Vaula, Giovanna; Talarico, Flavia; Mandich, Paola; Toro, Camilo; Pierre, Eleonore Eymard; Labauge, Pierre; Capellari, Sabina; Cortelli, Pietro; Vairo, Filippo... Journal: Human mutation Issue: Volume 35:Issue 1(2014:Jan.) Page Start: 149 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Analysis of LMNB1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele‐Specific Expression. Issue 8 (28th May 2013) Authors: Giorgio, Elisa; Rolyan, Harshvardhan; Kropp, Laura; Chakka, Anish Baswanth; Yatsenko, Svetlana; Gregorio, Eleonora Di; Lacerenza, Daniela; Vaula, Giovanna; Talarico, Flavia; Mandich, Paola; Toro, Camilo; Pierre, Eleonore Eymard; Labauge, Pierre; Capellari, Sabina; Cortelli, Pietro; Vairo, Filippo... Journal: Human mutation Issue: Volume 34:Issue 8(2013:Aug.) Page Start: 1160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Brain health for all on World Brain Day 2022. Issue 9 (September 2022) Authors: Wijeratne, Tissa; Bassetti, Claudio L A; Grisold, Wolfgang; Dodick, David; Rouleau, Guy; Lewis, Steven L; Stark, Richard; Freedman, Morris; Guekht, Alla; Gouider, Riadh; Medina, Marco T; Meshram, Chandrashekhar; Basri, Hamidon; Charway-Felli, Augustina; Abdel Naseer, Maged Journal: Lancet neurology Issue: Volume 21:Issue 9(2022) Page Start: 772 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy. Issue 8 (29th September 2020) Authors: Gauquelin, Laurence; Hartley, Taila; Tarnopolsky, Mark; Dyment, David A.; Brais, Bernard; Geraghty, Michael T.; Tétreault, Martine; Ahmed, Sohnee; Rojas, Samantha; Choquet, Karine; Majewski, Jacek; Bernier, François; Innes, Allan Micheil; Rouleau, Guy; Suchowersky, Oksana; Boycott, Kym M.; Yoon, ... Journal: Movement disorders clinical practice Issue: Volume 7:Issue 8(2020) Page Start: 940 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Characterisation of age and polarity at onset in bipolar disorder. (December 2021) Authors: Kalman, Janos L.; Olde Loohuis, Loes M.; Vreeker, Annabel; McQuillin, Andrew; Stahl, Eli A.; Ruderfer, Douglas; Grigoroiu-Serbanescu, Maria; Panagiotaropoulou, Georgia; Ripke, Stephan; Bigdeli, Tim B.; Stein, Frederike; Meller, Tina; Meinert, Susanne; Pelin, Helena; Streit, Fabian; Papiol, Sergi;... Other Names: collab.; collab.; collab. Journal: British journal of psychiatry Issue: Volume 219:Number 6(2021) Page Start: 659 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Characterization of human iPSC-derived astrocytes with potential for disease modeling and drug discovery. (13th July 2020) Authors: Soubannier, Vincent; Maussion, Gilles; Chaineau, Mathilde; Sigutova, Veronika; Rouleau, Guy; Durcan, Thomas M.; Stifani, Stefano Journal: Neuroscience letters Issue: Volume 731(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Cover Image, Volume 39, Issue 1. Issue 1 (7th December 2017) Authors: Marsh, Ashley P. L.; Edwards, Timothy J.; Galea, Charles; Cooper, Helen M.; Engle, Elizabeth C.; Jamuar, Saumya S.; Méneret, Aurélie; Moutard, Marie‐Laure; Nava, Caroline; Rastetter, Agnès; Robinson, Gail; Rouleau, Guy; Roze, Emmanuel; Spencer‐Smith, Megan; Trouillard, Oriane; Billette de Villeme... Journal: Human mutation Issue: Volume 39:Issue 1(2018) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome. Issue 1 (11th November 2017) Authors: Marsh, Ashley P. L.; Edwards, Timothy J.; Galea, Charles; Cooper, Helen M.; Engle, Elizabeth C.; Jamuar, Saumya S.; Méneret, Aurélie; Moutard, Marie‐Laure; Nava, Caroline; Rastetter, Agnès; Robinson, Gail; Rouleau, Guy; Roze, Emmanuel; Spencer‐Smith, Megan; Trouillard, Oriane; Billette de Villeme... Journal: Human mutation Issue: Volume 39:Issue 1(2018) Page Start: 23 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. DNA hypomethylation of Synapsin II CpG islands associates with increased gene expression in bipolar disorder and major depression. Issue 1 (December 2016) Authors: Cruceanu, Cristiana; Kutsarova, Elena; Chen, Elizabeth; Checknita, David; Nagy, Corina; Lopez, Juan; Alda, Martin; Rouleau, Guy; Turecki, Gustavo Journal: BMC psychiatry Issue: Volume 16:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗