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2023Phenotypic effects of genetic variants associated with autism., Nat Med 2023 Jun; (): .
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2021Operative list of genes associated with autism and neurodevelopmental disorders based on database review., Mol Cell Neurosci 2021 Jun; 113(): 103623.
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2019Both rare and common genetic variants contribute to autism in the Faroe Islands., NPJ Genom Med 2019 ; 4(): 1.
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2018Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology, J. Appl. Genet. 2019 Feb;60(1):49-56.
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2017Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population, Mov. Disord. 2017 Feb;32(2):292-295.
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2017A framework to identify contributing genes in patients with Phelan-McDermid syndrome., NPJ Genom Med 2017 ; 2(): 32.
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2016The dementia-associated APOE ε4 allele is not associated with rapid eye movement sleep behavior disorder, Neurobiol. Aging 2017 Jan;49:218.e13-218.e15.
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2016NEK1 variants confer susceptibility to amyotrophic lateral sclerosis, Nat. Genet. 2016 09;48(9):1037-42.
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2016Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson’s disease, Neurobiol. Aging 2016 09;45:212.e13-212.e17.
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2016CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia, Nat Commun 2016 Apr;7:11253.
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