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

Neurology, 2015-07, Vol.85 (1), p.89

2015

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

Movement disorders, 2013-12, Vol.28 (14), p.1966-1971

2013

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Familial aggregation of early‐ and late‐onset Parkinson's disease

Annals of neurology, 2003-10, Vol.54 (4), p.507-513

2003

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

Annals of clinical and translational neurology, 2014-09, Vol.1 (9), p.670-678

2014

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Pilot association study of the β-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity

Movement disorders, 2005-01, Vol.20 (1), p.100-103

2005

Volltextzugriff (PDF)

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

Human molecular genetics, 2014-09, Vol.23 (17), p.4693-4702

2014

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Progression in the LRRK2-Asssociated Parkinson Disease Population

JAMA neurology, 2018-03, Vol.75 (3), p.312

2018

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Estimation of genetic risk function with covariates in the presence of missing genotypes: A. J. LEE et al

Statistics in medicine, 2017-09, Vol.36 (22), p.3533-3546

2017

Volltextzugriff (PDF)

Non-motor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene

Movement disorders, 2015-03, Vol.30 (7), p.981-986

2015

Volltextzugriff (PDF)

REM Sleep Behavior Disorder, as assessed by the RBDSQ, in G2019S LRRK2 mutation PD and unaffected carriers

Movement disorders, 2015-09, Vol.30 (13), p.1834-1839

2015

Volltextzugriff (PDF)

Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease

Journal of clinical and experimental neuropsychology, 2010-08, Vol.32 (7), p.775-779

2010

Volltextzugriff (PDF)

Association of glucocerebrosidase mutations with dementia with lewy bodies

Archives of neurology (Chicago), 2009-05, Vol.66 (5), p.578

2009

Volltextzugriff (PDF)

Self-report of cognitive impairment and Mini-Mental State Exam performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson’s disease

Journal of clinical and experimental neuropsychology, 2010-02, Vol.32 (7), p.775-779

2010

Volltextzugriff (PDF)

Lack of familial aggregation of Parkinson disease and Alzheimer disease

Archives of neurology (Chicago), 2004-07, Vol.61 (7), p.1033

2004

Volltextzugriff (PDF)

Pilot association study of the b-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity

Movement disorders, 2005-01, Vol.20 (1), p.100-103

2005

Volltextzugriff (PDF)

Body mass index in essential tremor

Archives of neurology (Chicago), 2002-08, Vol.59 (8), p.1273

2002

Volltextzugriff (PDF)

Interval timing in GBA and parkin mutation-carrying, and idiopathic parkinson's disease patients

Journal of Cognitive Neuroscience. Supplement, 2013-01, p.116e-116e

2013

Volltextzugriff (PDF)

Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method

Archives of neurology (Chicago), 2008-04, Vol.65 (4), p.467

2008

Volltextzugriff (PDF)

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The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study

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

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

Familial aggregation of early‐ and late‐onset Parkinson's disease

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

Pilot association study of the β-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity

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

Progression in the LRRK2-Asssociated Parkinson Disease Population

Association of Olfactory Performance With Motor Decline and Age at Onset in People With Parkinson Disease and the LRRK2 G2019S Variant

Estimation of genetic risk function with covariates in the presence of missing genotypes: A. J. LEE et al

Cognitive and motor function in long-duration PARKIN-associated Parkinson disease

Non-motor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene

REM Sleep Behavior Disorder, as assessed by the RBDSQ, in G2019S LRRK2 mutation PD and unaffected carriers

Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease

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

Michael J. Fox Foundation Consortium: Geographical Differences in Returning Genetic Research Data to Study Participants

Association of glucocerebrosidase mutations with dementia with lewy bodies

Self-report of cognitive impairment and Mini-Mental State Exam performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson’s disease

Lack of familial aggregation of Parkinson disease and Alzheimer disease

Pilot association study of the b-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity

Body mass index in essential tremor

Interval timing in GBA and parkin mutation-carrying, and idiopathic parkinson's disease patients

Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method

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