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Neurogenetics|April 10, 2017
Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3Megha N Murthy, Cornelis Blauwendraat, , et al.
BMC Neurology|December 26, 2006
A common genetic factor for Parkinson disease in ethnic Chinese population in TaiwanHon-Chung Fung, Chiung-Mei Chen, John Hardy, et al.
European Heart Journal|May 14, 2009
Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older peopleAnna Murray, Christie Cluett, Stefania Bandinelli, et al.
F1000Research|May 31, 2016
Intracerebral haemorrhage in Down syndrome: protected or predisposed?Lewis Buss, Elizabeth Fisher, John Hardy, et al.
Glia|December 26, 2022
Human myeloid progenitor glucocorticoid receptor activation causes genomic instability, type 1 IFN- response pathway activation and senescence in differentiated microglia; an early life stress modelJingzhang Wei, Charles Arber, Selina Wray, et al.
Alzheimer Disease and Associated Disorders|February 24, 2006
Tangle diseases and the tau haplotypesJohn Hardy, Alan Pittman, Amanda Myers, et al.
Neurobiology of Aging|October 26, 2005
Characterization of two APP gene promoter polymorphisms that appear to influence risk of late-onset Alzheimer's diseaseDebomoy K Lahiri, Yuan-Wen Ge, Bryan Maloney, et al.
Neurobiology of Disease|March 1, 2006
A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementiaRoneil Malkani, Ian D'Souza, Katrina Gwinn-Hardy, et al.
JAMA Neurology|May 28, 2014
Insights from cerebellar transcriptomic analysis into the pathogenesis of ataxiaConceição Bettencourt, Mina Ryten, Paola Forabosco, et al.
JMIR Research Protocols|April 7, 2025
Racial Disparities in Parkinson Disease Clinical Phenotype, Management, and Genetics: Protocol for a Prospective Observational StudyDeborah A Hall, Josh M Shulman, Andrew Singleton, et al.
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