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CYRUS ZABETIAN, MD

MD

Neurology Physician

NPI: 1538267190Individual

Specialties, Licenses & Credentials

Neurology PhysicianPrimary

Psychiatry & Neurology — Neurology

Code: 2084N0400X

MD00035514(WA)

Research & Publications (20)

LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.
PMID 19343804·Mov Disord·2009
8-other
Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.
PMID 17514749·Ann Neurol·2007
8-other
Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease.
PMID 16728648·Neurology·2006
2-rct
LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.
PMID 16960813·Am J Hum Genet·2006
8-other
A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations.
PMID 16157909·Neurology·2005
8-other
Visualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's disease.
PMID 19582778·Genet Epidemiol·2010
8-other
Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain.
PMID 19308469·Neurogenetics·2009
8-other
LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay.
PMID 18980856·Parkinsonism Relat Disord·2009
8-other
Genetic polymorphism at codon 129 of the prion protein gene is not associated with multiple sclerosis.
PMID 19204171·Arch Neurol·2009
8-other
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
PMID 18952485·Parkinsonism Relat Disord·2009
8-other
Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries.
PMID 19283415·Neurogenetics·2009
8-other
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.
PMID 18337586·Neurology·2008
4-observational
Genetic association between alpha-synuclein and idiopathic Parkinson's disease.
PMID 18404644·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders.
PMID 18332251·Arch Neurol·2008
4-observational
Exploring gene-environment interactions in Parkinson's disease.
PMID 18210157·Hum Genet·2008
4-observational
Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk.
PMID 17987647·Mov Disord·2008
8-other
Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease.
PMID 18093156·Eur J Neurol·2008
8-other
Application of targeted quantitative proteomics analysis in human cerebrospinal fluid using a liquid chromatography matrix-assisted laser desorption/ionization time-of-flight tandem mass spectrometer (LC MALDI TOF/TOF) platform.
PMID 18186601·J Proteome Res·2008
8-other
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.
PMID 18539534·Lancet Neurol·2008
4-observational
DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease.
PMID 17503507·Ann Neurol·2007
8-other

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
1660 S COLUMBIAN WAY, GRECC (S-182), VA PUGET SOUND HEALTH CARE SYSTEM
SEATTLE, WA 98108

Location

Practice Location

1660 S COLUMBIAN WAY, SEATTLE, WA
(206) 277-6167

Quick Facts

NPI
1538267190
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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