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Alexandre Dionne-Laporte

Montreal Neurological Institute and Hospital
McGill University

62

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1709

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Machine learning analysis of exome trios to contrast the genomic architecture of autism and schizophrenia.

2020 BMC Psychiatry
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DOORS syndrome and a recurrent truncating ATP6V1B2 variant

2020 Genetics in Medicine
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Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant (Genetics in Medicine, (2020), 10.1038/s41436-020-00950-9)

2020 Genetics in Medicine
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Oligogenicity, C9orf72 expansion, and variant severity in ALS.

2020 Neurogenetics
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Multi-omics integration of the phenome, transcriptome and genome highlights genes and pathways relevant to essential tremor

2019 bioRxiv
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SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegia

2019 Journal of Human Genetics
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SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease: SMPD1 MUTATIONS, α-SYNUCLEIN, AND PD

2019 Movement Disorders
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Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression

2019 PLOS ONE
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Whole exome sequencing identifies novel predisposing genes in neural tube defects

2019 Molecular Genetics & Genomic Medicine
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51IDENTIFICATION OF NEW GENES ASSOCIATED WITH CHILDHOOD-ONSET SCHIZOPHRENIA: ATP1A3 AND THE FXYD GENE FAMILY

2019 European Neuropsychopharmacology
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