Found: 18
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Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Genome-wide association study in essential tremor identifies three new loci.
- Published in:
- Brain: A Journal of Neurology, 2016, v. 139, n. 12, p. 3163, doi. 10.1093/brain/aww242
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- Publication type:
- Article
Absence of Mutation Enrichment for Genes Phylogenetically Conserved in the Olivocerebellar Motor Circuitry in a Cohort of Canadian Essential Tremor Cases.
- Published in:
- Molecular Neurobiology, 2019, v. 56, n. 6, p. 4317, doi. 10.1007/s12035-018-1369-1
- By:
- Publication type:
- Article
A New ELOVL4 Mutation in a Case of Spinocerebellar Ataxia With Erythrokeratodermia.
- Published in:
- JAMA Dermatology, 2015, v. 151, n. 8, p. 942
- By:
- Publication type:
- Article
Exome sequencing of sporadic childhood‐onset schizophrenia suggests the contribution of X‐linked genes in males.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 6, p. 335, doi. 10.1002/ajmg.b.32683
- By:
- Publication type:
- Article
Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophrenia.
- Published in:
- Frontiers in Cellular Neuroscience, 2015, v. 9, p. 1, doi. 10.3389/fncel.2015.00386
- By:
- Publication type:
- Article
FAMILIAL AGGREGATION OF ATYPICAL DEMENTIA IN A LARGE CANADIAN FAMILY: THE MISSING GENE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P302, doi. 10.1016/j.jalz.2017.06.223
- By:
- Publication type:
- Article
Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia?
- Published in:
- Annals of the New York Academy of Sciences, 2022, v. 1517, n. 1, p. 279, doi. 10.1111/nyas.14883
- By:
- Publication type:
- Article
LINGO1 Variants in the French-Canadian Population.
- Published in:
- PLoS ONE, 2011, v. 6, n. 1, p. 1, doi. 10.1371/journal.pone.0016254
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- Publication type:
- Article
Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy.
- Published in:
- EMBO Reports, 2014, v. 15, n. 7, p. 766, doi. 10.15252/embr.201438840
- By:
- Publication type:
- Article
Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome.
- Published in:
- Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03231-0
- By:
- Publication type:
- Article
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals.
- Published in:
- PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0164212
- By:
- Publication type:
- Article
Investigation of the RFC1 Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations.
- Published in:
- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01219
- By:
- Publication type:
- Article
A New ELOVL4 Mutation in a Case of Spinocerebellar Ataxia With Erythrokeratodermia.
- Published in:
- JAMA Neurology, 2015, v. 72, n. 8, p. 942, doi. 10.1001/jamaneurol.2015.0888
- By:
- Publication type:
- Article
SYNE1 Mutations in Autosomal Recessive Cerebellar Ataxia.
- Published in:
- JAMA Neurology, 2013, v. 70, n. 10, p. 1296, doi. 10.1001/jamaneurol.2013.3268
- By:
- Publication type:
- Article
Mutation Burden of Rare Variants in Schizophrenia Candidate Genes.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0128988
- By:
- Publication type:
- Article
Increased Missense Mutation Burden of Fatty Acid Metabolism Related Genes in Nunavik Inuit Population.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0128255
- By:
- Publication type:
- Article