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Neurology. Genetics|October 20, 2018
Plasticity-related gene 3 (<i>LPPR1</i>) and age at diagnosis of Parkinson diseaseZachary D Wallen, Honglei Chen, Erin M Hill-Burns, et al.
Frontiers in Neurology|February 15, 2021
Resting-State Cerebello-Cortical Dysfunction in Parkinson's DiseaseWilliam C Palmer, Brenna A Cholerton, Cyrus P Zabetian, et al.
Genetic Epidemiology|July 8, 2009
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 diseaseHaydeh Payami, Denise M Kay, Cyrus P Zabetian, et al.
Brain Connectivity|May 28, 2019
Effect of Dopaminergic Medications on Blood Oxygen Level-Dependent Variability and Functional Connectivity in Parkinson's Disease and Healthy AgingTrevor K M Day, Tara M Madhyastha, Adél Lee, et al.
Parkinsonism & Related Disorders|June 20, 2020
Arterial spin labeling detects perfusion patterns related to motor symptoms in Parkinson's diseaseSwati Rane, Natalie Koh, John Oakley, et al.
BMC Genomics|February 12, 2014
Identification of a novel Parkinson's disease locus via stratified genome-wide association studyErin M Hill-Burns, William T Wissemann, Taye H Hamza, et al.
Biological Psychiatry|April 18, 2006
A single nucleotide polymorphism at DBH, possibly associated with attention-deficit/hyperactivity disorder, associates with lower plasma dopamine beta-hydroxylase activity and is in linkage disequilibrium with two putative functional single nucleotide polymorphismsYilang Tang, Sarah G Buxbaum, Irwin Waldman, et al.
NPJ Parkinson'S Disease|August 19, 2021
Exploring human-genome gut-microbiome interaction in Parkinson's diseaseZachary D Wallen, William J Stone, Stewart A Factor, et al.
American Journal of Human Genetics|May 6, 2003
The structure of linkage disequilibrium at the DBH locus strongly influences the magnitude of association between diallelic markers and plasma dopamine beta-hydroxylase activityCyrus P Zabetian, Sarah G Buxbaum, Robert C Elston, et al.
American Journal of Medical Genetics|February 22, 2002
Mutations in the dopamine beta-hydroxylase gene are associated with human norepinephrine deficiencyChun-Hyung Kim, Cyrus P Zabetian, Joseph F Cubells, et al.
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