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De novo variants in sporadic cases of childhood onset schizophrenia.. Eur J Hum Genet. 24(6):944-8.. 2016.
The dementia-associated APOE ε4 allele is not associated with rapid eye movement sleep behavior disorder.. Neurobiol Aging. 49:218.e13-218.e15.. 2017.
Exome sequencing of sporadic childhood-onset schizophrenia suggests the contribution of X-linked genes in males.. Am J Med Genet B Neuropsychiatr Genet.. 2018.
Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression.. PLoS One. 14(11):e0225186.. 2019.
Mutation burden of rare variants in schizophrenia candidate genes.. PLoS One. 10(6):e0128988.. 2015.
No evidence for GADL1 variation as a bipolar disorder susceptibility factor in a Caucasian lithium-responsive cohort.. Am J Psychiatry. 172(1):94-5.. 2015.