List of works - Jennifer A Ruskey

Age at Onset of Parkinson's Disease Among Ashkenazi Jewish Patients: Contribution of Environmental Factors, LRRK2 p.G2019S and GBA p.N370S Mutations

scientific article published on 09 April 2020

Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease

scientific article published on 13 July 2020

Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson's Disease

scientific article published on 24 September 2020

Analysis of common and rare VPS13C variants in late-onset Parkinson disease

scientific article published on 09 January 2020

Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease

scientific article published on 31 October 2020

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

scientific article published on 17 December 2018

Carriers of both GBA and LRRK2 mutations, compared to carriers of either, in Parkinson's disease: Risk estimates and genotype-phenotype correlations

scientific article published on 13 December 2018

Common and rare GCH1 variants are associated with Parkinson's disease

scientific article published on 15 September 2018

Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder

scientific article published on 01 October 2020

Development and characterization of twenty-five microsatellite markers for the longnose dace (Cyprinidae: Rhinichthys) using paired-end Illumina shotgun sequencing

article

Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies

scientific article published on 12 February 2020

Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder

scholarly article by Jiao Li et al published July 2018 in Movement Disorders

GBA variants in REM sleep behavior disorder: a multicenter study

scientific article published on 26 June 2020

Genetic and epidemiological characterization of restless legs syndrome in Québec

scientific article published on 30 October 2019

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia

scientific article published on 01 January 2020

Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies

scientific article published on 18 November 2019

Glucocerebrosidase mutations and phenoconversion of REM sleep behavior disorder to parkinsonism and dementia

scientific article published on 27 April 2019

Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder

scientific article

Increased yield of full GBA sequencing in Ashkenazi Jews with Parkinson's disease

scientific article published on 26 May 2018

LRRK2 protective haplotype and full sequencing study in REM sleep behavior disorder.

scientific article published on 21 March 2018

Morphological and genetic analysis of sympatric dace within theRhinichthys cataractaespecies complex: a case of isolation lost

scientific article published on 21 September 2015

Novel Associations of <i>BST1</i> and <i>LAMP3</i> with Rapid Eye Movement Sleep Behavior Disorder

scientific article published on 04 January 2021

SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease

scientific article published on 20 February 2019

SMPD1 variants do not have a major role in rapid eye movement sleep behavior disorder

scientific article published on 18 April 2020

Sequencing of the GBA coactivator, Saposin C, in Parkinson disease

scholarly article by Bouchra Ouled Amar Bencheikh et al published 2 July 2018 in Neurobiology of Aging

TOX3 Variants Are Involved in Restless Legs Syndrome and Parkinson's Disease with Opposite Effects

scientific article

Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations

scientific article published on 22 December 2020

The GBA p.Trp378Gly mutation is a probable French-Canadian founder mutation causing Gaucher disease and synucleinopathies

article

Triple A syndrome presenting as complicated hereditary spastic paraplegia

article

Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson's disease

scientific article published on 08 April 2020

List of works by Jennifer A Ruskey

Age at Onset of Parkinson's Disease Among Ashkenazi Jewish Patients: Contribution of Environmental Factors, LRRK2 p.G2019S and GBA p.N370S Mutations

Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease

Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson's Disease

Analysis of common and rare VPS13C variants in late-onset Parkinson disease

Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease

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

Carriers of both GBA and LRRK2 mutations, compared to carriers of either, in Parkinson's disease: Risk estimates and genotype-phenotype correlations

Common and rare GCH1 variants are associated with Parkinson's disease

Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder

Development and characterization of twenty-five microsatellite markers for the longnose dace (Cyprinidae: Rhinichthys) using paired-end Illumina shotgun sequencing

Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies

Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder

GBA variants in REM sleep behavior disorder: a multicenter study

Genetic and epidemiological characterization of restless legs syndrome in Québec

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia

Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies

Glucocerebrosidase mutations and phenoconversion of REM sleep behavior disorder to parkinsonism and dementia

Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder

Increased yield of full GBA sequencing in Ashkenazi Jews with Parkinson's disease

LRRK2 protective haplotype and full sequencing study in REM sleep behavior disorder.

Morphological and genetic analysis of sympatric dace within theRhinichthys cataractaespecies complex: a case of isolation lost

Novel Associations of <i>BST1</i> and <i>LAMP3</i> with Rapid Eye Movement Sleep Behavior Disorder

SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease

SMPD1 variants do not have a major role in rapid eye movement sleep behavior disorder

Sequencing of the GBA coactivator, Saposin C, in Parkinson disease

TOX3 Variants Are Involved in Restless Legs Syndrome and Parkinson's Disease with Opposite Effects

Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations

The GBA p.Trp378Gly mutation is a probable French-Canadian founder mutation causing Gaucher disease and synucleinopathies

Triple A syndrome presenting as complicated hereditary spastic paraplegia

Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson's disease