Alexandre D. Laporte
Montreal, QC, Canada
Last Updated: 09/26/2026
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Found 8 publications
Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: November 25, 2019
Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infantile-Onset Cerebellar Ataxia.
Journal: Journal of child neurology
Published: October 17, 2019
Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes.
Journal: Nature communications
Published: May 29, 2019
Pathogenic variants in AIMP1 cause pontocerebellar hypoplasia.
Journal: Neurogenetics
Published: December 23, 2018
Prospective head-to-head comparison of accuracy of two sequencing platforms for screening for fetal aneuploidy by cell-free DNA: the PEGASUS study.
Journal: European journal of human genetics : EJHG
Published: December 20, 2018
Investigating the association and causal relationship between restless legs syndrome and essential tremor.
Journal: Parkinsonism & related disorders
Published: June 28, 2018
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.
Journal: American journal of human genetics
Published: June 27, 2017
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Last Updated: 09/26/2026