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List of works by Oksana Suchowersky

A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study.

scientific article

Assessing non-Mendelian inheritance in inherited axonopathies

scientific article published on 03 August 2020

Bilateral impairments of skilled reach-to-eat in early Parkinson's disease patients presenting with unilateral or asymmetrical symptoms

scientific article published on 22 July 2008

CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia

scientific article published on 17 December 2018

Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset

scientific article

Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy

scientific article published on 29 September 2020

Clinical and genetic study of hereditary spastic paraplegia in Canada

scientific article published on 5 December 2016

Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials

scientific article

Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region

scientific article

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

scientific article

Exome sequencing as a diagnostic tool for pediatric-onset ataxia

scientific article published in January 2014

Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study

scientific article

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study

scientific article

Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study

scientific article

Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study

scientific article published on June 2006

Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease

scientific article published on 01 June 2003

KCNA2 mutations are rare in hereditary spastic paraplegia

scientific article published on 26 December 2016

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

scientific article published on May 2016

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

scientific article published on June 2016

PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study

scientific article published on 27 March 2002

POLR3A variants in hereditary spastic paraplegia and ataxia

scientific article published on 8 December 2017

Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset

scientific article

Replication of association between ELAVL4 and Parkinson disease: the GenePD study

scientific article

Serotonin syndrome and the combined use of deprenyl and an antidepressant in Parkinson's disease. Parkinson Study Group

scientific article published in April 1997

TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease

scientific article

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