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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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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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2016De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopia, Neurol Genet 2016 Apr;2(2):e63.
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2016Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD, Acta Neuropathol Commun 2016 Feb;4:18.
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201511q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures., Am J Med Genet A 2015 Dec; 167A(12): 3019-30.
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