Publications by authors named "Alexandre D Laporte"

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Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor.
Calwing Liao, Faezeh Sarayloo, Daniel Rochefort, Gabrielle Houle, Fulya Akçimen, Alexandre D Laporte

Mov Disord· July 2020

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Transcriptomic Changes Resulting From Overexpression Identify Pathways Potentially Relevant to Essential Tremor.
Calwing Liao, Faezeh Sarayloo, Veikko Vuokila, Daniel Rochefort, Fulya Akçimen, Alexandre D Laporte

Front Genet· July 2020

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Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infantile-Onset Cerebellar Ataxia.
Andrea Accogli, Judith St-Onge, Nassima Addour-Boudrahem, Joël Lafond-Lapalme, Alexandre Dionne Laporte

J Child Neurol· February 2020

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Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes.
Calwing Liao, Alexandre D Laporte, Dan Spiegelman, Fulya Akçimen, Ridha Joober

Nat Commun· October 2019

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Pathogenic variants in AIMP1 cause pontocerebellar hypoplasia.
Andrea Accogli, Laura Russell, Guillaume Sébire, Jean-Baptiste Rivière, Judith St-Onge, Alexandre Dionne Laporte

Neurogenetics· May 2019

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Investigating the association and causal relationship between restless legs syndrome and essential tremor.
Calwing Liao, Gabrielle Houle, Qin He, Alexandre D Laporte, Simon L Girard

Parkinsonism Relat Disord· April 2019

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High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.
Fadi F Hamdan, Candace T Myers, Patrick Cossette, Philippe Lemay, Dan Spiegelman, Alexandre Dionne Laporte

Am J Hum Genet· November 2017

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