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List of works by Ronald G. Lafrenière

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura

scientific article

A population genetic approach to mapping neurological disorder genes using deep resequencing

scientific article

De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy

scientific article published in June 2009

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment

scientific article

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

scientific article

De novo truncating mutation in Kinesin 17 associated with schizophrenia

scientific article published on 19 June 2010

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

scientific article

Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability

scientific journal article

Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder

scientific article published on 17 September 2013

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation

scientific article

Mutations in the calcium-related gene IL1RAPL1 are associated with autism

scientific article published on 18 September 2008

No association between SRGAP3/MEGAP haploinsufficiency and mental retardation.

scientific article published in May 2009

Novel de novo SHANK3 mutation in autistic patients

scientific article

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

scientific article

WNK1/HSN2 mutation in human peripheral neuropathy deregulates KCC2 expression and posterior lateral line development in zebrafish (Danio rerio)

scientific article

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