Eric Yu
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Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's diseaseNeurobiol Aging. 2021 04; 100:119. e7-119. e13. . View in PubMed
Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson's diseaseNeurobiol Aging. 2020 09; 93:143. e1-143. e4. . View in PubMed
LRRK2 pM1646T is associated with glucocerebrosidase activity and with Parkinson's disease. Neurobiol Aging. 2021 07; 103:142. e1-142. e5. . View in PubMed
HLA in isolated REM sleep behavior disorder and Lewy body dementia medRxiv. 2023 Apr 03. . View in PubMed
Neuroanatomical correlates of genetic risk for obesity in children Transl Psychiatry. 2023 01 03; 13(1):1. . View in PubMed
GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson's disease Brain. 2022 Nov 11. . View in PubMed
Gene-based burden analysis of damaging private variants in PRKN, PARK7 and PINK1 in Parkinson's disease cohorts of European descent Neurobiol Aging. 2022 11; 119:136-138. . View in PubMed
Genetic, structural and clinical analysis of spastic paraplegia 4 Parkinsonism Relat Disord. 2022 05; 98:62-69. . View in PubMed
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects Nat Commun. 2022 12 05; 13(1):7496. . View in PubMed
Axial Impairment Following Deep Brain Stimulation in Parkinson's Disease: A Surgicogenomic Approach J Parkinsons Dis. 2022; 12(1):117-128. . View in PubMed
Rare PSAP Variants and Possible Interaction with GBA in REM Sleep Behavior Disorder J Parkinsons Dis. 2022; 12(1):333-340. . View in PubMed
Alzheimer's Disease Polygenic Risk Score Is Not Associated With Cognitive Decline Among Older Adults With Type 2 Diabetes Front Aging Neurosci. 2022; 14:853695. . View in PubMed
Fine mapping of the HLA locus in Parkinson's disease in Europeans NPJ Parkinsons Dis. 2021 Sep 21; 7(1):84. . View in PubMed
Lack of Causal Effects or Genetic Correlation between Restless Legs Syndrome and Parkinson's Disease Mov Disord. 2021 08; 36(8):1967-1972. . View in PubMed
Common X-Chromosome Variants Are Associated with Parkinson Disease Risk Ann Neurol. 2021 07; 90(1):22-34. . View in PubMed
Evidence for Non-Mendelian Inheritance in Spastic Paraplegia 7 Mov Disord. 2021 07; 36(7):1664-1675. . View in PubMed
Association of the CD2AP locus with cognitive functioning among middle-aged individuals with a family history of Alzheimer's disease Neurobiol Aging. 2021 05; 101:50-56. . View in PubMed
Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson's Disease Mov Disord. 2021 01; 36(1):178-187. . View in PubMed
Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder Mov Disord. 2021 01; 36(1):235-240. . View in PubMed
Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease Front Neurol. 2021; 12:656342. . View in PubMed
Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations Brain. 2021 03 03; 144(2):462-472. . View in PubMed
Novel Associations of BST1 and LAMP3 With REM Sleep Behavior Disorder Neurology. 2021 03 09; 96(10):e1402-e1412. . View in PubMed
No Evidence for a Causal Relationship Between Cancers and Parkinson's Disease J Parkinsons Dis. 2021; 11(2):801-809. . View in PubMed
Contrast echocardiography: putting things into perspective - a Canadian Cardiovascular Society/Canadian Society of Echocardiography joint commentary Can J Cardiol. 2008 Nov; 24(11):835-7. . View in PubMed
