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Lista de obras de Cyrus P Zabetian

A Peruvian family with a novel PARK2 mutation: Clinical and pathological characteristics

artículo científico publicado en 2015

A Single Nucleotide Polymorphism at DBH, Possibly Associated with Attention-Deficit/Hyperactivity Disorder, Associates with Lower Plasma Dopamine β-Hydroxylase Activity and is in Linkage Disequilibrium with Two Putative Functional Single Nucleotide

artículo científico publicado en 2006

A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations

article

A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2

artículo científico publicado en 2010

A genetic basis for the variable effect of smoking/nicotine on Parkinson's disease.

artículo científico publicado en 2012

A genotype-controlled analysis of plasma dopamine beta-hydroxylase in healthy and alcoholic subjects: evidence for alcohol-related differences in noradrenergic function

artículo científico publicado en 2002

A novel X-linked four-repeat tauopathy with Parkinsonism and spasticity

artículo científico publicado en 2010

A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology

artículo científico publicado en 2007

A quantitative-trait analysis of human plasma-dopamine beta-hydroxylase activity: evidence for a major functional polymorphism at the DBH locus

artículo científico publicado en 2001

A revised allele frequency estimate and haplotype analysis of the DBH deficiency mutation IVS1+2T → C in African- and European-Americans

article

APOE ε4 increases risk for dementia in pure synucleinopathies

artículo científico publicado en 2013

APOE, MAPT, and SNCA genes and cognitive performance in Parkinson disease

artículo científico publicado en 2014

Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS).

artículo científico publicado en 2013

An alpha-synuclein MRM assay with diagnostic potential for Parkinson's disease and monitoring disease progression

artículo científico publicado en 2017

An attempt to replicate interaction between coffee and CYP1A2 gene in connection to Parkinson's disease

artículo científico publicado en 2011

Analysis of the LRRK2 G2019S mutation in Alzheimer Disease

artículo científico publicado en 2006

Apolipoprotein E-ε4 increases the risk for dementia in the ‘pure’ synucleopathies

scholarly article by Debby Tsuang et al published July 2012 in Alzheimer's and Dementia

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

artículo científico publicado en 2008

Arguing against the proposed definition changes of PD

artículo científico publicado en 2016

Arterial spin labeling detects perfusion patterns related to motor symptoms in Parkinson's disease

scientific article published on 11 May 2020

Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries

artículo científico publicado en 2009

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease

artículo científico publicado en 2007

Association between the ubiquitin carboxyl-terminal esterase L1 gene (UCHL1) S18Y variant and Parkinson's Disease: a HuGE review and meta-analysis

scientific article published on 28 October 2009

Association mapping of the PARK10 region for Parkinson's disease susceptibility genes

artículo científico publicado en 2013

Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease

artículo científico publicado en 2016

Association of Parkinson disease with structural and regulatory variants in the HLA region

artículo científico publicado en 2013

Association of a neuronal nitric oxide synthase gene polymorphism with levodopa-induced dyskinesia in Parkinson's disease.

artículo científico publicado en 2017

Association of cognitive domains with postural instability/gait disturbance in Parkinson's disease.

artículo científico publicado en 2015

C9orf72 hexanucleotide repeat expansion and Guam amyotrophic lateral sclerosis-Parkinsonism-dementia complex

artículo científico publicado en 2013

CNS tau efflux via exosomes is likely increased in Parkinson's disease but not in Alzheimer's disease

artículo científico publicado en 2016

CSF Aβ(42) and tau in Parkinson's disease with cognitive impairment.

artículo científico publicado en 2010

Cerebrospinal fluid Aβ42 levels and APP processing pathway genes in Parkinson's disease

artículo científico publicado en 2015

Cerebrospinal fluid amyloid β and tau in LRRK2 mutation carriers

artículo científico publicado en 2011

Cerebrospinal fluid biomarkers and cognitive performance in non-demented patients with Parkinson's disease.

artículo científico publicado en 2010

Cerebrospinal fluid peptides as potential Parkinson disease biomarkers: a staged pipeline for discovery and validation.

artículo científico publicado en 2015

Characterizing dysbiosis of gut microbiome in PD: evidence for overabundance of opportunistic pathogens

scientific article published on 12 June 2020

Cheek cell-derived α-synuclein and DJ-1 do not differentiate Parkinson's disease from control

artículo científico publicado en 2013

Clinical and biochemical differences in patients having Parkinson disease with vs without GBA mutations.

artículo científico publicado en 2013

Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations

artículo científico publicado en 2006

Cognitive associations with comprehensive gait and static balance measures in Parkinson's disease

artículo científico publicado en 2019

Cognitive impairment and dementia in patients with Parkinson disease.

artículo científico publicado en 2009

Cognitive profile of LRRK2-related Parkinson's disease

artículo científico publicado en 2015

Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk

artículo científico publicado en 2008

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease

artículo científico publicado en 2010

Common variant rs356182 near SNCA defines a Parkinson's disease endophenotype

artículo científico publicado en 2016

Common variation in the LRRK2 gene is a risk factor for Parkinson's disease

artículo científico publicado en 2012

Comparative sensitivity of the MoCA and Mattis Dementia Rating Scale-2 in Parkinson's disease

artículo científico publicado en 2018

Complement 3 and factor h in human cerebrospinal fluid in Parkinson's disease, Alzheimer's disease, and multiple-system atrophy

artículo científico publicado en 2011

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

artículo científico publicado en 2012

DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease.

artículo científico publicado en 2007

DJ-1 and alpha-synuclein in human cerebrospinal fluid as biomarkers of Parkinson's disease

artículo científico publicado en 2010

DJ-1 and αSYN in LRRK2 CSF do not correlate with striatal dopaminergic function

artículo científico publicado en 2011

DJ-1 isoforms in whole blood as potential biomarkers of Parkinson disease

artículo científico publicado en 2012

DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient

artículo científico publicado en 2016

Detecting Mild Cognitive Deficits in Parkinson's Disease: Comparison of Neuropsychological Tests

scientific article published on 14 September 2018

Detection of biomarkers with a multiplex quantitative proteomic platform in cerebrospinal fluid of patients with neurodegenerative disorders.

artículo científico publicado en 2006

Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study

artículo científico publicado en 2015

Diagnostic Validation for Participants in the Washington State Parkinson Disease Registry

scholarly article by Hojoong M Kim et al published 2018 in Parkinson's disease

Diagnostic prediction model for levodopa-induced dyskinesia in Parkinson's disease

scientific article published on 09 April 2020

Disease-related and genetic correlates of psychotic symptoms in Parkinson's disease

artículo científico publicado en 2011

Effect of Dopaminergic Medications on Blood Oxygen Level-Dependent Variability and Functional Connectivity in Parkinson's Disease and Healthy Aging

artículo científico publicado en 2019

Effects of Environmental Salinity on Pituitary Growth Hormone Content and Cell Activity in the Euryhaline Tilapia, Oreochromis mossambicus

artículo científico publicado en 1994

Erratum: Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry.

artículo científico publicado en 2018

Erythrocytic α-synuclein contained in microvesicles regulates astrocytic glutamate homeostasis: a new perspective on Parkinson's disease pathogenesis

artículo científico publicado en 2020

Escaping Parkinson's disease: a neurologically healthy octogenarian with the LRRK2 G2019S mutation

artículo científico publicado en 2005

Evaluation of mild cognitive impairment subtypes in Parkinson's disease.

artículo científico publicado en 2014

Evidence for more than one Parkinson's disease-associated variant within the HLA region

artículo científico publicado en 2011

Exploring gene-environment interactions in Parkinson’s disease

article

Exploring human-genome gut-microbiome interaction in Parkinson's disease

artículo científico publicado en 2021

Functional variants at CYP2A6: new genotyping methods, population genetics, and relevance to studies of tobacco dependence

artículo científico publicado en 2000

GBA Variants are associated with a distinct pattern of cognitive deficits in Parkinson's disease

artículo científico publicado en 2015

GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology

artículo científico publicado en 2012

Genetic association between α-synuclein and idiopathic parkinson's disease

article

Genetic polymorphism at codon 129 of the prion protein gene is not associated with multiple sclerosis

artículo científico publicado en 2009

Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients

artículo científico publicado en 2020

Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee

artículo científico publicado en 2011

Genotype-controlled analysis of plasma dopamine beta-hydroxylase activity in psychotic unipolar major depression

artículo científico publicado en 2002

Genotypic and haplotypic associations of the DBH gene with plasma dopamine beta-hydroxylase activity in African Americans

artículo científico publicado en 2007

Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders

artículo científico publicado en 2008

Glutamate receptor gene GRIN2A, coffee, and Parkinson disease

artículo científico publicado en 2014

Glycoproteomics in neurodegenerative diseases

artículo científico publicado en 2010

Hallucinations and Development of Dementia in Parkinson's Disease

artículo científico publicado en 2020

Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism

scientific article published on 26 October 2008

Haplotype-controlled analysis of the association of a non-synonymous single nucleotide polymorphism atDBH (+ 1603C → T) with plasma dopamine β-hydroxylase activity

article

Haptoglobin phenotype modifies serum iron levels and the effect of smoking on Parkinson disease risk

artículo científico publicado en 2015

Heterozygousparkinpoint mutations are as common in control subjects as in Parkinson's patients

article

Homocysteine and cognitive function in Parkinson's disease.

artículo científico publicado en 2017

Human PON1, a biomarker of risk of disease and exposure

artículo científico publicado en 2010

Human genetics of plasma dopamine beta-hydroxylase activity: applications to research in psychiatry and neurology

artículo científico publicado en 2004

Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease

article

Identification of a Japanese family with LRRK2 p.R1441G-related Parkinson's disease

artículo científico publicado en 2014

Identification of a novel Parkinson's disease locus via stratified genome-wide association study

artículo científico publicado en 2014

Identification of genetic modifiers of age-at-onset for familial Parkinson's disease

artículo científico publicado en 2016

Impact of Pre-Analytical Differences on Biomarkers in the ADNI and PPMI Studies: Implications in the Era of Classifying Disease Based on Biomarkers

artículo científico publicado en 2019

Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: first report in South America.

artículo científico publicado en 2017

LARGE-PD: Examining the genetics of Parkinson's disease in Latin America

artículo científico publicado en 2017

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.

artículo científico publicado en 2006

LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease

artículo científico publicado en 2009

LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay

artículo científico publicado en 2008

Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease

artículo científico publicado en 2007

Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

artículo científico publicado en 2006

Large-scale exploratory genetic analysis of cognitive impairment in Parkinson's disease

artículo científico

Letter to the Editor: Hypothesis: Somatic Mosaicism and Parkinson Disease

artículo científico publicado en 2015

Lower plasma apolipoprotein A1 levels are found in Parkinson's disease and associate with apolipoprotein A1 genotype

artículo científico publicado en 2014

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.

artículo científico publicado en 2008

Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain

artículo científico publicado en 2009

Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin America

artículo científico publicado en 2011

Memory, mood, and vitamin D in persons with Parkinson's disease

artículo científico publicado en 2013

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

artículo científico publicado en 2012

Molecular Genetic Analysis of Plasma Dopamine β-Hydroxylase in Depression

scholarly article by Joseph F. Cubells et al published 2002 in Advances in behavioral biology

Mosaicism of alpha-synuclein gene rearrangements: report of two unrelated cases of early-onset parkinsonism

artículo científico publicado en 2013

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

artículo científico publicado en 2009

Multivariate prediction of dementia in Parkinson's disease

scientific article published on 25 August 2020

Mutations in the dopamine beta-hydroxylase gene are associated with human norepinephrine deficiency

artículo científico publicado en 2002

Neuropathological and genetic correlates of survival and dementia onset in synucleinopathies: a retrospective analysis

artículo científico publicado en 2017

Neuropsychologic assessment in collaborative Parkinson's disease research: a proposal from the National Institute of Neurological Disorders and Stroke Morris K. Udall Centers of Excellence for Parkinson's Disease Research at the University of Pennsy

artículo científico publicado en 2012

New windows into the brain: Central nervous system-derived extracellular vesicles in blood

scientific article published on 25 January 2019

Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain.

artículo científico publicado en 2013

Novel compound heterozygous FBXO7 mutations in a family with early onset Parkinson's disease

artículo científico publicado en 2020

Pacific Northwest Udall Center of excellence clinical consortium: study design and baseline cohort characteristics

artículo científico publicado en 2013

Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics

artículo científico publicado en 2006

Parkinson's disease and Parkinson's disease medications have distinct signatures of the gut microbiome

artículo científico publicado en 2017

Participant and Study Partner Reported Impact of Cognition on Functional Activities in Parkinson's Disease

artículo científico publicado en 2019

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

artículo científico publicado en 2008

Phosphorylated α-synuclein in Parkinson's disease

artículo científico publicado en 2012

Phosphorylated α-synuclein in Parkinson's disease: correlation depends on disease severity

artículo científico publicado en 2015

Plasma apolipoprotein A1 as a biomarker for Parkinson disease

artículo científico publicado en 2013

Plasma exosomal α-synuclein is likely CNS-derived and increased in Parkinson's disease.

artículo científico publicado en 2014

Plasticity-related gene 3 () and age at diagnosis of Parkinson disease

article

Postural instability/gait disturbance in Parkinson's disease has distinct subtypes: an exploratory analysis

artículo científico publicado en 2010

Precision Medicine: Clarity for the Complexity of Dementia.

artículo científico publicado en 2015

Prediction of cognitive progression in Parkinson's disease using three cognitive screening measures

artículo científico publicado en 2019

Regulation of drug reward by cAMP response element-binding protein: evidence for two functionally distinct subregions of the ventral tegmental area.

artículo científico publicado en 2005

Relationship between Sensorimotor Inhibition and Mobility in Older Adults with and without Parkinson's Disease

artículo científico publicado en 2020

Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease.

artículo científico publicado en 2011

Response to the letter "Haptoglobin phenotype and Parkinson disease risk" by Delanghe et al.

artículo científico publicado en 2016

Revisiting protein aggregation as pathogenic in sporadic Parkinson and Alzheimer diseases

artículo científico publicado en 2019

Risk prediction for complex diseases: application to Parkinson disease.

artículo científico publicado en 2012

Salivary α-synuclein and DJ-1: potential biomarkers for Parkinson's disease.

artículo científico publicado en 2011

Screening of cognitive impairment in patients with Parkinson's disease: diagnostic validity of the Brazilian versions of the Montreal Cognitive Assessment and the Addenbrooke's Cognitive Examination-Revised

artículo científico publicado en 2015

Sensorimotor Inhibition and Mobility in Genetic Subgroups of Parkinson's Disease

scientific article published on 04 September 2020

Serotonin and dopamine transporter PET changes in the premotor phase of LRRK2 parkinsonism: cross-sectional studies

artículo científico publicado en 2017

Sex differences in progression to mild cognitive impairment and dementia in Parkinson's disease

artículo científico publicado en 2018

Sigma receptors are associated with cortical limbic areas in the primate brain

artículo científico publicado en 1992

Significance and confounders of peripheral DJ-1 and alpha-synuclein in Parkinson's disease.

artículo científico publicado en 2010

Smoking and haptoglobin phenotype modulate serum ferritin and haptoglobin levels in Parkinson disease

artículo científico publicado en 2016

Soluble TREM2 is elevated in Parkinson's disease subgroups with increased CSF tau

artículo científico publicado en 2020

Some aspects of the validity of the Montreal Cognitive Assessment (MoCA) for evaluating cognitive impairment in Brazilian patients with Parkinson's disease

artículo científico publicado en 2016

Stool immune profiles evince gastrointestinal inflammation in Parkinson's disease

artículo científico publicado en 2018

Targeted discovery and validation of plasma biomarkers of Parkinson's disease

artículo científico publicado en 2014

The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease

artículo científico publicado en 2015

The UCHL1 S18Y polymorphism and Parkinson's disease in a Japanese population

artículo científico publicado en 2011

The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot

artículo científico publicado en 2016

The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot

artículo científico publicado en 2016

The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru

scientific article published on 04 February 2019

The effect of LRRK2 mutations on the cholinergic system in manifest and premanifest stages of Parkinson's disease: a cross-sectional PET study

artículo científico publicado en 2018

The genetics of Parkinson disease

artículo científico publicado en 2010

The structure of linkage disequilibrium at the DBH locus strongly influences the magnitude of association between diallelic markers and plasma dopamine beta-hydroxylase activity

artículo científico publicado en 2003

Transcriptomic Profiling of Extracellular RNAs Present in Cerebrospinal Fluid Identifies Differentially Expressed Transcripts in Parkinson's Disease

artículo científico publicado en 2016

Validity and Utility of a LRRK2 G2019S Mutation Test for the Diagnosis of Parkinson's Disease

article

Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry.

artículo científico publicado en 2017

Variations in the dopamine ?-hydroxylase gene are not associated with the autonomic disorders, pure autonomic failure, or multiple system atrophy

article

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

artículo científico publicado en 2010

Visuospatial functioning is associated with sleep disturbance and hallucinations in nondemented patients with Parkinson's disease

scientific article published on 10 June 2019

White Matter Lesions in Mild Cognitive Impairment and Idiopathic Parkinson's Disease: Multimodal Advanced MRI and Cognitive Associations

scientific article published on 16 September 2020

[3H]-(+)-pentazocine binding to sigma recognition sites in human cerebellum

artículo científico publicado en 1994

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