SNCA 3′UTR genetic variants in patients with Parkinson’s disease and REM sleep behavior disorder

Analysis of protein-coding genetic variation in 60,706 humans

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A global reference for human genetic variation

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Rapid Eye Movement Sleep Behavior Disorder and Neurodegenerative Disease

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Clinical features associated with sleep disturbances in Parkinson’s disease

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REM Sleep Behavior Disorder in Parkinson's Disease: A Questionnaire-Based Survey

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Variants in the 3′UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression

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MicroRNAs in Parkinson's disease

(2012) M. Maral Mouradian   NEUROBIOLOGY OF DISEASE

A Search for SNCA 3′ UTR Variants Identified SNP rs356165 as a Determinant of Disease Risk and Onset Age in Parkinson’s Disease

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Utility of the REM sleep behavior disorder screening questionnaire (RBDSQ) in Parkinson’s disease patients

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The effect of SNCA 3′ region on the levels of SNCA-112 splicing variant

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Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

(2009) Wataru Satake et al.   NATURE GENETICS

Genome-wide association study reveals genetic risk underlying Parkinson's disease

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Multiplealpha-synucleingene polymorphisms are associated with Parkinson’s disease in a Norwegian population

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Quantifying the risk of neurodegenerative disease in idiopathic REM sleep behavior disorder

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Genetic variability in the SNCA gene influences α-synuclein levels in the blood and brain

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