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List of works by Deborah Raymond

A Case of Myoclonus-Dystonia Responding to Low-frequency Pallidal Stimulation

scientific article

Age-specific penetrance of LRRK2 G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium

scientific article published on 10 June 2015

Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers

scientific article published on 30 March 2018

Arm swing as a potential new prodromal marker of Parkinson's disease

scientific article published on 19 July 2016

Benign SLC39A14 Course of Dystonia-Parkinsonism Secondary to Inherited Manganese Accumulation

scientific article published on 07 May 2020

Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controls

scientific article published on 26 July 2019

Clinical and neurophysiological improvement of SGCE myoclonus-dystonia with GPi deep brain stimulation

scientific article

Complex and Dynamic Chromosomal Rearrangements in a Family With Seemingly Non-Mendelian Inheritance of Dopa-Responsive Dystonia

scientific article published in July 2017

DYT1 dystonia increases risk taking in humans

scientific article published on June 2016

Deep Brain Stimulation in Isolated Dystonia With a GNAL Mutation

scientific article published on 10 December 2018

Digitized spiral analysis may be a potential biomarker for brachial dystonia

scientific article published on 20 July 2018

Disclosure of research results in genetic studies of Parkinson's disease caused by LRRK2 mutations

scientific article published on 7 May 2015

Dysregulation of mitochondrial and proteolysosomal genes in Parkinson's disease myeloid cells

scientific article published on 14 September 2021

Evidence for increased completed suicide in first-degree relatives of G2019S mutation Parkinson's disease

scientific article published on 08 November 2018

Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia ⬇️

scientific article published on October 15, 2010

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes

scientific article

Glucocerebrosidase enzyme activity in GBA mutation Parkinson's disease

scientific article published on 5 February 2016

Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites

scientific article

Increased substantia nigra echogenicity in LRRK2 family members without mutations

scientific article published on 25 August 2018

Interest in genetic testing in Ashkenazi Jewish Parkinson's disease patients and their unaffected relatives

scientific article

LRRK2 G2019S mutations are associated with an increased cancer risk in Parkinson disease

scientific article

LRRK2 G2019S mutations may be increased in Puerto Ricans ⬇️

scientific article published on March 29, 2011

Low-variance RNAs identify Parkinson's disease molecular signature in blood

scientific article published on 18 March 2015

Metabolic changes in DYT11 myoclonus-dystonia

scientific article published on 2 January 2013

Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants

scientific article

Mood and cognition in leucine‐rich repeat kinase 2 G2019S Parkinson's disease ⬇️

scientific article published on May 24, 2011

Mutations in GNAL cause primary torsion dystonia

scientific article

Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study

scientific article published on April 2009

Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia

scientific article

Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish-Mennonites

scientific article published in September 2007

Neuropsychiatric characteristics of GBA-associated Parkinson disease

scientific article

Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's disease

scientific article

Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene

scientific article published on 21 March 2015

Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?

scientific article

Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations

scientific article published on 15 October 2013

Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with ɛ-sarcoglycan mutations

scientific article published on 01 March 2008

Primary dystonia: is abnormal functional brain architecture linked to genotype?

scientific article published in December 2002

Progression in the LRRK2-Asssociated Parkinson Disease Population

scientific article published on 8 January 2018

REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers

scientific article

Responsiveness to levodopa in epsilon-sarcoglycan deletions

scientific article published in February 2009

SGCE Myoclonus-Dystonia

scientific article published on 8 August 2019

Spatial Discrimination Threshold Abnormalities are not Detected in a Pilot Study of DYT6 Dystonia Mutation Carriers ⬇️

scientific article published on September 17, 2012

Substantia nigra hyperechogenicity in DYT6 dystonia: a pilot study

scientific article

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations

scientific article

The metabolic pathology of dopa-responsive dystonia

scientific article published in April 2005

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

scientific article

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene

scientific article

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