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Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach – CORRIGENDUM
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- The British Journal of Psychiatry / Volume 221 / Issue 2 / August 2022
- Published online by Cambridge University Press:
- 04 May 2022, p. 494
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- August 2022
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Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach
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- The British Journal of Psychiatry / Volume 220 / Issue 4 / April 2022
- Published online by Cambridge University Press:
- 28 February 2022, pp. 219-228
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- April 2022
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Characterisation of age and polarity at onset in bipolar disorder
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- The British Journal of Psychiatry / Volume 219 / Issue 6 / December 2021
- Published online by Cambridge University Press:
- 25 August 2021, pp. 659-669
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- December 2021
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Genetic and Epidemiological Study of Adult Ataxia and Spastic Paraplegia in Eastern Quebec
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- Canadian Journal of Neurological Sciences / Volume 48 / Issue 5 / September 2021
- Published online by Cambridge University Press:
- 05 January 2021, pp. 655-665
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A Founder Mutation in French-Canadian Families with X-linked Hereditary Neuropathy
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- Canadian Journal of Neurological Sciences / Volume 28 / Issue 1 / February 2001
- Published online by Cambridge University Press:
- 02 March 2017, pp. 51-55
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Linkage to the CCM2 Locus and Genetic Heterogeneity in Familial Cerebral Cavernous Malformation
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- Canadian Journal of Neurological Sciences / Volume 30 / Issue 2 / May 2003
- Published online by Cambridge University Press:
- 16 December 2016, pp. 122-128
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Relative Localizing Value of Common Tests used in the Preoperative Investigation of Epileptic Patients
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- Canadian Journal of Neurological Sciences / Volume 18 / Issue S4 / November 1991
- Published online by Cambridge University Press:
- 18 September 2015, pp. 598-600
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Newborn Apnea Caused by a Neurofibroma at the Craniocervical Junction
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- Canadian Journal of Neurological Sciences / Volume 21 / Issue 1 / February 1994
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- 18 September 2015, pp. 64-66
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Glucocerebrosidase Mutations in a French-Canadian Parkinson's Disease Cohort
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- Canadian Journal of Neurological Sciences / Volume 38 / Issue 5 / September 2011
- Published online by Cambridge University Press:
- 02 December 2014, pp. 772-773
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Hereditary Ataxia, Spastic Paraparesis and Neuropathy in the French-Canadian Population
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- Canadian Journal of Neurological Sciences / Volume 33 / Issue 2 / May 2006
- Published online by Cambridge University Press:
- 02 December 2014, pp. 149-157
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CYP7B1 Mutations in French-Canadian Hereditary Spastic Paraplegia Subjects
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- Canadian Journal of Neurological Sciences / Volume 39 / Issue 1 / January 2012
- Published online by Cambridge University Press:
- 02 December 2014, pp. 91-94
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ADVANCES IN RESEARCH ON NEURODEGENERATION. VOLUME 7. 2000. Edited by Y. Mizuno, D.B. Calne, R. Horowski, W. Poewe, P. Riederer and M.B.H. Youdim Published by Springer-Verlag/Wien. 214 pages. C$139.65 approx.
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- Canadian Journal of Neurological Sciences / Volume 29 / Issue 4 / November 2002
- Published online by Cambridge University Press:
- 02 December 2014, p. 408
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Purification of the NF2 Tumor Suppressor Protein from Human Erythrocytes
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- Canadian Journal of Neurological Sciences / Volume 33 / Issue 4 / November 2006
- Published online by Cambridge University Press:
- 02 December 2014, pp. 394-402
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Genome-Wide TDT Analysis in French-Canadian Families with Tourette Syndrome
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- Canadian Journal of Neurological Sciences / Volume 37 / Issue 1 / January 2010
- Published online by Cambridge University Press:
- 02 December 2014, pp. 110-112
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A Novel PLP1 Mutation Further Expands the Clinical Heterogeneity at the Locus
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- Canadian Journal of Neurological Sciences / Volume 39 / Issue 2 / March 2012
- Published online by Cambridge University Press:
- 02 December 2014, pp. 220-224
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SOD1 Mutations: More to Learn
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- Canadian Journal of Neurological Sciences / Volume 39 / Issue 2 / March 2012
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- 02 December 2014, pp. 132-133
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A Novel Mutation in a Large French-Canadian Family with LGMD1B
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- Canadian Journal of Neurological Sciences / Volume 35 / Issue 3 / July 2008
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- 02 December 2014, pp. 331-334
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SPG4 Founder Effect in French Canadians with Hereditary Spastic Paraplegia
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- Canadian Journal of Neurological Sciences / Volume 34 / Issue 2 / May 2007
- Published online by Cambridge University Press:
- 02 December 2014, pp. 211-214
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Progress in Understanding the Pathogenesis of Oculopharyngeal Muscular Dystrophy
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- Canadian Journal of Neurological Sciences / Volume 30 / Issue 1 / February 2003
- Published online by Cambridge University Press:
- 02 December 2014, pp. 8-14
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hnRNP A1 and A/B Interaction with PABPN1 in Oculopharyngeal Muscular Dystrophy
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- Canadian Journal of Neurological Sciences / Volume 30 / Issue 3 / August 2003
- Published online by Cambridge University Press:
- 02 December 2014, pp. 244-251
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